Dipartimento di Scienze del Farmaco and Centro di Ricerca Interdipartimentale di Farmacogenetica e Farmacogenomica (CRIFF), Università del Piemonte Orientale "A. Avogadro", Largo Donegani 2, 28100 Novara, Italy.
Dipartimento di Scienze del Farmaco and Centro di Ricerca Interdipartimentale di Farmacogenetica e Farmacogenomica (CRIFF), Università del Piemonte Orientale "A. Avogadro", Largo Donegani 2, 28100 Novara, Italy.
Eur Psychiatry. 2016 Mar;33:45-53. doi: 10.1016/j.eurpsy.2015.12.001. Epub 2016 Feb 6.
The polymorphic brain-derived neurotrophic factor (BDNF) gene has been postulated to be involved in inter-individual variability response to antipsychotic drugs.
To perform a qualitative and quantitative synthesis of studies evaluating the influence of BDNF genetic variation on clinical response to antipsychotics.
The review protocol was published in the PROSPERO database (Reg. n(o) CRD42015024614). A comprehensive search was performed through PubMed, Web of Knowledge and Cochrane databases up to July 2015. The methodological quality of identified studies was assessed using the MINORS criteria. Publication bias was estimated and potential sources of heterogeneity were investigated via meta-regression, subgroup and sensitivity analyses.
Nine studies including a total of 2461 antipsychotic-treated patients fulfilled inclusion criteria for meta-analysis of BDNF Val66Met. Using the random-effects model, the pooled results showed no significant association with antipsychotic response for the dominant (Met carriers vs Val/Val, OR: 0.93, 95% CI: 0.72-1.19, P=0.55), codominant (Met/Met vs Val/Val, OR: 0.82, 95% CI: 0.59-1.15, P=0.25), recessive (Met/Met vs Val carriers, OR: 0.81, 95% CI 0.60-1.10, P=0.18) or the allelic contrast (Met vs Val, OR: 0.92, 95% CI 0.76-1.10, P=0.34). Visual inspection of funnel plots and further evaluation with Egger's test did not suggest evidence of publication bias. Despite lack of significant heterogeneity in most comparisons, no evidence of association also emerged in the subgroup and sensitivity analyses conducted.
The present meta-analysis excludes a clinically relevant effect of BDNF Val66Met on antipsychotic drug response per se. Nevertheless, further investigation is still needed to clarify in well-designed, large sample-based studies, the impact of BDNF haplotypes containing the Val66Met polymorphism.
多态性脑源性神经营养因子(BDNF)基因被认为与抗精神病药物个体间疗效差异有关。
对评估 BDNF 基因变异对抗精神病药临床疗效影响的研究进行定性和定量综合分析。
综述方案发表于 PROSPERO 数据库(注册号 CRD42015024614)。通过 PubMed、Web of Knowledge 和 Cochrane 数据库进行全面检索,检索时限截至 2015 年 7 月。使用 MINORS 标准评估纳入研究的方法学质量。采用漏斗图分析和 Egger 检验评估发表偏倚,并通过亚组分析和敏感性分析探索异质性来源。
纳入 9 项研究共 2461 例接受抗精神病药物治疗的患者,进行 BDNF Val66Met 荟萃分析。采用随机效应模型,汇总结果显示,在抗精神病药疗效方面,BDNF Val66Met 多态性的显性遗传模式(Met 携带者与 Val/Val,OR:0.93,95%CI:0.72-1.19,P=0.55)、共显性遗传模式(Met/Met 与 Val/Val,OR:0.82,95%CI:0.59-1.15,P=0.25)、隐性遗传模式(Met/Met 与 Val 携带者,OR:0.81,95%CI 0.60-1.10,P=0.18)和等位基因对比(Met 与 Val,OR:0.92,95%CI 0.76-1.10,P=0.34)均无显著相关性。漏斗图的直观检查和 Egger 检验进一步评估均未提示存在发表偏倚。尽管大多数比较的异质性较小,但在亚组和敏感性分析中也未发现相关性。
本荟萃分析排除了 BDNF Val66Met 对抗精神病药疗效的临床相关影响。尽管如此,仍需在设计良好、样本量大的研究中进一步明确 BDNF 包含 Val66Met 多态性的单倍型对抗精神病药疗效的影响。