- Department of Psychology, Tianjin Medical University General Hospital, Tianjin, China
Objective: Major depressive disorder (MDD) has a relapse rate that cannot be ignored and places a tremendous burden on the patient in the prevention and treatment process. Yoga, a combination of physical and mental exercises, is effective and acceptable for the adjunctive treatment of MDD. This study aimed to explore further the evidence of yoga’s efficacy for patients with MDD.
Methods: PubMed, Embase, Cochrane library, PsycINFO, SinoMed, CNKI, Wanfang, and VIP databases from their inception to 13 October 2022 were searched by a pre-defined search strategy. RCTs of patients with MDD who met diagnostic criteria for yoga treatment were included. RoB2.0 was used to evaluate the quality of the literature. Improvement in depressive symptoms was assessed by the Beck Depression Inventory (BDI), Hamilton Depression Rating Scale (HAMD), or other scales were used as primary outcome indicators, and improvement in anxiety was assessed by the Hamilton Anxiety Scale (HAMA) and State–Trait Anxiety Inventory (STAI) scale as secondary outcome indicators. RR and Cohen’s d at 95% CI were used as effect size estimates, and Q and I2 were used to evaluate the size of heterogeneity, with a p-value less than 0.05 indicating statistical significance.
Results: Thirty-four RCT studies, including 1,269 patients in the treatment group and 1,072 patients in the control group, 48.4% of whom were women, were included in the study. Compared to the control group, the BDI-II results yielded a moderate effect of yoga on the improvement of depressive symptoms (Cohen’s d = −0.60; 95% CI: −1.00 to −0.21; p < 0.01), the HAMD results yielded a moderate improvement of yoga on the severity of depressive symptoms (Cohen’s d = −0.64; 95% CI: −0.98 to −0.30; p < 0.01), and the STAI results can be concluded that yoga had a negligible effect on the improvement of the level of anxiety (Cohen’s d = −0.26; 95% CI: −0.48 to −0.04; p = 0.02). No adverse events occurred in the yoga group during the treatment.
Conclusion: Yoga can improve depressive symptoms and anxiety in patients with MDD and has a safe and wide patient acceptance.
Systematic review registration: [https://www.crd.york.ac.uk/prospero/], identifier [PROSPERO, CRD42022373282].
1. Introduction
Major depression disorder is a type of depression with a high degree of severity and accompanying symptoms and is one of the most common psychiatric disorders, with a prevalence of 2–20% in the general population (1). According to the surveys of diagnostic data, patients with MDD will experience one or more episodes of depression during their lifetime, with an estimated lifetime prevalence of 16.6% and a relapse rate of between 35 and 80% within 1 year of remission (2, 3). According to statistics, depression ranks as the sixth leading cause of disease in the 10–49 years age group, affecting about 17% of the population, with a considerable disease burden (4). Suicide rates are generally elevated in MDD, especially among younger patients, with at least 10% experiencing suicidal ideation and suicidal behavior (5).
Antidepressant medication (ADM) is currently one of the most commonly prescribed medications for MDD, with 10% or more of the general population taking antidepressants yearly in some high-income countries (6). However, side effects of antidepressants are frequently reported in studies, including central nervous system abnormalities, gastrointestinal reactions, weight changes, and allergic reactions. In one study, electroconvulsive therapy (ECT) was potentially superior to ketamine in improving the severity of depression in the acute phase. Still, both ketamine and ECT have unique adverse reaction profiles (7). In a true sense, relapse prevention is a critical task in the successful treatment of MDD. Clinical guidelines (8) tend to recommend long-term treatment of ADM for relapse prevention and additional psychotherapy for patients with depression at significant risk of relapse, such as those with more previous depressive episodes or those who still have residual symptoms (9). Therefore, continuing psychotherapy or pharmacotherapy after remission or adding psychotherapy sequentially to pharmacotherapy could reduce depression relapse rates during the maintenance of treatment period (10).
Yoga is an integrated model of mind–body practice that includes physical postures, movement, breath control and techniques, relaxation, mindfulness, and meditation (11), which is effective in improving exercise adherence and compliance and is readily accepted by most people (12). In clinical studies, yoga has been applied to Parkinson’s disease (13), chronic pain (14), cancer (15), psychiatric disorders such as anxiety and depression (16, 17), and chronic diseases (18) as an adjunctive therapy. Notable that yoga is well tolerated by patients with MDD while having a high-safety profile (19). However, there is a lack of evidence that yoga is effective in treating MDD. A previous review exploring the effectiveness and safety of yoga interventions for treating patients with depression found some evidence of positive effects superior to placebo (20). Still, the method is unclear due to the small number of randomized trials and patients included in this review. The risk–benefit ratio of the intervention is also dark, meta-analysis cannot be performed, and there are significant limitations. In addition, there was no previous meta-analysis of yoga as an adjunctive treatment for MDD. Consequently, it is necessary to verify the therapeutic effect and safety of yoga on MDD. This study aimed to validate the evidence that yoga could be used as an adjunctive intervention to improve outcomes and reduce relapse rates in the treatment of patients with major depressive disorder.
2. Methods
This review was conducted in accordance with the report review under the Preferred Reporting Items for Systematic Evaluation and Meta-Analysis (PRISMA) statement (Supplementary Table 1) (21), and the registration number is CRD42022373282 (22).
2.1. Search strategy
The literature search was conducted independently by two researchers, and disagreements were resolved through consultation and discussion with a third researcher. PubMed, Embase, Cochrane library, PsycINFO, SinoMed, CNKI, Wanfang, and VIP databases were searched for randomized controlled trials (RCTs) on yoga for MDD by combining the mesh terms and keywords (“yoga,” “major depression disorder,” etc.). The search time was from each database establishment to 13 October 2022, with no language, region, or sample size restrictions. The PubMed search strategy is shown in Supplementary Table 2.
2.2. Eligible criteria
The inclusion criteria are as follows:
1. Type of the study: randomized controlled trials (RCTs) and without language restriction.
2. Type of subjects: (a) All patients with MDD were diagnosed by the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) or the International Classification of Disease 10 (ICD-10). (b) All patients with severe levels were diagnosed by validated clinician-based or self-report depression symptom questionnaire, such as the Hamilton Rating Scale for Depression (23), the Beck Depression Inventory-II (24), or the Center for Epidemiological Studies Depression Scale (CES-D). (c) All patients with major depressive disorder were diagnosed using any other clinician-based diagnosis criterion.
The exclusion criteria are as follows: (a) Type of the study: non-randomized controlled trials (RCTs), duplicate publications, animal studies, reviews, and case reports. (b) Type of subjects: patients diagnosed with other mental disorders.
3. Types of intervention: Yoga intervention measures include breath control suggestions, traditional yoga meditation, or a way of life.
4. Types of outcome measure: (a) Primary outcomes: Improvement in depressive symptom severity was assessed by clinician-rated scales such as the Hamilton Rating Scale for Depression or any other validated scales. Primary indicators included both the BDI-II and the HAMD scale, which assess the degree of depression or symptoms. (b) Secondary indicators: Improvement in anxiety symptoms was assessed by the Hamilton Anxiety Scale (HAMA) or State–Trait Anxiety Inventory (STAI).
