Causes & Risk Factors
Nutrition therapy for depression 
Suggested Supplementation


Depression is a state of psyche characterized by a spectrum of negative feelings ranging from minor unhappiness to overwhelming despair. Though generally associated with emotional or psychological symptoms, depression can be accompanied by severe pain or other physical symptoms as well.

Recent data estimate the overall prevalence of depression at about 11.1% of the American population, or nearly 35 million individuals (CDC 2010), and predictive models suggest that up to 50% of the population will experience at least one episode of depression during their lives (Andrews 2005).

The framework underlying the pathogenesis of depression is complex and variable among individuals; both psychological and biological factors influence a person’s state of mind at any given time. Emergent research links depression with several metabolic phenomena, including inflammationinsulin resistance, and oxidative stress. Intriguing preliminary data also suggest that mitochondrial dysfunction plays a role in depression. Moreover, the role of hormones in depression is considerable, including stress hormones (glucocorticoids) and sex hormones (testosterone, estrogen). Many people affected by depression may be suffering from hormonal imbalances that are significantly contributing to their symptoms (Howland 2010).

Mainstream medicine relies heavily upon psychoactive drugs that manipulate brain chemistry as the frontline treatment (ICSI 2011). Unfortunately, the success rate of pharmacologic intervention for depression is a mere 50% or less and these medications are fraught with potential side effects, including a proclivity to increase suicidal ideation with some anti-depressant drugs (Prescrire Int. 2011).

We need to acknowledge the complex nature of depression and advocate a comprehensive management strategy that includes proactive lifestyle changes, behavioral therapy, hormone restoration, and targeted nutritional support to complement conventional antidepressant treatment and balance brain chemistry holistically.

Types of Depression and Associated Symptoms

Although depression is a clearly defined disorder with mental and physical symptoms, unlike other disorders, doctors cannot diagnose it using blood test. Instead, they use carefully developed clinical guidelines as defined in the Diagnostic and Statistical Manual of Mental Disorders (DSM).

Depression is distinguished into various forms. The most common are major depressive disorder and dysthymic disorder.

Major depressive disorder (major depression): Major depressive disorder can be very disabling, preventing the patient from functioning normally. A combination of symptoms sabotages the patient’s ability to sleep, study, work, eat, and enjoy pleasurable activities. Some people may experience only a single episode, while others experience recurrent episodes.

Dysthymic disorder (dysthymia): Dysthymia, also known as chronic mild depression, lasts longer than two years. Symptoms are not disabling or as severe as those of major depression, however the patient finds it difficult to function normally and does not feel well. A person with dysthymia may also experience periods of major depression.

Psychotic depression: Psychotic depression is a severe depressive illness that includes hallucinations, delusions, or withdrawal from reality.

Postpartum depression (postnatal depression): Postpartum depression, also known as postnatal depression (PND), affects 10% to 15% of all women after giving birth. This is not to be confused with the “baby blues,” which a mother may feel briefly after giving birth. The development of a major depressive episode within a few weeks of giving birth likely indicates PND. Sadly, many of these women go undiagnosed and suffer for long periods without treatment and support.

Seasonal affective disorder (SAD): The incidence of SAD increases along with the distance from the equator. A person who develops a depressive illness during the winter months with symptoms that go away during spring or summer may have SAD. Accumulating evidence points to vitamin D deficiency as a contributing factor in SAD and in other forms of depression (Parker 2011).

Bipolar disorder (manic-depressive illness): A patient with bipolar disorder experiences (extreme) highs (mania) and lows (depression) in mood.


Diagnosing Depression

A diagnosis of clinical depression requires that the patient experience at least five of the nine symptoms below, as described by the DSM, for most of the day, nearly every day, for at least two weeks. One of the symptoms must be either a constant feeling of sadness, anxiety, and emptiness, or loss of interest in formerly pleasurable activities.

If any of these symptoms affects your relationships and your ability to function at home or work, consult with a health care practitioner qualified to assess and treat depression.

Emotional Symptoms

  • Constant or transient feelings of sadness, anxiety, and emptiness
  • Feeling restless; may experience irritability
  • Feeling hopeless
  • Feeling worthless or guilty for no reason; suicidal thoughts may occur
  • Loss of interest in activities or hobbies once enjoyed; may lose interest in sex

Physical Symptoms

  • Disturbed sleep patterns; may sleep too little or too much
  • Low energy; fatigue
  • Significant weight loss or gain due to a change in eating habits; either loss of appetite or eating too much
  • Difficulty concentrating, remembering details, or making decisions




Research spanning the last 20 to 30 years has examined a range of influences that contribute to depression. These include genetics, brain chemistry, early life trauma, negative thinking, one’s personality and temperament, stress, and difficulty relating to others (Liu 2010). Moreover, emerging scientific research suggests that metabolic phenomenon such as inflammation, oxidative stress, and hormonal imbalances can cause or exacerbate depression as well (Maes 2011; Wolkowitz 2011).

Impaired Stress Response

When a person experiences stress—whether it’s physical or emotional, internal or external—the body copes through a complex system of adaptive reactions. This response involves the release of glucocorticoids, or stress hormones, which stimulate adaptive changes throughout the body.

A stress response is designed to help us confront or escape danger by redirecting blood flow to the muscles, dilating the pupils, inhibiting digestion, and releasing stored fatty acids and glucose (blood sugar) to be used by the muscles. This process is known as the fight-or-flight response.

The fight-or-flight response originates in the brain. When the hypothalamus, the brain’s “control tower,” perceives a threat, it sends chemical signals to the brain’s pituitary gland, also known as the master hormone gland. The pituitary gland then sends chemical signals to the adrenal glands, which sit atop the kidneys. The adrenal glands then release the stress hormone cortisol, which triggers many of the physiological responses to danger.

Modern humans cope with relentless stress. Such things as financial worries, deadline pressures at work or school, emotional challenges, excessive caloric intake, poor diet, obesity, inactivity, and environmental toxins chronically activate the hypothalamic-pituitary-adrenal axis, keeping us in a perpetual fight-or-flight response. The result is an increased rate of cardiovascular disease, diabetes, and mood disorders such as depression and anxiety.

The relationship between chronic stress, depression, and anxiety is complex, but incredibly powerful. For instance, the chronic elevation of glucocorticoids (primarily cortisol) caused by chronic stress actually changes the physical structure of the brain.

New findings strongly support the importance of controlling the stress response in order to alleviate mood disorders. Indeed, several genetic and epidemiological studies have linked excessive stress, and the inability to adapt efficiently to stress, with increased rates of anxiety and depression (Ströhle 2003; Binder 2010; Bennett 2008).

Fortunately, a number of relaxation techniques and coping styles can improve depression, further emphasizing the role of stress in depression. These approaches include Mindfulness-Based Stress Reduction (McCown 2010), meditation (Newberg 2010), biofeedback (Katsamanis 2007), progressive muscle relaxation (Dusek 2008) and an integrative health approach that combines relaxation, nutrition, and exercise (Dusek 2009).

Traumatic events and Post-Traumatic Stress Disorder

Research establishes that trauma, such as the sudden loss of a family member, sexual abuse, or war-related traumas, contributes significantly to prolonged periods of depression. The effects are more pronounced when the trauma occurs in childhood; childhood trauma can considerably alter the structure and function of the brain, increasing susceptibility to depression and anxiety later in life (Nemeroff 2003).

Social network and personal relationships

Lack of meaningful social contact with others has been linked to depression, while evidence increasingly shows that close personal relationships and social networks positively affect mood and health (Grav 2011). Loving relationships, social connection and support, work-related passion and recognition, and a good marriage help prevent depression (Kiecolt-Glaser 2010; Coughlin 2010).

Neurotransmitter imbalances

Magnetic resonance imaging (MRI) shows that the areas of the brain that orchestrate thinking, sleep, mood, appetite, and behavior function abnormally in depressed patients compared to non-depressed individuals. In addition, an imaging technique called single-photon emission computed tomography (SPECT) shows changes in brain blood flow and neurotransmitter activity in the depressed person’s brain (Yang 2008 Joensuu 2007). Although imaging technology can identify neurotransmitter imbalances, it cannot reveal why depression has occurred.

Comorbid Conditions

Research shows a person with both depression and a serious illness is more likely to experience severe symptoms and find it harder to adapt to the medical condition. Studies also show that treating depression in this population may improve symptoms of the co-occurring illness in some instances.

Additionally, people dependent on alcohol or narcotics are significantly more likely to be depressed (Shibasaki 2011).


Biological Factors

  • Hormonal imbalances
  • Nutritional deficiencies
  • Oxidative stress and mitochondrial dysfunction
  • Insulin resistance and chronic inflammation

Hormonal influences

Balanced and youthful concentrations of hormones can help control depression, and astute clinicians often find hormonal imbalances in patients with depression. Because a wide range of hormones can influence depression, it is important to discern which hormone(s) may be an underlying factor when considering depression.

For example, thyroid function directly affects metabolism and brain function, and low thyroid activity can contribute to depression. Conventional medicine relies on overly broad thyroid lab ranges, failing to recognize many cases of sub-optimal thyroid function.

Because the brain requires sufficient thyroid hormones to function optimally, a low thyroid hormone status can contribute to overall loss of function and degeneration in the brain, including the areas of the brain that govern mood (Davis 2007). Hashimoto’s thyroiditis, an autoimmune thyroid disease, can cause a person’s metabolism to swing between overly active to overly depressed. These swings can mimic the symptoms of bipolar disorder and cause misdiagnosis and inappropriate treatment (Chang 1998; Kupka 2002; Cole 2002; Frye 1999).

Sex hormones also influence mood and depression. Women are more susceptible to anxiety than men and also experience more depression when they are pregnant, postpartum, premenstrual and menopausal than at other times in life.

It is well known that most steroid hormones (e.g., pregnenolone, estrogen, progesterone, testosterone, and DHEA) are neurologically active. In fact, the brain contains large numbers of receptors for DHEA, estrogen, and progesterone. These hormones affect many functions in the brain, including the regulation of mood.

