Discriminative accuracy of genomic profiling comparing multiplicative and additive risk models

Eur J Hum Genet. 2011 Feb;19(2):180-5. doi: 10.1038/ejhg.2010.165. Epub 2010 Nov 17.

Abstract

Genetic prediction of common diseases is based on testing multiple genetic variants with weak effect sizes. Standard logistic regression and Cox Proportional Hazard models that assess the combined effect of multiple variants on disease risk assume multiplicative joint effects of the variants, but this assumption may not be correct. The risk model chosen may affect the predictive accuracy of genomic profiling. We investigated the discriminative accuracy of genomic profiling by comparing additive and multiplicative risk models. We examined genomic profiles of 40 variants with genotype frequencies varying from 0.1 to 0.4 and relative risks varying from 1.1 to 1.5 in separate scenarios assuming a disease risk of 10%. The discriminative accuracy was evaluated by the area under the receiver operating characteristic curve. Predicted risks were more extreme at the lower and higher risks for the multiplicative risk model compared with the additive model. The discriminative accuracy was consistently higher for multiplicative risk models than for additive risk models. The differences in discriminative accuracy were negligible when the effect sizes were small (<1.2), but were substantial when risk genotypes were common or when they had stronger effects. Unraveling the exact mode of biological interaction is important when effect sizes of genetic variants are moderate at the least, to prevent the incorrect estimation of risks.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gene Expression Profiling*
  • Genetic Markers / genetics*
  • Genetic Markers / physiology
  • Genetic Predisposition to Disease*
  • Genome, Human*
  • Genotype
  • Humans
  • Logistic Models
  • Male
  • Models, Genetic*
  • Predictive Value of Tests
  • Prostatic Neoplasms / genetics*
  • ROC Curve
  • Reproducibility of Results
  • Risk
  • Sensitivity and Specificity

Substances

  • Genetic Markers