Dietary Supplementations and Depression

Abstract

Depression is a mood disturbance condition that occurs for more than two weeks in a row, leading to suicide. Due to adverse effects of depression, antidepressants and adjunctive therapies, such as dietary supplementation, are used for treatment. Therefore, this review explored and summarized dietary supplements’ types, dosages, and effectiveness in preventing and treating depression. A literature search of the PubMed database was conducted in August 2021 to identify studies assessing depression, after which scale measurements based on dietary supplements were identified. From the obtained 221 studies, we selected 63 papers. Results showed PUFA (EPA and DHA combination), vitamin D, and probiotics as the most common supplementation used in clinical studies to reduce depressive symptoms. We also observed that although the total daily PUFA dosage that exhibited beneficial effects was in the range of 0.7–2 g EPA and 0.4–0.8 g DHA daily, with an administration period of three weeks to four months, positive vitamin D-based supplementation effects were observed after administering doses of 2000 IU/day or 50,000 IU/week between 8 weeks and 24 months. Alternatively, microbes from the genus Lactobacillus and Bifidobacterium in the probiotic group with a minimum dose of 10⁸ CFU in various dose forms effectively treated depression. Besides, a depression scale was helpful to assess the effect of an intervention on depression. Hence, PUFA, vitamin D, and probiotics were proposed as adjunctive therapies for depression treatment based on the results from this study.

Keywords:

• depression
• dietary supplementation
• clinical studies
• PUFA
• vitamin D
• probiotics

Introduction

Depression is a mood disturbance condition that lasts for more than two weeks in a row. As per the United States Department of Health and Human Services, the prevalence of depression is 8.7% in individuals aged between 18 and 25 years.¹ Approximately, 264 million people worldwide suffer from this disorder.² It is characterized by sadness, feelings of worthlessness or guilt, appetite changes, sleep problems, fatigue, loss of interest, aimless physical activities or slowed movements, thinking challenges, and worst of all, suicidal thoughts.³ Depression can also lead to reduced activities levels, hampering the ability to work and study. Suicide is the worst impact of depression, causing the deaths of; >700,000 people every year. Suicide is the fourth leading cause of death among 15–29-year-olds.⁴

Depression has several types, including depressive disorder (clinical depression), bipolar disorder (manic depression), persistent depressive disorder (dysthymia), and seasonal affective disorder (SAD).⁵ A potential cause of major depressive disorder (MDD) is an inflammatory reaction in the hippocampus.⁶ MDD can also occur due to bad life experiences. Child abuse, neglect, and loss increase the risk of MDD in adulthood.⁷ The exact cause of bipolar disorder (manic depression) is unknown, but several factors may contribute such as biological differences and genetics. Biological differences include circadian dysregulation of mood disorders, Circadian Locomotor Output Cycles Kaput (CLOCK) protein and Brain and Muscle ARNT-like Protein 1 (BMAL1), and pharmacological triggers like tricyclic antidepressants (TCAs).⁸ The existence of complex interactions between neurotransmitters and receptors that affect the brain’s chemical moods play a role in persistent depressive disorder. Neurotransmitters that affect mood include dopamine, epinephrine, norepinephrine, GABA, and glutamate,⁹ which are the neurotransmitters in question. The exact cause of SAD is unclear, but it may be due to chemical changes in the brain attributable to inadequate sunlight and shorter days. Additionally, melatonin may also be associated with SAD.¹⁰

Depression can be treated with antidepressants that are categorized into five groups, including tricyclic antidepressants (TCAs), selective serotonin reuptake inhibitors (SSRIs), monoamine oxidase inhibitors (MAOIs), serotonin-norepinephrine reuptake inhibitors, and non-TCA antidepressants.¹¹ These treatments are effective;^12,13 however, meta-analytical studies have found low remission rates,¹⁴ and antidepressants and placebo drugs only provide clinically significant differences in patients with upper-end severe depression. The reason for the skepticism with regard to the prescription of antidepressant drugs is their addictive effect. A study revealed that female patients and patients from ethnic minorities often choose complementary and alternative medicine (CAM) as the first step in treating depression.¹⁴ This skepticism refers to the trend of using CAM. One type of CAM approach includes natural products like dietary supplements (vitamins, minerals, and probiotics).¹⁵

Dietary supplements are orally consumed products, such as vitamins, herbs, minerals, amino acids, enzymes, metabolites, probiotics, and other substances for supplementing typical diets.¹⁶ Several dietary supplements have also been commonly used for reducing depression symptoms. For example, Kazemi et al¹⁷ explained that dietary supplementation, such as prebiotic use, significantly decreased the Beck Depression Inventory (BDI) scores compared with the placebo group, after eight weeks of intervention. Other dietary supplementations, such as polyunsaturated fatty acid (PUFA), vitamin D,¹⁸ B12,¹⁹ magnesium, zinc,²⁰ and curcumin,²¹ have also been studied for their efficacy and effects as add-on supplements for depression treatment. In a review conducted by Hoffman et al,¹⁸ vitamin D and PUFA supplementation had complementarily positive effects on depressive symptoms, anxiety, and pain. Therefore, this review explored and summarized clinical study updates on dietary supplements’ types, dosages, and effectiveness to reduce symptoms of depression.

Methods

Search Strategy and Selection Criteria

The search of the PubMed database was conducted in August 2021, using the terms “(dietary supplementation) AND (depression)” on the advanced query box. Afterward, some criteria were put in place to choose relevant articles, including only articles published in English, article types reporting clinical studies or randomized controlled trials, and those with a maximum publication date of 10 years.

The Review Process

Extracted article references were manually searched and screened for relevance. Then, we collected the following information: country of study, type of supplementation, the dosage used, the scale of depression, and results.

Clinical Studies on Dietary Supplementations for Treating Depression

Although we finally identified 221 article records from the advanced search data, 137 articles were excluded because the studies did not focus on depression or the journal had incomplete titles and abstracts. Likewise, 21 articles were excluded due to ineligibility (Figure 1). Therefore, we included 63 articles and further grouped these studies into five broad groups based on the number of supplements used in the research. The five groups were PUFA, vitamin D, probiotics, a combination of vitamins and nutrients, and other supplements.

Figure 1 Literature search results.