Accordingly, a number of studies link hormonal imbalances to various depressive disorders (Cunningham 2009; Parcells 2010; Bloch 2011; Sundermann 2010). In the follicular phase of menses, when estrogen levels are high, women produce more serotonin and experience an improved mood. When estrogen decreases during the premenstrual period, serotonin levels drop, contributing to the negative mood and personality shifts associated with PMS (Kikuchi 2010).

Likewise, the drop in estrogen during menopause is associated with reduced serotonin production and a negative impact on mood and cognition. This is evidenced by the fact that SSRIs have been shown to improve mood and cognitive function in menopausal women (Cubeddu 2010).

In addition, testosterone deficiency has been linked with depression in men, which is not surprising since testosterone plays an important role in brain function, including mood regulation (Zitzmann 2006; Delhez 2003). In studies, select populations of men were more likely to be depressed if their total and/or free testosterone levels are low; these included those with heart disease, HIV/AIDS, and the elderly (Jankowska 2010; Zarrouf 2009).

Medical research acknowledges the link between hormonal imbalances and depression; however, conventional doctors rarely evaluate and address hormone status when treating depression.


Nutritional deficiency or insufficiency

Nutrition plays an essential role in brain function, and poor nutrition significantly increases one’s risk for depression. Dietary nutrients influence nervous system function in multiple ways. Important dietary nutrients include:

  • B-complex vitamins: B-complex vitamins serve as cofactors for the production of neurotransmitters. Inadequate levels of B-vitamins, especially folate, vitamin B12, niacin, and vitamin B6, can disrupt neurotransmitter synthesis. This not only may lead to mood alterations, but also can impact overall brain function, memory, and cognition.
  • Optimal balance of omega-3 and omega-6 fatty acids: Fatty acids are critical components of nerve cell membranes and play an important role in neuronal communication. Fatty acid imbalances can impair the transmission of messages between nerve cells, leading to cognitive deficits and mood alterations, including depression (Yehuda 2005).
  • Vitamin D activity: A vitamin-D insufficiency, which is very common (Faloon 2010), is linked with seasonal depression. Recent evidence suggests that it also may contribute to general depression through its considerable influence on genetic activity, its ability to control inflammation, and other mechanisms.

It is important to remember that optimal brain function necessitates all of these nutritional aspects be addressed simultaneously.


Oxidative Stress and Mitochondrial Dysfunction

Brain tissue is particularly susceptible to oxidative damage due to its high concentrations of phospholipids and the exhaustive metabolic rate among neurons. A growing body of research suggests that oxidative stress contributes to depression and other brain-related disorders (Hovatta 2010). This is thought to result from either an increase in damaging reactive oxygen species, a decrease in antioxidant defense mechanisms, or a combination of the two. These mechanisms become especially important with advancing age (Wolkowitz 2011).

Newer research sheds light on the critical role of mitochondria and neurotransmission and mood regulation. Mitochondria are the “powerhouses” in each cell that generate energy. In an intriguing study, researchers measured the content of mitochondrial DNA within white blood cells in aging patients who were depressed, and in an age-matched group who were not depressed. The subjects with depression had significantly fewer mitochondria than non-depressed controls, leading researchers to suggest, “mitochondrial dysfunction could be a mechanism of geriatric depression” (Kim 2011). In a similar study, greater numbers of mitochondria in peripheral cells were associated with improved cognitive function in healthy elderly women (Lee 2010).

Preliminary research suggests that two nutrients, coenzyme Q10 and acetyl-L-carnitine, which support mitochondrial function, may influence depression. A small study of 35 depressed patients in comparison to 22 healthy volunteer controls showed that plasma CoQ10 levels were significantly lower in the depressed patients. Levels were also lower in treatment-resistant patients, as well as those with chronic fatigue (Maes, 2009).

Several studies of geriatric depression have investigated acetyl-L-carnitine (Pettigrew 2000). One study compared treatment with acetyl-L-carnitine to the medication amisulpride, an antipsychotic medication commonly used to treat depression. In 204 patients with chronic depression, both acetyl-L-carnitine and the pharmaceutical drug improved symptoms (Zanardi, 2006). Acetyl-L-carnitine also has been found to relieve depression and improve quality of life in patients with liver disease (Malaguarnera 2011), and to ease depressive symptoms significantly in patients with fibromyalgia (Rossini 2007).

Another nutrient, pyrroloquinoline quinine (PQQ), is an enzyme involved in the generation of new mitochondria and the maintenance of antioxidant defense systems (Chowanadisai 2010; Rucker 2009; Tachaparian 2010). Supplemental PQQ has been shown to increase mitochondrial activity levels and to be neuroprotective in animal models (Bauerly 2011; zhang 2006; Zhang 2009). Since fewer mitochondria have been observed in depressed patients (Kim 2011), PQQ may be supportive in this population.


Insulin Resistance

Recent data suggest a direct link between insulin resistance and depression. In a small clinical study, treatment of depressed patients with the insulin-sensitizing drug pioglitazone alleviated depression while simultaneously improving their cardio-metabolic risk profiles (Kemp 2011). Evidence suggests that another popular glucose control agent, metformin, may influence psychiatric health as well (Ohaeri 2011). Individuals who are overweight, have suboptimal glucose control, or have diabetes with concurrent depression may find that losing weight and gaining control over their glucose levels eases their depressive symptoms.

Scientific literature indicates that for optimal health, fasting glucose levels should fall between 70 and 85mg/dL,.


Chronic Inflammation

Several studies support the role of inflammation and immune system deregulation in depression. Studies have found elevated levels of inflammatory cytokines (signaling molecules with which immune cells communicate) in patients suffering from major depression (Tsao et al 2006), late-life depression (Craddock et al, 2006), and in patients who do not respond to SSRIs (O’Brien 2007).

Studies show an association between the systemic inflammation marker C-reactive protein (C-RP) and major depression (Cizza 2009). Moreover, elevated CRP levels are associated with a number of other significant health problems such as cardiovascular disease. Women should target a CRP blood level of less than 1.0 mg/L and men should target a level of less than 0.55 mg/L.


Medications Used to Treat Depression

Several classes of medications may be employed to treat depression; depending on the patients symptoms and history medications from the following classes are typically utilized.

Most antidepressant medications work by altering signaling within the brain. They do so by manipulating the level of neurotransmitters in the synaptic junction, the finite space between two neurons in which signaling molecules are released and reabsorbed to facilitate neuronal communication.

While antidepressants may temporarily improve mood, they do so in a way that is somewhat artificial and unlikely to be effective for an extended time. There is disturbing evidence that some antidepressants may cause the brain to adapt to their presence, requiring increasing dosage and leading to withdrawal symptoms upon cessation.

Moreover, a condition known as antidepressant discontinuation syndrome may arise in as many as 20% of patients upon abrupt discontinuation of an antidepressant medication. This phenomenon is likely the result of the brain having adapted to the medication, and now being deprived of it, malfunctions for a time until it can readapt to the lack of the drug. Symptoms of antidepressant discontinuation syndrome include flu-like symptoms, insomnia, nausea, hyperactivity, and sensory disturbances, among others (Warner 2006).

Antidepressants (depending on type) may be associated with a number of side effects: decreased libido, digestive symptoms, headaches, insomnia, dry mouth, etc.


Other Therapies

Cognitive Behavioral Therapy

Cognitive behavioral therapy (CBT) is a non-pharmacologic means of therapy often employed to relieve depression. CBT is typically initiated if primary treatment with antidepressant medications fail, but it is sometimes used as part of first-line treatment alongside antidepressants.

CBT is centered upon the belief that depression is closely linked with negative thinking (i.e. thought patterns that negatively reinforce depressed mood). The goal of CBT is to help the patient recognize and replace negative thinking with more positive, constructive thoughts. CBT has been studied in various settings and has shown efficacy both independently and in combination with other conventional treatment regimens.

Physical activity

Research supports the use of exercise, primarily aerobic or weight training, as a preventive and adjuvant treatment (used in conjunction with medication) of mood disorders and depression. Some studies have found exercise alone is as effective as medication for relieving depression (Freeman, 2010) and that exercise can reduce depression recurrence rates (Babyak et al 2000). A recent study looked at 202 adults with major depression,  and the one-year follow up showed that exercise was as effective as the medication at relieving depression and that exercise during the follow-up period extended the benefits (Hoffman et al 2011).

Light Therapy

Research shows morning light therapy from a light-therapy lamp is effective at treating seasonal affective disorder (seasonal depression), and that it is equally or possibly even more effective than antidepressants, in this type of depression (Freeman, 2010). A study of 98 patients with seasonal depression illustrated this. Depressed subjects were randomly assigned to 8 weeks of therapy with light in the morning (30 minutes, 10,000 lux, and a placebo pill) or 30 minutes of dim light (100 lux and 20 mg of fluoxitine), with both groups experiencing a 67 % response rate (Lam et al 2006).

Transcranial Magnetic Stimulation

A new procedure called transcranial magnetic stimulation (TMS), which uses magnetic fields to stimulate nerve cells in the brain, is widely researched and showing promising results as a treatment for depression.  A recent study of 190 patients with major depression treated with TMS showed a clinically significant improvement in symptoms (George 2010). In a recent review, TMS was concluded to be as effective as cognitive behavioral therapy or pharmacotherapy for relieving depression (Schutter 2011).


Dietary Considerations for Depression

Dietary factors should always be addressed when managing depression, as evidence demonstrates that various aspects of diet can affect the disorder.

Individuals with depression may consume too many inflammatory omega-6 fatty acids and saturated fats, so increasing consumption of omega-3's and decreasing consumption of trans-fats, saturated fat, and excess omega-6 fatty acids is recommended (McNamara 2008).

Omega-3 fatty acids (Lin, 2007) and folate (Tolmunen 2004) both appear to be very important in mood management. Although the role of these nutrients in the diet is important, one should augment the diet with supplements as described below for maximum benefit in addressing symptoms of depression or in trying to prevent a recurrence. Foods high in omega-3's include deep-water fish such as salmon, mackerel, sardines, and tuna, as well as flax seeds, and some nuts (e.g., walnuts).

Evidence suggests that limiting sugar intake to control blood sugar levels is another important approach to depression. This would include addressing hyperglycemia (high blood sugar), hypoglycemia (low blood sugar), or reactive hypoglycemia (low blood sugar that occurs within 4 hours of eating). To address high or low blood sugar, it is important to limit or avoid sugar and refined carbohydrates, eat small meals 4–6 times per day, eat a balance of healthy proteins, fats, and complex carbohydrates, and decrease caffeine. The nutrients magnesium and chromium also help manage hypoglycemia.