2.3. Study screening and data extraction
Literature screening was done independently by two authors (Y.F. and D.N.). After abstract title screening, it was then screened by full-text reading, and any disagreements were resolved through discussion. Data extraction included patient information (e.g., age, sex, and diagnosis), method (e.g., randomization), intervention (e.g., type, frequency, and duration of yoga), control intervention (e.g., type, frequency, and time), and outcome (e.g., outcome assessment scales).
2.4. Quality assessment
The quality of the literature was evaluated using the Cochrane risk of bias tool (RoB2.0) (25), which includes the bias during randomization, the bias for deviation from established interventions, the bias for missing outcome data, the bias for outcome measures, the bias for selective reporting of outcomes, and an overall bias. The evaluation levels include low risk, high risk, and some concerns. Publication bias refers to the fact that among similar studies, the results of studies with negative statistical significance are more difficult to be published than those with positive statistical significance. Visual analysis of funnel plots was used to assess the symmetry of this study, and Egger testing was used to quantify publication bias. The study sample size increases the accuracy of estimates of intervention effectiveness. Therefore, the estimated value of efficacy of the study with a large sample size is narrow at the bottom of the funnel plot, while the study with a small sample size is more scattered. Egger’s and Begg’s test and funnel plots are shown in Supplementary Figure 2 and Supplementary Table 4.
2.5. Risk of bias
All studies were assessed as biased with uncertain risk for at least one domain. Figures 1, 2 show an overall risk of bias assessment across domains and the risk of bias in each included study. There was not enough information in 12 studies to judge whether the studies were at high risk or low risk for selection bias. Researchers rated five studies as uncertain risks for bias owing to participant exclusion without explanation, loss of follow-up imbalance, self-selection bias, self-reported compliance, and a lack of clarity in the management of yoga interventions to measure outcomes.
Figure 1. Risk of bias graph: review authors’ judgments about each risk of bias item, presented as a percentage of included studies.
Figure 2. Risk of bias summary: a review of the authors’ judgments about each risk of bias item for each included study.
2.6. Assessment of the quality of the evidence—GRADE
Grading of Recommendations Assessment, Development and Evaluation (GRADE) was used to evaluate the quality of data evidence. Evidence from low- and moderate-quality studies suggests yoga interventions are effective for each of the outcomes examined. A detailed assessment of the evidence is contained in Supplementary Figures 3A–F.
2.7. Data analysis
After extracting the data, two researchers decided which outcome to include in the meta-analysis that was performed by Stata 17.0 software. We calculated and compared the standardized mean difference (Cohen’s d), standard deviation (SD), or 95% confidence interval (95% CI), and the number of participants for each intervention group before and after the intervention (pre and post) in each study. Heterogeneity was evaluated using the I2 and Q test. I2 < 25% was considered low heterogeneity, between 25 and 50% was considered moderate heterogeneity, and > 75% was considered significant heterogeneity. It is generally believed that I2 > 50% indicates apparent heterogeneity, and the random effects model is used. If I2 ≤ 50%, the fixed effects model is used (26). In this study, we used random effects models. The research results were represented in a forest plot. In addition, meta-regression or subgroup analysis was conducted to evaluate meta-analysis with high heterogeneity (I2 > 75%).
2.8. Sensitivity analysis
A sensitivity analysis shall be conducted with the results to determine the robustness of the results. We conducted a sensitivity analysis on the results one by one and generate sensitivity figures, representing the result of removing the total effect from each article. Excluded items may result in biased results, i.e., deleted things can significantly impact the actual outcome and re-merge the data. The meta-analysis results are relatively stable if there is no substantial change in the pre- and post-combined effect. If there are significant differences or even diametrically opposite conclusions then in that case, the stability of the results of meta-analysis is worse, and it is necessary to be careful when interpreting the results and making a conclusion.
2.9. Subgroup analysis
We conducted four subgroup analyses of studies with the Hamilton Depression Assessment Scale as the primary outcome to investigate the impact of specific geographic location, type, duration of intervention, and frequency of intervention on the effectiveness of improving depressive symptoms or degrees in patients with major depressive disorder.
3. Results
3.1. Literature search
The literature search initially detected 842 studies, and after stepwise screening based on the title, abstract, and full text, 34 studies were finally included (19, 27–59). This included 1,269 patients in the treatment group and 1,072 patients in the control group, which met our pre-defined inclusion criteria and were included in the final meta-analysis. The literature screening flowchart is shown in Figure 3.
3.2. Characteristics
Of the 34 RCTs included, 11 (27–30, 32, 43, 44, 47, 49, 52, 53) were from India, 13 (31, 33, 35, 36, 38–42, 46, 50, 54, 55) were from the United States, two (37, 38) were from Germany, two (19, 34) were from the United Kingdom, one (51) was from Canada, and five (45, 56–59) were from China. One study (29) included only male participants, nine studies (31, 33–36, 38, 55, 57, 59) included only female participants, three studies (31, 33, 34) had only women with prenatal depression, and one study (59) included postpartum depression. Eleven RCTs (19, 27, 28, 37, 40, 42, 49, 50, 53, 55) included patients with a DSM-IV diagnosis of MDD, six RCTs (41, 48, 52) included patients with a score greater than or equal to 24 on the Hamilton Depression Inventory for patients with MDD, two RCTs (33, 44) included patients with DSM-V diagnosis of MDD, and two RCTs (35, 36) included patients with the MINI diagnosis of MDD. Of the four studies from China, two (56, 57) met the CCMD-3 diagnostic criteria for depression, one (58) used the CCMD-10 diagnostic criteria, and the others (59) included the EPDS diagnostic criteria for depression. The mean age of the patients in the intervention group was 34.66 years, the mean age of the patients in the control group was 31.13 years, and the median age was 32.90 years. Female patients in each study ranged from 0 to 100.0% (median: 54.12%) (Table 1).
Among all randomized controlled trials included, four (19, 41, 46, 55) used Iyengar yoga, seven (35–37, 39, 42, 43, 50) used Hatha yoga, eight (30, 38, 44, 51, 56–59) used self-designed yoga based on breathing, meditation, and mindfulness, four (27, 29, 40, 52) used Sudarshan Kriya yoga, three (31, 33, 34) used yoga specially designed for the middle and late pregnancy, one (28) used SAHAJ yoga, one (48) used Ashtanga yoga, one (45) used Laugher yoga, one (32) used Yoga Nidra, and four (47, 49, 53, 54) studies did not mention yoga methods. Seven studies (28, 32, 37, 44, 52, 56, 58) added yoga as an adjunct to regular treatment, nine studies (28, 35, 36, 39, 40, 52, 56–58) had a duration of 8 weeks, 14 studies (19, 31, 33, 34, 38, 41, 43, 44, 46–49, 53, 55) had a more extended study duration of 12 weeks, and one study (41) had a maximum period of 28 months. The mean study duration of the studies included here was 10 weeks. Combined pharmacological/psychotherapeutic interventions were allowed in 11 studies (28, 32, 37, 48, 51–53, 56, 58) and no combined intervention in four RCTs (27, 43–45). The specific characteristics of the included studies are detailed in Table 2.