Table 1 summarizes the study characteristics of the 63 selected articles. We observed that the most common supplementation used was that of the PUFA group and its combination (n = 17, 26.9%), followed by vitamin D (n = 15, 23.8%), probiotics (n = 8, 12.7%), then combination of vitamins and nutrients (n = 6, 9.5%). Furthermore, most clinical studies were conducted in Iran (41.3%), with adult participants aged above 18 (98.4%). From all studies, the most commonly used scale was the BDI and its respective version (47.6%).

Table 1 Study Characteristics

Characteristics/Country of Study	Number of Studies (%)
Iran	26 (41.3)
Australia	6 (9.5)
America	5 (7.9)
Netherlands	5 (7.9)
France	3 (4.8)
China	3 (4.8)
Brazil	2 (3.2)
Japan	2 (3.2)
Denmark	1 (1.6)
Nigeria	1 (1.6)
Norway	1 (1.6)
Italy	1 (1.6)
Taiwan	1 (1.6)
Korea	1 (1.6)
Austria	1 (1.6)
Ghana	1 (1.6)
Sweden	1 (1.6)
Poland	1 (1.6)
Spain	1 (1.6)
Vietnam	1 (1.6)
Age of Subject Studied
<18 years old	1 (1.6)
≥18 years old	62 (98.4)
The type of Supplementation Studied
PUFA	17 (26.9)
Vitamin D	15 (23.8)
Probiotic	8 (12.7)
Combination of vitamins and nutrients	6 (9.5)
Vitamin B	4 (6.3)
Vitamin E	3 (4.8)
Zinc	2 (3.2)
Curcumin	2 (3.2)
Nanocurcumin	1 (1.6)
Vitamin A	1 (1.6)
Vitamin C	1 (1.6)
ALA (Alpha-lipoic acid)	1 (1.6)
Ferrous sulfate	1 (1.6)
Magnesium oxide	1 (1.6)
Melatonin	1 (1.6)
Myo-inositol	1 (1.6)
Sumac (Rhus coriaria L)	1 (1.6)
Zinc sulfate	1 (1.6)
Caffeine	1 (1.6)
Carnitine	1 (1.6)
Coenzyme Q10	1 (1.6)
Scale of Depression
Beck Depression Inventory (BDI, BDI-II)	30 (47.6)
Hamilton Depression Rating Scale (HDRS, HDRS-17)	9 (14.3)
Geriatric Depression Scale (GDS, GDS-15)	7 (11.1)
Depression Anxiety Stress Scale (DASS, DASS-21	6 (9.5)
Personal Health Questionnaire (PHQ-8, PHQ-9)	5 (7.9)
Edinburgh Postnatal Depression Scale (EPDS)	5 (7.9)
Center for Epidemiologic Studies Depression (CES-D)	4 (6.3)
Hospital Anxiety and Depression Scale (HADS)	3 (4.8)
Montgomery-Asberg Depression Rating Scale (MADRS)	3 (4.8)
Global Seasonality Score (GSS)	1 (1.6)
Children’s Depression Rating Scale (CDRS)	1 (1.6)
Child PTSD Symptom Scale (CPSS)	1 (1.6)
Profile of Mood State (PMOS)	1 (1.6)
State-Trait Personality Inventory (STPI)	1 (1.6)

The Polyunsaturated Fatty Acid (PUFA) Group

This review found that the most commonly used supplementation in treating depression was the PUFA group, which was a combination of Docosahexaenoic acid (DHA) and Eicosapentaenoic acid (EPA). Table 2 shows that from the twelve clinical studies that used PUFA supplementation for depression, eight studies showed positive effects in improving depression symptoms and reducing the scale of depression. However, the other four had no significant impact on the scale of depression, meaning that most of the studies agreed that PUFA was beneficial as a treatment for depression.

Table 2 Effects of Using PUFA Supplements for Treating Depression

Author	Year	Country	Dosage	Duration	Scale of Depression	Result
Nishi et al^Citation23	2019	Japan and Taiwan	134 mg EPA + 67.7 mg DHA (9 times daily)	12 weeks	HDRS, EPDS, and BDI-II	Had beneficial effects, decreased overall score by 59.5%
Ravi et al^Citation27	2016	Iran	1 capsule = 360 mg EPA + 240 mg DHA (twice daily)	8 weeks	BDI-II, HADS, and PHQ-9	Had beneficial effects, decreased overall score by 47.86%
Gharekhani et al^Citation85	2014	Iran	180 mg EPA + 120 mg DHA (6 times daily)	16 weeks	BDI	Had beneficial effects, decreased BDI score by 42.86%
McNamara et al^Citation22	2016	America	Group 1: 1.6 g EPA + 0.8 g DHA (4 capsules/day) Group 2: 10.8 g EPA + 5.4 g DHA (2 tbsp/day)	10 weeks	CDRS	Had beneficial effects, decreased CDRS score by 40%
Keshavarz et al^Citation86	2018	Iran	1 capsule contains 180 mg EPA + 120 mg DHA (6 capsule/day)	12 weeks	BDI	Had beneficial effects, decreased BDI score by 32.48%
Rizzo et al^Citation87	2012	Italy	2.5 g (with EPA:DHA 2:1) per day	8 weeks	GDS	Had beneficial effects, decreased GDS score by 32.16%
Jiang et al^Citation88	2018	America	Group 1: 400 mg EPA + 200 mg DHA Group 2: 500 mg EPA (4 times daily)	12 weeks	HDRS and BDI-II	Had beneficial effects, decreased overall score by 28.35%
Ginty et al^Citation29	2015	America	1000 mg EPA + 400 mg DHA per day	21 days	BDI	Had beneficial effects, 67% of the subject no longer met criteria of depression
Vaz et al^Citation89	2017	Brazil	1.08 g EPA + 0.72 g DHA per day	16 weeks	EPDS	No significant effect
Antypa et al^Citation90	2012	Netherlands	1.74 g EPA + 0.25g DHA per day	4 weeks	BDI-II	No significant effect
Maltais et al^Citation91	2019	France	400 mg DHA + 112.5 mg EPA, twice a day	3 years	GDS	No significant effect
Park et al^Citation26	2015	Korea	1140 mg EPA + 600 mg DHA (3 times daily)	12 weeks	CES-D and HDRS	No significant effect

Abbreviations: BDI, beck depression inventory; EPDS, Edinburgh postnatal depression scale; HDRS, Hamilton depression rating scale; GDS, geriatric depression scale; CES-D, center for epidemiologic studies depression; HADS, hospital anxiety and depression scale; PHQ, personal health questionnaire depression scale; CDRS, children’s depression rating scale.