Evidence also suggests that an anti-inflammatory Mediterranean Diet may help prevent or manage depression (Sanchez-Villegas 2006). A Mediterranean diet, which is rich in omega-3 fatty acids and polyphenolic antioxidants, could serve as a foundation to which targeted dietary supplements are added for maximum response. The diet generally includes good quantities of fish, vegetables, unrefined grains, beans or legumes, fruit, and olive oil. It includes moderate amounts of dairy (mostly cheese and yogurt) and red wine, and limits meats to small portions.




Hormone Restoration

Hormones may play an important role in depression management. Doctors should investigate hormonal imbalance when treating patients with depression.


Thyroid dysfunction may be a significantly underappreciated cause of depressive symptoms. In one study, thyroid disorders were associated with a 22% higher likelihood of depression in women (Fuller-Thomson 2011).

Studies have shown that treating subjects within so-called “normal” thyroid hormone levels may still be beneficial. In one such pilot study involving 17 female patients with depression, 11 (64.7%) saw significant improvement in response to a moderate dose of l-thyroxine (Lojko 2007). Similarly, in a study of 225 subjects with treatment resistant depression, augmenting primary antidepressant therapy with thyroid hormone was found to be roughly as effective as adding a second antidepressant medication for providing relief of symptoms (Fang 2011).

Maintain a TSH (thyroid stimulating hormone) of 1 – 2 µIU/mL (typical lab normal range 0.45- 4.5 µIU/mL) to avoid the consequences of subclinical thyroid dysfunction, which may include depression.


Studies indicate that some depressed men have low levels of testosterone (Barrett-Connor 1999; Schweiger 1999). In addition, several clinical trials have shown that testosterone replacement therapy, usually transdermal testosterone gel, can relieve depression in men with low testosterone, metabolic syndrome, and HIV/AIDS (Giltay 2010; Shores 2009; Zarrouf 2009; Pope 2003).


Estrogen is critically important for brain function and linked to depression, especially in peri-menopausal or postmenopausal women (Grigoriadis 2002). Women using estrogen replacement therapy to alleviate menopause symptoms appear to experience reduced depression (Miller 2002). In some older women being treated for depression, estrogen replacement therapy may actually improve the effects of conventional antidepressants (Schneider 2001).

Estrogen is thought to prevent depression through its association with serotonin regulation in the brain (Osterlund 2010; Joffe 1998; Rubinow 1998).


Melatonin is a hormone produced in the pineal gland in the brain; it is involved in sleep-wake function and other circadian rhythms. Melatonin decreases with age and some studies link low levels of melatonin with symptoms of depression.

A double-blind placebo-controlled pilot study of peri-menopausal and post-menopausal women who took 3 mg of melatonin at bedtime for 6 months showed significant improvement in depressive symptoms (Bellipanni 2001). Recently, another well-controlled preliminary study looked at 33 participants with major depression and early morning waking who took 6 mg of melatonin for 4 weeks. The results suggested improvement in sleep and depressive symptoms (Serafty 2010).


Nutrients to Balance Brain Chemistry

Depression is a multifactorial condition, and efficient relief requires addressing multiple neurochemical and metabolic imbalances that may underlie mood disturbances. The nutrients listed in the protocol are categorized according to their evidence-based mechanisms of action in brain health and mood regulation. The categories are:

  1. Broad-range nervous system function (omega-3 fatty acids, magnesium);
  2. Neurotransmitter synthesis (SAMe, folate, B12 , B6, tryptophan);
  3. Blood-sugar regulation (chromium, green coffee extract);
  4. Antioxidant effects (lipoic acid, NAC, selenium); and
  5. Others (St. John's Wort, vitamin D, zinc, inositol, iron).


1. Broad-Range Nervous System Effects:

Omega-3 fatty acids

Omega-3 fatty acids are long-chain polyunsaturated fatty acids found in fish and various oils, such as flaxseed or canola oil (Logan 2003). The brain has a high concentration of polyunsaturated fatty acids, which are found mostly in cell membranes. They affect adaptability of the nervous system, nerve cell conduction and function, and neurotransmitter synthesis (Yehuda 2005; Bourre 1991). Several research models exhibit the influence of omega-3 fatty acids in depression including: (a) dietary studies (Tanskanen 2001); (b) nutritional status studies showing positive effects associated with higher omega-3 to omega-6 fatty acid ratios (Tiemeier 2003); and (c) intervention studies that look at both eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) taken as a stand-alone treatment and as an adjunct to medication (Lin 2007).

One investigation showed that adding the omega-3 fatty acid EPA to conventional antidepressant treatment relieved depressive symptoms (Puri 2001).

Omega-3 fatty acids are counterbalanced with the inflammatory omega-6 fatty acids. Typically, people consume far too many omega-6's and not nearly enough omega-3's.



Magnesium is a cofactor for more than 300 enzymes in the body; it is important for blood-sugar regulation, and has a calming effect on the nervous system (Nadler 1995). Some evidence shows a link between magnesium deficiency and depression (Whittle 2011), and a recent, comprehensive review in the Journal of Medical Hypotheses suggests that magnesium supplementation is a viable approach for depressive symptoms (Eby 2010).

A major hurdle for supplemental magnesium historically has been delivery into the brain. This is a barrier that has limited the ability of typical magnesium supplements to target conditions that arise from within the central nervous system such as depression and anxiety. However, in a recent scientific breakthrough, researchers collaborating from Beijing, Ontario, the University of Texas, and the Massachusetts Institute of Technology have developed a highly advanced form of supplemental magnesium called magnesium-L-threonate.

Magnesium-L-threonate was shown in multiple animal models to not only effectively penetrate deep into the brain, but also to trigger enhancements in learning and memory by optimizing neuronal communication and reinforcing brain structure in key areas of the cortex, the most advanced aspect of the human brain (Slutsky 2010; Abumaria 2011). Since magnesium-L-threonate is readily able to diffuse across the blood brain barrier, while other forms of magnesium are not, it appears to be the ideal form of supplemental magnesium for those with depression of other mood disorders.


2.   Supporting Neurotransmitter Synthesis:


L-tryptohan is essential for the brain to synthesize serotonin, and several studies have shown that acute tryptophan depletion can cause depression in humans. In fact, some foreign countries license L-tryptophan as an antidepressant (Murphy 2006).

In one study, healthy women given L-tryptophan for 14 days experienced increased recognition of happy faces and words, and decreased recognition of negative words. The research team concluded L-tryptophan had improved the study participants' supply of serotonin in a manner similar to that of SSRIs (Murphy 2006). In another study of the effects of acute tryptophan depletion on healthy women and on patients with bulimia nervosa, both groups were given amino acid mixtures to decrease their plasma L-tryptophan levels. Both groups experienced an increase in depression.


Methylation (a biochemical building block process for producing neurotransmitters):

Methylation is a process in which a molecule passes a methyl group to another molecule. Methylation is essential to multiple functions in the body, including the production of neurotransmitters. One can supply raw materials to support methylation reactions by supplementing with S-adenosyl-methionine (SAMe) or by providing metabolic cofactors such as folate, vitamin B12, and vitamin B6. These nutrients are necessary for neurotransmitter production and have other regulating effects.


S-Adenosylmethionine (SAMe)

SAMe, which can be found in almost every tissue in the body, assists with production of creatine, glutathione, taurine, L-carnitine, and melatonin.

Research shows SAMe can benefit depressed patients who do not respond to SSRIs. In a well-controlled, 6-week, double-blind trial, 73 subjects with treatment resistant depression were treated with an SSRI plus placebo, or an SSRI plus 1,600 mg SAMe daily. The group receiving the SAMe experienced significantly better response rates and remission compared to the placebo control group (Papakostas 2010). Intriguingly, the group that received SAMe also displayed improved memory function over those receiving placebo. A smaller 6-week study revealed a response rate of 50% and a remission rate of 43% in subjects taking 800–1,600 mg a day of SAMe as an adjunct to their antidepressants (Alpert 2004).



Research shows that low blood levels of folate are associated with depression (Alpert 2000), and may also be predictive of poor response to antidepressant medication (Fava 1997). Clinical trials have also demonstrated that folic acid both relieves depression on its own and enhances the effect of antidepressants. Because relapse is associated with low serum folate, it is important to maintain folate supplementation for a year following a depressive episode (Morris 2003).

The form of supplemental folate is important since a considerable portion of people may have a genetic polymorphism that impairs folate metabolism (Willems 2004). In fact, mutations in the gene (MTHFR) that converts folic acid into the active 5-methyltetrahydrofolate (5-MTHF) are associated with depression (Lewis 2006). Therefore, taking supplemental 5-MTHFdirectly, which can cross the blood-brain barrier, may be more effective in supporting healthy neurotransmission and decreasing potentially neurotoxic homocysteine levels.


Vitamin B12

Vitamin B12 should always be measured in the event of depression (or any other psychological problems) as a vitamin B12 deficiency can be a reversible cause of various neuropsychiatric disorders (Hector 1988). One should also consider whether a vegetarian diet or malabsorption due to celiac disease or gluten enteropathy is a factor in B12 deficiency.

Weaker digestion, reduced absorption of nutrients, and hypochlorhydria (inadequate stomach acid needed to break down proteins that contain vitamin B12) are common in the aging population and associated with a B12 deficiency; B12 levels should be tested in an older person with symptoms of depression. Evidence suggests that the methylcobalamin form of B12may have more beneficial metabolic effects than cyanocobalamin (Sun et al 2005; Bertoglio et al 2010).


Vitamin B6

Vitamin B6 is a cofactor for the production of most neurotransmitters, but it is particularly important for serotonin synthesis (Baldewicz 2000). B6 levels are often low in women taking oral contraceptives and research has shown that B6 supplementation in these women can improve mood. For example, one study showed 22 women who had depression associated with oral contraceptive use and a B6 deficiency saw significant improvement in their symptoms with B6 supplementation (Adams et al 1973).

