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Powerful and Efficient Strategies for Genetic Association Testing of Symptom and Questionnaire Data in Psychiatric Genetic Studies.
Holleman, Aaron M; Broadaway, K Alaine; Duncan, Richard; Todor, Andrei; Almli, Lynn M; Bradley, Bekh; Ressler, Kerry J; Ghosh, Debashis; Mulle, Jennifer G; Epstein, Michael P.
Affiliation
  • Holleman AM; Department of Epidemiology, Emory University, Atlanta, GA, USA.
  • Broadaway KA; Center for Computational and Quantitative Genetics, Emory University, Atlanta, GA, USA.
  • Duncan R; Department of Human Genetics, Emory University, Atlanta, GA, USA.
  • Todor A; Department of Human Genetics, Emory University, Atlanta, GA, USA.
  • Almli LM; Center for Computational and Quantitative Genetics, Emory University, Atlanta, GA, USA.
  • Bradley B; Department of Human Genetics, Emory University, Atlanta, GA, USA.
  • Ressler KJ; Department of Psychiatry and Behavioral Sciences, Emory University, Atlanta, GA, USA.
  • Ghosh D; Department of Psychiatry and Behavioral Sciences, Emory University, Atlanta, GA, USA.
  • Mulle JG; Clinical Psychologist, Mental Health Service Line, Department of Veterans Affairs Medical Center, Atlanta, GA, USA.
  • Epstein MP; Department of Psychiatry, McLean Hospital, Harvard Medical School, Belmont, MA, USA.
Sci Rep ; 9(1): 7523, 2019 05 17.
Article in En | MEDLINE | ID: mdl-31101869
Genetic studies of psychiatric disorders often deal with phenotypes that are not directly measurable. Instead, researchers rely on multivariate symptom data from questionnaires and surveys like the PTSD Symptom Scale (PSS) and Beck Depression Inventory (BDI) to indirectly assess a latent phenotype of interest. Researchers subsequently collapse such multivariate questionnaire data into a univariate outcome to represent a surrogate for the latent phenotype. However, when a causal variant is only associated with a subset of collapsed symptoms, the effect will be challenging to detect using the univariate outcome. We describe a more powerful strategy for genetic association testing in this situation that jointly analyzes the original multivariate symptom data collectively using a statistical framework that compares similarity in multivariate symptom-scale data from questionnaires to similarity in common genetic variants across a gene. We use simulated data to demonstrate this strategy provides substantially increased power over standard approaches that collapse questionnaire data into a single surrogate outcome. We also illustrate our approach using GWAS data from the Grady Trauma Project and identify genes associated with BDI not identified using standard univariate techniques. The approach is computationally efficient, scales to genome-wide studies, and is applicable to correlated symptom data of arbitrary dimension.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Genetic Association Studies / Mental Disorders Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Sci Rep Year: 2019 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Genetic Association Studies / Mental Disorders Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Sci Rep Year: 2019 Type: Article Affiliation country: United States