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基因多态性 () 与亚洲人群阿片类药物使用障碍显著相关,但与高加索人群无关:一项荟萃分析。

Significant Association of the Gene Polymorphism () and Opioid Use Disorder in Asian Populations, but not Caucasian Populations: A Meta-analysis.

机构信息

Department of Psychiatry, Wuchang Hospital, Wuhan, China.

出版信息

Genet Test Mol Biomarkers. 2022 Jun;26(6):316-323. doi: 10.1089/gtmb.2021.0280.

Abstract

Previous studies have reported on the association between the polymorphism in the () gene and opioid use disorder (OUD) with inconsistent outcomes. The goal of this study was to examine the correlation of the polymorphism and OUD using a meta-analysis approach. Six electronic databases, including PubMed, Web of Science, Cochrane Library, EMBASE, Wanfang and CNKI, were searched thoroughly for relevant studies on the association of the polymorphism and OUD up to September, 2021. Summary odds ratios (ORs) with 95% confidence intervals (CIs) were utilized to test the association. Statistical analyses was performed using RevMan 5.3 software. Eleven studies with 13 independent cohorts encompassing 2538 cases and 2519 controls were included in this study. In the overall analysis, the polymorphism was not associated with OUD susceptibility. Subgroup analyses suggested that was significantly correlated with OUD in Asian populations: VV vs. MM, OR = 1.46, 95% CI 1.05-2.02,  = 0.02; VM vs. MM, OR = 1.44, 95% CI 1.04-2.00,  = 0.03; VV+VM vs. MM, OR = 1.45, 95% CI 1.07-1.99,  = 0.02. However, the pooled data did not suggest any significant association in the Caucasian population. This meta-analysis supports a significant association between the polymorphism and predisposition to OUD in Asians, carriers of VV and VM genotypes appear to have an increased susceptibility to OUD. However, the association does not exist in Caucasians.

摘要

先前的研究报告了基因多态性与阿片类药物使用障碍(OUD)之间的关联,但结果不一致。本研究旨在通过荟萃分析方法研究多态性与 OUD 的相关性。我们全面检索了 PubMed、Web of Science、Cochrane 图书馆、EMBASE、万方和中国知网等 6 个电子数据库,以获取截至 2021 年 9 月关于多态性与 OUD 关联的相关研究。采用汇总优势比(ORs)及其 95%置信区间(CIs)来检验相关性。采用 RevMan 5.3 软件进行统计分析。本研究纳入了 11 项研究,包含 13 个独立队列,共纳入 2538 例病例和 2519 例对照。在总体分析中,该多态性与 OUD 易感性无关。亚组分析表明,在亚洲人群中,与 OUD 显著相关:VV 与 MM 相比,OR=1.46,95%CI 为 1.05-2.02,=0.02;VM 与 MM 相比,OR=1.44,95%CI 为 1.04-2.00,=0.03;VV+VM 与 MM 相比,OR=1.45,95%CI 为 1.07-1.99,=0.02。然而,在白种人群中,汇总数据并未提示存在显著相关性。本荟萃分析支持该多态性与亚洲人群 OUD 易感性之间存在显著关联,携带 VV 和 VM 基因型的个体似乎对 OUD 的易感性增加。然而,这种关联在白种人群中并不存在。

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