A more recent study examined blood levels of pyridoxal-5-phosphate (P5P), a metabolically active form of B6, in the blood of 251 elderly individuals living is Massachusetts. The investigators found that deficient levels of P5P doubled the likelihood of depression in this population. Accordingly, when dietary composition was assessed, those with higher daily B6 intakes were less likely to be depressed (Merete 2008).


3. Blood sugar regulation and insulin resistance:

Green Coffee

Conventional coffee preparation, which involves roasting the green coffee beans at high temperatures to attain the desired flavor profile, dramatically lowers levels of health-promoting coffee constituents called chlorogenic acids.

Chlorogenic acids have been shown in several studies to aid in controlling blood sugar levels; especially those glucose spikes which occur after a high-carbohydrate meal (Tunnicliffe 2011; Zhang 2011). In a 12-week study, consumption of chlorogenic acid-fortified instant coffee led to a considerable reduction in the absorption of glucose when compared to regular instant coffee (Thom 2007). As elevated glucose levels are common among depressives, chlorogenic acids may help combat some symptoms of depression tied to insulin resistance and irregularities in glucose metabolism.

Green coffee, the primary source of chlorogenic acids, cannot be consumed as a beverage due to its extremely bitter taste. Consuming a green coffee extract standardized to chlorogenic acids is an effective means of obtaining biologically active concentrations of chlorogenic acids.

The potential role of chlorogenic acids in mediating the mood boost associated with coffee consumption, and their thoroughly studied antihyperglycemic properties give rise to promising multimodal depression protection.



Chromium has been studied for its role in regulating blood sugar by facilitating the uptake of glucose into cells, and some research indicates that it may be beneficial in depression as well (McCarty 1994).

In one case series of five patients with minor depression, chromium supplementation led to remission (MacLeod 1999). Two other pilot studies found chromium picolinate supplementation benefited atypical depression (Davidson et al 2003; Docherty et al 2005).


4.Antioxidant Effects: N-Acetyl-cysteine, Lipoic acid, vitamins C and E, and Selenium

One of the best-researched antioxidants for depression is N-acetyl cysteine (NAC). NAC is a precursor to glutathione, one of the body's most powerful antioxidants. Research has found glutathione depletion and oxidative stress in people with bipolar depression. Two recent studies showed NAC is a safe and effective adjunctive treatment that improves depression in patients with bipolar disorder (Berk 2011).

Although lipoic acid has not been well studied for depression, it is one of the most effective supplemental antioxidants, since it helps recycle other antioxidants, such as vitamin C (May 2010). It also may benefit blood sugar regulation and neurological function, as evidence shows it can help diabetic neuropathy (Jin et al 2007).

In general, antioxidants may help buffer nerve cell damage in cases of chronic or recurrent depression, although they also serve other roles in brain health. For example, the antioxidant vitamin C is an important cofactor in the synthesis of serotonin, norepinephrine, and adrenal hormones that mediate stress. Vitamin E helps protect nerve cell membranes, and low selenium levels are associated with depression (Hawkes WC, Hornbostel L 1996).


5.Additional nutrients:


Curcumin is a phytoceutical derived from turmeric, a spice used often in preparation of Indian cuisine. It belongs to a class of compounds called polyphenols, which have been extensively studied and shown to exert an array of health benefits. One of the most intriguing properties of polyphenols, and curcumin in particular, is the ability to positively influence mood (Pathak 2013). Indeed, mounting evidence suggests curcumin might represent an important novel modality for the treatment of depression (Lopresti 2012).

Curcumin appears to modulate several aspects of neurobiology involved in mood and behavior. Experimental evidence from an animal model of depression suggests curcumin can preserve levels of a protein important for healthy neuronal function (brain-derived neurotrophic factor [BDNF]) in a region of the brain called the amygdala, which is involved in mood regulation (Zhang 2014). Curcumin appears to manipulate neurotransmitter signaling as well. In another animal model, mice with neuropathy (who are prone to depression) were treated for 3 weeks with 45 mg/kg of curcumin twice daily (about 583 mg daily for an 80 kg adult human). While these mice normally exhibit depressive-like symptoms, curcumin treatment ameliorated this behavior. Interestingly, the researchers found that curcumin may have eased the rodent’s depression by altering serotonin and gamma-aminobutyric acid (GABA) signaling in their central nervous systems (Zhao 2013). Curcumin also helps relieve pain, which may be helpful for some individuals with depression because pain, especially of chronic nature, is closely – and potentially causally – associated with depression (Finan 2013; Ong 2003; Zhao 2013; Arora 2011). Other studies show that curcumin’s powerful anti-inflammatory properties may also underlie its ability to elevate mood. Curcumin considerably eased inflammation by suppressing activation of nuclear factor-kappa B (NF-κB), a master regulator of inflammation; the researchers concluded that curcumin’s antidepressant effects were due in part to its anti-inflammatory action (Jiang 2013).

Evidence for a potent antidepressant effect of curcumin among animals has been partially confirmed in at least one human study. In a randomized, double-blind, placebo-controlled trial, 40 people with new-onset depression were treated with antidepressants (escitalopram [Lexapro®] or venlafaxine [Effexor®]) together with either curcumin (500 mg per day) or placebo for 5 weeks. Researchers then tracked subjects’ depression severity using several standardized assessments. Although subjects in both groups experienced comparable relief of their depression, those who received curcumin tended to achieve faster relief than those who received a placebo (Bergman 2013).

A plethora of animal data indicate curcumin may be a powerful tool in the treatment of depression, and, as of the time of this writing, additional human studies are ongoing to assess its effects on mood (SHSC 2014). Most importantly, curcumin, unlike conventional antidepressant medications, has an excellent safety and side-effect profile (Gupta 2013; Noorafshan 2013; Whiskey 2013; Henry 2012; Asher 2013).


St. John's Wort

St. John's wort (Hypericum perforatum) is a medicinal herb used to treat neurological and psychiatric disorders, including depression (Nangia M et al 2000). Compared to a placebo, H. perforatum extract is more effective at targeting mild to moderate depression, and reducing symptoms and recurrence rate (Lecrubier Y et al 2002). Its effectiveness is considered comparable to antidepressant medications, but its actions are more complex (Schrader E et al 2000; Szegedi A et al 2005).

St. John's wort's mechanism of action on depression is not entirely understood, even though it is one of the most researched herbs for depression. St. John's wort has been shown to inhibit serotonin and norephinephrine reuptake, thus increasing their availability at the synapse (Nangia M et al 2000). Other investigators found it influences dopamine and GABA activity. Its antidepressant qualities also can be linked to its antioxidant and anti-inflammatory properties that normalize an overactive hypothalamus-pituitary-adrenal axis and stress response (Butterweck 2003).

While additional research is on-going to identify all of the anti-depressant mechanisms of action, experimental models and clinical trials alike have shown that treatment with St. John's wort delivers positive response rates for mild to moderate depression (Can 2011; Kim 1999; Linde 1996).

Unfortunately, potential side effects associated with St. John's Wort deprive many depressives of its benefits.


Vitamin D

Growing evidence suggests that vitamin D significantly affects depression. This is not surprising in seasonal depression, since the skin synthesizes vitamin D in response to sunlight, which is less available in the winter (Namri et al 2009; Shipowick 2009). However, vitamin D has been found to play other roles in depression. For example, in a study of 7,358 patients age 50 and over with a cardiovascular diagnosis and no a history of depression, low vitamin D levels significantly increased the risk of developing depression (May et al 2010).

Studies also find that vitamin D3 (cholecalciferol) supplementation can improve symptoms of depression. One well-controlled study of 441 overweight and obese participants showed an association between low vitamin D levels and depression. High dose vitamin D supplementation (20,000–40,000 IUs per week or 2,800–6,000 IUs per day) for one year improved mood (Jorde 2008). Another pilot study noted significant improvement in depression in six of nine women with low levels of vitamin D upon supplementation (Shipowick 2009).

Vitamin D's effectiveness may be related to the high prevalence of vitamin-D deficiency in the general population, its importance in blood-sugar regulation, and its importance in overall regulation of genetic activity.



Zinc is a trace element known to help regulate the nervous system (Nowak G 2002) and may be specifically related to depression (Levenson 2006). Increasing evidence shows that decreased blood levels of zinc are associated with depression (Maes M et al 1994, 1997; McLoughlin 1990), and, in depressed subjects, lower levels of zinc are associated with worse depression (Nowak et al 1999). One pilot study of 20 depressed patients also showed that 25 mg a day of zinc augmented benefits of antidepressant medication (Nowak et al 2003).



Inositol levels in the brain and cerebrospinal fluid were found to be lower in subjects with depression. One well-controlled trial showed that taking 12 grams a day of inositol helped relieve symptoms in 39 patients with depression (Levine 1995).

Inositol, a second-messenger precursor, has important cellular communication functions in the nervous system. Interestingly, inositol is also involved with insulin signaling and function. It therefore may have more of an effect on overweight or obese individuals, as well as those who are insulin resistant, such as those with metabolic syndrome or women with polycystic ovarian syndrome (PCOS). These findings require further research and replication.



Depression is a multifactorial condition, and efficient relief requires addressing neurochemical and metabolic imbalances that may underlie mood disturbances. The nutrients listed in this protocol are categorized according to their evidence-based mechanisms of action in brain health and mood regulation.

Many of these suggestions may serve as adjuvants to conventional therapies for depression. Always consult a qualified healthcare professional before combining any supplements with an antidepressant medication.

Broad-Range Nervous System Effects

  • Fish oil (with olive polyphenols): 1400 mg EPA and 1000 mg DHA daily
  • Magnesium L-Threonate: 2000 mg daily (supplying 144 mg elemental magnesium)

Supporting Neurotransmitter Synthesis

  • Tryptophan: 1000 – 2000 mg daily

Supporting Methylation Reactions

  • S-Adenosylmethionine (SAMe): 400 – 1200 mg daily
  • L-methylfolate: 1000 mcg daily
  • Vitamin B12 (as methylcobalamin): 1000 – 8000 mcg daily
  • Vitamin B6 (as pyridoxal 5-phosphate): 100 mg daily

Supporting Blood Sugar Regulation

  • Chromium: 500 mcg daily
  • Green Coffee Bean extract (standardized 50% to chlorogenic acid): 400 mg before each meal, up to three times daily.

