An Atlas Characterizing the Shared Genetic Architecture of Inflammatory Bowel Disease with Clinical and Behavioral Traits

Author:

Shaw Vikram R1ORCID,Byun Jinyoung123,Pettit Rowland W1,Hou Jason K4,Walsh Kyle M5,Han Younghun12,Amos Christopher I123ORCID

Affiliation:

1. Institute for Clinical and Translational Research, Baylor College of Medicine , Houston, TX , USA

2. Section of Epidemiology and Population Sciences, Department of Medicine, Baylor College of Medicine , Houston, TX , USA

3. Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine , Houston, TX , USA

4. Department of Medicine-Gastroenterology, Baylor College of Medicine , Houston, TX , USA

5. Division of Neuro-epidemiology, Department of Neurosurgery, Duke University School of Medicine , Durham, NC , USA

Abstract

Abstract Background Inflammatory bowel disease (IBD) development is a complex, multifactorial process that involves extrinsic and intrinsic factors such as host genetics, the immune system, the gut microbiome, and environmental risks. To help understand the genetic contribution of clinical, behavioral, psychiatric, and diet-related traits, we aim to provide a deep and comprehensive characterization of the shared genetic architecture between IBD and hundreds of potentially related traits. Methods Utilizing publicly available summary statistics from a previously published IBD genome-wide association study and hundreds of traits from the United Kingdom BioBank (UKBB), we performed linkage disequilibrium score regression (LDSR) analysis to estimate cross-trait genetic correlations between Crohn’s disease (CD), ulcerative colitis (UC), and IBD summary statistics with the UKBB traits of interest. Results Nominally significant (P < .05) genetic correlations were observed for 181 traits in overall IBD, 239 traits in CD, and 94 traits in UC. We replicate the known association between smoking behavior and CD/UC, namely that current tobacco smoking has a positive genetic correlation with CD (rg = 0.12, P = 4.2 × 10-4), while “ever smoking” has a negative genetic correlation with UC (rg = −0.07, P = .042). Globally, all 3 strata (IBD, CD, and UC) demonstrated increased genetic correlations for psychiatric-related traits related to anxiety and depression. Conclusion The present analysis reveals the shared genetic architecture between multiple traits and IBD, CD, and UC. Understanding the relevance of joint occurrences of IBD with psychiatric diseases may moderate management of these diseases for individuals jointly affected by them.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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