3.3. Methodological quality
Of the 34 included RCTs, 22 studies mentioned randomization (19, 32, 35, 36, 38, 39, 41–47, 49–51, 54–59), 13 studies reported allocation concealment (19, 32, 39, 41, 43, 46, 47, 49, 55–59), 18 studies mentioned blinding (three single-blind (32, 41, 51), four studies mentioned double-blind (39, 42, 50, 54), 11 studies mentioned unblind (27, 38, 40, 43–47, 52, 55)), and the remaining six studies did not mention blinding; all 35 studies clearly had no other sources of bias and selective reporting of risk (Supplementary Table 3).
3.4. Meta-analysis
The improvement in depressive symptom severity was assessed separately by clinician-administered rating scales, and six studies yielded moderate effects of yoga on depressive symptom severity when assessed by the BDI-II (Cohen’s d = −0.60; 95% CI: −1.00 to −0.21; p < 0.01; heterogeneity: I2 = 66.77%; Q (5) = 14.69, p = 0.01) (Figure 4). Eight studies could conclude moderate improvement of yoga on the severity of depressive symptoms when assessed by HAMD (Cohen’s d = −0.64; 95% CI: −0.98 to −0.30; p < 0.01; heterogeneity: I2 = 55.48%; Q (7) = 15.01, p = 0.04) (Figure 5). When the two studies were assessed by CES-D, it could be concluded that yoga had a moderate improvement in the severity of depressive symptoms (Cohen’s d = −0.55; 95% CI: −0.89 to −0.22; p < 0.01; heterogeneity: I2 = 0.00%; Q (1) = 0.033, p = 0.86) (Figure 6).
One study had no significant evidence that yoga improved anxiety levels as assessed by the HAMA scale (Cohen’s d = −0.49; 95% CI: −1.23 to 0.25; p = 0.19; I2 = 68.48%; Q (1) = 3.17, p = 0.07) (Figure 7). Four studies assessed by the STAI scale showed that yoga had a small effect on the improvement of anxiety levels (Cohen’s d = −0.26; 95% CI: −0.48 to −0.04; p = 0.02; heterogeneity: I2 = 0; Q (4) = 3.25, p = 0.52) (Figure 8). In two RCTs, there was no significant evidence of improvement in yoga-related quality of life as assessed by relationships (Cohen’s d = 0.10; 95% CI: −0.28 to 0.47; p = 0.62; heterogeneity: I2 = 44.04%; Q (2) = 3.59, p = 0.17) (Figure 9).
In all, one RCT (42) reported that 42% of patients in the yoga group had a 50% reduction in depressive symptoms at a 6-month follow-up compared to 31% in the control group. In addition, yoga had a significant improvement in depressive symptoms, body cortisol concentration, and IL-6 concentration levels but no statistically significant improvement in anxiety levels (Supplementary Figure 1 and Supplementary Table 5).
3.5. Subgroup analysis
3.5.1. Subgroup analysis regarding the area of study
To determine whether the place where the RCT was conducted was effective in improving the symptoms or degree of depression in patients with MDD, we conducted a subgroup analysis. Six studies were from Asia, and two studies were from the Americas. In the former subgroup: Cohen’s d = −0.51; 95% CI: −0.79 to −0.24; p < 0.05; I2 = 18.76%; Q (5) = 3.17, p = 0.26, and in the latter subgroup: Cohen’s d = −1.24; 95% CI: −2.73 to 0.25; p = 0.1; I2 = 85.39%; Q (1) = 6.84, p = 0.01 (Figure 10). The results showed that studies from Asia were less heterogeneous than those from the Americas and had a moderately positive effect on improving depressive symptoms.
3.5.2. Subgroup analysis regarding intervention type
To determine whether the experimental intervention in a different way for improving the depressive symptoms of patients with severe depression or level effectively, we conducted a subgroup analysis. Group intervention into only yoga and yoga as an aid in the treatment of drugs. There were only three studies with yoga as an intervention and five with yoga and meditation as an intervention. The results show that the intervention included both yoga and meditation (Cohen’s d = −0.58; 95% CI: −0.85 to −0.30; p = 0.1; I2 = 13.29%; Q (4) = 4.66, p = 0.32) compared with the experimental group that received only yoga (Cohen’s d = −0.83; 95% CI: −1.94 to 0.29; p < 0.0001; I2 = 85.69%; Q (2) = 10.31, p = 0.01), depressive symptoms improved significantly (Figure 11).
3.5.3. Subgroup analysis regarding intervention duration
To determine whether the duration of the intervention in the trial group was effective in improving depressive symptoms or severity in patients with major depressive disorder, we performed a subgroup analysis. An intervention duration of fewer than 8 weeks was defined as a short-range intervention, and an intervention duration of more than 15 weeks was defined as a long-range intervention. There were six studies on short-term intervention and two studies on long-term intervention. The results showed that the short-term intervention (Cohen’s d = −0.70; 95% CI: −1.18 to −0.22; p = 0.001; I2 = 73.89%; Q (5) = 14.95, p = 0.01) and the long-term intervention (Cohen’s d = −0.53; 95% CI: −1.04 to −0.02; p = 0.05; I2 = 0.00%; Q (1) = 0.00, p = 0.96) had a moderate effect on the improvement of depressive symptoms or severity. In contrast, the impact of the short-term intervention was more significant (Figure 12).
3.5.4. Subgroup analysis regarding intervention frequency
We conducted a subgroup analysis to determine whether the frequency of the intervention in the trial group was effective in improving symptoms or the degree of depression in patients with MDD. Intervention frequency less than four times per week was defined as low-frequency intervention, and intervention frequency more than four times per week was described as high-frequency intervention. There were three studies with low-frequency interventions and five studies with high-frequency interventions. The results showed that the low-frequency intervention (Cohen’s d = −1.18; 95% CI: −2.02 to −0.33; I2 = 73.32%; Q (2) = 7.33, p = 0.03) and the high-frequency intervention (Cohen’s d = −0.45; 95% CI: −0.70 to −0.19; I2 = 4.50%; Q (4) = 3.26, p = 0.51) had a moderate effect on the improvement of depressive symptoms or severity. In contrast, the impact of the high-frequency intervention was more significant (Figure 13).
3.6. Sensitivity analysis and publication bias
The funnel plot shows some asymmetry (Supplementary Figures 2A–E). The Egger test confirmed that yoga improved MDD without potential publication bias (Supplementary Table 4).