Antioxidant Effects

  • R-lipoic acid: 300 – 600 mg daily
  • Vitamin C: 1000 – 2000 mg daily
  • Vitamin E (as gamma tocopherol mix): 350 mg daily
  • Selenium (as Se-methylselenocysteine): 200 mcg daily

Supporting Mitochondrial Health

  • Coenzyme Q10 (as ubiquinol): 100 – 200 mg daily
  • Pyrroloquinoline quinine (PQQ): 10 – 20 mg daily
  • Acetyl-L-Carnitine: 1000 – 2000 mg daily

Address hormonal insufficiency if relevant.

Address thyroid hormone irregularities if relevant.

Miscellaneous Mechanisms of Relief

  • Vitamin D: 5000 – 8000 IU daily (depending on blood test results)
  • Zinc: 30 mg daily
  • Inositol: 2000 – 10 000 mg daily
  • Comprehensive multivitamin formula: Per label instructions
  • St. John's Wort; standardized extract: 300 – 600 mg daily
  • Curcumin (as highly absorbed phospholipid blend): 630 mg daily



Abadie JM, Wright B et al. Effect of dehydroepiandrosterone on neurotransmitter levels and appetite regulation of the obese Zucker rat. The Obesity Research Program. Diabetes. 1993 May;42(5):662–9.

Abumaria N et al. Effects of elevation of brain magnesium on fear conditioning, fear extinction, and synaptic plasticity in the infralimbic prefrontal cortex and lateral amygdala. J Neurosci. 2011 Oct 19;31(42):14871-81.

Adams PW, Rose DP, et al. Effect of pyridoxine hydrochloride (vitamin B6) upon depression associated with oral contraceptives. Lancet 1973;1:897-904.

Alpert JE, Papakostas G, et al. S-adenosyl-methionine (SAMe) as an adjunct for reistant major depressive disorder. J of Clin Psycopharmacol 2004;24:661-4.

Alpert, J. E., Mischoulon, D., Nierenberg, A. A., & Fava, M. (2000). Nutrition and depression: Focus on folate. Nutrition, 16, 544–546.

Anacker C, Zunszain PA, Carvalho LA, et al. The glucocorticoid receptor: pivot of depression and of antidepressant treatment? Psychoneuroendocrinology. 2011 Apr;36(3):415-25.

Andrews G et al. Lifetime risk of depression: restricted to a minority or waiting for most? Br J Psychiatry. 2005 Dec;187:495-6.

Arora V, Kuhad A, Tiwari V, Chopra K. Curcumin ameliorates reserpine-induced pain-depression dyad: behavioural, biochemical, neurochemical and molecular evidences. Psychoneuroendocrinology. Nov 2011;36(10):1570-1581.

Asher GN, Spelman K. Clinical utility of curcumin extract. Alternative therapies in health and medicine. Mar-Apr 2013;19(2):20-22.

Babyak M, Blumenthal JA, et al. Exercise treatment for major depression: maintenance of therapeutic benefit at 10 months. Psychosom Med 2000;62:633-8.

Baldewicz, T. T., Goodkin, K., Blaney, N. T., Shor-Posner, G., Kumar, M., Wilkie, F. L., et al. (2000). Cobalamin level is related to self-reported and clinically rated mood and to syndromal depression in bereaved HIV-1+ and HIV-1- homosexual men. Journal of Psychosomatic Research, 48(2), 177–185.

Barha CK and Galea LA. Influence of different estrogens on neuroplasticity and cognition in the hippocampus. Biochim Biophys Acta. 2010 Oct;1800(10):1056-67. Epub 2010 Jan 25.

Barrett-Connor E, Von Muhlen DG et al. Bioavailable testosterone and depressed mood in older men: The Rancho Bernardo Study. J Clin Endocrinol Metab. 1999 Feb;84(2):573–7.

Bauerly K et al. Altering pyrroloquinoline quinone nutritional status modulates mitochondrial, lipid, and energy metabolism in rats. PLoS One. 2011;6(7):e21779. Epub 2011 Jul 21.

Bellipanni G, Bianchi P, et al. Effects of melatonin in perimenopausal and menopausal women: a randomized and placebo controlled study. Exp Gerontol 2001;36:297-310.

Bennett AO MR. Stress and anxiety in schizophrenia and depression: glucocorticoids, corticotrophin-releasing hormone and synapse regression. Aust N Z J Psychiatry. 2008; 42(12):995-1002.

Bergman J, Miodownik C, Bersudsky Y, Sokolik S, Lerner PP, Kreinin A, . . . Lerner V. Curcumin as an add-on to antidepressive treatment: a randomized, double-blind, placebo-controlled, pilot clinical study. Clinical neuropharmacology. May-Jun 2013;36(3):73-77.

Berk M, Dean O, et al. The efficacy of N-acetycysteine as an adjunctive treatment in bipolar depression: an open label trial. J Afect Disord 2011;Jun 28[Epub ahead of print].

Bertoglio K, James JS, et al. Pilot study of the effect of methyl B12 treatment on behavioral and biomarker measures in children with autism. J Altern Complement Med 2010;16:555-60.

Bethea CL, Pecins-Thompson M et al. Ovarian steroids and serotonin neural function. Mol Neurobiol. 1998 Oct;18(2):87-123. Review.

Binder EB, Nemeroff CB. The CRF system, stress, depression and anxiety-insights from human genetic studies. Mol Psychiatry. 2010 Jun;15(6):574-88.

Bloch M, Aharonov I, Ben Avi I, et al. Gonadal steroids and affective symptoms during in vitro fertilization: implication for reproductive mood disorders. Psychoneuroendocrinology. 2011 Jul;36(6):790-6.

Booij L, Swenne CA, et al. Tryptophan depletion affects heart rate variability and impulsivity in remitted depressed patients with a history of suicidal ideation. Biol Psychiatry 2006;60:507-14.

Bourre JM, Dumont O et al. Essentiality of omega 3 fatty acids for brain structure and function. World Rev Nutr Diet. 1991;66:103–17.

Burr ML, Fehily AM et al. Effects of changes in fat, fish, and fibre intakes on death and myocardial reinfarction: Diet and reinfarction trial (DART). Lancet. 1989 Sep 30;2(8666):757–61.

Butterweck V. Mechanism of action of St John’s wort in depression: what is known? CNS Drugs 2003;17:539-62.

Calev A et al. ECT and non-memory cognition: a review. Br J Clin Psychol. 1995 Nov;34 ( Pt 4):505-15.

Can OD et al. Effects of Insulin and St. John's Wort Treatments on Anxiety, Locomotory Activity, Depression, and Active Learning Parameters of Streptozotocin-Diabetic Rats. Planta Med. 2011 Aug 19. [Epub ahead of print]

CDC. Centers for Disease Control and Prevention. Current Depression among Adults – united states, 2006 and 2008 Morbidity and Mortality weekly Report October 1, 2010 Erratum. Availble at: Accessed 10/31/2011.

Chang KD et al. Differences in thyroid function between bipolar manic and mixed states. Biol Psychiatry. 1998 May 15;43(10):730-3.

Chengappa KN, Levine J, et al. Inositol as an add-on treatment for bipolar depression. Bipolar Disord 2000;2:46-55.

Chowanadisai W et al. Pyrroloquinoline quinone stimulates mitochondrial biogenesis through cAMP response element-binding protein phosphorylation and increased PGC-1alpha expression. J Biol Chem. 2010 Jan 1;285(1):142-52. Epub 2009 Oct 27.

Christmas DM et al. A biological pathway linking inflammation and depression: activation of indoleamine 2,3-dioxygenase. Neuropsychiatr Dis Treat. 2011;7:431-9. Epub 2011 Jul 13.

Cizza G et al. Plasma CRP levels in premenopausal women with major depression: a 12-month controlled study. Horm Metab Res. 2009 Aug;41(8):641-8. Epub 2009 Apr 30.

Cole DP et al. Slower treatment response in bipolar depression predicted by lower pretreatment thyroid function. Am J Psychiatry. 2002 Jan;159(1):116-21.

Coppen A, Bailey J. Enhancement of the antidepressant action of fluoxetine by folic acid: A randomised, placebo controlled trial. J Affect Disord. 2000 Nov;60(2):121–30.

Coughlin PA. Facilitating emotional health and well-being. In Monti DA, Beitman BD (eds), Integrative Psychiatry. Oxford, England: Oxford University Press, Inc., pp. 383-407, 2010.

Craddock D, Thomas A. Cytokines and late-life depression. Essent Psychopharmacol 2006;7:42-52.

Cubeddu A, Giannini A, Bucci F, Merlini S, Casarosa E, Pluchino N, Luisi S, Luisi M, Genazzani AR. Paroxetine increases brain-derived neurotrophic factor in postmenopausal women. Menopause. 2010 Mar;17(2):338-43.

Cunningham J, Yonkers KA, O'Brien S, Eriksson E. Update on research and treatment of premenstrual dysphoric disorder. Harv Rev Psychiatry. 2009;17(2):120-37.

Dantzer R et al. Inflammation-associated depression: from serotonin to kynurenine. Psychoneuroendocrinology. 2011 Apr;36(3):426-36. Epub 2010 Oct 30.

Davidson JR, Abraham K, et al. Efectiveness ofchromium in atypical depression. Biol Psychiatry 2003;53:261-4.

Davis JD et al. Neuropsychiatric aspects of hypothyroidism and treatment reversibility. Minerva Endocrinol. 2007 Mar;32(1):49-65.

Delhez M et al. [Testosterone and depression in men aged over 50 years. Andropause and psychopathology: minimal systemic work-up]. Ann Endocrinol (Paris). 2003 Apr;64(2):162-9.

Docherty JP, Sack DA, et al. A double-blind, placebo controlled, exploratory trial of chromium picolinate inatypical depression: effect on carbohydrate craving. 2005;11:302-14.

Dusek JA et al. Mind-body medicine: a model of the comparative clinical impact of the acute stress and relaxation responses. Minn Med. 2009 May;92(5):47-50.

Dusek JA, Otu HH, Wohlhueter AL, et al. Genomic counter-stress changes induced by the relaxation response. PLoS One. 2008 Jul;3(7):e2576.