From the eight studies that showed PUFA’s beneficial effects on depression, we observed that the range of the total daily dosage of the EPA ranged from 0.7 g to 2 g and DHA was from 0.4 g to 0.8 g. Moreover, the frequency of PUFA supplement intake varied from one to nine times daily, within a 3-week to 4-month administration period. Most studies showed beneficial effects in a total daily dose of PUFA supplementation and a total daily dose of 180 mg of EPA and 120 mg of DHA, with an intake frequency of six times daily. However, the studies with no significant impact used a higher dosage with higher study durations of up to three years. However, we identified one study by McNamara et al²² that stated that PUFA had a beneficial effect on depression, with a total daily dosage that was higher than the other studies, more specifically, at 16.2 grams daily (10.8-g EPA + 5.4 g DHA, divided to 2 tablespoons/day). This dosing was based on a previous study that reported supplementation’s efficacy and safety data in patients with attention deficit hyperactivity disorder. Moreover, only one study of the eight,²³ wherein the subjects were pregnant women at various stages of pregnancy, also showed beneficial effects of PUFA’s supplementation on pregnancy depression. A review conducted by Hsu et al²⁴ also supported this result, which explained that in addition to preventing pregnancy-related depression, sufficient consumption of omega-3 fatty acid supplements such as EPA during pregnancy was important, because they served as the critical building blocks of the fetal brain and retina. They also determine the pregnancy length.

Omega-3 fatty acids are substrates that affect the formation of neurotransmitters and prostaglandins. Therefore, they have extensively functions with regard to the maintenance and regulation of a healthy brain. Furthermore, it has been reported that depression rates can increase with lower levels of membrane-related omega-3 fatty acids.²⁵ The main pathway target of omega-3, which is also linked to the inflammatory hypothesis of depression,²⁶ is the arachidonic acid inflammatory pathway.²⁷ Two possible pathways exist in the reduced synthesis of eicosanoids from arachidonic acid by DHA and EPA, as explained by Wani et al.²⁵ First, they combine with arachidonic acid for amalgamation into membrane-based phospholipids, thereby reducing both cellular and plasma concentrations of arachidonic acid. DHA and EPA, which hinder the release of pro-inflammatory cytokines (interferon-γ, tumor necrosis factor [TNF]-α, interleukin [IL]-1β, IL-2, and IL-6), are determined by the eicosanoid discharge. The other possible way is that of the cyclooxygenase enzyme system. Here, EPA can compete with arachidonic acid to block the pro-inflammatory eicosanoid synthesis from arachidonic acid, prostaglandin E2, and thromboxanes B2²⁵ by inhibiting the action of phospholipase A2, as shown in Figure 2.²⁶ Additionally, Lotrich et al²⁸ reported that the elevated ratio of arachidonic acid to omega-3 fatty acid was linked to depression. The observation from other intervention studies also indicated that administering omega-3 fatty acids can decrease this ratio and improve depressive symptoms.

Figure 2 The proposed mechanism of EPA in inhibiting phospholipase A2 and preventing depression.

Additionally, in the pathophysiology of depression, the upregulation of 5-HT2A/C receptors is proposed to play a significant role. From the previous study, it was observed that for an individual with chronic stage omega-3 fatty acid deficiencies, changes in the concentration of brain fatty acids can result in an altered serotonergic or dopaminergic neurotransmission, increase in 5-HT2,²⁷ and decrease in serotonin and dopamine in the prefrontal cortex,²⁹ thereby indicating the importance of adequate PUFA intake. A few studies we obtained also investigated the efficacy of PUFA combined with other dietary supplements, such as 5-aminolevulinic acid (ALA), curcumin, vitamin E, and vitamin B on depression (Table 3). From the five studies obtained, the overall result was that those combinations showed no significant effect. From these studies, only one study showed beneficial supplement effects on depression, which was the combination of PUFA and vitamin E.³⁰ The study used 1000-mg PUFA with 400 IU vitamin E daily for twelve weeks, with the subjects being women with polycystic ovary syndrome (PCOS). Jamilian et al stated that compared to a single supplementation, combining supplements gave better and more significant treatment results, including improved mental health parameters. Alternatively, the other four studies obtained showed statistically non-significant results with the use of PUFA combined with other supplements in treating depression, thereby proposing that PUFA use during depression conditions was preferred without any supplement combination.

Table 3 Effects of Combined PUFA Supplementations for Treating Depression

Author	Year	Country	Combination	Dosage	Duration	Scale of Depression	Result
Jamilian M et al^Citation30	2018	Iran	PUFA and vitamin E	1000-mg of PUFA + 400 IU vitamin E per day	12 weeks	BDI	Had beneficial effects decreased BDI score by 13.33%
Giltay et al^Citation92	2011	America	PUFA and ALA	400 mg EPA-DHA/day, 2 g ALA/day, or both combination EPA-DHA and ALA	40 months	GDS	No significant effect
Kuszewski et al^Citation93	2020	Australia	PUFA and Curcumin	400 mg EPA + 2000 mg DHA/day + 160 mg curcumin/day	16 weeks	PMOS	No significant effect
Meyer et al^Citation94	2013	Australia	PUFA and vitamin E	2 g DHA + 0.6 g EPA + 10 mg vitamin E (8 x 1 g capsules per day)	16 weeks	HDRS	No significant effect
Andreeva et al^Citation95	2012	France	PUFA and vitamin B	Vitamin B [5-methyl-tetrahydrofolate (0.56 mg) and vitamins B-6 (3 mg) and B-12 (0.02 mg)] + PUFAs [600 mg EPA and DHA in a 2:1 ratio] in 2 capsules per day	5 years	GDS	No significant effect

Abbreviations: GDS, geriatric depression scale; PMOS, profile of mood states; BDI, beck depression inventory; HDRS, Hamilton depression rating scale.

