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候选基因关联资源(CARe):设计、方法及概念验证

Candidate gene association resource (CARe): design, methods, and proof of concept.

作者信息

Musunuru Kiran, Lettre Guillaume, Young Taylor, Farlow Deborah N, Pirruccello James P, Ejebe Kenechi G, Keating Brendan J, Yang Qiong, Chen Ming-Huei, Lapchyk Nina, Crenshaw Andrew, Ziaugra Liuda, Rachupka Anthony, Benjamin Emelia J, Cupples L Adrienne, Fornage Myriam, Fox Ervin R, Heckbert Susan R, Hirschhorn Joel N, Newton-Cheh Christopher, Nizzari Marcia M, Paltoo Dina N, Papanicolaou George J, Patel Sanjay R, Psaty Bruce M, Rader Daniel J, Redline Susan, Rich Stephen S, Rotter Jerome I, Taylor Herman A, Tracy Russell P, Vasan Ramachandran S, Wilson James G, Kathiresan Sekar, Fabsitz Richard R, Boerwinkle Eric, Gabriel Stacey B

机构信息

Broad Institute, Cambridge, MA 02142, USA.

出版信息

Circ Cardiovasc Genet. 2010 Jun;3(3):267-75. doi: 10.1161/CIRCGENETICS.109.882696. Epub 2010 Apr 17.

Abstract

BACKGROUND

The National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe), a planned cross-cohort analysis of genetic variation in cardiovascular, pulmonary, hematologic, and sleep-related traits, comprises >40,000 participants representing 4 ethnic groups in 9 community-based cohorts. The goals of CARe include the discovery of new variants associated with traits using a candidate gene approach and the discovery of new variants using the genome-wide association mapping approach specifically in African Americans.

METHODS AND RESULTS

CARe has assembled DNA samples for >40,000 individuals self-identified as European American, African American, Hispanic, or Chinese American, with accompanying data on hundreds of phenotypes that have been standardized and deposited in the CARe Phenotype Database. All participants were genotyped for 7 single-nucleotide polymorphisms (SNPs) selected based on prior association evidence. We performed association analyses relating each of these SNPs to lipid traits, stratified by sex and ethnicity, and adjusted for age and age squared. In at least 2 of the ethnic groups, SNPs near CETP, LIPC, and LPL strongly replicated for association with high-density lipoprotein cholesterol concentrations, PCSK9 with low-density lipoprotein cholesterol levels, and LPL and APOA5 with serum triglycerides. Notably, some SNPs showed varying effect sizes and significance of association in different ethnic groups.

CONCLUSIONS

The CARe Pilot Study validates the operational framework for phenotype collection, SNP genotyping, and analytic pipeline of the CARe project and validates the planned candidate gene study of approximately 2000 biological candidate loci in all participants and genome-wide association study in approximately 8000 African American participants. CARe will serve as a valuable resource for the scientific community.

摘要

背景

美国国立心肺血液研究所的候选基因关联资源(CARe)计划对心血管、肺部、血液和睡眠相关性状的基因变异进行跨队列分析,涵盖了9个社区队列中代表4个种族群体的40,000多名参与者。CARe的目标包括使用候选基因方法发现与性状相关的新变异,以及特别是在非裔美国人中使用全基因组关联图谱方法发现新变异。

方法与结果

CARe已收集了超过40,000名自我认定为欧洲裔美国人、非裔美国人、西班牙裔或华裔美国人的个体的DNA样本,以及数百种已标准化并存储在CARe表型数据库中的表型数据。所有参与者都对基于先前关联证据选择的7个单核苷酸多态性(SNP)进行了基因分型。我们按性别和种族分层,对这些SNP与脂质性状进行关联分析,并对年龄和年龄平方进行了校正。在至少2个种族群体中,CETP、LIPC和LPL附近的SNP与高密度脂蛋白胆固醇浓度的关联得到了强烈重复,PCSK9与低密度脂蛋白胆固醇水平的关联,以及LPL和APOA5与血清甘油三酯的关联。值得注意的是,一些SNP在不同种族群体中显示出不同的效应大小和关联显著性。

结论

CARe试点研究验证了CARe项目的表型收集、SNP基因分型和分析流程的操作框架,并验证了在所有参与者中对约2000个生物学候选基因座进行计划中的候选基因研究以及在约8000名非裔美国参与者中进行全基因组关联研究。CARe将成为科学界的宝贵资源。

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