Eby GA, Eby KL. Magnesium for treatment-resistant depression: a review and hypothesis. Medical Hypotheses 2010;74(4):649-60.

Evins, A. E., Demopulos, C., Yovel, I., Culhane, M., Ogutha, J., Grandin, L. D., et al. (2006). Inositol augmentation of lithium or valproate for bipolar depression. Bipolar Disorders, 8, 168–174.

Faloon W. “Startling Findings About Vitamin D Levels in Life Extension® Members” Life Extension Magazine. January 2010.

Fang Y et al. A pilot study of the efficacy and safety of paroxetine augmented with risperidone, valproate, buspirone, trazodone, or thyroid hormone in adult Chinese patients with treatment-resistant major depression. J Clin Psychopharmacol. 2011 Oct;31(5):638-42.

Fava M et al. Folate, vitamin B12, and homocysteine in major depressive disorder. American Journal of Psychiatry, 1997 Mar;154(3), 426–428.

Finan PH, Smith MT. The comorbidity of insomnia, chronic pain, and depression: dopamine as a putative mechanism. Sleep medicine reviews. Jun 2013;17(3):173-183.

Freeman MP, Fava M, et al. Complementary and Alternative Medicine in major depressive disorder: the American psychiatric association task force report. J Clin Psychiatry 2010;71:669-81.

Frye MA et al. Association between lower serum free T4 and greater mood instability and depression in lithium-maintained bipolar patients. Am J Psychiatry. 1999 Dec;156(12):1909-14.

Fuller-Thomson E et al. The association between depression and thyroid disorders in a regionally representative Canadian sample. Psychol Health Med. 2011 Sep 26. [Epub ahead of print]

George MS, Lisanby SH, et al. Daily left prefrontal transcranial magnetic stimulation therapy for major depressive disorder. Arch Gen Psychiatry 2010; 67:507-16.

Giltay EJ, Tishova YA, et al. Effects of testosterone supplementation on depressive syptoms and sexual dysfunction in hypogonadal men with metabolic syndrome. J Sex Med 2010;7:2572-82.

Girdler SS et al. A history of depression in women is associated with an altered GABAergic neuroactive steroid profile. Psychoneuroendocrinology. 2011 Sep 2. [Epub ahead of print]

Grav S et al. Association between social support and depression in the general population: the HUNT study, a cross-sectional survey. J Clin Nurs. 2011 Oct 24. doi: 10.1111/j.1365-2702.2011.03868.x. [Epub ahead of print]

Green B. Focus on agomelatine. Curr Med Res Opin 2011;27:745-9.

Grigoriadis S, Kennedy SH. Role of estrogen in the treatment of depression. Am J Ther. 2002 Nov;9(6):503–9.

Gupta SC, Kismali G, Aggarwal BB. Curcumin, a component of turmeric: from farm to pharmacy. BioFactors (Oxford, England). Jan-Feb 2013;39(1):2-13.

Hawkes WC, Hornbostel L. Effects of dietary selenium on mood in healthy men living in a metabolic research unit. Biol Psychiatry 1996;39:121-8.

Hector, M., & Burton, J. R. (1988). What are the psychiatric manifestations of vitamin B12 deficiency? Journal of the American Geriatrics Society, 36(12), 1105–1112.

Hemmerle AM et al. Stress, depression and Parkinson's disease. Exp Neurol. 2011 Oct 6. [Epub ahead of print]

Henry A, Kisicki MD, Varley C. Efficacy and safety of antidepressant drug treatment in children and adolescents. Molecular psychiatry. Dec 2012;17(12):1186-1193.

Hickie IB et al. Novel melatonin-based therapies: potential advances in the treatment of major depression. Lancet. 2011 Aug 13;378(9791):621-31. Epub 2011 May 17.

Hoffman BM, Babyak MA, et al. Exercise and pharmacotherapy in patients with major depression: one-year follow-up of the SMILE study. Psychosom Med 2011;73:127-33.

Hovatta I, Juhila J, Donner J. Oxidative stress in anxiety and comorbid disorders. Neurosci Res 2010; 68:261-75.

Howland RH. Use of endocrine hormones for treating depression. J Psychosoc Nurs Ment Health Serv. 2010 Dec;48(12):13-6. doi: 10.3928/02793695-20101105-01. Epub 2010 Nov 22.

Hynninen MJ et al. A randomized controlled trial of cognitive behavioral therapy for anxiety and depression in COPD. Respir Med. 2010 Jul;104(7):986-94. Epub 2010 Mar 25.

ICSI. Institute for Clinical Systems Improvement. Health care Guideline: Major Depression in Adults in Primary Care. May 2011. Available at Accessed 11/2/2011.

Inoue K. [Cognitive-behavioral therapy for treatment-resistant depression]. Seishin Shinkeigaku Zasshi. 2010;112(11):1097-104.

Jankowska EA, Drohomirecka A, Ponikowska B, et al. Deficiencies in circulating testosterone and dehydroepiandrosterone sulphage, and depression in men with systolic chronic heart failure. Eur J Heart Fail. 2010 Sep;12(9):966-73.

Jayadevappa R et al. The burden of depression in prostate cancer. Psychooncology. 2011 Aug 12. doi: 10.1002/pon.2032. [Epub ahead of print]

Jiang H, Wang Z, Wang Y, Xie K, Zhang Q, Luan Q, . . . Liu D. Antidepressant-like effects of curcumin in chronic mild stress of rats: involvement of its anti-inflammatory action. Progress in neuro-psychopharmacology & biological psychiatry. Dec 2 2013;47:33-39.

Jin HY, Joung SJ, et al. The effect of alpha-lipoic acid on sumptoms and skin blood flow in diabetic neuropathy. Diabet Med 2007;24:1034-8.

Joëls M. Impact of glucocorticoids on brain function: relevance for mood disorders. Psychoneuroendocrinology. 2011 Apr;36(3):406-14.  

Joensuu M, Tomunen T, Saarinen PI et. al. Reduced midbrain serotonin transporter availability in drug-naïve patients with depression measured by SERT-specific [(123)I] nor beta CIT SPECT imaging. Psychiatry 2007 154 (2): 125-31

Joffe H, Cohen LS. Estrogen, serotonin, and mood disturbance: Where is the therapeutic bridge? Biol Psychiatry. 1998 Nov 1;44(9):798–811.

Jorde R, Sneve M, et al. Effects of vitamin D supplementation on symptoms of depression in overweight and obese subjects: randomized double blind trial. J Intern Med 2008;264:599-609.

Karishma KK, Herbert J. Dehydroepiandrosterone (DHEA) stimulates neurogenesis in the hippocampus of the rat, promotes survival of newly formed neurons and prevents corticosterone-induced suppression. Eur J Neurosci. 2002 Aug;16(3):445–53.

Karten YJ, Nair SM, van Essen L, et al. Long-term exposure to high corticosterone levels attenuates serotonin responses in rat hippocampal CA1 neurons. Proc Natl Acad Sci USA. 1999 Nov;96(23):13456-61.

Katsamanis MK, Lehrer PM, et al. Preliminary results of an open label study of heart rate variability biofeedback for major depression. Appl Psychophys Biofeedback 2007;32:19-30.

Kaye WH et al. Effects of acute tryptophan depletion on mood in bulimia nervosa. Biol Psychiatry. 2000 Jan 15;47(2):151-7.

Kemp DE et al. Use of insulin sensitizers for the treatment of major depressive disorder: A pilot study of pioglitazone for major depression accompanied by abdominal obesity. J Affect Disord. 2011 Jul 20. [Epub ahead of print]

Kendall DA, Stancel GM et al. The influence of sex hormones on antidepressant-induced alterations in neurotransmitter receptor binding. J Neurosci. 1982 Mar;2(3):354–60.

Kiecolt-Glaser JK, Gouin JP, et al. Close relationships, inflammation and health. Neurosci Biobehav Rev 2010;35:33-8.

Kikuchi H, Nakatani Y, Seki Y, Yu X, Sekiyama T, Sato-Suzuki I, Arita H. Decreased blood serotonin in the premenstrual phase enhances negative mood in healthy women.J Psychosom Obstet Gynaecol. 2010 Jun;31(2):83-9.

Kim HL, Streltzer J et al. St. John’s wort for depression: A meta-analysis of well-defined clinical trials. J Nerv Ment Dis. 1999 Sep;187(9):532–8.

Kim MY et al. Leukocyte mitochondrial DNA (mtDNA) content is associated with depression in old women. Arch Gerontol Geriatr. 2011 Sep-Oct;53(2):e218-21. Epub 2010 Dec 14.

Kroczka B, Branski P et al. Antidepressant-like properties of zinc in rodent forced swim test. Brain Res Bull. 2001 May 15;55(2):297–300.

Kupka RW et al. High rate of autoimmune thyroiditis in bipolar disorder: lack of association with lithium exposure. Biol Psychiatry. 2002 Feb 15;51(4):305-11.

Lam RW, Levitt AJ, et al. The Can-SAD study: a randomized controled trial of the effectiveness of light therapy and fluoxetine in patients with winter seasonal affective disorder. Am J Psychiatry 2006;163:805-12.

Lecrubier Y, Clerc G, Didi R, et al. Efficacy of St. John’s wort extract WS 5770 in major depression: a double-blind, placebo-controlled trial. Am J Psychiatry. 2002 Aug;159(8):1361-6.

Lee JW et al. Mitochondrial DNA copy number in peripheral blood is associated with cognitive function in apparently healthy elderly women. n Chim Acta. 2010 Apr 2;411(7-8):592-6. Epub 2010 Jan 28.

Levenson CW. Zinc: the new antidepressant? Nutrition Reviews 2006;64:39-42.

Levine J, Barak Y et al. Double blind controlled trial of inositol treatment of depression. Am J Psychiatry 1995;152:1084-6.

Lewis SJ et al. The thermolabile variant of MTHFR is associated with depression in the British Women's Heart and Health Study and a meta-analysis. Mol Psychiatry. 2006 Apr;11(4):352-60.

Lin, P., & Su, K. (2007). A meta-analytic review of double-blind, placebo-controlled trials of antidepressant efficacy of omega-3 fatty acids. Journal of Clinical Psychiatry, 68(7), 1056–1061.

