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弗雷明汉心脏研究中与心血管相关数量性状的全基因组关联分析。

Genome-wide association analysis of cardiovascular-related quantitative traits in the Framingham Heart Study.

作者信息

Roslin Nicole M, Hamid Jemila S, Paterson Andrew D, Beyene Joseph

机构信息

Program in Genetics and Genome Biology, MaRS Centre, The Hospital for Sick Children Research Institute, 101 College Street, Toronto, Ontario M5G 1L7, Canada.

出版信息

BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S117. doi: 10.1186/1753-6561-3-s7-s117.

Abstract

Multivariate linear growth curves were used to model high-density lipoprotein (HDL), low-density lipoprotein (LDL), triglycerides (TG), and systolic blood pressure (SBP) measured during four exams from 1659 independent individuals from the Framingham Heart Study. The slopes and intercepts from each of two phenotype models were tested for association with 348,053 autosomal single-nucleotide polymorphisms from the Affymetrix Gene Chip 500 k set. Three regions were associated with LDL intercept, TG slope, and SBP intercept (p < 1.44 x 10-7). We observed results consistent with previously reported associations between rs599839, on chromosome 1p13, and LDL. We note that the association is significant with LDL intercept but not slope. Markers on chromosome 17q25 were associated with TG slope, and a single-nucleotide polymorphism on chromosome 7p11 was associated with SBP intercept. Growth curve models can be used to gain more insight on the relationships between SNPs and traits than traditional association analysis when longitudinal data has been collected. The power to detect association with changes over time may be limited if the subjects are not followed over a long enough time period.

摘要

多元线性生长曲线用于对来自弗雷明汉心脏研究的1659名独立个体在四次检查期间测量的高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、甘油三酯(TG)和收缩压(SBP)进行建模。对两个表型模型中每个模型的斜率和截距进行测试,以确定其与Affymetrix基因芯片500k组中的348,053个常染色体单核苷酸多态性的关联。三个区域与LDL截距、TG斜率和SBP截距相关(p < 1.44 x 10-7)。我们观察到的结果与先前报道的1号染色体1p13上的rs599839与LDL之间的关联一致。我们注意到该关联在LDL截距上显著,但在斜率上不显著。17号染色体17q25上的标记与TG斜率相关,7号染色体7p11上的一个单核苷酸多态性与SBP截距相关。当收集了纵向数据时,与传统关联分析相比,生长曲线模型可用于更深入了解单核苷酸多态性(SNP)与性状之间的关系。如果对受试者的随访时间不够长,检测与随时间变化的关联的能力可能会受到限制。

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