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利用酒精使用障碍研究结果进行的多特征全基因组关联分析,在百万退伍军人计划中为吸烟行为确定了新的基因座。

Multi-trait genome-wide association analyses leveraging alcohol use disorder findings identify novel loci for smoking behaviors in the Million Veteran Program.

机构信息

Yale School of Public Health, New Haven, CT, 06511, USA.

VA Connecticut Healthcare System, West Haven, CT, 06516, USA.

出版信息

Transl Psychiatry. 2023 May 5;13(1):148. doi: 10.1038/s41398-023-02409-2.

Abstract

Smoking behaviors and alcohol use disorder (AUD), both moderately heritable traits, commonly co-occur in the general population. Single-trait genome-wide association studies (GWAS) have identified multiple loci for smoking and AUD. However, GWASs that have aimed to identify loci contributing to co-occurring smoking and AUD have used small samples and thus have not been highly informative. Applying multi-trait analysis of GWASs (MTAG), we conducted a joint GWAS of smoking and AUD with data from the Million Veteran Program (N = 318,694). By leveraging GWAS summary statistics for AUD, MTAG identified 21 genome-wide significant (GWS) loci associated with smoking initiation and 17 loci associated with smoking cessation compared to 16 and 8 loci, respectively, identified by single-trait GWAS. The novel loci for smoking behaviors identified by MTAG included those previously associated with psychiatric or substance use traits. Colocalization analysis identified 10 loci shared by AUD and smoking status traits, all of which achieved GWS in MTAG, including variants on SIX3, NCAM1, and near DRD2. Functional annotation of the MTAG variants highlighted biologically important regions on ZBTB20, DRD2, PPP6C, and GCKR that contribute to smoking behaviors. In contrast, MTAG of smoking behaviors and alcohol consumption (AC) did not enhance discovery compared with single-trait GWAS for smoking behaviors. We conclude that using MTAG to augment the power of GWAS enables the identification of novel genetic variants for commonly co-occuring phenotypes, providing new insights into their pleiotropic effects on smoking behavior and AUD.

摘要

吸烟行为和酒精使用障碍(AUD)都是具有中度遗传倾向的特征,在普通人群中通常同时存在。单特征全基因组关联研究(GWAS)已经确定了多个与吸烟和 AUD 相关的基因座。然而,旨在确定导致同时发生的吸烟和 AUD 的基因座的 GWAS 使用的样本量较小,因此信息含量不高。通过应用 GWAS 的多特征分析(MTAG),我们利用百万退伍军人计划(N = 318694)的数据对吸烟和 AUD 进行了联合 GWAS。通过利用 AUD 的 GWAS 汇总统计数据,MTAG 确定了 21 个与吸烟起始相关的全基因组显著(GWS)基因座,以及 17 个与戒烟相关的基因座,而单特征 GWAS 分别确定了 16 个和 8 个基因座。MTAG 确定的与吸烟行为相关的新基因座包括先前与精神或物质使用特征相关的基因座。共定位分析确定了 AUD 和吸烟状态特征共享的 10 个基因座,这些基因座在 MTAG 中均达到 GWS,包括 SIX3、NCAM1 和 DRD2 附近的变体。MTAG 变体的功能注释突出了 ZBTB20、DRD2、PPP6C 和 GCKR 上对吸烟行为有重要影响的生物学区域。相比之下,MTAG 对吸烟行为和酒精摄入(AC)的分析与单特征 GWAS 相比并没有增强对吸烟行为的发现。我们得出结论,使用 MTAG 增强 GWAS 的效力可以确定与常见共现表型相关的新遗传变异,为它们对吸烟行为和 AUD 的多效性影响提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afa/10162964/23a53b3391e0/41398_2023_2409_Fig1_HTML.jpg

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