Linde K, Ramirez G et al. St John’s wort for depression: An overview and meta-analysis of randomised clinical trials. BMJ. 1996 Aug 3;313(7052):253–8.

Lisanby SH et al. The effects of electroconvulsive therapy on memory of autobiographical and public events. Arch Gen Psychiatry. 2000 Jun;57(6):581-90.

Liu RT, Alloy LB. Stress generation in depression: a systematic review of the empirical literature and recommendations for future study. Clin Psychol Rev 2010a;30:582-93.

Liu SS et al. Depression in patients with heart disease: the case for more trials. Future Cardiol. 2010b Jul;6(4):547-56.

Logan AC. Neurobehavioral aspects of omega-3 fatty acids: Possible mechanisms and therapeutic value in major depression. Altern Med Rev. 2003 Nov;8(4):410–25.

Lojko D, Rybakowski JK. L-thyroxine augmentation of serotonergic antidepressants in female patients with refractory depression. J Affect Disord 2007;103:253-6.

Lopresti AL, Hood SD, Drummond PD. Multiple antidepressant potential modes of action of curcumin: a review of its anti-inflammatory, monoaminergic, antioxidant, immune-modulating and neuroprotective effects. Journal of psychopharmacology (Oxford, England). Dec 2012;26(12):1512-1524.

Lucas M et al. Coffee, caffeine, and risk of depression among women. Arch Intern Med. 2011 Sep 26;171(17):1571-8.

MacLeod MN, Gaynes BN, et al. Chromium potentiation of antidepressant pharmacotherapy for dysthymic disorder in 5 patients. J Clin Psychiatry1999;60:237-40.

Maes M et al. Activation of cell-mediated immunity in depression: Association with inflammation, melancholia, clinical staging and the fatigue and somatic symptom cluster of depression. Prog Neuropsychopharmacol Biol Psychiatry. 2011 Sep 16. [Epub ahead of print]

Maes M, D’Haese PC et al. Hypozincemia in depression. J Affect Disord. 1994 Jun;31(2):135–40.

Maes M, Mihaylova I, et al. Lower plasma coenzyme Q10 in depression: a marker for treatment resistance and chronic fatigue in depression and a risk factor to cardiovascular disorder in that illness. Neuro Endocrinol Lett 2009;30:462-9.

Maes M, Vandoolaeghe E et al. Lower serum zinc in major depression is a sensitive marker of treatment resistance and of the immune/inflammatory response in that illness. Biol Psychiatry. 1997 Sep 1;42(5):349–58.

Malaguarnera M et al. Acetyl-L-carnitine reduces depression and improves quality of life in patients with minimal hepatic encephalopathy. Scand J Gastroenterol. 2011 Jun;46(6):750-9. Epub 2011 Mar 28.

May HT, Bair TL, et al. Association of vitamin D levels with incident depression among a general cardiovascular population. Am Heart J 2010;159:1037-43.

May JM et al. Assessing the reductive capacity of cells by measuring the recycling of ascorbic and lipoic acids. Methods Mol Biol. 2010;610:229-43.

McCarty MF et al. Enhancing central and peripheral insulin activity as a strategy for the treatment of endogenous depression--an adjuvant role for chromium picolinate? Med Hypotheses. 1994 Oct;43(4):247-52.

McCown D, Reibel DK, Micozzi MS. Teaching mindfulness: a practical guide for clinicians and educators. Springer Science and Business Media, LLC, New York, 2010.

McLoughlin IJ, Hodge JS. Zinc in depressive disorder. Acta Psychiatr Scand. 1990 Dec;82(6):451–3.

McNamara RK et al. Deficits in docosahexaenoic acid and associated elevations in the metabolism of arachidonic acid and saturated fatty acids in the postmortem orbitofrontal cortex of patients with bipolar disorder. Psychiatry Res. 2008 Sep 30;160(3):285-99. Epub 2008 Aug 20.

Merete C et al. Vitamin B6 is associated with depressive symptomatology in Massachusetts elders. J Am Coll Nutr. 2008 Jun;27(3):421-7.

Miller KJ, Conney JC et al. Mood symptoms and cognitive performance in women estrogen users and nonusers and men. J Am Geriatr Soc. 2002 Nov;50(11):1826–30.

Morris MS, Fava M et al. Depression and folate status in the US population. Psychother Psychosom. 2003 Mar;72(2):80–7.

Morris R et al. Depression and anxiety screening after stroke: adherence to guidelines and future directions. Disabil Rehabil. 2011 Oct 17. [Epub ahead of print]

Murphy SE, Longhitano C et al. Tryptophan supplementation induces a positive bias in the processing of emotional material in healthy female volunteers. Psychopharmacology (Berl). 2006 Jul;187(1):121–30.

Nadler JL, Rude RK. Disorders of magnesium metabolism. Endocrinol Metab Clin North Am 1995;24:623-41.

Namri A, Mizoue T, et al. Association between serum 25-hydroxyvitamin D and depressive symptoms in Japanese: analysis by survey season. Eur J Clin Nutr 2009;63:1444-7.

Nangia M, Syed W et al. Efficacy and safety of St. John’s wort for the treatment of major depression. Public Health Nutr. 2000 Dec;3(4A):487–94.

Nemeroff CB. Improving antidepressant adherence. J Clin Psychiatry. 2003;64 Suppl 18:25–30.

Nemets H, Nemets R et al. Omega-3 treatment of childhood depression: a controlled, double-blind pilot study. Am J Psychiatry. 2006 Jun;163(6):1098-100.

Neumeister A, Turner EH, et al. Effects of tryptophan depletion vs. catecholamine depletion in patients with seasonal affective disorder in remission with light therapy. Arch Gen Psychiatry 1998;55:524-30.

Newberg AB. The neurobiology of meditation. In Monti DA, Beitman BD (eds), Integrative Psychiatry. Oxford, England: Oxford University Press, Inc., pp. 339-58, 2010.

Noorafshan A, Ashkani-Esfahani S. A review of therapeutic effects of curcumin. Current pharmaceutical design. 2013;19(11):2032-2046.

Nowak G, Schlegel-Zawadzka M. Alterations in serum and brain trace element levels after antidepressant treatment: Part I. Zinc. Biol Trace Elem Res. 1999 Jan;67(1):85–92.

Nowak G, Schlegel-Zawadzka M. Alterations in serum and brain trace element levels after antidepressant treatment: part 1. Zinc. Biol Trace Elem Res. 1999 Jan;67(1):85-92.

Nowak G, Siwek M, et al. Effect of zinc supplementation on antidepressant therapy in unipolar depression: a preliminary placebo-contolled study. Pol J Pharmacol 2003;55:1143-7.

Nowak G, Szewczyk B. Mechanisms contributing to antidepressant zinc actions. Pol J Pharmacol. 2002 Nov;54(6):587–92.

O’Brien SM, Scully P, et al. Plasma cytokine profiles in depressed patients who fail to respond to selective serotonin reuptake inhibitor therapy. J Psychiatr Res 2007;41:326-31.

Ohaeri JU et al. Metabolic syndrome in severe mental disorders. Metab Syndr Relat Disord. 2011 Apr;9(2):91-8. Epub 2010 Oct 21.

Ong KS, Keng SB. The biological, social, and psychological relationship between depression and chronic pain.Cranio : the journal of craniomandibular practice. Oct 2003;21(4):286-294.

Osterlund MK. Underlying mechanisms mediating the antidepressant effects of estrogens. Biochim Biophys Acta. 2010;1800:1136-44.

Papakostas GI, Mishoulon D, et al. S-adenosyl methionine (SAMe) augmentation of serotonin reuptake inhibitors for antidepressant nonresponders with major depressive disorder: a double-blind randomized clinical trial. Am J Psychiatry 2010; 167:942-8.

Parcells DA. Women's mental health nursing: depression, anxiety and stress during pregnancy.J Psychiatr Ment Health Nurs. 2010 Nov;17(9):813-20.

Parker G et al. 'D' for depression: any role for vitamin D? 'Food for Thought' II. Acta Psychiatr Scand. 2011 Oct;124(4):243-9. doi: 10.1111/j.1600-0447.2011.01705.x. Epub 2011 Apr 12.

Pathak L, Agrawal Y, Dhir A. Natural polyphenols in the management of major depression. Expert opinion on investigational drugs. Jul 2013;22(7):863-880.

Pettigrew JW, Levine J, et al. P-MRS study of acetyl-L-carnitine treatment in geriatric depression: preliminary results. Bipolar Disorders 2000;4:61-6.

Pope HG Jr, Cohane GH et al. Testosterone gel supplementation for men with refractory depression: A randomized, placebo-controlled trial. Am J Psychiatry. 2003 Jan;160(1):105–11.

Prescrire Int. Treatment-resistant depression: no panacea, many uncertainties. Adverse effects are a major factor in treatment choice. Prescrire Int. 2011 May;20(116):128-33.

Puri BK, Counsell SJ et al. Eicosapentaenoic acid in treatment-resistant depression associated with symptom remission, structural brain changes and reduced neuronal phospholipid turnover. Int J Clin Pract. 2001 Oct;55(8):560–3.

Rabkin JG, McElhiney MC et al. Placebo-controlled trial of dehydroepiandrosterone (DHEA) for treatment of nonmajor depression in patients with HIV/AIDS. Am J Psychiatry. 2006 Jan;163(1):59–66.

Rossini M et al. Double-blind, multicenter trial comparing acetyl l-carnitine with placebo in the treatment of fibromyalgia patients. Clin Exp Rheumatol. 2007 Mar-Apr;25(2):182-8.

Rubinow DR, Schmidt PJ et al. Estrogen-serotonin interactions: Implications for affective regulation. Biol Psychiatry. 1998 Nov 1;44(9):839–50.

Rucker R et al. Potential physiological importance of pyrroloquinoline quinone. Altern Med Rev. 2009 Sep;14(3):268-77.

Ruusunen A et al. Coffee, tea and caffeine intake and the risk of severe depression in middle-aged Finnish men: the Kuopio Ischaemic Heart Disease Risk Factor Study. Public Health Nutr. 2010 Aug;13(8):1215-20. Epub 2010 Apr 1.

