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本文引用的文献

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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.与人类血液中低密度脂蛋白胆固醇、高密度脂蛋白胆固醇或甘油三酯相关的六个新基因座。
Nat Genet. 2008 Feb;40(2):189-97. doi: 10.1038/ng.75. Epub 2008 Jan 13.
2
Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.弗雷明汉心脏研究10万项目:血压和动脉僵硬度的全基因组关联研究
BMC Med Genet. 2007 Sep 19;8 Suppl 1(Suppl 1):S3. doi: 10.1186/1471-2350-8-S1-S3.
3
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.弗雷明汉心脏研究中血脂表型的全基因组关联研究。
BMC Med Genet. 2007 Sep 19;8 Suppl 1(Suppl 1):S17. doi: 10.1186/1471-2350-8-S1-S17.
4
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.弗雷明汉心脏研究10万个单核苷酸多态性全基因组关联研究资源:17个表型工作组报告综述。
BMC Med Genet. 2007;8 Suppl 1(Suppl 1):S1. doi: 10.1186/1471-2350-8-S1-S1.
5
An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study.降脂药物效果的调查:HyperGEN研究中血脂的全基因组连锁分析
BMC Genet. 2007 Sep 10;8:60. doi: 10.1186/1471-2156-8-60.
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PLINK: a tool set for whole-genome association and population-based linkage analyses.PLINK:一个用于全基因组关联分析和基于群体的连锁分析的工具集。
Am J Hum Genet. 2007 Sep;81(3):559-75. doi: 10.1086/519795. Epub 2007 Jul 25.
7
Genomewide association analysis of coronary artery disease.冠状动脉疾病的全基因组关联分析。
N Engl J Med. 2007 Aug 2;357(5):443-53. doi: 10.1056/NEJMoa072366. Epub 2007 Jul 18.
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The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: design, recruitment, and initial examination.美国国立心肺血液研究所弗雷明汉心脏研究的第三代队列研究:设计、招募与初始检查。
Am J Epidemiol. 2007 Jun 1;165(11):1328-35. doi: 10.1093/aje/kwm021. Epub 2007 Mar 19.
9
Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure.在数量性状研究中对治疗效果进行校正:抗高血压治疗与收缩压
Stat Med. 2005 Oct 15;24(19):2911-35. doi: 10.1002/sim.2165.
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A note on exact tests of Hardy-Weinberg equilibrium.关于哈迪-温伯格平衡精确检验的一则注释。
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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.

DOI:10.1186/1753-6561-3-s7-s117
PMID:20017982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2795889/
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。