Association of Thyroid Function Genetic Predictors With Atrial Fibrillation
Year: 2019
Type: review
Study design: Observational Study
Abstract: Importance: Thyroid hormone levels are tightly regulated through feedback inhibition by thyrotropin, produced by the pituitary gland. Hyperthyroidism is overwhelmingly due to thyroid disorders and is well recognized to contribute to a wide spectrum of cardiovascular morbidity, particularly the increasingly common arrhythmia atrial fibrillation (AF). Objective: To determine the association between genetically determined thyrotropin levels and AF. Design, Setting, and Participants: This phenome-wide association study scanned 1318 phenotypes associated with a polygenic predictor of thyrotropin levels identified by a previously published genome-wide association study that included participants of European ancestry. North American individuals of European ancestry with longitudinal electronic health records were analyzed from May 2008 to November 2016. Analysis began March 2018. Main Outcomes and Measures: Clinical diagnoses associated with a polygenic predictor of thyrotropin levels. Exposures: Genetically determined thyrotropin levels. Results: Of 37 154 individuals, 19 330 (52%) were men. The thyrotropin polygenic predictor was positively associated with hypothyroidism (odds ratio [OR], 1.10; 95% CI, 1.07-1.14; P = 5 × 10-11) and inversely associated with diagnoses related to hyperthyroidism (OR, 0.64; 95% CI, 0.54-0.74; P = 2 × 10-8 for toxic multinodular goiter). Among nonthyroid associations, the top association was AF/flutter (OR, 0.93; 95% CI, 0.9-0.95; P = 9 × 10-7). When the analyses were repeated excluding 9801 individuals with any diagnoses of a thyroid-related disease, the AF association persisted (OR, 0.91; 95% CI, 0.88-0.95; P = 2.9 × 10-6). To replicate this association, we conducted an inverse-variance weighted average meta-analysis using AF single-nucleotide variant weights from a genome-wide association study of 17 931 AF cases and 115 142 controls. As in the discovery analyses, each SD increase in predicted thyrotropin was associated with a decreased risk of AF (OR, 0.86; 95% CI, 0.79-0.93; P = 4.7 × 10-4). In a set of AF cases (n = 745) and controls (n = 1680) older than 55 years, directly measured thyrotropin levels that fell within the normal range were inversely associated with AF risk (OR, 0.91; 95% CI, 0.83-0.99; P = .04). Conclusions and Relevance: This study suggests a role for genetically determined variation in thyroid function within a physiologically accepted normal range as a risk factor for AF. The clinical decision to treat subclinical thyroid disease should incorporate the risk for AF as antithyroid medications to treat hyperthyroidism may reduce AF risk and thyroid hormone replacement for hypothyroidism may increase AF risk.
Source: JAMA Cardiology
Authors: Joe-Elie Salem, M. Benjamin Shoemaker, Lisa Bastarache, Christian M. Shaffer, Andrew M. Glazer, Brett Kroncke, Quinn S. Wells, Mingjian Shi, Peter Straub, Gail P. Jarvik, Eric B. Larson, Digna R. Velez Edwards, Todd L. Edwards, Lea K. Davis, Hakon Hakonarson, Chunhua Weng, David Fasel, Bjorn C. Knollmann, Thomas J. Wang, Joshua C. Denny, Patrick T. Ellinor, Dan M. Roden, Jonathan D. Mosley
Institutions: Inserm, Sorbonne Université, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Fondation pour l’innovation en Cadiométabolisme et Nutrition, CIC Paris-est, Vanderbilt University Medical Center, University of Washington, Kaiser Permanente Washington Health Research Institute, Children's Hospital of Philadelphia, Columbia University, Broad Institute, Massachusetts General Hospital
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: American Heart Association, National Institutes of Health, National Heart, Lung, and Blood Institute, National Human Genome Research Institute, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke, U.S. National Library of Medicine, National Center for Research Resources, National Center for Advancing Translational Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1855952650, G1967470738, Understanding the genetic risk underlying racial disparities in uterine fibroids, G2310098089, G2328519459, G2505793412, G25420283, G3420921512, G4538165758, Genetic Epidemiology of Multiple Sclerosis, Beyond PheWAS: Recognition of Phenotype Patterns for Discovery and Translation, The Vanderbilt Institute for Clinical and Translational Research (VICTR) UL1, Delineating epidemiological and genetic factors associated with cardiac diastolic dysfunction, High-throughput Discovery of Pathogenic Cardiac Sodium Channel Variants, The Vanderbilt Institute for Clinical and Translational Research (VICTR), Vanderbilt Genome Electronic Records Project, Molecular and Cellular Basis for the Efficacy of Bariatric Surgery, Epidemiologic Architecture for Genes Linked to Environment (EAGLE), Vanderbilt Institute for Clinical and Translational Research (VICTR), G949362299, G95160140, G96670786
OpenAlex ID: W2913258494