Sairanen M, Lucas G, et al. Brain-derived neurotrophic factor and antidepressant drugs have different but coordinated effects on neuronal turnover, proliferation and survival in the adult dentate gyrus. J Neurosci 2005;25:1089-94.

Sanchez-Villegas, A., Henriquez, P., Bes-Rastrollo, M., & Doreste, J. (2006). Mediterranean diet and depression. Public Health Nutrition, 9, 1104–1109.

Schmidt PJ, Daly RC et al. Dehydroepiandrosterone monotherapy in midlife-onset major and minor depression. Arch Gen Psychiatry. 2005 Feb;62(2):154–62.

Schneider C, Lovett E. Depression. In: Integrative Medicine. Rakel D (ed). Saunders Elsevier, Philadelphia, pp.78, 2007.

Schneider LS, Small GW et al. Estrogen replacement therapy and antidepressant response to sertraline in older depressed women. Am J Geriatr Psychiatry. 2001;9(4):393–9.

Schrader E. Equivalence of St John’s wort extract (Ze 117) and fluoxitine: a randomized controlled study in mild-moderate depression. Int Clin Psychopharmacol 2000:15:61-8.

Schutter DJ. [Transcranial magnetic stimulation as a treatment for depression]. Tijdschr Psychiatr. 2011;53(6):343-53.

Schweiger U, Deuschle M et al. Testosterone, gonadotropin, and cortisol secretion in male patients with major depression. Psychosom Med. 1999 May;61(3):292–6.

Serafty MA, Osborne D, et al. A randomized double-blind placebo-controlled trial of treatment as usual plus exogenous slow-release melatonin (6mg) or placebo for sleep disturbance and depressed mood. Int Clin Psychopharmacol 2010;25:132-42.

Shibasaki M et al. [Functional homology between alcohol dependence and mood disorder]. Nihon Arukoru Yakubutsu Igakkai Zasshi. 2011 Jun;46(3):337-46.

Shipowick CK, Moore CB, et al. Vitamin D and depressive symptoms in women during the winter: a pilot study. Appl Nurs Res 2009;22:221-5.

Shores MM, Kivlahan DR, et al. A randomized, double-blind, placebo-controlled study of testosterone treatment in hypogonadal older men with subthreshold depression (dysthymia or minor depression). J Clin Psychiatry 2009;70:1009-16.

Singh RB, Niaz MA et al. Randomized, double-blind, placebo-controlled trial of fish oil and mustard oil in patients with suspected acute myocardial infarction: The Indian experiment of infarct survival—4. Cardiovasc Drugs Ther. 1997 Jul;11(3):485–91.

Slutsky L et al. Enhancement of learning and memory by elevating brain magnesium. Neuron. 2010 Jan 28;65(2):165-77.

Stipcevic T et al. Platelet serotonin concentration and monoamine oxidase activity in hypothyroid patients. Horm Res. 2009;71(4):207-12. Epub 2009 Mar 4.

Ströhle A, Holsboer F. Stress responsive neurohormones in depression and anxiety. Pharmacopsychiatry. 2003 Nov;36 Suppl 3:S207-14.

Stuart MJ et al. Depression and type 2 diabetes: Inflammatory mechanisms of a psychoneuroendocrine co-morbidity. Neurosci Biobehav Rev. 2011 Oct 14. [Epub ahead of print]

Sun, Y., Lai, M., & Lu, C. (2005). Effectiveness of vitamin B12 on diabetic neuropathy: Systematic review of clinical controlled trials. Acta Neurologica Taiwanica, 14(2), 48–54.

Sundermann EE, Maki PM, Bishop JR.A review of estrogen receptor alpha gene (ESR1) polymorphisms, mood, and cognition. Menopause. 2010 Jul;17(4):874-86.

Sunnybrook Health Sciences Centre (SHSC). Adjunctive Curcumin for Symptomatic Adolescents With Bipolar Disorder: Brain and Body Considerations. In: [Internet]. Available at: Accessed 2/17/2014. NLM Identifier: NCT01928043.

Szegedi A, Kohnen R et al. Acute treatment of moderate to severe depression with Hypericum extract WE 5570 (St John’s wort): Randomized controlled double-blind non-inferiority trial versus paroxetine. BMJ 2005;330:503.

Tachaparian E et al. Identification of transcriptional networks responding to pyrroloquinoline quinone dietary supplementation and their influence on thioredoxin expression, and the JAK/STAT and MAPK pathways. Biochem J. 2010 Aug 1;429(3):515-26.

Tanskanen A, Hibbeln JR, Hintikka J, et al. Fish Consumption, Depression, and Suicidality in a General Population. Arch Gen Psychiatry. 2001;58(5):512-13.

Thom E. The effect of chlorogenic acid enriched coffee on glucose absorption in healthy volunteers and its effect on body mass when used long-term in overweight and obese people. J Int Med Res. 2007 Nov-Dec;35(6):900-8.

Tiemeier, H., Van Tuijl, H. R., Hofman, A., Kiliaan, A. J., & Breteler, M. M. B. (2003). Plasma fatty acid composition and depression are associated in the elderly: The Rotterdam study. American Journal of Clinical Nutrition, 78(1), 40–46.

Tolmunen, T., Hintikka, J., Ruusunen, A., Voutilainen, S., Tanskanen, A., Valkonen, V. P., et al. (2004). Dietary folate and the risk of depression in Finnish middle-aged men. A prospective follow-up study. Psychotherapy and Psychosomatics, 73, 334–339.

Tsao CW, Lin YS, et al. Cytokines and serotonin transporter in patients with major depression. Prog Neuropsychopharmacol Biol Psychiatry 2006;30:899-905.

Tunnicliffe JM et al. Chlorogenic acid differentially affects postprandial glucose and glucose-dependent insulinotropic polypeptide response in rats. Appl Physiol Nutr Metab. 2011 Oct;36(5):650-9. Epub 2011 Oct 6.

van Riel E, Meijer OC, Steenbergen PJ, et al. Chronic unpredictable stress causes attenuation of serotonin responses in cornu ammonis 1 pyramidal neurons. Neuroscience. 2003;120(3):649-58.

Vidailhet P. [Depressive recurrence: cognitive alterations and neuroplasticity]. Encephale. 2010 Dec;36 Suppl 5:S140-4.

Warner CH et al. Antidepressant Discontinuation Syndrome. Am Fam Physician. 2006 Aug 1;74(3):449-456.

Weisz JR et al. Cognitive-behavioral therapy versus usual clinical care for youth depression: an initial test of transportability to community clinics and clinicians. J Consult Clin Psychol. 2009 Jun;77(3):383-96.

Whittle N et al. Changes in brain protein expression are linked to magnesium restriction-induced depression-like behavior. Amino Acids. 2011 Apr;40(4):1231-48. Epub 2011 Feb 11.

Whiskey E, Taylor D. A review of the adverse effects and safety of noradrenergic antidepressants. Journal of psychopharmacology (Oxford, England). Aug 2013;27(8):732-739.

Willems FF et al. Pharmacokinetic study on the utilisation of 5-methyltetrahydrofolate and folic acid in patients with coronary artery disease. Br J Pharmacol. 2004 Mar;141(5):825-30. Epub 2004 Feb 9.

Williams AL, Katz D et al. Do essential fatty acids have a role in the treatment of depression? J Affect Disord. 2006 Jul;93(1-3):117-23. Epub 2006 May 2.

Wilson K, Mottram P. A comparison of side effects of selective serotonin reuptake inhibitors and tricyclic antidepressants in older depressed patients: A meta-analysis. Int J Geriatr Psychiatry. 2004 Aug;19(8):754–62.

Wolff LC et al. [Depression in HIV infection: prevalence, risk factors and management]. Rev Chilena Infectol. 2010 Feb;27(1):65-74. Epub 2010 Feb 3.

Wolkowitz OM et al. Leukocyte telomere length in major depression: correlations with chronicity, inflammation and oxidative stress--preliminary findings. PLoS One. 2011a Mar 23;6(3):e17837.

Wolkowitz OM, Reus VI, Mellon SH. Of sound mind and body: depression, disease, and accelerated aging. Dialogues Clin Neurosci 2011b;13:25-39.

Yang YK, Yeh TL, Yao WJ et al. Greater availability of dopamine transporters in patients with major depression a dual isotope SPECT study. Psychiatry Res. 2008 162 (15):230-5.

Yehuda S et al. Essential fatty acids and the brain:from infancy to aging. Neurobiology of Aging. 2005; 26 (Suppl 1), 98–102.

Zanardi R, Smeraldi E. A double-blind, randomised, controlled clinical trial of acetyl-L-carnitine vs. amisulpride in the treatment of dysthymia. Eur Neruopsychopharmacol 2006;16:281-7.

Zarrouf FA, Artz S, et al. Testosterone and depression: systematic review and meta-analysis. J Psychiatr Pract 2009;15:289-305.

Zhang JJ et al. Protective effect of pyrroloquinoline quinone against Abeta-induced neurotoxicity in human neuroblastoma SH-SY5Y cells. Neurosci Lett. 2009 Oct 30;464(3):165-9. Epub 2009 Aug 20.

Zhang L, Luo J, Zhang M, Yao W, Ma X, Yu SY. Effects of curcumin on chronic, unpredictable, mild, stress-induced depressive-like behaviour and structural plasticity in the lateral amygdala of rats. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP). Jan 9 2014:1-14.

Zhang LT et al. [Effect of chlorogenic acid on disordered glucose and lipid metabolism in db/db mice and its mechanism]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2011 Jun;33(3):281-6.

Zhang Y et al. Neuroprotection by pyrroloquinoline quinone (PQQ) in reversible middle cerebral artery occlusion in the adult rat. Brain Res. 2006 Jun 13;1094(1):200-6. Epub 2006 May 18.

Zhao X, Wang C, Zhang JF, Liu L, Liu AM, Ma Q, . . . Xu Y. Chronic curcumin treatment normalizes depression-like behaviors in mice with mononeuropathy: involvement of supraspinal serotonergic system and GABA receptor. Psychopharmacology. Dec 3 2013.

Zitzmann M. Testosterone and the brain. Aging Male. 2006 Dec;9(4):195-9.