Set-Based Tests for Genetic Association in Longitudinal Studies

被引:12
作者
He, Zihuai [1 ]
Zhang, Min [1 ]
Lee, Seunggeun [1 ]
Smith, Jennifer A. [2 ]
Guo, Xiuqing [3 ]
Palmas, Walter [4 ]
Kardia, Sharon L. R. [2 ]
Roux, Ana V. Diez [5 ]
Mukherjee, Bhramar [1 ]
机构
[1] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Epidemiol, Ann Arbor, MI 48109 USA
[3] Harbor UCLA Med Ctr, Dept Pediat, Torrance, CA 90509 USA
[4] Columbia Univ, Dept Med, New York, NY USA
[5] Drexel Univ, Dept Epidemiol, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
Genetic association; Generalized estimating equations; Generalized score test; Longitudinal study; Multimarker test; Random field; GENOME-WIDE ASSOCIATION;
D O I
10.1111/biom.12310
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genetic association studies with longitudinal markers of chronic diseases (e.g., blood pressure, body mass index) provide a valuable opportunity to explore how genetic variants affect traits over time by utilizing the full trajectory of longitudinal outcomes. Since these traits are likely influenced by the joint effect of multiple variants in a gene, a joint analysis of these variants considering linkage disequilibrium (LD) may help to explain additional phenotypic variation. In this article, we propose a longitudinal genetic random field model (LGRF), to test the association between a phenotype measured repeatedly during the course of an observational study and a set of genetic variants. Generalized score type tests are developed, which we show are robust to misspecification of within-subject correlation, a feature that is desirable for longitudinal analysis. In addition, a joint test incorporating gene-time interaction is further proposed. Computational advancement is made for scalable implementation of the proposed methods in large-scale genome-wide association studies (GWAS). The proposed methods are evaluated through extensive simulation studies and illustrated using data from the Multi-Ethnic Study of Atherosclerosis (MESA). Our simulation results indicate substantial gain in power using LGRF when compared with two commonly used existing alternatives: (i) single marker tests using longitudinal outcome and (ii) existing gene-based tests using the average value of repeated measurements as the outcome.
引用
收藏
页码:606 / 615
页数:10
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