The results of the sensitivity analysis showed that on the sensitivity analysis chart of HAMD, the combined effect was −0.63, 95% CI (−0.96, −0.30), and the combined effect size did not change significantly after excluding any study (Supplementary Figure 4A). This indicates that the meta-analysis results are relatively stable. The sensitivity analysis showed that on the sensitivity analysis chart of BDI-II, the combined effect was −0.60, 95% CI (−1.00, −0.21). The combined effect size did not change significantly after excluding any study (Supplementary Figure 4B). This indicates that the results of the meta-analysis are stable. The sensitivity analysis showed that on the sensitivity analysis chart of STAI, the combined effect was −0.24, 95% CI (−0.48, −0.01), and the combined effect size did not change significantly after excluding any study (Supplementary Figure 4C). This indicates that the results of this meta-analysis are stable. The sensitivity analysis showed that on the sensitivity analysis chart of the relationship, the combined effect was 0.10, 95% CI (−0.28, 0.47), and the combined effect size did not change significantly after excluding any study (Supplementary Figure 4D). This indicates that the results of the meta-analysis are stable. The results of the sensitivity analysis showed that on the sensitivity analysis chart of STAIX, the combined effect was −0.32, 95% CI (−0.60, −0.04), and the combined effect size did not change significantly after excluding any study (Supplementary Figure 4E). This indicates that the results of the meta-analysis are stable.
4. Discussion
This study systematically evaluates the effectiveness of yoga in improving depressive symptoms in patients with MDD. It validates the evidence for the efficacy of yoga for short-term improvements in depressive symptoms and anxiety levels in patients with MDD. Patients diagnosed with MDD in the included studies were recruited from inpatient and outpatient psychiatric services in North America, India, Europe, and China. The participants had the general population, prenatal women, postpartum women, and students, with the majority of participants being female and with a mean age of 32.39 years. Subjects in all nine studies were female, thus, the evidence appears to be more applicable to female patients. This study still has some limitations. First, a moderate number of studies were included in this article, but some of the included articles were published long ago and were of low quality. Second, we did not conduct a subgroup analysis to compare the differences between yoga alone and yoga as an adjunct to psychotherapy. Third, we could not conclude the optimal duration and frequency of exercise for yoga to improve depressive symptoms.
The second subgroup analysis showed that yoga as an adjunct combination with medication was more effective in improving severe depression alone. With the subgroup analysis of the study (60) result is consistent. As well as in the review (61) also mentioned yoga as a supplement to antipsychotic medications to help reduce psychopathology and improve socio-occupational functioning. The third subgroup analysis showed that the effect of randomized controlled trials for short yoga intervention (<8 weeks) was more significant, indicating that brief yoga intervention can improve symptoms of severe depression in a short period. Still, some studies suggested that yoga must be performed for a certain period to obtain the maximum benefit. Most studies described here had a maximum intervention period of 6 months. Therefore, the optimal course of yoga intervention is still an issue worth discussing. The fourth subgroup analysis showed that a weekly high-frequency yoga intervention significantly improved severe depression. However, it is unclear how the various postures used in these studies resulted in therapeutic effects, possibly involving concentration and control of breathing (62).
The pathogenesis of MDD has not been elucidated and is now thought to be caused by biological, genetic, environmental, and psychosocial factors. Early on, MDD was supposed to be associated with abnormalities in monoamine neurotransmitters such as serotonin, norepinephrine, 5-HT, and dopamine. Thus, the mechanisms underlying many clinical treatments for depression were based on this. In contrast, recent theories suggest that it is related to more complex neuromodulator systems and neural circuits. Some scholars suggest that psychological stress, inflammatory cytokines, and hypothalamic–pituitary–adrenal axis dysfunction may trigger depression (63–65). In addition, it has also been recommended that MDD results from disruption of homeostatic mechanisms controlling synaptic plasticity, including reduced synaptic connections between the frontal lobe and other brain regions, neurotrophic and altered dendritic numbers, and increased connectivity within the DMN (66–68). In clinical practice, less than 40% of patients with MDD achieve remission with initial treatment, and approximately 20–30% of patients with MDD do not respond adequately to standard therapy. In one clinical trial, antidepressants had substantial antidepressant effects that exceeded the placebo effect in approximately 15% of patients with MDD compared with placebo in a clinical trial (69). A study conducted in Denmark describing treatment patterns in patients with refractory depression (TRD) and MDD showed that 15% of patients with MDD met the diagnostic criteria for TRD and that treatment for this group of patients was haphazard and did not follow the first treatment guidelines for MDD, probably because of the lack of specific procedures (70).
The number of studies addressing yoga to improve symptoms of depression has been gradually increasing in recent years. A recent Cochrane review and meta-analysis found (71) that exercise was moderately effective in reducing depressive symptoms in depressed adults compared to controls [standardized mean difference (SMD) = −0.62 (95% CI: −0.81 to −0.42)], and that yoga as a soothing exercise and its-based interventions have good therapeutic research. The research has shown that yoga-based interventions are a safe and effective treatment for depression as well as other psychiatric disorders, and a recent meta-analysis (18) whose included 13 studies with conditions such as depression, posttraumatic stress, schizophrenia, anxiety, alcohol dependence, and bipolar disorder, this meta found that yoga provided more relief from depressive symptoms than did waiting for conventional treatment and attentional control (standardized mean difference = 0.41; 95% CI −0.65 to −0.17; p < 0.001). Depressive symptoms were significantly reduced with the higher frequency of weekly yoga practice (β = −0.44, p < 0.01), and yoga was more acceptable and more accessible to adhere to than electroconvulsive therapy. Yoga is an exercise for both young and old, and of the 34 RCTs included in this article, nine were conducted with female subjects. The participants in three of the studies were pregnant, showing that yoga is effective in improving depression in women with perinatal depression (72), postpartum depression (73), and adolescent children (74). More recently, studies have demonstrated the effectiveness of yoga and mindfulness in the treatment of refractory depression and the prevention of relapse (75). In another study, yoga was evaluated for adverse effects, safety, and potential effects on suicidal ideation. Thirty-two patients with MDD were randomized to a high-dose group (HDG) and a low-dose group (LDG) for 12 weeks of intervention. The HDG group consisted of three 90-min yoga sessions per week, while the LDG group consisted of two 90-min yoga sessions per week for 12 weeks of intervention. A total of 30 participants completed the intervention. The most common adverse effect was musculoskeletal soreness, which was reported by 16 of the 30 participants, but all resolved throughout the study; other than that, no other serious adverse effects were reported. No patients withdrew midway through the study due to skeletal pain or other adverse effects, and no risk of worsening psychiatric symptoms was observed, suggesting that the side effects of yoga are incredibly mild and well tolerated by patients with MDD while having a high-safety profile (19). There are nine (19, 39–43, 47, 48, 51) studies that evaluated adverse reactions, and no serious adverse events were found. Among them, mild musculoskeletal soreness occurred in four (19, 39, 41, 47) studies, but all were relieved during the study, and no subjects were withdrawn. In total, two (19, 41) studies were assessed weekly using adverse event forms filled out by subjects and assessed using adverse event forms at the fourth, eighth, and 12th week (the end point of intervention) of the intervention by physicians or psychologists. Overall, one (42) study was assessed every 3 weeks, while the other six did not mention the specific evaluation method. A previous review (76) looked at the safety of yoga interventions and the frequency of adverse events from randomized controlled trials and found that the frequency and severity of yoga-related adverse events were comparable to that associated with physical activity or usual care. However, yoga may be associated with more frequent non-serious adverse events than psychological or educational interventions (i.e., interventions that typically do not involve physical activity). Consistent with this article, limited evidence shows that yoga is still a safe intervention, with only a tiny proportion of serious adverse events occurring. Therefore, it is necessary to report comprehensive and detailed safety-related data in randomized controlled trials with yoga as the intervention method in the future, including evaluating the time point when adverse events occurred and the frequency of all adverse events. In addition, reporting adverse events should follow international guidelines (77), and further studies with larger sample sizes are needed.
