Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, United States; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, United States.
Lindner Center of HOPE, Mason, OH, United States; University of Cincinnati College of Medicine, Cincinnati, OH, United States; The Bipolar Collaborative Network, Bethesda, MD, United States.
J Affect Disord. 2012 Jan;136(1-2):e21-e29. doi: 10.1016/j.jad.2011.05.038. Epub 2011 Jun 15.
Antidepressants can trigger a rapid mood switch from depression to mania. Identifying genetic risk factors associated with antidepressant induced mania (AIM) may enable individualized treatment strategies for bipolar depression. This review and meta-analysis evaluates the evidence for association between the serotonin transporter gene promoter polymorphism (5HTTLPR) and AIM.
Medline up to November 2009 was searched for key words bipolar, antidepressant, serotonin transporter, SLC6A4, switch, and mania.
Five studies have evaluated the SLC6A4 promoter polymorphism and AIM in adults (total N=340 AIM+ cases, N=543 AIM- controls). Although a random effects meta-analysis showed weak evidence of association of the S allele with AIM+ status, a test of heterogeneity indicated significant differences in estimated genetic effects between studies. A similar weak association was observed in a meta-analysis based on a subset of three studies that excluded patients on mood stabilizers; however the result was again not statistically significant.
Few pharmacogenomic studies of antidepressant treatment of bipolar disorder have been published. The completed studies were underpowered and often lacked important phenotypic information regarding potential confounders such as concurrent use of mood stabilizers or rapid cycling.
There is insufficient published data to confirm an association between 5HTTLPR and antidepressant induced mania. Pharmacogenomic studies of antidepressant induced mania have high potential clinical impact provided future studies are of adequate sample size and include rigorously assessed patient characteristics (e.g. ancestry, rapid cycling, concurrent mood stabilization, and length of antidepressant exposure).
抗抑郁药可能会导致情绪从抑郁迅速转变为躁狂。确定与抗抑郁药引起的躁狂(AIM)相关的遗传风险因素,可能会为双相情感障碍的抑郁提供个体化的治疗策略。本综述和荟萃分析评估了 5-羟色胺转运体基因启动子多态性(5HTTLPR)与 AIM 之间关联的证据。
截至 2009 年 11 月,通过搜索 Medline 中的关键词“双相情感障碍、抗抑郁药、5-羟色胺转运体、SLC6A4、转换、躁狂”,来寻找相关文献。
五项研究评估了 SLC6A4 启动子多态性与成人的 AIM(共 340 例 AIM+病例,543 例 AIM-对照)。虽然随机效应荟萃分析显示 S 等位基因与 AIM+状态存在弱关联的证据,但异质性检验表明,研究之间的遗传效应估计存在显著差异。在一项基于排除心境稳定剂的三项研究子集的荟萃分析中也观察到类似的弱关联;然而,结果仍无统计学意义。
关于双相情感障碍抗抑郁治疗的药物基因组学研究发表较少。已完成的研究缺乏动力,并且常常缺乏关于潜在混杂因素(如同时使用心境稳定剂或快速循环)的重要表型信息。
目前尚缺乏确认 5HTTLPR 与抗抑郁药引起的躁狂之间存在关联的充分数据。抗抑郁药引起的躁狂的药物基因组学研究具有很高的潜在临床影响,前提是未来的研究具有足够的样本量,并包括严格评估的患者特征(例如,祖先、快速循环、同时的心境稳定和抗抑郁药暴露时间)。