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Non-invasive brain stimulation significantly increases peripheral BDNF levels and reduces depressive symptoms in MDDBrain Stimulation May Increase BDNF Levels in Depression Patients

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Key Takeaway
Note that NIBS significantly increases BDNF levels and reduces symptoms in MDD, suggesting BDNF as a potential biomarker.

This meta-analysis evaluated the effects of non-invasive brain stimulation (NIBS), including repetitive transcranial magnetic stimulation (rTMS) and transcranial direct current stimulation (tDCS), on peripheral BDNF levels and depressive symptoms in patients with major depressive disorder (MDD). The study included a total of 1271 patients compared against sham stimulation.

The analysis found that NIBS significantly increased peripheral BDNF levels (SMD = 1.05; 95% CI: 0.57 to 1.52, p < 0.001). Additionally, NIBS was associated with a significant reduction in depressive symptoms (SMD = -0.90; 95% CI: -1.13 to -0.67, p < 0.001). A positive association was observed between BDNF elevation and antidepressant effects. Specifically, rTMS significantly increased BDNF levels, whereas tDCS did not. Furthermore, extended rTMS protocols of 4 weeks or more were associated with greater BDNF increases compared to shorter durations.

While the findings suggest that BDNF could serve as a biomarker for neuromodulation efficacy, the authors note that the relationship between BDNF elevation and antidepressant effects is an association rather than a proven cause. The study does not report specific limitations or safety data. Clinical application of BDNF as a definitive biomarker for treatment response is not yet established.

How this fits prior evidence

This meta-analysis extends prior evidence regarding the role of neuromodulation in MDD. It builds upon findings that transcranial magnetic stimulation modulates transcriptomic and connectomic changes in treatment-resistant depression. While the previous evidence focused on neural architecture, this study provides evidence that NIBS, specifically rTMS, increases peripheral BDNF levels (SMD = 1.05) and reduces symptoms (SMD = -0.90), potentially offering a biochemical marker for the efficacy of these interventions.

Researchers analyzed data from 1,271 patients with major depressive disorder to see how non-invasive brain stimulation (NIBS) affects the body. This included methods like repetitive transcranial magnetic stimulation (rTMS) and transcranial direct current stimulation (tDCS). The study looked specifically at BDNF, a protein that plays a role in brain health.

The results showed that NIBS significantly increased BDNF levels in the blood. Specifically, rTMS was shown to increase these levels, while tDCS did not show the same effect. Additionally, longer treatment periods of four weeks or more were linked to higher BDNF levels. The study also found a link between higher BDNF levels and a greater reduction in depressive symptoms.

Because this was a meta-analysis of existing data, the results suggest that BDNF could be a useful marker to see if brain stimulation is working. However, the study does not prove that BDNF is the direct cause of the improvement in mood. It only shows a link between the two. Patients should talk to their doctors about how these findings might apply to their specific treatment plans.

What this means for you:
Brain stimulation may increase BDNF levels, which are linked to better outcomes for those with depression.

Common questions

What is BDNF and why does it matter for depression?

BDNF is a protein that is important for brain health. This study found that non-invasive brain stimulation (NIBS) significantly increased BDNF levels in patients with major depressive disorder. Higher levels of BDNF were linked to a greater reduction in depressive symptoms.

Is there a difference between rTMS and tDCS for BDNF?

Yes, the study found a difference between the two types of stimulation. Repetitive transcranial magnetic stimulation (rTMS) significantly increased BDNF levels, while transcranial direct current stimulation (tDCS) did not show the same increase in this analysis.

Does the length of treatment affect the results?

The study found that longer treatment plans can make a difference. Specifically, extended rTMS protocols of 4 weeks or more were associated with greater increases in BDNF levels compared to shorter treatment durations.

Study Details

Study typeMeta analysis
EvidenceLevel 1
Follow-up0.9 mo
PublishedNov 2026
View Original Abstract ↓
BACKGROUND: Brain-derived neurotrophic factor (BDNF), a critical modulator of neuroplasticity, has been strongly implicated in the pathophysiology of major depressive disorder (MDD). Non-invasive brain stimulation (NIBS), including repetitive transcranial magnetic stimulation (rTMS) and transcranial direct current stimulation (tDCS), shows therapeutic promise for MDD. However, their impact on peripheral BDNF levels remains inconclusive. OBJECTIVE: This meta-analysis aimed to quantify the effects of NIBS on peripheral BDNF levels in MDD patients and to evaluate BDNF as a potential biomarker of treatment response. METHODS: Following PRISMA guidelines, randomized controlled trials (RCTs) comparing NIBS with sham stimulation in MDD were identified through a systematic search of five databases. Sixteen RCTs (n = 1271) were included. Random-effects models were used to estimate pooled standardized mean differences (SMDs) for peripheral BDNF levels and depressive symptom severity. Subgroup and moderator analyses examined the effects of BDNF elevation, stimulation modality, and treatment duration. RESULTS: NIBS significantly increased peripheral BDNF levels (SMD = 1.05, 95% CI: 0.57 to 1.52, p < 0.001) and reduced depressive symptoms (SMD = -0.90, 95% CI: -1.13 to -0.67, p < 0.001). Moderator analyses demonstrated that BDNF elevation was associated with greater antidepressant effects. Subgroup analyses revealed that rTMS significantly increased BDNF levels, whereas tDCS did not. Extended rTMS protocols (≥4 weeks) were associated with greater BDNF increases than shorter durations. CONCLUSION: NIBS is associated with increased peripheral BDNF levels and improved depressive symptoms in MDD patients, suggesting the potential utility of BDNF as a biomarker for neuromodulation efficacy. PROSPERO REGISTRATION: CRD42025630845.
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