Sequence kernel association test for survival traits

Genet Epidemiol. 2014 Apr;38(3):191-7. doi: 10.1002/gepi.21791. Epub 2014 Jan 26.

Abstract

Rare variant tests have been of great interest in testing genetic associations with diseases and disease-related quantitative traits in recent years. Among these tests, the sequence kernel association test (SKAT) is an omnibus test for effects of rare genetic variants, in a linear or logistic regression framework. It is often described as a variance component test treating the genotypic effects as random. When the linear kernel is used, its test statistic can be expressed as a weighted sum of single-marker score test statistics. In this paper, we extend the test to survival phenotypes in a Cox regression framework. Because of the anticonservative small-sample performance of the score test in a Cox model, we substitute signed square-root likelihood ratio statistics for the score statistics, and confirm that the small-sample control of type I error is greatly improved. This test can also be applied in meta-analysis. We show in our simulation studies that this test has superior statistical power except in a few specific scenarios, as compared to burden tests in a Cox model. We also present results in an application to time-to-obesity using genotypes from Framingham Heart Study SNP Health Association Resource.

Keywords: Cox proportional hazard model; likelihood ratio test; rare variant analysis; variance component test.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cohort Studies
  • Genetic Association Studies*
  • Genotype
  • Heart
  • Humans
  • Logistic Models
  • Models, Genetic*
  • Obesity / genetics
  • Phenotype*
  • Polymorphism, Single Nucleotide / genetics
  • Proportional Hazards Models
  • Research Design
  • Software*
  • Survival Analysis
  • Survival*
  • Time Factors