The utility of empirically assigning ancestry groups in cross‐population genetic studies of addiction. (17th July 2017)

• Record Type: Journal Article
• Authors: Peterson, Roseann E.; Edwards, Alexis C.; Bacanu, Silviu‐Alin; Dick, Danielle M.; Kendler, Kenneth S.; Webb, Bradley T.
• Other Names: Chartier Karen G. guestEditor.; Hesselbrock Michie N. guestEditor.; Hesselbrock Victor guestEditor.
• Is Part Of: American journal on addictions. Volume 26:Number 5(2017)
• Page Start: 494
• Page End: 501
• Publication Date: 2017-07-17
• Subjects: Substance abuse -- Periodicals; Substance abuse -- Treatment -- Periodicals; 616.86005
• DOI: 10.1111/ajad.12586
• Languages: English
• ISSNs: 1055-0496

Abstract

Abstract : Background and Objectives: Given moderate heritability and significant heterogeneity among addiction phenotypes, successful genome‐wide association studies (GWAS) are expected to need very large samples. As sample sizes grow, so can genetic diversity leading to challenges in analyzing these data. Methods for empirically assigning individuals to genetically informed ancestry groups are needed. Methods: We describe a strategy for empirically assigning ancestry groups in ethnically diverse GWAS data including extensions of principal component analysis (PCA) and population matching through minimum Mahalanobis distance. We apply these methods to data from Spit for Science (S4S): the University Student Survey, a study following college students longitudinally that includes genetic and environmental data on substance use and mental health ( n = 7, 603). Results: The genetic‐based population assignments for S4S were 48.7% European, 22.5% African, 10.4% Americas, 9.2% East Asian, and 9.2% South Asian descent. Self‐reported census categories "More than one race" and "Unknown"as well as "Hawaiian/Pacific Islander" and "American‐Indian/Native Alaskan" were empirically assigned representing a +9% sample retention over conventional methods. Although there was high concordance between self‐reported race and empirical population‐match (+.924), there was reduction in variance for most ancestry PCs for genetic‐based population assignments. Conclusions: We were able to create more genetically homogenous groups and reduce sample and marker loss through cross‐ancestry meta‐analysis, potentially increasing power to detect etiologically relevant variation. Our approach provides a framework for empirically assigning genetic ancestry groups which can be applied to other ethnically diverse genetic studies. Scientific Significance: Given the important public health impact and demonstrable gains in statistical power from studying diverse populations, empirically sound practices for genetic studies are needed. (Am J Addict 2017;26:494–501)