Konigorski Stefan, Yilmaz Yildiz E, Bull Shelley B
Dalla Lana School of Public Health, University of Toronto, 155 College Street, Toronto, ON, M5T 3M7, Canada.
Current address: Molecular Epidemiology Group, Max Delbrück Center for Molecular Medicine (MDC), Robert-Rössle-Straße 10, 13125 Berlin, Germany.
BMC Proc. 2014 Jun 17;8(Suppl 1):S72. doi: 10.1186/1753-6561-8-S1-S72. eCollection 2014.
We conduct genetic association analysis in the subset of unrelated individuals from the San Antonio Family Studies pedigrees, applying a two-stage approach to take account of the dependence between systolic and diastolic blood pressure (SBP and DBP). In the first stage, we adjust blood pressure for the effects of age, sex, smoking, and use of antihypertensive medication based on a novel modification of censored regression. In the second stage, we model the bivariate distribution of the adjusted SBP and DBP phenotypes by a copula function with interpretable SBP-DBP correlation parameters. This allows us to identify genetic variants associated with each of the adjusted blood pressures, as well as variants that explain the association between the two phenotypes. Within this framework, we define a pleiotropic variant as one that reduces the SBP-DBP correlation. Our results for whole genome sequence variants in the gene ULK4 on chromosome 3 suggest that inference obtained from a copula model can be more informative than findings from the SBP-specific and DBP-specific univariate models alone.
我们在圣安东尼奥家族研究系谱中的非亲属个体子集中进行基因关联分析,采用两阶段方法来考虑收缩压和舒张压(SBP和DBP)之间的相关性。在第一阶段,我们基于截尾回归的一种新修正,对年龄、性别、吸烟和使用抗高血压药物对血压的影响进行调整。在第二阶段,我们通过具有可解释SBP-DBP相关参数的Copula函数对调整后的SBP和DBP表型的双变量分布进行建模。这使我们能够识别与每种调整后血压相关的基因变异,以及解释两种表型之间关联的变异。在此框架内,我们将多效性变异定义为一种能降低SBP-DBP相关性的变异。我们对3号染色体上ULK4基因全基因组序列变异的研究结果表明,从Copula模型获得的推断可能比仅从SBP特异性和DBP特异性单变量模型得出的结果更具信息量。