Brunoni André R, Baeken Chris, Machado-Vieira Rodrigo, Gattaz Wagner F, Vanderhasselt Marie-Anne
Laboratory of Neuroscience (LIM27), Department and Institute of Psychiatry, University of São Paulo , São Paulo , Brazil.
World J Biol Psychiatry. 2015 Feb;16(2):114-22. doi: 10.3109/15622975.2014.958101. Epub 2014 Sep 29.
To evaluate whether the antidepressant effects of novel non-invasive brain stimulation (NIBS) therapies are associated with neurotrophic effects, indexed by peripheral brain-derived neurotrophic factor (BDNF) levels.
Systematic review and meta-analysis. We included trials published in PubMed/Medline from the first date available to June 2014 measuring BDNF blood levels before and after repetitive transcranial magnetic stimulation or transcranial direct current stimulation in depression.
Eight datasets (n = 259) were included. These studies enrolled mostly treatment-resistant depression patients, who received daily stimulation sessions on the left dorsolateral prefrontal cortex. BDNF did not increase after NIBS (Hedges' g = 0.03, 95% CI = -0.21 to 0.27), even when examining each intervention separately. Meta-regressions did not identify the influence of any clinical and demographic predictors on the outcome. Finally, Begg's funnel plot did not suggest publication bias and results were robust according to sensitivity analysis.
Peripheral BDNF levels do not increase after NIBS in depression. Such biomarker might, therefore, not be suitable to index NIBS antidepressant response. Further trials are needed, particularly exploring non-medicated populations, performing subsequent BDNF assessments in a larger timeframe and employing more intensive NIBS treatment protocols.
评估新型非侵入性脑刺激(NIBS)疗法的抗抑郁作用是否与神经营养作用相关,以外周脑源性神经营养因子(BDNF)水平为指标。
系统评价和荟萃分析。我们纳入了从可获取的首日至2014年6月在PubMed/Medline上发表的试验,这些试验测量了抑郁症患者在重复经颅磁刺激或经颅直流电刺激前后的BDNF血液水平。
纳入了8个数据集(n = 259)。这些研究主要纳入了难治性抑郁症患者,他们接受了左侧背外侧前额叶皮质的每日刺激疗程。即使分别检查每种干预措施,NIBS后BDNF也未升高(Hedges' g = 0.03,95% CI = -0.21至0.27)。Meta回归未发现任何临床和人口统计学预测因素对结果的影响。最后,Begg漏斗图未提示发表偏倚,根据敏感性分析结果稳健。
抑郁症患者接受NIBS后外周BDNF水平未升高。因此,这种生物标志物可能不适用于作为NIBS抗抑郁反应的指标。需要进一步的试验,特别是探索未用药人群,在更长时间内进行后续BDNF评估,并采用更强化的NIBS治疗方案。