Methotrexate use, MTHFR polymorphisms and traditional risk factors in predicting cardiovascular events in elderly males with rheumatoid arthritis (RA). (22nd February 2011)

• Record Type: Journal Article
• Authors: Davis, Lisa A; Cannon, Grant W; Pointer, Lauren M; Wolff, Roger K; Mikuls, Ted R; Haverhals, Leah; Reimold, Andreas M; Kerr, Gail S; Richards, J Steuart; Johnson, Dannette S; Caplan, Liron
• Is Part Of: Annals of the rheumatic diseases. Volume 70(2011)Supplement 2
• Page Start: A92
• Page End: A93
• Publication Date: 2011-02-22
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/ard.2011.151209.1
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Objective: The enzyme methylenetetrahydrofolate reductase (MTHFR) has been implicated in the metabolism of methotrexate (MTX) – the most common disease modifying antirheumatic drug used to treat rheumatoid arthritis (RA). MTHFR C677T and A1298C polymorphisms have been associated with increased cardiovascular (CV) events in non-RA populations. We explored the potential associations of MTHFR C677T, A1298C and MTX with decreased time-to-CV event in the prospective Veterans Affairs Rheumatoid Arthritis (VARA) registry. Methods: VARA participants were genotyped for MTHFR polymorphisms. Demographic information, RA duration and auto-antibody status were collected upon enrolment into the registry. Disease activity was recorded at baseline and at follow-up visits. Patients' baseline comorbidities and the outcome variable were defined using ICD-9 and CPT codes recorded in inpatient and outpatient patient treatment files. The combined CV event outcome included: myocardial infarction (MI), percutaneous transluminal coronary angioplasty, coronary artery bypass graft and stroke. Multivariable Cox proportional-hazards regression was used to model the time-to-CV event. Results: Data were available for 1047 subjects. Post-enrolment CV events occurred in 406 patients. Prior MI was strongly associated with time-to-CV event (HR 6.65 (CI 5.31 to 8.33)), as was hyperlipidaemia (HR 1.64 (CI 1.32 to 2.05)). Methotrexate use was associated with a substantial decline in first CV events (HR 0.76 (CI 0.62 to 0.92)). MTHFR polymorphisms were not associated with decreased time-to-CV event. Conclusions: Although MTHFR polymorphisms have previously been associated with increased CV events, we found no evidence that MTHFR status was associated with VARA patients' time-to-CV event. Traditional CV risk factors conferred substantial CV risk, while methotrexate use was protective.