For noninvasive brain stimulation, a hot topic in recent years, in a recent meta-analysis of the variability of the treatment effect of noninvasive brain stimulation, no significant improvement in the treatment effect of noninvasive stimulation compared to sham stimulation was found in the depression group of patients, and individual differences in the influencing factors are essential. Thus, personalizing treatment remains an open question (78). Although most patients with MDD can benefit from established treatments, some symptoms remain resistant to treatment. For patients suffering from major depressive disorder, new therapies are urgently needed. Studies have shown that depression is often highly comorbid with other psychiatric disorders, such as anxiety disorders (79). A total of 65% of patients with depression also have physical comorbidities, often including obesity, type 2 diabetes, metabolic syndrome, and cardiovascular disease (80). In patients with MDD, physical inactivity and a sedentary lifestyle are strongly associated with depressive symptoms. Current international guidelines for treating mental disorders now recommend physical activity-based interventions as part of routine psychiatric treatment (81). Although these recommendations exist, their actual application to treatment is not easy (82), which should also receive adequate attention.
5. Conclusion
Yoga presents a non-negligible clinical effect in improving depressive symptoms during treatment and has a safe and wide patient acceptance. RCTs with larger sample sizes and better clinical method designs are still needed to evaluate the level of evidence.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.
Author contributions
YW and DY collected the data, prepared the manuscript, revised the manuscript, carried out the supervision, checked, verified all data, and finalized the approval of the manuscript. YW created figures and conducted the quality assessment. JY designed and supervised the work. All authors contributed to the manuscript and approved the submitted version.
Acknowledgments
The authors thank all the researchers involved in this study. A special thanks to YW for efficiently collecting and analyzing data, to DY for the revision and improvement of the manuscript, and to JY for his research support. The authors also thank all the institutions and researchers who provided data for this meta-analysis study.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpsyt.2023.1138205/full#supplementary-material
References
1. Monroe, SM, and Harkness, KL. Major depression and its recurrences: Life course matters. Annu Rev Clin Psychol. (2022) 18:329–57. doi: 10.1146/annurev-clinpsy-072220-021440
2. Fekadu, A, Wooderson, SC, Markopoulo, K, Donaldson, C, Papadopoulos, A, and Cleare, AJ. What happens to patients with treatment-resistant depression? A systematic review of medium to long term outcome studies. J Affect Disord. (2009) 116:4–11. doi: 10.1016/j.jad.2008.10.014
3. Snyder, HR. Major depressive disorder is associated with broad impairments on neuropsychological measures of executive function: A meta-analysis and review. Psychol Bull. (2013) 139:81–132. doi: 10.1037/a0028727
4. GBD 2019 Diseases and Injuries Collaborators. Global burden of 369 diseases and injuries in 204 countries and territories, 1990-2019: A systematic analysis for the global burden of disease study 2019. Lancet. (2020) 396:1204–22. doi: 10.1016/s0140-6736(20)30925-9
5. Mangione, CM, Barry, MJ, Nicholson, WK, Cabana, M, Chelmow, D, Coker, TR, et al. Screening for depression and suicide risk in children and adolescents: Us preventive services task force recommendation statement. JAMA. (2022) 328:1534–42. doi: 10.1001/jama.2022.16946
6. Jorm, AF, Patten, SB, Brugha, TS, and Mojtabai, R. Has increased provision of treatment reduced the prevalence of common mental disorders? Review of the evidence from four countries. World Psychiatry. (2017) 16:90–9. doi: 10.1002/wps.20388
7. Rhee, TG, Shim, SR, Forester, BP, Nierenberg, AA, McIntyre, RS, Papakostas, GI, et al. Efficacy and safety of ketamine vs electroconvulsive therapy among patients with major depressive episode: A systematic review and meta-analysis. JAMA Psychiat. (2022) 79:1162–72. doi: 10.1001/jamapsychiatry.2022.3352
8. Shah, BN. National Institute for Health and Care Excellence (NICE) guidance on heart valve disease. Heart. (2022) 18:heartjnl-2022-321095. doi: 10.1136/heartjnl-2022-321095
9. Bockting, CLH, Klein, NS, Elgersma, HJ, van Rijsbergen, GD, Slofstra, C, Ormel, J, et al. Effectiveness of preventive cognitive therapy while tapering antidepressants versus maintenance antidepressant treatment versus their combination in prevention of depressive relapse or recurrence (DRD study): A three-group, multicentre, randomised controlled trial. Lancet Psychiatry. (2018) 5:401–10. doi: 10.1016/s2215-0366(18)30100-7
10. Furukawa, TA, Shinohara, K, Sahker, E, Karyotaki, E, Miguel, C, Ciharova, M, et al. Initial treatment choices to achieve sustained response in major depression: A systematic review and network meta-analysis. World Psychiatry. (2021) 20:387–96. doi: 10.1002/wps.20906
11. Saeed, SA, Cunningham, K, and Bloch, RM. Depression and anxiety disorders: Benefits of exercise, yoga, and meditation. Am Fam Physician. (2019) 99:620–7.