Vitamin D

Table 4 shows that nine of the 15 vitamin D studies reported beneficial effects on improving depression symptoms. These studies showed that vitamin D supplementation at 2000 IU/day–50,000 IU/week for eight weeks (two months) to 24 months of supplementation positively affected depression. However, although the exact dosage was used in one study, no significant impact on depression was observed since the study included a dialysis patients. Furthermore, the duration of the study was from eight weeks (2 months) to 24 months of supplementation before a positive result. Two studies were also observed in addition to a single supplementation, which combined vitamin D supplementation with probiotics³¹ and zinc.³² The findings of both studies showed that the combined supplementation had positive effects on depression. Therefore, since probiotics and zinc influence depression, its proposed action mechanism is discussed below. Notably, seven of 15 findings mentioned that vitamin D supplementation had no significant effect on depression, which was attributed to the low intervention impact, compared to efficient treatment standards like antidepressants.³³

Table 4 Effects of Vitamin D Supplementation on Depression

Author	Year	Country	Dosage	Duration	Scale of Depression	Result
Sepehrmanesh Z et al^Citation96	2016	Iran	50 kIU/week	8 weeks	BDI	Had beneficial effects, decreased score by 31.75%
Vaziri F et al^Citation97	2016	Iran	2000 IU/day	±15 weeks	EPDS	Had beneficial effects, decreased score by 50.36%
Kjærgaard M et al^Citation98	2012	Norway	20,000 IU/week	6 months	1. BDI-II 2. HADS 3. MADRS 4. GSS	Had beneficial effects, decreased score by 25%
Zheng S et al^Citation99	2018	Australia	50,000 IU/month	24 months	PHQ-9	Had beneficial effects, decreased score by 14.71%
Sharifi A et al^Citation100	2018	Iran	300,000 IU (injection one time)	3 months	BDI	Had beneficial effects, decreased score by 33.59%
Omidian M et al^Citation101	2019	Iran	4000 IU/day	12 weeks	BDI-II	Had beneficial effects, decreased score by 35.53%
Raygan F et al^Citation31	2018	Iran	Every two weeks: Vit. D: 50,000 IU + Probiotic: 8×10^9 CFU/g	12 weeks	BDI	Had beneficial effects, decreased score by 12.07%
Yosaee S et al^Citation32	2019	Iran	Group: 1. 2000 IU/day Vit. D + daily zinc placebo 2. 30 mg zinc gluconate/day + placebo Vit.D/day 3. Vit. D 2000 IU/day + 30 mg/day zinc gluconate 4. Identical matching placebos for vitamin D and zinc	12 weeks	BDI-II	Had beneficial effects. Change in BDI-II: a) Zinc: −7.02 b) Vitamin D: −3.87 c) Zinc+Vitamin D: −7.62
Alavi NM et al^Citation102	2018	Nigeria	● 50,000 IU/week	8 weeks	GDS-15	Had beneficial effects, decreased score by 19.14%
Hansen JP et al^Citation103	2019	Denmark	● 2800 IU/day	12 weeks	HDRS17	No significant effect
Okereke OI et al^Citation104	2020	America	● 2000 IU/day	5.3 years	PHQ-8	No significant effect
De Koning EJ et al^Citation105	2019	Netherlands	● 1200 IU/day	12 months	CES-D	No significant effect
Rolf L et al^Citation106	2017	Netherlands	● 7000 IU/day (first four weeks) ● 14,000 IU/day (up to 48 weeks)	48 weeks	HADS	No significant effect
Mousa A et al^Citation107	2017	Australia	● 100,000 IU followed by 4,000 IU daily	16 weeks	BDI	No significant effect
Wang Y et al^Citation108	2016	China	● 50,000 IU/week	52 weeks	BDI-II	No significant effect

Abbreviations: HDRS, Hamilton depression rating scale; PHQ, personal health questionnaire depression scale; CES-D, center for epidemiologic studies depression; HADS, hospital anxiety and depression scale; GDS, geriatric depression scale; BDI, beck depression inventory; EPDS, Edinburgh postnatal depression scale; HADS, hospital anxiety and depression scale; MADRS, Montgomery-asberg depression rating scale; GSS, global seasonality score.

The potential function of vitamin D is to regulate calcium-phosphate homeostasis.³⁴ Its mechanism is through the vitamin D receptor, which affects most physiological systems, including the brain.³⁵ Some studies have mentioned that lower serum levels of 25(OH) D3 were associated with depression.³⁶ Furthermore, depression results from some pathways, including chronic inflammation, formation of serotonin, expression of mitochondrial proteins, Ca²⁺ homeostasis, and antioxidant gene expression,³⁷ which are indirectly related to vitamin D. Chronic inflammation accounts for depression in the presence of inflammatory cytokine expression, which can be reduced with vitamin D supplementation.^38–40

The lack of vitamin D in the serum can also lead to depression through mitochondrial function and serotonin formation pathways. In the serotonin formation pathway, vitamin D fails to induce the serotonin-synthesized gene of tryptophan hydroxylase 2 (TPH-2) while repressing the expression of TPH-1.⁴¹ Its consequence is a decline in plasma tryptophan levels; tryptophan cannot be transferred into the brain. This inhibition results in low serotonin levels in the brain, causing depression.⁴² Additionally, mitochondrial function will be impaired in the presence of low serum vitamin D levels,⁴³ resulting in elevated reactive oxygen species (ROS) and reduced ATP formation, impacting Ca²⁺ and antioxidant gene (GSH) homeostasis. Significant antioxidants in neurons are GSH or glutathione. They are depleted when ROS is high,⁴⁴ resulting in depression. Both the elevation of ROS and glutamate, which leads to higher Ca²⁺ levels, causes a decline in the number and size of GABAergic neurons. This decline accounts for the imbalance in excitatory and inhibitory neurons that leads to depression.³⁷ Studies showed that vitamin D supplementation normalized vitamin D levels in the serum to prevent depression. Figure 3 depicts the proposed vitamin D pathway to prevent depression. Toxic doses of vitamin D are been considered to be >50 × 10³ IU/day⁴⁵ and are detailed in Table 5.

