Department of Medicine, Washington University School of Medicine, St, Louis, MO, USA.
BMC Psychiatry. 2013 Nov 12;13:304. doi: 10.1186/1471-244X-13-304.
Debate is ongoing about what role, if any, variation in the serotonin transporter linked polymorphic region (5-HTTLPR) plays in depression. Some studies report an interaction between 5-HTTLPR variation and stressful life events affecting the risk for depression, others report a main effect of 5-HTTLPR variation on depression, while others find no evidence for either a main or interaction effect. Meta-analyses of multiple studies have also reached differing conclusions.
METHODS/DESIGN: To improve understanding of the combined roles of 5-HTTLPR variation and stress in the development of depression, we are conducting a meta-analysis of multiple independent datasets. This coordinated approach utilizes new analyses performed with centrally-developed, standardized scripts. This publication documents the protocol for this collaborative, consortium-based meta-analysis of 5-HTTLPR variation, stress, and depression.
Our goal is to invite all datasets, published or unpublished, with 5-HTTLPR genotype and assessments of stress and depression for at least 300 subjects. This inclusive approach is to minimize potential impact from publication bias.
This project currently includes investigators from 35 independent groups, providing data on at least N = 33,761 participants.The analytic plan was determined prior to starting data analysis. Analyses of individual study datasets will be performed by the investigators who collected the data using centrally-developed standardized analysis scripts to ensure a consistent analytical approach across sites. The consortium as a group will review and interpret the meta-analysis results.
Variation in 5-HTTLPR is hypothesized to moderate the response to stress on depression. To test specific hypotheses about the role of 5-HTTLPR variation on depression, we will perform coordinated meta-analyses of de novo results obtained from all available data, using variables and analyses determined a priori. Primary analyses, based on the original 2003 report by Caspi and colleagues of a GxE interaction will be supplemented by secondary analyses to help interpret and clarify issues ranging from the mechanism of effect to heterogeneity among the contributing studies. Publication of this protocol serves to protect this project from biased reporting and to improve the ability of readers to interpret the results of this specific meta-analysis upon its completion.
关于 5-羟色胺转运体基因(5-HTTLPR)多态性区域的变异在抑郁症中起何种作用(如果有的话),目前仍存在争议。一些研究报告称,5-HTTLPR 变异与应激性生活事件之间存在相互作用,从而影响抑郁症的发病风险,另一些研究则报告称 5-HTTLPR 变异对抑郁症有主要影响,还有一些研究则没有发现主要影响或相互作用的证据。对多项研究的荟萃分析也得出了不同的结论。
方法/设计:为了更好地了解 5-HTTLPR 变异和应激在抑郁症发展中的综合作用,我们正在对多个独立数据集进行荟萃分析。这种协调的方法利用了新的分析,这些分析是使用中央开发的标准化脚本进行的。本出版物记录了基于合作、联盟的 5-HTTLPR 变异、应激和抑郁荟萃分析的方案。
我们的目标是邀请所有已发表或未发表的数据集,这些数据集包含 5-HTTLPR 基因型以及至少 300 名受试者的应激和抑郁评估。这种包容性的方法是为了最大限度地减少发表偏倚的潜在影响。
该项目目前包括来自 35 个独立小组的研究人员,提供了至少 N=33761 名参与者的数据。分析计划是在开始数据分析之前确定的。使用中央开发的标准化分析脚本,由收集数据的研究人员对个别研究数据集进行分析,以确保各站点的分析方法一致。该联盟将作为一个整体,对荟萃分析结果进行审查和解释。
5-HTTLPR 的变异被假设为调节对压力的反应,从而影响抑郁。为了检验 5-HTTLPR 变异对抑郁症的作用的具体假设,我们将使用预先确定的变量和分析方法,对来自所有可用数据的新结果进行协调荟萃分析。基于 Caspi 等人 2003 年报告的 GxE 相互作用的主要分析,将辅以次要分析,以帮助解释和阐明从作用机制到参与研究之间的异质性等问题。本方案的发表有助于防止该项目出现有偏报告,并提高读者在完成该特定荟萃分析后解释结果的能力。