12. Thornton, JS, Frémont, P, Khan, K, Poirier, P, Fowles, J, Wells, GD, et al. Physical activity prescription: A critical opportunity to address a modifiable risk factor for the prevention and Management of Chronic Disease: A position statement by the Canadian academy of sport and exercise medicine. Br J Sports Med. (2016) 50:1109–14. doi: 10.1136/bjsports-2016-096291
13. Kwok, JYY, Kwan, JCY, Auyeung, M, Mok, VCT, Lau, CKY, Choi, KC, et al. Effects of mindfulness yoga vs stretching and resistance training exercises on anxiety and depression for people with Parkinson disease: A randomized clinical trial. JAMA Neurol. (2019) 76:755–63. doi: 10.1001/jamaneurol.2019.0534
14. Wieland, LS, Skoetz, N, Pilkington, K, Harbin, S, Vempati, R, and Berman, BM. Yoga for chronic non-specific low back pain. Cochrane Database Syst Rev. (2022) 11:Cd010671. doi: 10.1002/14651858.CD010671.pub3
15. Cramer, H, Lauche, R, Klose, P, Lange, S, Langhorst, J, and Dobos, GJ. Yoga for improving health-related quality of life, mental health and cancer-related symptoms in women diagnosed with breast cancer. Cochrane Database Syst Rev. (2017) 1:Cd010802. doi: 10.1002/14651858.CD010802.pub2
16. Cramer, H, Lauche, R, Anheyer, D, Pilkington, K, de Manincor, M, Dobos, G, et al. Yoga for anxiety: A systematic review and meta-analysis of randomized controlled trials. Depress Anxiety. (2018) 35:830–43. doi: 10.1002/da.22762
17. Cramer, H, Lauche, R, Langhorst, J, and Dobos, G. Yoga for depression: A systematic review and meta-analysis. Depress Anxiety. (2013) 30:1068–83. doi: 10.1002/da.22166
18. Brinsley, J, Schuch, F, Lederman, O, Girard, D, Smout, M, Immink, MA, et al. Effects of yoga on depressive symptoms in people with mental disorders: A systematic review and meta-analysis. Br J Sports Med. (2021) 55:992–1000. doi: 10.1136/bjsports-2019-101242
19. Nyer, M, Gerbarg, PL, Silveri, MM, Johnston, J, Scott, TM, Nauphal, M, et al. A randomized controlled dosing study of Iyengar yoga and coherent breathing for the treatment of major depressive disorder: Impact on suicidal ideation and safety findings. Complement Ther Med. (2018) 37:136–42. doi: 10.1016/j.ctim.2018.02.006
20. Cramer, H, Anheyer, D, Lauche, R, and Dobos, G. A systematic review of yoga for major depressive disorder. J Affect Disord. (2017) 213:70–7. doi: 10.1016/j.jad.2017.02.006
21. Shamseer, L, Moher, D, Clarke, M, Ghersi, D, Liberati, A, Petticrew, M, et al. Preferred reporting items for systematic review and meta-analysis protocols (Prisma-P) 2015: Elaboration and explanation. BMJ. (2015) 350:g7647. doi: 10.1136/bmj.g7647
22. Page, MJ, McKenzie, JE, Bossuyt, PM, Boutron, I, Hoffmann, TC, Mulrow, CD, et al. The Prisma 2020 statement: An updated guideline for reporting systematic reviews. BMJ. (2021) 372:n71. doi: 10.1136/bmj.n71
23. Hamilton, M. A rating scale for depression. J Neurol Neurosurg Psychiatry. (1960) 23:56–62. doi: 10.1136/jnnp.23.1.56
24. Beck, AT, Ward, CH, Mendelson, M, Mock, J, and Erbaugh, J. An inventory for measuring depression. Arch Gen Psychiatry. (1961) 4:561–71. doi: 10.1001/archpsyc.1961.01710120031004
25. Shuster, JJ. Review: Cochrane handbook for systematic reviews for interventions, Version 5.1.0, Published 3/2011. Julian P.T. Higgins and Sally Green, Editors. Res Synth Methods. (2011) 2:126–30. doi: 10.1002/jrsm.38
26. Higgins, JP, Thompson, SG, Deeks, JJ, and Altman, DG. Measuring inconsistency in meta-analyses. BMJ. (2003) 327:557–60. doi: 10.1136/bmj.327.7414.557
27. Janakiramaiah, N, Gangadhar, BN, Naga Venkatesha Murthy, PJ, Harish, MG, Subbakrishna, DK, and Vedamurthachar, A. Antidepressant efficacy of Sudarshan Kriya Yoga (Sky) in melancholia: A randomized comparison with electroconvulsive therapy (Ect) and imipramine. J Affect Disord. (2000) 57:255–9. doi: 10.1016/s0165-0327(99)00079-8
28. Sharma, VK, Das, S, Mondal, S, Goswampi, U, and Gandhi, A. Effect of Sahaj yoga on depressive disorders. Indian J Physiol Pharmacol. (2005) 49:462–8.
29. Vedamurthachar, A, Janakiramaiah, N, Hegde, JM, Shetty, TK, Subbakrishna, DK, Sureshbabu, SV, et al. Antidepressant efficacy and hormonal effects of Sudarshana Kriya Yoga (Sky) in alcohol dependent individuals. J Affect Disord. (2006) 94:249–53. doi: 10.1016/j.jad.2006.04.025
30. Srivastava, M, Talukdar, U, and Lahan, V. Meditation for the management of adjustment disorder anxiety and depression. Complement Ther Clin Pract. (2011) 17:241–5. doi: 10.1016/j.ctcp.2011.04.007
31. Field, T, Diego, M, Hernandez-Reif, M, Medina, L, Delgado, J, and Hernandez, A. Yoga and massage therapy reduce prenatal depression and prematurity. J Bodyw Mov Ther. (2012) 16:204–9. doi: 10.1016/j.jbmt.2011.08.002
32. Rani, K, Tiwari, S, Singh, U, Singh, I, and Srivastava, N. Yoga Nidra as a complementary treatment of anxiety and depressive symptoms in patients with menstrual disorder. Int J Yoga. (2012) 5:52–6. doi: 10.4103/0973-6131.91715
33. Field, T, Diego, M, Delgado, J, and Medina, L. Yoga and social support reduce prenatal depression, anxiety and cortisol. J Bodyw Mov Ther. (2013) 17:397–403. doi: 10.1016/j.jbmt.2013.03.010
34. Field, T, Diego, M, Delgado, J, and Medina, L. Tai Chi/Yoga reduces prenatal depression, anxiety and sleep disturbances. Complement Ther Clin Pract. (2013) 19:6–10. doi: 10.1016/j.ctcp.2012.10.001
35. Kinser, PA, Bourguignon, C, Whaley, D, Hauenstein, E, and Taylor, AG. Feasibility, acceptability, and effects of gentle hatha yoga for women with major depression: Findings from a randomized controlled mixed-methods study. Arch Psychiatr Nurs. (2013) 27:137–47. doi: 10.1016/j.apnu.2013.01.003
36. Kinser, PA, Elswick, RK, and Kornstein, S. Potential long-term effects of a mind-body intervention for women with major depressive disorder: Sustained mental health improvements with a pilot yoga intervention. Arch Psychiatr Nurs. (2014) 28:377–83. doi: 10.1016/j.apnu.2014.08.014
37. Sarubin, N, Nothdurfter, C, Schüle, C, Lieb, M, Uhr, M, Born, C, et al. The influence of hatha yoga as an add-on treatment in major depression on hypothalamic-pituitary-adrenal-axis activity: A randomized trial. J Psychiatr Res. (2014) 53:76–83. doi: 10.1016/j.jpsychires.2014.02.022