Table 5 Dietary Supplementation Permissible Levels

Dietary Supplementation	Description
Vitamin D	>50,000 IU/day (Toxic level of Vitamin D)^Citation45
PUFA: Omega-3 fatty acids, mainly the combination of Docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA)	Daily intake of EPA and DHA higher than 2 g is not recommended^Citation121
Caffeine	Recommended daily intake is low dose 60 mg/day but Not recommended at high dose intake (>120 mg)^Citation116
Carnitine	Recommended daily intake around 250 mg–2000 mg per day^Citation60
Coenzyme Q10 (CoQ10)	Recommended doses from previous study around 150–1200 mg per day^Citation61,Citation122
Nanocurcumin	Recommended doses from previous study is 80 mg per day^Citation62,Citation65
Curcumin	Recommended dose based previous clinical trials is around 250–1000 mg/day^Citation62
Magnesium oxide	Recommended dose from previous study was around 125–500 mg/day^Citation68
Melatonin	Recommended doses based previous study around 5–10 mg/day^Citation117
Myo-inositol	Recommended doses from previous study around 2 gram per day^Citation60
Sumac (Rhus coriaria L)	Recommended doses from previous study around 1000–3000 gram per day^Citation73
Vitamin A (retinyl palmitate)	Tolerable Upper Intake Level (UL) for Vitamin A is 3000 μg per day for >18 years^Citation123
Vitamin B12	No tolerable upper intake level have been determined. Recommended Dietary Allowances 2.4 μg per day for >18 years^Citation123
Folic acid	Tolerable upper intake level for folic acid was at 1000 μg per day^Citation124
Zinc	Recommended Dietary Intake around 8–12 mg per day. Tolerable Upper Intake Level (UL) for Zinc is 40 mg per day for >18 years^Citation123
Vitamin C and Vitamin E	Tolerable Upper Intake Level (UL) for Vitamin C is 2000 mg/day for >18 years and 1000 mg Vitamin E per day for >18 years^Citation123
Iron	Tolerable Upper Intake Level (UL) for Iron is 45 mg/day^Citation125

Figure 3 The proposed vitamin D pathway to prevent depression.

Probiotics

Other supplementations studied for reducing depression are probiotics. Probiotics are live microorganisms that can improve gut health. Lately, they have been used to manage and treat various diseases, one of which is depression.⁴⁶ Table 6 shows eight studies reporting the usage of probiotic supplementation in depression. While five of these studies showed beneficial effects on depression symptoms and measured improvements using a depression scale, the other three showed no significant impact on depression.

Table 6 Effects of Probiotic Supplementation for Treating Depression

Author	Year	Country	Species, Dosage	Duration	Scale of Depression	Result
Moludi et al^Citation109	2019	Iran	L. rhamnosus 1.6×10^9 CFU per capsule per day	12 weeks	BDI	Had beneficial effects, decreased BDI score by 28.36%
Inoue et al^Citation110	2018	Japan	Various Bifidobacteria species, each 1.25×10^10 CFU per sachet per day	12 weeks	PHQ-9	Had beneficial effects, decreased PHQ-9 score by 26.92%
Mohammadi et al^Citation111	2016	Iran	Group 1 100 g/day probiotic yogurt with L. acidophilus and B. lactis 1×10^7 CFU + one placebo capsule Group 2 100 g/day conventional yogurt with S. thermophilus and L. bulgaricus + one probiotic capsule Group 3 100 g/day conventional yogurt + one placebo capsule The probiotic capsule contained Lactobacillus casei 3 × 10^3, L. acidophilus 3 × 10^7, L. rhamnosus 7 × 10^9, L. bulgaricus 5 × 10^8, Bifidobacterium breve 2 × 10^10, B. longum 1 × 10^9, S. thermophilus 3×10^8 CFU/g	6 weeks	DASS	Had beneficial effects with DASS score decreased by 8.83 for overall intervention group.
Kouchaki et al^Citation112	2017	Iran	One capsule containing Lactobacillus acidophilus, Lactobacillus casei, Bifidobacterium bifidum, and Lactobacillus fermentum each 2×10^9 CFU/g per day	12 weeks	BDI	Had beneficial effects with BDI score decreased by 5.5±0.8
Akkasheh et al^Citation113	2016	Iran	One capsule daily containing Lactobacillus acidophilus (2×10^9 CFU/g) Lactobacillus casei (2×10^9 CFU/g) Bifidobacterium bifidum (2×10^9 CFU/g)	8 weeks	BDI	Had beneficial effects with BDI score decreased by 5.3±1.2
Louzada et al^Citation49	2020	Brazil	L. paracasei 10^9–10^8 CFU + L. rhamnosus 10^9–10^8 CFU + L. acidophilus 10^9–10^8 CFU + B. lactis 10^9–10^8 CFU consumed orally twice a day	24 weeks	GDS-15	No significant effect
Kazemi et al^Citation17	2018	Iran	Probiotic Groups: Lactobacillus helveticus and Bifidobacterium longum Prebiotic: Galactooligosaccharide Dosage: ⩾10 × 10^9 CFU per 5 g sachet consumed orally per day	8 weeks	BDI	No significant effect
Reininghaus et al^Citation114	2020	Austria	Probiotic oral supplement that contains nine bacterial strains at least 7.5 billion organisms per 1 sachet (3g). Also contains 125 mg vitamin B7 + 30 mg horsetail + 30 mg fish collagen + 30 mg keratin, consumed once daily.	4 weeks	HDRS and BDI-II	No significant effect

Abbreviations: BDI, beck depression inventory; PHQ, personal health questionnaire depression scale; HDRS, Hamilton depression rating scale; DASS, depression anxiety stress scales; GDS, geriatric depression scale.

The microbe species included in the studies with positive results comprised various bacteria from the genus Lactobacillus (L. acidophilus, L. casei, L. fermentum, L.rhamnosus, and L. bulgaricus) and the genus Bifidobacterium (Bifidobacterium bifidum and Bifidobacterium lactis) with various dosage ranges above 10⁸ CFU in the form of yogurt, capsules, and sachets. The positive effect of using probiotic supplementations in depression was also supported by a meta-analysis conducted by Chao et al.⁴⁷ The study explained that probiotics were adjunct therapies that can improve depressive symptoms in patients diagnosed with depression. Yong et al⁴⁸ explained another advantage of probiotics as an antidepressive treatment. According to his study, although probiotics are primarily safe to be consumed and socially help patients, they are proposed not to receive the negative stigma associated with standard antidepressants.

In studies with negative results, Louzada et al⁴⁹ explained that compared to previous studies wherein probiotics simultaneously had significant effects on depression parameter scores, the negative outcome could be attributed to the characteristics of participants included in their research, which are proposed to not have been clinically diagnosed as depressed. Moreover, other uncontrolled events could have interfered with the study result.⁴⁹ It was also explained by Kazemi et al¹⁷ that probiotics were only beneficial when used as an additive to regular antidepressants as compared to probiotics that were used as primary therapy for depression.¹⁷

Although an in-depth mechanism explaining probiotics’ effect on depression is not fully understood yet,⁴⁶ a possible pathway is connected to the microbiota–gut–brain (MGB) axis in the pathophysiology of depression. The MGB axis allows two-way communication between the gut microbiota and the human brain. Depression is therefore developed when the MGB axis becomes maladaptive, adversely affecting the host physiology, which eventually leads to depression. Hence, probiotics also help alleviate depression by modulating the MGB axis. Nevertheless, a few challenges have been observed in explaining the complete mechanism that contributes to the effectiveness of probiotics in depression, including the heterogeneity of depression and the gut microbiota’s complexity.⁴⁸ However, despite these challenges and the unclear mechanism, increasing evidence supports that probiotics are an excellent alternative for depression treatment, compared to standard antidepressants.

