TY - JOUR
T1 - Covariate-based linkage analysis
T2 - Application of a propensity score as the single covariate consistently improves power to detect linkage
AU - Doan, Betty Q.
AU - Sorant, Alexa J.M.
AU - Frangakis, Constantine E.
AU - Bailey-Wilson, Joan E.
AU - Shugart, Yin Y.
N1 - Funding Information:
The results of this paper were obtained by using the program package S.A.G.E., which is supported by a US Public Health Service Resource Grant (RR03655) from the National Center for Research Resources. YYS is partially supported by an American Cancer Society Grant, IRG-58-005-40 and by the Department of Epidemiology, JHBPSH. BQD is supported by a NHGRI pre-doctoral IRTA fellowship. The authors would like to thank the late Jane Olson without whom much of this work would not have been possible, and the two anonymous reviewers for their critical insights.
PY - 2006/9
Y1 - 2006/9
N2 - Successful identification of genetic risk loci for complex diseases has relied on the ability to minimize disease and genetic heterogeneity to increase the power to detect linkage. One means to account for disease heterogeneity is by incorporating covariate data. However, the inclusion of each covariate will add one degree of freedom to the allele sharing based linkage test, which may in fact decrease power. We explore the application of a propensity score, which is typically used in causal inference to combine multiple covariates into a single variable, as a means of allowing for multiple covariates with the addition of only one degree of freedom. In this study, binary trait data, simulated under various models involving genetic and environmental effects, were analyzed using a nonparametric linkage statistic implemented in LODPAL. Power and type I error rates were evaluated. Results suggest that the use of the propensity score to combine multiple covariates as a single covariate consistently improves the power compared to an analysis including no covariates, each covariate individually, or all covariates simultaneously. Type I error rates were inflated for analyses with covariates and increased with increasing number of covariates, but reduced to nominal rates with sample sizes of 1000 families. Therefore, we recommend using the propensity score as a single covariate in the linkage analysis of a trait suspected to be influenced by multiple covariates because of its potential to increase the power to detect linkage, while controlling for the increase in the type I error.
AB - Successful identification of genetic risk loci for complex diseases has relied on the ability to minimize disease and genetic heterogeneity to increase the power to detect linkage. One means to account for disease heterogeneity is by incorporating covariate data. However, the inclusion of each covariate will add one degree of freedom to the allele sharing based linkage test, which may in fact decrease power. We explore the application of a propensity score, which is typically used in causal inference to combine multiple covariates into a single variable, as a means of allowing for multiple covariates with the addition of only one degree of freedom. In this study, binary trait data, simulated under various models involving genetic and environmental effects, were analyzed using a nonparametric linkage statistic implemented in LODPAL. Power and type I error rates were evaluated. Results suggest that the use of the propensity score to combine multiple covariates as a single covariate consistently improves the power compared to an analysis including no covariates, each covariate individually, or all covariates simultaneously. Type I error rates were inflated for analyses with covariates and increased with increasing number of covariates, but reduced to nominal rates with sample sizes of 1000 families. Therefore, we recommend using the propensity score as a single covariate in the linkage analysis of a trait suspected to be influenced by multiple covariates because of its potential to increase the power to detect linkage, while controlling for the increase in the type I error.
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U2 - 10.1038/sj.ejhg.5201650
DO - 10.1038/sj.ejhg.5201650
M3 - Article
C2 - 16736037
AN - SCOPUS:33747785249
SN - 1018-4813
VL - 14
SP - 1018
EP - 1026
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
IS - 9
ER -