The Collaborative Study on the Genetics of Alcoholism: Overview

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2023-09-22 DOI:10.1111/gbb.12864
Arpana Agrawal, Sarah J. Brislin, Kathleen K. Bucholz, Danielle Dick, Ronald P. Hart, Emma C. Johnson, Jacquelyn Meyers, Jessica Salvatore, Paul Slesinger, COGA Collaborators, Laura Almasy, Tatiana Foroud, Alison Goate, Victor Hesselbrock, John Kramer, Samuel Kuperman, Alison K. Merikangas, John I. Nurnberger, Jay Tischfield, Howard J. Edenberg, Bernice Porjesz
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引用次数: 2

Abstract

Alcohol use disorders (AUD) are commonly occurring, heritable and polygenic disorders with etiological origins in the brain and the environment. To outline the causes and consequences of alcohol-related milestones, including AUD, and their related psychiatric comorbidities, the Collaborative Study on the Genetics of Alcoholism (COGA) was launched in 1989 with a gene-brain-behavior framework. COGA is a family based, diverse (~25% self-identified African American, ~52% female) sample, including data on 17,878 individuals, ages 7–97 years, in 2246 families of which a proportion are densely affected for AUD. All participants responded to questionnaires (e.g., personality) and the Semi-Structured Assessment for the Genetics of Alcoholism (SSAGA) which gathers information on psychiatric diagnoses, conditions and related behaviors (e.g., parental monitoring). In addition, 9871 individuals have brain function data from electroencephalogram (EEG) recordings while 12,009 individuals have been genotyped on genome-wide association study (GWAS) arrays. A series of functional genomics studies examine the specific cellular and molecular mechanisms underlying AUD. This overview provides the framework for the development of COGA as a scientific resource in the past three decades, with individual reviews providing in-depth descriptions of data on and discoveries from behavioral and clinical, brain function, genetic and functional genomics data. The value of COGA also resides in its data sharing policies, its efforts to communicate scientific findings to the broader community via a project website and its potential to nurture early career investigators and to generate independent research that has broadened the impact of gene-brain-behavior research into AUD.

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酗酒遗传学合作研究综述。
酒精使用障碍(AUD)是常见的、可遗传的和多基因的疾病,其病因起源于大脑和环境。为了概述酒精相关里程碑(包括AUD)的原因和后果及其相关的精神合并症,1989年启动了酒精中毒遗传学合作研究(COGA),该研究采用了基因-大脑行为框架。COGA是一个以家庭为基础的多样化样本(约25%为非裔美国人,约52%为女性),包括17878名7-97岁个体的数据 在2246个家庭中,有一部分家庭受到AUD的严重影响。所有参与者都对问卷(如性格)和酒精中毒遗传学半结构评估(SSAGA)进行了回答,该评估收集了有关精神病诊断、病情和相关行为的信息(如父母监测)。此外,9871人从脑电图(EEG)记录中获得了脑功能数据,12009人在全基因组关联研究(GWAS)阵列中进行了基因分型。一系列功能基因组学研究考察了AUD背后的特定细胞和分子机制。这一综述为COGA在过去三十年中作为科学资源的发展提供了框架,个别综述对行为和临床、大脑功能、遗传和功能基因组学数据的数据和发现进行了深入描述。COGA的价值还在于其数据共享政策、通过项目网站向更广泛的社区传达科学发现的努力,以及培养早期职业调查人员和开展独立研究的潜力,这些研究将基因-大脑行为研究的影响扩大到AUD。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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