38. Schuver, KJ, and Lewis, BA. Mindfulness-based yoga intervention for women with depression. Complement Ther Med. (2016) 26:85–91. doi: 10.1016/j.ctim.2016.03.003
39. Prathikanti, S, Rivera, R, Cochran, A, Tungol, JG, Fayazmanesh, N, and Weinmann, E. Treating major depression with yoga: A prospective, randomized, controlled pilot trial. PLoS One. (2017) 12:e0173869. doi: 10.1371/journal.pone.0173869
40. Sharma, A, Barrett, MS, Cucchiara, AJ, Gooneratne, NS, and Thase, ME. A breathing-based meditation intervention for patients with major depressive disorder following inadequate response to antidepressants: A randomized pilot study. J Clin Psychiatry. (2017) 78:e59–63. doi: 10.4088/JCP.16m10819
41. Streeter, CC, Gerbarg, PL, Whitfield, TH, Owen, L, Johnston, J, Silveri, MM, et al. Treatment of major depressive disorder with Iyengar yoga and coherent breathing: A randomized controlled dosing study. Altern Complement Ther. (2017) 23:236–43. doi: 10.1089/act.2017.29134.ccs
42. Uebelacker, LA, Tremont, G, Gillette, LT, Epstein-Lubow, G, Strong, DR, Abrantes, AM, et al. Adjunctive yoga V. health education for persistent major depression: A randomized controlled trial. Psychol Med. (2017) 47:2130–42. doi: 10.1017/s0033291717000575
43. Tolahunase, MR, Sagar, R, and Dada, R. 5-Httlpr and Mthfr 677c>T polymorphisms and response to yoga-based lifestyle intervention in major depressive disorder: A randomized active-controlled trial. Indian J Psychiatry. (2018) 60:410–26. doi: 10.4103/psychiatry.IndianJPsychiatry_398_17
44. Tolahunase, MR, Sagar, R, Faiq, M, and Dada, R. Yoga- and meditation-based lifestyle intervention increases neuroplasticity and reduces severity of major depressive disorder: A randomized controlled trial. Restor Neurol Neurosci. (2018) 36:423–42. doi: 10.3233/rnn-170810
45. Bressington, D, Mui, J, Yu, C, Leung, SF, Cheung, K, Wu, CST, et al. Feasibility of a group-based laughter yoga intervention as an adjunctive treatment for residual symptoms of depression, anxiety and stress in people with depression. J Affect Disord. (2019) 248:42–51. doi: 10.1016/j.jad.2019.01.030
46. Scott, TM, Gerbarg, PL, Silveri, MM, Nielsen, GH, Owen, L, Nyer, M, et al. Psychological function, Iyengar yoga, and coherent breathing: A randomized controlled dosing study. J Psychiatr Pract. (2019) 25:437–50. doi: 10.1097/pra.0000000000000435
47. Bhargav, PH, Reddy, PV, Govindaraj, R, Gulati, K, Ravindran, A, Gayathri, D, et al. Impact of a course of add-on supervised yoga on cortical inhibition in major depressive disorder: A randomized controlled trial. Can J Psychiatr. (2021) 66:179–81. doi: 10.1177/0706743720953247
48. Bieber, M, Görgülü, E, Schmidt, D, Zabel, K, Etyemez, S, Friedrichs, B, et al. Effects of body-oriented yoga: A RCT study for patients with major depressive disorder. Eur Arch Psychiatry Clin Neurosci. (2021) 271:1217–29. doi: 10.1007/s00406-021-01277-5
49. Gulati, K, Bhargav, PH, Reddy, PV, Govindaraj, R, Ravindran, A, Gayathri, D, et al. Adjunct yoga therapy: Influence on heart rate variability in major depressive disorder - a randomized controlled trial. Asian J Psychiatr. (2021) 65:102832. doi: 10.1016/j.ajp.2021.102832
50. Nugent, NR, Brick, L, Armey, MF, Tyrka, AR, Ridout, KK, and Uebelacker, LA. Benefits of yoga on Il-6: Findings from a randomized controlled trial of yoga for depression. Behav Med. (2021) 47:21–30. doi: 10.1080/08964289.2019.1604489
51. Ravindran, AV, McKay, MS, Silva, TD, Tindall, C, Garfinkel, T, Paric, A, et al. Breathing-focused yoga as augmentation for unipolar and bipolar depression: A randomized controlled trial: Le Yoga Axé Sur La Respiration Comme Traitement D'appoint Pour La Dépression Unipolaire Et Bipolaire: Un Essai Randomisé Contrôlé. Can J Psychiatr. (2021) 66:159–69. doi: 10.1177/0706743720940535
52. Srivastava, A, Kuppili, PP, Gupta, T, Nebhinani, N, and Chandani, A. Kriya yoga in patients with depressive disorders: A pilot study. J Neurosci Rural Pract. (2021) 12:362–7. doi: 10.1055/s-0041-1726618
53. Subbanna, M, Talukdar, PM, Abdul, F, Debnath, M, Reddy, PV, Arasappa, R, et al. Long-term add-on yoga therapy offers clinical benefits in major depressive disorder by modulating the complement pathway: A randomized controlled trial. Asian J Psychiatr. (2021) 66:102876. doi: 10.1016/j.ajp.2021.102876
54. West, JL, Tremont, G, Miller, IW, Uebelacker, LA, and Yoga, V. Health education for attentional processes relevant to major depressive disorder. Mindfulness. (2021) 12:604–12. doi: 10.1007/s12671-020-01519-y
55. Streeter, CC, Gerbarg, PL, Brown, RP, Scott, TM, Nielsen, GH, Owen, L, et al. Thalamic gamma aminobutyric acid level changes in major depressive disorder after a 12-week Iyengar yoga and coherent breathing intervention. J Altern Complement Med. (2020) 26:190–7. doi: 10.1089/acm.2019.0234
56. Yi-huan, L, Jun-qing, W, and Hua-na, Z. Effect of yoga relaxationon anxiety and somatic symptoms in patients with depression. Chin J Prac Nurs. (2010) 35:45–7. doi: 10.3760/cma.j.issn.1672-7088.2010.12.062
57. Wenjuan, W, Qin, P, and Huimin, Z. Effects of yoga intervention nursing activities on female patients with severe depression. Chin J Mod Nurs. (2020) 26:2348–51. doi: 10.3760/cma.j.cn115682-20191213-04573
58. Jinmei, L, Xingxing, K, and We, J. The effect of yoga skill training therapy in Im proving the clinical SYM Ptoms and the quality of life of patients with depression. IMHGN. (2017) 23:3288–90. doi: 10.3760/cma.j.issn.1007-1245.2017.20.050
59. Li, L, and Lin, G. Effects of yoga combined with psychological counseling on mental health, body type and pelvic floor function recovery of primiparas with postpartum depression. Chin J Health Psychol. (2019) 27:118–23. doi: 10.13342/j.cnki.cjhp.2019.01.035
60. Seshadri, A, Adaji, A, Orth, SS, Singh, B, Clark, MM, Frye, MA, et al. Exercise, yoga, and tai chi for treatment of major depressive disorder in outpatient settings: A systematic review and meta-analysis. Prim Care Companion CNS Disord. (2020) 23:20r02722. doi: 10.4088/PCC.20r02722
