4.4 Article

Transformation of Summary Statistics from Linear Mixed Model Association on All-or-None Traits to Odds Ratio

期刊

GENETICS
卷 208, 期 4, 页码 1397-1408

出版社

GENETICS SOCIETY AMERICA
DOI: 10.1534/genetics.117.300360

关键词

complex diseases; genome-wide association studies; summary statistics; OR; linear mixed models

资金

  1. Australian Research Council [DP160102400]
  2. Australian National Health and Medical Research Council [1113400, 1078037]
  3. National Institutes of Health [R21 ES025052]
  4. Sylvia & Charles Viertel Charitable Foundation
  5. RC2 Grand Opportunity grant
  6. University of California, San Francisco Institute for Human Genetics [AG036607]
  7. Welsh Assembly Government
  8. British Heart Foundation
  9. Diabetes UK
  10. Medical Research Council [MC_qA137853] Funding Source: researchfish

向作者/读者索取更多资源

Genome-wide association studies (GWAS) have identified thousands of loci that are robustly associated with complex diseases. The use of linear mixed model (LMM) methodology for GWAS is becoming more prevalent due to its ability to control for population structure and cryptic relatedness and to increase power. The odds ratio (OR) is a common measure of the association of a disease with an exposure (e.g., a genetic variant) and is readably available from logistic regression. However, when the LMM is applied to all-or-none traits it provides estimates of genetic effects on the observed 0-1 scale, a different scale to that in logistic regression. This limits the comparability of results across studies, for example in a meta-analysis, and makes the interpretation of the magnitude of an effect from an LMM GWAS difficult. In this study, we derived transformations from the genetic effects estimated under the LMM to the OR that only rely on summary statistics. To test the proposed transformations, we used real genotypes from two large, publicly available data sets to simulate all-or-none phenotypes for a set of scenarios that differ in underlying model, disease prevalence, and heritability. Furthermore, we applied these transformations to GWAS summary statistics for type 2 diabetes generated from 108,042 individuals in the UK Biobank. In both simulation and real-data application, we observed very high concordance between the transformed OR from the LMM and either the simulated truth or estimates from logistic regression. The transformations derived and validated in this study improve the comparability of results from prospective and already performed LMM GWAS on complex diseases by providing a reliable transformation to a common comparative scale for the genetic effects.

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