重度抑郁症患者的 5-HTR1A 基因 C-1019G 多态性与抗抑郁药反应之间的关系:荟萃分析

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-19 DOI:10.5498/wjp.v14.i10.1573
Huai-Neng Wu, Shuang-Yue Zhu, Li-Na Zhang, Bian-Hong Shen, Lian-Lian Xu
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引用次数: 0

摘要

背景:重度抑郁障碍(MDD)是全球关注的重大健康问题,其治疗因个体对抗抑郁药反应的差异而变得复杂。目的:整合研究并阐明基因变异对MDD治疗结果的影响:根据《系统综述和元分析首选报告项目》(Preferred Reporting Items for Systematic Reviews and Meta-Analyses)指南,利用与 MDD、5-羟色胺 1A 受体多态性 (5-HTR1A)、C-1019G 多态性和抗抑郁药反应相关的关键术语,在 PubMed、EMBASE、Web of Science 和 Cochrane 图书馆进行了系统检索,没有日期限制。对符合纳入标准的研究进行了全面筛选,并使用纽卡斯尔-渥太华量表对研究质量进行了评估。统计分析(包括 χ 2 和 I² 值)用于评估异质性,并相应采用固定效应或随机效应模型:初步检索共获得 1216 篇文章,其中 11 项研究符合纳入标准。对各种遗传模型的分析表明,5-HTR1A C-1019G 多态性与抗抑郁药效之间没有显著关联。异质性为低度至中度,通过漏斗图对称性以及Egger和Begg检验未发现发表偏倚:这项荟萃分析不支持 5-HTR1A C-1019G 多态性与 MDD 抗抑郁剂疗效之间存在显著关联。这些研究结果要求对更大规模的队列进行进一步研究,以证实这些结果并加深对抗抑郁药物遗传学的理解。
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Association between 5-HTR1A gene C-1019G polymorphism and antidepressant response in patients with major depressive disorder: A meta-analysis.

Background: Major depressive disorder (MDD) is a substantial global health concern, and its treatment is complicated by the variability in individual response to antidepressants.

Aim: To consolidate research and clarify the impact of genetic variation on MDD treatment outcomes.

Methods: Adhering to Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, a systematic search across PubMed, EMBASE, Web of Science, and the Cochrane Library was conducted without date restrictions, utilizing key terms related to MDD, serotonin 1A receptor polymorphism (5-HTR1A), C-1019G polymorphism, and antidepressant response. Studies meeting inclusion criteria were thoroughly screened, and quality assessed using the Newcastle-Ottawa Scale. Statistical analyses, including χ 2 and values, were used to evaluate heterogeneity and fixed-effect or random-effect models were applied accordingly.

Results: The initial search yielded 1216 articles, with 11 studies meeting criteria for inclusion. Analysis of various genetic models showed no significant association between the 5-HTR1A C-1019G polymorphism and antidepressant efficacy. The heterogeneity was low to moderate, and no publication bias was detected through funnel plot symmetry and Egger's and Begg's tests.

Conclusion: This meta-analysis does not support a significant association between the 5-HTR1A C-1019G polymorphism and the efficacy of antidepressant treatment in MDD. The findings call for further research with larger cohorts to substantiate these results and enhance the understanding of antidepressant pharmacogenetics.

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