TY - BOOK AU - Epstein, Stephen E TI - Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease SN - 1061-4036 PY - 2017/// KW - *Coronary Disease/ge [Genetics] KW - *Diabetes Mellitus, Type 2/ge [Genetics] KW - *Genome-Wide Association Study KW - Asia/ep [Epidemiology] KW - Asian Continental Ancestry Group/ge [Genetics] KW - Biomarkers KW - Comorbidity KW - Coronary Disease/ep [Epidemiology] KW - Coronary Disease/et [Etiology] KW - Diabetes Mellitus, Type 2/dt [Drug Therapy] KW - Diabetes Mellitus, Type 2/ep [Epidemiology] KW - Diabetes Mellitus, Type 2/et [Etiology] KW - Europe/ep [Epidemiology] KW - European Continental Ancestry Group/ge [Genetics] KW - Genetic Loci/ge [Genetics] KW - Genetic Predisposition to Disease KW - HLA-DRB5 Chains/ge [Genetics] KW - Humans KW - Metabolic Networks and Pathways/ge [Genetics] KW - Metabolic Syndrome X/ep [Epidemiology] KW - Metabolic Syndrome X/ge [Genetics] KW - Molecular Targeted Therapy KW - Mutation, Missense KW - Polymorphism, Single Nucleotide KW - Risk Factors KW - MedStar Health Research Institute KW - Journal Article N2 - To evaluate the shared genetic etiology of type 2 diabetes (T2D) and coronary heart disease (CHD), we conducted a genome-wide, multi-ancestry study of genetic variation for both diseases in up to 265,678 subjects for T2D and 260,365 subjects for CHD. We identify 16 previously unreported loci for T2D and 1 locus for CHD, including a new T2D association at a missense variant in HLA-DRB5 (odds ratio (OR) = 1.29). We show that genetically mediated increase in T2D risk also confers higher CHD risk. Joint T2D-CHD analysis identified eight variants-two of which are coding-where T2D and CHD associations appear to colocalize, including a new joint T2D-CHD association at the CCDC92 locus that also replicated for T2D. The variants associated with both outcomes implicate new pathways as well as targets of existing drugs, including icosapent ethyl and adipocyte fatty-acid-binding protein UR - https://dx.doi.org/10.1038/ng.3943 ER -