The Combination of Vitamins and Nutrients

Table 7 shows six studies reporting a combination of vitamin and nutrient supplementation in depression. We observed that four studies conducted by Nguyen,⁵⁰ Berens,⁵¹ Oliver-Baxter,⁵² and Harris⁵³ revealed beneficial effects of these classes on depression. Nguyen et al⁵⁰ reported that the intervention of multiple micronutrient and iron-folic acid groups had a significant impact on lowering depression scores during the first and second trimesters of pregnancy compared to folic acid alone (P < 0.05) among women in the highest tertile for CES-D scores. Multiple micronutrients, such as vitamin B12, vitamin D, folates, zinc, and selenium, have been recommended for preventing maternal depression.

Table 7 Effects of Combining Vitamins and Nutrient Supplementation as Depression Treatments

Author	Year	Country	Supplementation	Dosage	Duration	Scale of Depression	Result
Nguyen et al^Citation50	2017	Vietnam	Pre-pregnancy: 1. Multiple micronutrients 2. Iron and folic acid 3. Folic acid During pregnancy: iron+ folic acid	Pre-Pregnancy Group: Group 1: 2800 μg folic acid Group 2: 2800 μg folic acid + 60 mg iron Group 3: 15 micronutrients including 2800 μg folic acid + 60 mg iron During Pregnancy: 60 mg iron + 400 μcg folic acid	Pre-pregnancy: weekly until conception During pregnancy: daily until delivery	Preconception: CES-D During Pregnancy and 3 Months Postpartum: EPDS	Had beneficial effects, decreased EPDS score during first and second trisemester in group 1 and 2 compare to group 3 (p<0.05)
Berens et al^Citation51	2018	Sweden	Nutritional supplementation	119mL nutritional supplementation (150 kcal 20 g whey protein 800 IU vitamin D Combination of vitamins and minerals) daily	6 months	CES-D	Had beneficial effects, decreased CES-D score by 26.80%
Oliver-Baxter et al^Citation52	2018	Australia	Supplements containing 12 vitamins, minerals, and herbs	1 tablet/day	8 weeks	STPI	Had beneficial effects, decreased STPI score by 16.66%
Harris et al^Citation53	2011	Australia	Supplements containing 53 vitamins, minerals, antioxidants, and herbs	One tablet after meal	8 weeks	DASS	Had beneficial effects, decreased DASS score by 50%
Bot et al^Citation115	2019	Netherlands	PUFA, selenium, folic acid, vitamin D3 coupled with calcium	1412 mg PUFA, 30 μg selenium, 400 μg of folic acid, 20 μg of vitamin D3 coupled with 100-mg calcium (2 pills/day)	1 year	PHQ-9	No significant effect
Okronipa et al^Citation56	2018	Ghana	1. Iron 2. Folic acid 3. Calcium 4. Multiple micronutrient capsule (MMN) 5. SQ-LNS supplement (contained similar as the MMN capsule, plus other four minerals (Ca, P, K, Mg) and essential fatty acids	Group 1: 60 mg iron and 400 μg folic acid capsule daily during pregnancy with calcium (Ca) for the first six months postpartum Group 2: Multiple micronutrient capsules (18 vitamins and 20 mg iron daily) daily during pregnancy and the first six months postpartum Group 3: 20 g SQ-LNS during pregnancy and the first six months postpartum	6 months postpartum	EPDS	No significant effect

Abbreviations: PHQ, personal health questionnaire depression scale; EPDS, Edinburgh postnatal depression scale; CES-D, center for epidemiologic studies depression; STPI, state-trait personality inventory; DASS, depression anxiety stress scales.

Oliver-Baxter⁵² also reported that the consumption of supplements containing 12 vitamins, minerals, and herbs within eight weeks to have significant results in decreasing depression scores and all pro-inflammatory cytokines levels related to depression, such as IL-1β, IL-5, IL-6, TNF-α, and TNF-β. Significant changes in IL-1, TNF-α, and TNF-β caused supplement effects on TNF-related cytokines that modulated fundamental cellular processes, such as inflammation. Withania somnifera, one of the active ingredients, has shown effects on proinflammatory cytokines that interfere with hypothalamic-pituitary-gonadal axis down-regulation of local inflammatory.⁵² When the hypothalamic-pituitary-adrenal axis is repeatedly activated, interrelated systems produce by-products to compensate for failure in other systems, such as decreased lymphocytes and increased pro-inflammatory activities that resulted in inflammation.⁵⁴ Previous studies have shown that depression is highly associated with increased inflammatory marker levels, such as IL-1 and IL-6.⁵²

Several ingredients in multivitamin supplements can potentially improve symptoms of depression, such as folate, vitamin C, vitamin D, and herbal ingredients (Ginseng and Ginkgo biloba), by oxidative-stress reduction and mood enhancement. Zinc, vitamin D, and α-tocopherol have antioxidant and anti-inflammatory activities linked to the mechanism of increased telomere length of leukocyte DNA.⁵⁵

The findings of another study indicated that a small quantity of lipid-based nutrient supplement (SQ-LNS) containing vitamin, mineral, and essential fatty acids did not affect maternal postpartum depression (PDD),⁵⁶ which was proposed to be a result of the dosage of essential fatty acids (alpha-linolenic acid [ALA] and linoleic acid) in SQ-LNS formulation was insufficient to treat depression.⁵⁶ Results from this study are in concurrence with a meta-analysis study where EPA/DHA supplements with substantially greater dosages (>60%) of high dose EPA (0.2–2.2 gram/day) were found to offer more significant results in treating depression than supplements with a lower dosage (<60%).⁵⁷

Other Supplementations

Table 8 shows other supplementations that significantly reduced depression scores, such as carnitine, coenzyme Q10, nanocurcumin, curcumin, magnesium oxide, melatonin, myo-inositol, sumac (Rhus coriaria L.), vitamin A, vitamin B, folic acid, zinc, and zinc sulfate. However, other supplementations, such as vitamin E, C, and ferrous sulfate, did not offer a significant reduction in the depression score in this study due to many factors, such as the short trial duration, limited sample size in each group, low effective doses, and inadequate measurement at the start and end of the trial.^58,59

