Suppr超能文献

与阿片类药物成瘾相关的基因变异:一项全基因组关联研究

Genetic Variants Linked to Opioid Addiction: A Genome-Wide Association Study.

作者信息

Panday Shailesh Kumar, Shankar Vijay, Lyman Rachel Ann, Alexov Emil

机构信息

Department of Physics and Astronomy, Clemson University, Clemson, SC 29634, USA.

Center for Human Genetics, Clemson University, Greenwood, SC 29646, USA.

出版信息

Int J Mol Sci. 2024 Nov 21;25(23):12516. doi: 10.3390/ijms252312516.

Abstract

Opioid use disorder (OUD) affects millions of people worldwide. While it is known that OUD originates from many factors, including social and environmental factors, the role of genetic variants in developing the disease has also been reported. This study aims to investigate the genetic variants associated with the risk of developing OUD upon exposure. Twenty-three subjects who had previously been given opioid-based painkillers to undergo minor surgical treatment were recruited at Prisma Health Upstate clinic and elsewhere. Eleven were considered nonpersistent opioid users (controls), and 12 were persistent opioid users (cases) at the time of sample collection after an initial surgery. The subjects were asked to provide saliva samples, which were subjected to DNA sequencing at Clemson University Center for Human Genetics, and variant calling was performed. The genome-wide association studies (GWASs) for genes known to be associated with OUD resulted in 13 variants (intronic or SNV) with genome-wide significance (raw -value < 0.01) and two missense variants, rs6265 (p.Val66Met in BNDF isoform a) and rs1799971 (p.Asn40Asp) in , previously reported in the literature. Furthermore, extending the GWASs to find all genomic variants and filtering the variants to include only variants found in cases (persistent opioid users) but not in controls (nonpersistent opioid users) resulted in 11 new variants (-value < 0.005). Considering that OUD is a complex disease and the effect might come from different variants in the same genes, we performed a co-occurrence analysis of variants on the genes. We identified eight additional genes that harbor multiple variants, including four genes: , , , and , with three or more variants in the case subjects but not in the control individuals. The performed PPI network construction, along with functional enrichment, indicated that the variants occur in calcium signaling, circadian entrainment, morphine addiction, alcoholism, and opioid signaling pathways, which are closely related to OUD or addiction in general.

摘要

阿片类药物使用障碍(OUD)影响着全球数百万人。虽然已知OUD源于多种因素,包括社会和环境因素,但基因变异在该疾病发生中的作用也有相关报道。本研究旨在调查与接触阿片类药物后发生OUD风险相关的基因变异。在普isma健康上州诊所及其他地方招募了23名曾接受基于阿片类药物的止痛药进行小手术治疗的受试者。在初次手术后样本采集时,11人被视为非持续性阿片类药物使用者(对照组),12人是持续性阿片类药物使用者(病例组)。受试者被要求提供唾液样本,这些样本在克莱姆森大学人类遗传学中心进行DNA测序,并进行变异检测。对已知与OUD相关基因的全基因组关联研究(GWAS)产生了13个具有全基因组显著性的变异(内含子或单核苷酸变异,原始P值<0.01)以及两个错义变异,即文献中先前报道的rs6265(脑源性神经营养因子a亚型中的p.Val66Met)和rs1799971(p.Asn40Asp)。此外,扩展GWAS以寻找所有基因组变异,并筛选变异使其仅包括在病例组(持续性阿片类药物使用者)中发现而不在对照组(非持续性阿片类药物使用者)中发现的变异,结果产生了11个新变异(P值<0.005)。考虑到OUD是一种复杂疾病,其影响可能来自同一基因中的不同变异,我们对基因上的变异进行了共现分析。我们确定了另外八个含有多个变异的基因,包括四个基因:……,在病例组受试者中有三个或更多变异,但在对照组个体中没有。所进行的蛋白质-蛋白质相互作用网络构建以及功能富集分析表明,这些变异发生在钙信号传导、昼夜节律调节、吗啡成瘾、酒精中毒和阿片类药物信号通路中,这些通路总体上与OUD或成瘾密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aaa/11641826/81431c112f52/ijms-25-12516-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验