Genome‐wide polygenic risk score for rheumatoid arthritis prediction in postmenopausal women

Author:

Xu Yingke12,Wu Qing3ORCID

Affiliation:

1. Nevada Institute of Personalized Medicine, College of Science University of Nevada Las Vegas NV USA

2. Department of Epidemiology and Biostatistics, School of Public Health the University of Nevada Las Vegas Las Vegas NV USA

3. Department of Biomedical Informatics, College of Medicine The Ohio State University Columbus OH USA

Abstract

AbstractBackgroundRheumatoid arthritis (RA), a common autoimmune disease, exhibits a vital genetic component. Polygenic risk scores (PRS) derived from genome‐wide association studies (GWAS) offer potential utility in predicting disease susceptibility. The present study aimed to develop and validate a PRS for predicting RA risk in postmenopausal women.MethodsThe study developed a novel PRS using 225,000 genetic variants from a GWAS dataset. The PRS was developed in a cohort of 8967 postmenopausal women and validated in an independent cohort of 6269 postmenopausal women. Among the development cohort, approximately 70% were Hispanic and approximately 30% were African American. The testing cohort comprised approximately 50% Hispanic and 50% Caucasian individuals. Stratification according to PRS quintiles revealed a pronounced gradient in RA prevalence and odds ratios.ResultsHigh PRS was significantly associated with increased RA risk in individuals aged 60–70 years, ≥ 70 years, and overweight and obese participants. Furthermore, at age 65 years, individuals in the bottom 5% of the PRS distribution have an absolute risk of RA at 30.6% (95% confidence interval = 18.5%–42.6%). The risk increased to 53.8% (95% confidence interval = 42.8%–64.9%) for those in the top 5% of the PRS distribution.ConclusionsThe PRS developed in the present study is significantly associated with RA risk, showing the potential for early screening of RA in postmenopausal women. This work demonstrates the feasibility of personalized medicine in identifying high‐risk individuals for RA, indicating the need for further studies to test the utility of PRS in other populations.

Funder

National Institute of General Medical Sciences

Publisher

Wiley

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