Table 8 Effects of Other Supplements in Treating Depression

Author	Year	Country	Supplementation	Dosage	Duration	Scale of Depression	Result
Liu et al^Citation116	2017	China	Caffeine	Group 1: 60 mg caffeine daily Group 2: 120 mg caffeine daily	4 weeks	HDRS-17 and MADRS	Had beneficial effects, 60 mg caffeine decreased HDRS-17 score by 25.2% and MADRS score by 20.61%, 120 mg caffeine did not result any beneficial effects
Jamilian et al^Citation60	2017	Iran	Carnitine	250 mg/day	12 weeks	BDI and DASS	Had beneficial effects, decreased BDI score by 19.85% and DASS score by 9.27%
Sanoobar et al^Citation61	2015	Iran	Coenzyme Q10 (CoQ10)	500mg/day	12 weeks	BDI	Had beneficial effects, decreased BDI score by 28.18%
Asadi et al^Citation62	2020	Iran	Nanocurcumin	One capsule of nanocurcumin, 80 mg daily	8 weeks	DASS-21	Had beneficial effects, decreased DASS-21 score by 8.38%
Yu et al^Citation63	2015	China	Curcumin	Two capsules of curcumin, 1000 mg daily with escitalopram orally, 5–15 mg daily	6 weeks	HDRS-17 and MADRS	Had beneficial effects, decreased HDRS-17 score by 4.52 (3.17) and MADRS score by 6.26 (4.03)
Rajizadeh et al^Citation68	2017	Iran	Magnesium Oxide	250 mg magnesium oxide twice daily	8 weeks	BDI-II	Had beneficial effects, decreased BDI-II score by 58.14%
Shabani et al^Citation117	2019	Iran	Melatonin	10-mg melatonin daily	12 weeks	BDI	Had beneficial effects, decreased BDI score by 23.53%
Jamilian et al^Citation72	2018	Iran	Myo-inositol	2 g Myo-inositol + 200 microgram folate twice daily	12 weeks	BDI and DASS	Had beneficial effects, decreased BDI score by 6.4% and DASS score by 4.3%
Hariri et al^Citation73	2020	Iran	Sumac (Rhus coriaria L)	Three capsules of sumac, 1 gram/capsule daily	12 weeks	BDI-II	Had beneficial effects, decreased BDI-II score by 41.1%
Bitarafan et al^Citation76	2016	Iran	Vitamin A (retinyl palmitate)	25,000 IU/day for six months and continued by 10,000 IU/day for six months	12 months	BDI-II	Had beneficial effects, decreased BDI-11 score by 95.41%
de Koning et al^Citation118	2016	Netherlands	Vitamin B (B12 and folic acid)	500 µg vitamin B12 and 400 µg folic acid daily	Two years	GDS-15	Had beneficial effects, resulted logistic regression intervention result by 112 (8.6)
Bochyńska et al^Citation119	2012	Poland	Vitamin B	0.4 mg folate, magnesium with 50 mg vitamin B6, and 100 mg vitamin B12 daily	1 year	BDI	Had beneficial effects, decreased BDI score by 24.17% for all patients
Loria-Kohen et al^Citation120	2013	Spain	Vitamin B (folic acid)	10 mg daily	6 months	BDI	Had beneficial effects, decreased BDI score by 33.62%
Solati et al^Citation79	2015	Iran	Zinc	30 mg daily	12 weeks	BDI-II	Had beneficial effects, decreased BDI-II score by 30.5%
Ranjbar et al^Citation80	2014	Iran	Zinc Sulfate	25 mg zinc sulfate/day with citalopram20–60 mg/day or fluoxetine 20–60 mg/day	12 weeks	HDRS	Had beneficial effects, statistically significant difference with p<0.05 compared to placebo
Mazloom et al^Citation58	2013	Iran	Vitamin C & vitamin E	Group 1: one vitamin C capsule, 1000 mg daily Group 2: one vitamin E capsule, 400 IU daily	6 weeks	DASS-21	No significant effect
Vaucher et al^Citation59	2012	France	Ferrous Sulfate	80 mg/day prolonged-release ferrous sulfate for women who had a ferritin level less than 50 ug/L and	12 weeks	CPSS	No significant effect

Abbreviations: DAS, depression anxiety stress scales; HDRS, Hamilton depression rating scale; MADRS, Montgomery-asberg depression rating scale; BDI, beck depression inventory; CPSS, child PTSD symptom scale; GDS, geriatric depression scale.

Furthermore, we observed that carnitine’s effect in lowering depression parameter scores was linked to improved mitochondrial performance, antioxidant effects, increased cholinergic neurotransmission, enhanced protein, and gene expression, which affected brain metabolism, thereby aiding the improvement of neuropsychological function.⁶⁰

Coenzyme Q10, nanocurcumin, and curcumin also had neuroprotective properties, including antioxidant and anti-inflammatory activities. Previously, several studies reported that depression was associated with higher TNF-α levels in individuals with depression than in healthy controls. Therefore, these supplements effectively protect brain cells and neurons from significant neurotoxic damage and lower pro-inflammatory cytokine levels (TNF-α and IL-1β), thereby reducing the overproduction of circulating TNF-α and IL-1β caused by lipopolysaccharides.⁶¹ These regulatory effects would help develop depression treatments in the future. Additionally, the studies showed that curcumin and nanocurcumin protected the brain from oxidative stress and regulated serotonin and dopamine release.^62,63 The low oral bioavailability of curcumin in humans is the cause for low levels of curcumin in the plasma and insufficient pharmacological effects.⁶² Thus, many formulations, such as nanoparticles, liposomes, micelles, and phospholipid complexes, have been developed to address this issue and improve curcumin bioavailability. Nanocurcumin is more potential than curcumin in suppressing nuclear factor B and has a higher cellular absorption rate, offering better efficacy at the pharmacological level as compared to curcumin.^62,64 Previous studies have reported that different curcumin formulae administered result in effects of different magnitudes at the behavioral, electrophysiological, and molecular levels in depression. Therefore, future clinical trials on the effects of different curcumin formulations on depression are essential, to evaluate the potential difference in efficacy on depression.^65–67

