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创伤后应激障碍与 ADCYAP1R1 基因 rs2267735 多态性的关联:一项荟萃分析。

Association of Posttraumatic Stress Disorder With rs2267735 in the ADCYAP1R1 Gene: A Meta-Analysis.

机构信息

Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia, USA.

Bradley/Hasbro Children's Research Center of Rhode Island Hospital, Providence, Rhode Island, USA.

出版信息

J Trauma Stress. 2017 Aug;30(4):389-398. doi: 10.1002/jts.22211. Epub 2017 Jul 26.

Abstract

Recent studies point to the potential role of the (pituitary) adenylate cyclase activating polypeptide receptor 1 (ADCYAP1R1) gene, which has been implicated in stress response, in posttraumatic stress disorder (PTSD). Multiple genetic association studies have examined potential PTSD risk related to this gene, with mixed results. We conducted a meta-analysis of rs2267735 in ADCYAP1R1 in PTSD. A literature search was conducted using PubMed and PsycINFO, resulting in nine studies that met criteria for inclusion in analysis. Biostat's Comprehensive Meta-Analysis was used to conduct the main meta-analysis on the combined sex sample, as well as two subanalyses examining effects separately in female and male participants. Results indicated that the C allele of rs2267735 conferred significant risk for PTSD in the combined sex data, OR = 1.210, 95% CI [1.007, 1.454], p = .042, and in the subsample of women and girls, OR = 1.328, 95% CI [1.026, 1.719], p = .031; but not in the subsample of men and boys, OR = 0.964, 95% CI [0.733, 1.269], p = .796. These results provide evidence for an association between ADCYAP1R1 and PTSD and indicate that there may indeed be sex differences. Implications of these findings, including the role of rs2267735 as one modulator of the stress system, are discussed.

摘要

最近的研究表明,(垂体)腺苷酸环化酶激活多肽受体 1(ADCYAP1R1)基因可能在创伤后应激障碍(PTSD)中发挥作用,该基因已被牵涉到应激反应中。多项遗传关联研究检查了与该基因相关的潜在 PTSD 风险,结果喜忧参半。我们对 PTSD 中 ADACYAP1R1 的 rs2267735 进行了荟萃分析。使用 PubMed 和 PsycINFO 进行文献检索,结果有 9 项研究符合纳入分析的标准。Biostat 的 Comprehensive Meta-Analysis 用于对合并性别样本进行主要荟萃分析,以及对女性和男性参与者分别进行效应的两项子分析。结果表明,rs2267735 的 C 等位基因在合并性别数据中显著增加 PTSD 的风险,OR = 1.210,95%CI [1.007, 1.454],p =.042,在女性和女孩亚样本中,OR = 1.328,95%CI [1.026, 1.719],p =.031;但在男性和男孩亚样本中没有,OR = 0.964,95%CI [0.733, 1.269],p =.796。这些结果提供了 ADACYAP1R1 与 PTSD 之间存在关联的证据,并表明确实存在性别差异。讨论了这些发现的意义,包括 rs2267735 作为应激系统的一个调节剂的作用。

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