Psychiatric Neurogenetics Section, Campbell Family Research Institute Centre for Addiction and Mental Health, University of Toronto, Toronto, ON, Canada.
Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
Pharmacogenomics J. 2019 Jun;19(3):269-276. doi: 10.1038/s41397-018-0041-5. Epub 2018 Sep 5.
Brain-derived neurotrophic factor (BDNF) plays an important role in dopaminergic and serotonergic neurotransmission by modulating dopaminergic neuron differentiation and establishment. Multiple studies have analyzed the functional BDNF Val66Met variant in relation to antipsychotic response in schizophrenia (SCZ) patients, yielding mixed results. A meta-analysis was thus performed to examine the relationship between this variant and symptom improvement during antipsychotic treatment. Searches using PubMed, Web of Science, and PsycInfo until October 2017 yielded 11 studies that met inclusion criteria (total n = 3774). These studies investigated the BDNF Val66Met variant and antipsychotic response in patients with SCZ or schizoaffective disorder. Responders to antipsychotics were defined using the original criteria applied in each study. Effect sizes were computed using odds ratios, which were pooled according to the Mantel-Haenszel method. The BDNF Val66Met variant was not associated with the total number of responders and non-responders (p > 0.05) under dominant, recessive, or allelic models. Secondary analyses stratifying for individuals of each ethnicity and drug type also revealed no significant associations. Our findings suggest that the BDNF Val66Met variant is not associated with response to antipsychotics in individuals with SCZ. However, considering the current sample size, small effects cannot be ruled out. Moreover, recent studies have suggested that Val66Met forms haplotypes with other BDNF variants. Future studies should examine the Val66Met variant in conjunction with these other variants in relation to antipsychotic response. Moreover, since illness duration appears to influence BDNF levels in SCZ patients, future studies should aim to control for this potential confounding factor in response analyses.
脑源性神经营养因子(BDNF)通过调节多巴胺能神经元的分化和建立,在多巴胺能和血清素能神经传递中发挥重要作用。多项研究分析了功能性 BDNF Val66Met 变体与精神分裂症(SCZ)患者抗精神病反应的关系,结果喜忧参半。因此进行了荟萃分析以检查该变体与抗精神病治疗期间症状改善之间的关系。使用 PubMed、Web of Science 和 PsycInfo 进行搜索,直到 2017 年 10 月,共检索到符合纳入标准的 11 项研究(总 n=3774)。这些研究调查了 BDNF Val66Met 变体与 SCZ 或分裂情感障碍患者的抗精神病反应。根据每个研究中应用的原始标准定义抗精神病药物的反应者。使用优势、隐性或等位基因模型计算效应大小,根据 Mantel-Haenszel 方法进行汇总。BDNF Val66Met 变体与反应者和无反应者的总数无关(p>0.05)。按每种种族和药物类型分层的二次分析也未显示出显著关联。我们的研究结果表明,BDNF Val66Met 变体与 SCZ 个体对抗精神病药物的反应无关。然而,考虑到当前的样本量,不能排除小效应。此外,最近的研究表明 Val66Met 与其他 BDNF 变体形成单倍型。未来的研究应该检查 Val66Met 变体与这些其他变体结合,与抗精神病反应相关。此外,由于疾病持续时间似乎会影响 SCZ 患者的 BDNF 水平,未来的研究应该旨在控制反应分析中潜在的混杂因素。