Menu
GWAS Study

Shared genetic risk factors and causal association between psoriasis and coronary artery disease.

Patrick MT, Li Q, Wasikowski R et al.

36323703 PubMed ID
GWAS Study Type
211665 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PM
Patrick MT
LQ
Li Q
WR
Wasikowski R
MN
Mehta N
GJ
Gudjonsson JE
EJ
Elder JT
ZX
Zhou X
TL
Tsoi LC
Chapter II

Abstract

Summary of the research findings

Psoriasis and coronary artery disease (CAD) are related comorbidities that are well established, but whether a genetic basis underlies this is not well studied. We apply trans-disease meta-analysis to 11,024 psoriasis and 60,801 CAD cases, along with their associated controls, identifying one opposing and three shared genetic loci, which are confirmed through colocalization analysis. Combining results from Bayesian credible interval analysis with independent information from genomic, epigenomic, and spatial chromatin organization, we prioritize genes (including IFIH1 and IL23A) that have implications for common molecular mechanisms involved in psoriasis and CAD inflammatory signaling. Chronic systemic inflammation has been associated with CAD and myocardial infarction, and Mendelian randomization analysis finds that CAD as an exposure can have a significant causal effect on psoriasis (OR = 1.11; p = 3×10-6) following adjustment for BMI and waist-hip ratio. Together, these findings suggest that systemic inflammation which causes CAD can increase the risk of psoriasis.

11,024 psoriasis cases, 60,801 coronary artery disease cases, 139,840 controls

Chapter III

Study Statistics

Key metrics and study information

211665
Total Participants
GWAS
Study Type
No
Replicated
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.