61. Sathyanarayanan, G, Vengadavaradan, A, and Bharadwaj, B. Role of yoga and mindfulness in severe mental illnesses: A narrative review. Int J Yoga. (2019) 12:3–28. doi: 10.4103/ijoy.IJOY_65_17
62. Davidson, RJ, Kabat-Zinn, J, Schumacher, J, Rosenkranz, M, Muller, D, Santorelli, SF, et al. Alterations in brain and immune function produced by mindfulness meditation. Psychosom Med. (2003) 65:564–70. doi: 10.1097/01.psy.0000077505.67574.e3
63. Mao, L, Ren, X, Wang, X, and Tian, F. Associations between autoimmunity and depression: Serum Il-6 and Il-17 have directly impact on the HAMD scores in patients with first-episode depressive disorder. J Immunol Res. (2022) 2022:6724881. doi: 10.1155/2022/6724881
64. Morrens, M, Overloop, C, Coppens, V, Loots, E, Van Den Noortgate, M, Vandenameele, S, et al. The relationship between immune and cognitive dysfunction in mood and psychotic disorder: A systematic review and a meta-analysis. Mol Psychiatry. (2022) 27:3237–46. doi: 10.1038/s41380-022-01582-y
65. Shukla, R, Newton, DF, Sumitomo, A, Zare, H, McCullumsmith, R, Lewis, DA, et al. Molecular characterization of depression trait and state. Mol Psychiatry. (2022) 27:1083–94. doi: 10.1038/s41380-021-01347-z
66. Leung, E, Lau, EW, Liang, A, de Dios, C, Suchting, R, Östlundh, L, et al. Alterations in brain synaptic proteins and MRNAS in mood disorders: A systematic review and meta-analysis of postmortem brain studies. Mol Psychiatry. (2022) 27:1362–72. doi: 10.1038/s41380-021-01410-9
67. Vlainić, JV, Šuran, J, Vlainić, T, and Vukorep, AL. Probiotics as an adjuvant therapy in major depressive disorder. Curr Neuropharmacol. (2016) 14:952–8. doi: 10.2174/1570159x14666160526120928
68. Wang, G, Liu, Y, Zhu, X, Lin, K, Li, M, Wu, Z, et al. Knockdown of MIRNA-134-5p rescues dendritic deficits by promoting AMPK-mediated Mitophagy in a mouse model of depression. Neuropharmacology. (2022) 214:109154. doi: 10.1016/j.neuropharm.2022.109154
69. Stone, MB, Yaseen, ZS, Miller, BJ, Richardville, K, Kalaria, SN, and Kirsch, I. Response to acute monotherapy for major depressive disorder in randomized, placebo controlled trials submitted to the us Food and Drug Administration: Individual participant data analysis. BMJ. (2022) 378:e067606. doi: 10.1136/bmj-2021-067606
70. Gronemann, FH, Petersen, J, Alulis, S, Jensen, KJ, Riise, J, Ankarfeldt, MZ, et al. Treatment patterns in patients with treatment-resistant depression in Danish patients with major depressive disorder. J Affect Disord. (2021) 287:204–13. doi: 10.1016/j.jad.2021.03.029
71. Cooney, GM, Dwan, K, Greig, CA, Lawlor, DA, Rimer, J, Waugh, FR, et al. Exercise for depression. Cochrane Database Syst Rev. (2013) 2013:Cd004366. doi: 10.1002/14651858.CD004366.pub6
72. Wang, G, Liang, C, and Sun, G. Yoga's therapeutic effect on perinatal depression: A systematic review and meta-analysis. Psychiatr Danub. (2022) 34:195–204. doi: 10.24869/psyd.2022.195
73. Eustis, EH, Ernst, S, Sutton, K, and Battle, CL. Innovations in the treatment of perinatal depression: The role of yoga and physical activity interventions during pregnancy and postpartum. Curr Psychiatry Rep. (2019) 21:133. doi: 10.1007/s11920-019-1121-1
74. Re, P, McConnell, JW, Reidinger, G, Schweit, R, and Hendron, A. Effects of yoga on patients in an adolescent mental health hospital and the relationship between those effects and the patients’ sensory-processing patterns. J Child Adolesc Psychiatr Nurs. (2014) 27:175–82. doi: 10.1111/jcap.12090
75. Pradhan, B, Parikh, T, Makani, R, and Sahoo, M. Ketamine, transcranial magnetic stimulation, and depression specific yoga and mindfulness based cognitive therapy in management of treatment resistant depression: Review and some data on efficacy. Depress Res Treat. (2015) 2015:842817–4. doi: 10.1155/2015/842817
76. Cramer, H, Ward, L, Saper, R, Fishbein, D, Dobos, G, and Lauche, R. The safety of yoga: A systematic review and meta-analysis of randomized controlled trials. Am J Epidemiol. (2015) 182:281–93. doi: 10.1093/aje/kwv071
77. Administration UFaD. Safety [updated 2016 February 1; cited 2014 November 3] (2016). Available at: https://www.fda.gov/safety/reporting-serious-problems-fda/what-serious-adverse-event
78. Homan, S, Muscat, W, Joanlanne, A, Marousis, N, Cecere, G, Hofmann, L, et al. Treatment effect variability in brain stimulation across psychiatric disorders: A meta-analysis of variance. Neurosci Biobehav Rev. (2021) 124:54–62. doi: 10.1016/j.neubiorev.2020.11.033
79. Rebar, AL, Stanton, R, and Rosenbaum, S. Comorbidity of depression and anxiety in exercise research. Lancet Psychiatry. (2017) 4:519. doi: 10.1016/s2215-0366(17)30164-5
80. Vancampfort, D, Stubbs, B, Mitchell, AJ, De Hert, M, Wampers, M, Ward, PB, et al. Risk of metabolic syndrome and its components in people with schizophrenia and related psychotic disorders, bipolar disorder and major depressive disorder: A systematic review and meta-analysis. World Psychiatry. (2015) 14:339–47. doi: 10.1002/wps.20252
81. Stubbs, B, Vancampfort, D, Hallgren, M, Firth, J, Veronese, N, Solmi, M, et al. EPA guidance on physical activity as a treatment for severe mental illness: A meta-review of the evidence and position statement from the European psychiatric association (EPA), supported by the International Organization of Physical Therapists in Mental Health (IOPTMH). Eur Psychiatry. (2018) 54:124–44. doi: 10.1016/j.eurpsy.2018.07.004
Keywords: major depressive disorder, depression, anxiety, yoga, systematic review
Citation: Wu Y, Yan D and Yang J (2023) Effectiveness of yoga for major depressive disorder: A systematic review and meta-analysis. Front. Psychiatry. 14:1138205. doi: 10.3389/fpsyt.2023.1138205
Edited by:
Yifeng Shen, Shanghai Jiao Tong University, ChinaReviewed by:
Duan Zeng, Shanghai Changning Mental Health Center, ChinaCarmen Concerto, University of Catania, Italy
Copyright © 2023 Wu, Yan and Yang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jianli Yang, YWR5eTAwNUAxNjMuY29t
†These authors have contributed equally to this work and share first authorship