rs12188958 - CDH9
Magnitude 2.2 · 1 study on file
Reported associations
-
Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis - Unknown journal (n.d.) · Unknown authors · PubMed 37326842
ABSTRACT: Abstract Objectives To investigate the influence of genetic factors on persistence with treatment of early RA with MTX monotherapy. Methods We conducted a genome-wide association study (GWAS) in a sample of 3902 Swedish early-RA patients initiating MTX in DMARD monotherapy as their first-ever DMARD. The outcome, short- and long-term MTX treatment persistence, was defined as remaining on MTX at 1 and at 3 years, respectively, with no additional DMARDs added. As genetic predictors, we investigated individual SNPs, and then calculated a polygenic risk score (PRS) based on SNPs associated with RA risk. The SNP-based heritability of persistence was estimated overall and by RA serostatus. Results No individual SNP reached genome-wide significance (P < 5 × 10−8), either for per
Auto-generated from study metadata. AI-synthesised commentary is added when this entry is regenerated through content-service's LLM mode.
Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
-
Methotrexate response in rheumatoid arthritis Moderate
rs12188958 C allele is associated with improved persistence with methotrexate in early rheumatoid arthritis.
If diagnosed with RA, discuss this variant with your rheumatologist before starting methotrexate therapy.