Rajizadeh et al⁶⁸ investigated the consumption of 500 mg magnesium oxide daily for eight weeks in people with depression and hypomagnesemia. They observed that magnesium oxide improved depression by reducing BDI scores. Although the advised dose for treating depression ranged from 125 mg to 450 mg based on the previous study, the duration of therapeutic supplementation ranged from 7 to 20 months. Based on these findings, magnesium was proposed to be essential for improving synaptic functions, particularly in the hippocampal neurons of the brain. In addition to its role in blocking N-methyl-D- aspartate (NMDA) channels, magnesium also has an excitatory influence on the production of the brain-derived neurotrophic factor (BDNF) involved in brain function and neuron maintenance.⁶⁹ Additionally, magnesium influences the production of cyclic adenosine monophosphate response element-binding proteins that control genes related to brain function, particularly those involved in dopamine synthesis. Thus, magnesium can help alleviate depression.⁶⁸

Melatonin also has a similar mechanism in reducing depression. As observed, melatonin exerts its neuroprotective properties by controlling glutamate’s NMDA-mediated excitotoxic effects, such as through decreased BDNF signaling and necrosis in cells.⁷⁰ Furthermore, melatonin regulates dopamine signaling, which is a precursor of noradrenaline.

MDD has been linked to a decline in monoaminergic neurotransmitters, such as noradrenaline, dopamine, and serotonin.⁷¹ Jamalian et al⁷² observed that myo-inositol (2 g) with 200 ug folate twice a day compared to the metformin group significantly improved BDI and DASS scores in women with polycystic ovary syndrome (PCOS) after 12 weeks of supplementation. Furthermore, myo-inositol lowered the oxidation of thiol groups that prevented the progressive rise of oxidative stress in women with PCOS.

Likewise, Hariri et al⁷³ investigated the effects of sumac (Rhus coriaria L.) supplementation with a total dose of three grams daily in obese women. Although BDI scores reduced significantly in both groups, no significant difference compared with the placebo was observed. Sumac contains gallotannins that have anti-inflammatory activities through their ability to scavenge ROS and suppress inflammatory mediators (COX-2) linked with depression.^74,75

Some vitamin supplementations also help in depression treatment, such as vitamins A and B. Bitarafan et al,⁷⁶ reported that consuming a vitamin A (retinyl palmitate) dose of 2500 IU daily within six months continued by 10.000 IU per day for another six months, significantly improved depression scales in patients with multiple sclerosis. These patients had immune dysfunction and psychosocial stressors that can cause depression.⁷⁶ Therefore, vitamin A influences anti-inflammatory effects by suppressing the growth of inflammatory T-helper cells and lowering the gene expression of inflammatory cytokines.⁷⁷ This modulation can help reduce depression symptoms in patients with MS can be reduced. In contrast, vitamin B, such as B12, folic acid, and B6, also improves depression symptoms. It has been reported that combining vitamin B12 and folic acid lowered homocysteine levels, thereby lowering harmful effects and enhancing the efficacy of antidepressant treatments. In the brain, vitamin B12-dependent methylation influences neurological symptoms and disorders. Thus, vitamin B deficiency can increase homocysteine levels, resulting in increased oxidative stress that can cause depression.⁷⁸

Furthermore, Solati et al⁷⁹ reported that 30 mg of zinc daily in obese women for 12 weeks improved depression scores by increasing BDNF levels. Thus, zinc had a similar mechanism to antidepressants and other supplementations. In turn, the rise of BDNF levels in the hippocampus triggered therapeutic effects in depressed patients. Likewise, Ranjbar et al⁸⁰ investigated the consumption of 25 mg zinc sulfate daily in addition to antidepressants (SSRI citalopram or fluoxetine). As observed, depression scores were significantly different compared to the control group. Zinc also mediated antidepressant effects through other pathways, such as zinc antagonism of the NMDA receptor.⁸⁰ Zinc supplementation results in its storage in the synaptic vesicles of glutamatergic neurons and following neuronal activity that can be transferred into the synaptic cleft, inhibiting glutamate receptors like NMDA is observed.⁸¹

Alternatively, the study by Mazloom reported that although the effect of vitamins C and E did not have significant results on depression levels compared with the placebo in patients with diabetes type-2, vitamin C caused a substantial change in anxiety levels.⁵⁸ This change was proposed to be caused by the short duration of treatment and inadequate doses of vitamin C and E. However, Amr et al⁸² reported that vitamin C supplementation of 500 mg twice a day with fluoxetine (SSRI antidepressant) of 10 mg per day, administered orally in pediatric patients with MDDs, led to a significant reduction in depressive symptoms compared to the group given fluoxetine alone. This finding shows that vitamin C can be an adjunctive therapy for antidepressant drugs. Furthermore, vitamin C offers neuroprotective properties as an additional protection from oxidative free radicals that can cause brain damage and result in depression.⁸³ Similarly, a previous study observed that vitamin C modulated dopamine and glutamate-mediated neurotransmission as a neuromodulator in the brain. Moreover, the complicated connection of vitamin C with the dopaminergic pathway can be another potential mechanism of action, accounting for its efficacy in treating depression.⁸⁴

Implications and Future Directions

Given the positive results of the dietary supplements in reducing depressive symptoms, we suggest that people with depression consult with a specialist before selecting the type of supplementation. The lower and upper permissible levels of consumption of these supplementations also need to be considered (Table 5). Further studies focusing on substances that showed no positive results, with more carefully selected groups, doses, and combinations are needed to provide a more comprehensive and up-to-date overview of existing supplementations to reduce depressive symptoms.

Conclusion

Based on this study, we observed that the most common supplementation used in clinical studies for depression treatment was the PUFA group and its combination (n = 17, 26.98%), followed by vitamin D (n = 15, 23.81%), then probiotics (n = 8, 12.7%). The total daily dosage of PUFA showed its beneficial effect with 0.7–2 g EPA and 0.4–0.8 g DHA daily for three weeks to 4 months. Furthermore, its positive effect was 2000 IU/day–50,000 IU/week vitamin D for eight weeks to 24 months of supplementation. We also observed that microbes from the genus Lactobacillus and Bifidobacterium with various dosage ranges above 10⁸ CFU in yogurt, capsule, and sachets in the probiotic group showed beneficial adjunctive therapy effects in treating depression. The depression scale was therefore valuable to assess the effect of an intervention on depression. Nevertheless, we propose that PUFA, vitamin D, and probiotics be considered beneficial dietary supplementations in depression treatment and management.

Disclosure

The authors report no conflicts of interest in this work.

Additional information

Funding

This work is supported by Universitas Padjadjaran, Indonesia.