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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Systematic review and meta-analysis of serotonin transporter genotype and discontinuation from antidepressant treatment
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Systematic review and meta-analysis of serotonin transporter genotype and discontinuation from antidepressant treatment

机译:对血清素转运蛋白基因型和抗抑郁药停药的系统评价和荟萃分析

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There is evidence that 5-HTTLPR is associated with response following treatment from selective serotonin reuptake inhibitors (SSRIs). The short (S) allele has reduced serotonin transporter expression, compared to the long (L) allele, and has been reported to be associated with poorer response in Europeans, with the effect in other populations unclear. However the published literature is inconsistent. A systematic review and meta-analysis was performed to investigate the effect of 5-HTTLPR on discontinuation from antidepressant treatment. Data were obtained from 17 studies including 4309 participants. The principal outcome measure was the allelic odds ratio (OR) for the 5-HTTLPR S allele and discontinuation status. A random effects meta-analysis provided no evidence that the S allele was associated with increased odds of discontinuation from SSRIs in Europeans (OR 1.09, 95% CI 0.83-1.42, p=0.53; 10 studies, n=2504) but in East Asians there was evidence of a reduced odds of discontinuation (OR 0.28, 95% CI 0.12-0.64, p=0.002; 2 studies, n=136). There was a suggestion of small study bias (p=0.05). This meta-analysis provides no evidence of an association between 5-HTTLPR and discontinuation from antidepressant treatment in Europeans. The low number of studies in East Asian samples using SSRIs reduces confidence in our evidence that the S allele decreases the odds of discontinuation in this population. At present, there is no evidence of an association between 5-HTTLPR and discontinuation from SSRI treatment in a European population with further studies required to investigate its effects in different populations.
机译:有证据表明5-HTTLPR与选择性5-羟色胺再摄取抑制剂(SSRI)治疗后的反应有关。与长(L)等位基因相比,短(S)等位基因降低了血清素转运蛋白的表达,并且据报道与欧洲人的反应较弱有关,在其他人群中的影响尚不清楚。但是,已发表的文献并不一致。进行了系统的综述和荟萃分析,以研究5-HTTLPR对抗抑郁药治疗中止的影响。数据来自17项研究,包括4309名参与者。主要结果指标是5-HTTLPR S等位基因和终止状态的等位基因比值比(OR)。一项随机效应荟萃分析未提供证据,表明在欧洲人中,S等位基因与SSRI终止的可能性增加相关(OR 1.09,95%CI 0.83-1.42,p = 0.53; 10个研究,n = 2504),但在东亚人中有证据表明停药的几率降低了(OR 0.28,95%CI 0.12-0.64,p = 0.002; 2个研究,n = 136)。有研究偏倚小的建议(P = 0.05)。这项荟萃分析没有证据表明在欧洲人中5-HTTLPR与抗抑郁药的停用之间存在关联。在东亚地区使用SSRI进行的研究数量较少,这降低了我们对S等位基因降低了该人群中止机会的证据的信心。目前,在欧洲人群中,尚无证据表明5-HTTLPR与SSRI治疗终止之间存在关联,需要进一步研究以研究其在不同人群中的作用。

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