Rheumatoid arthritis (RA) patients who take methotrexate do so because they hope it will reduce pain and inflammation and slow the progression of the disease. But patients who take methotrexate for these reasons may experience an additional benefit when it comes to their heart health.
Methotrexate, a conventional disease-modifying antirheumatic drug (DMARD), has long been believed to be cardio-protective in people who have RA, and research has shown that RA patients who take it have a reduced risk of serious cardiovascular events like heart attacks and strokes. But is that heart protection really a direct benefit of methotrexate, or is it simply the result of getting RA disease activity under good control?
To find out, researchers led by Tate Johnson, MD, at the University of Nebraska Medical Center analyzed data on a large (2,168) group of U.S. Veterans who had RA and were considered high risk for cardiovascular events. The researchers focused on the patients’ health status (based on check-ups with medical providers), prescription use (including methotrexate), and cardiovascular events over a 10-year period (2005 to 2015).
As expected, the researchers found that cardiovascular events were less likely to occur in patients who had taken methotrexate. But they were also able to use statistical modeling to “reduce confounding by disease activity” and focus on the association between methotrexate and cardiovascular events.
According to their analysis, which was presented at the 2019 American College of Rheumatology/Association of Rheumatology Professionals Annual Meeting in Atlanta, RA patients who used methotrexate were 30 percent less likely to experience a cardiovascular event such as a heart attack, stroke, or heart failure that required hospitalization.
“We used statistical approaches that adjusted for known links between RA disease activity and cardiovascular risk, as well as RA disease activity and use of methotrexate. We also performed analyses evaluating cardiovascular risk that adjusted for disease activity before and after methotrexate use,” says Dr. Johnson. “Our findings suggest that, in addition to controlling RA disease activity, methotrexate may have other means of reducing cardiovascular disease risk in RA.”
Interesting, methotrexate might only protect the heart in certain populations. An unrelated large study (CIRT) that involved patients with cardiovascular disease (and who did not have RA) found that those who took methotrexate were not any less likely to avoid a heart attack, stroke, or other serious cardiovascular event.
“While the CIRT trial did not find methotrexate to be cardioprotective, not all subjects in the trial had systemic inflammation, in contrast to patients with RA,” says Dr. Johnson. “Potential cardiovascular benefits of methotrexate beyond lowering RA disease activity include lower systemic inflammation as well as improved lipoprotein and endothelial function. More research is needed to understand these mechanisms and whether they may be specific to patients with RA.”
Use Our ArthritisPower App to Manage Your Arthritis
Join CreakyJoints’ patient-centered research registry to track your symptoms, disease activity, and medications — and share with your doctor. Learn more and sign up here.
Keep Reading
Endothelial Function Testing. Cedars Sinai. https://www.cedars-sinai.org/programs/heart/clinical/womens-heart/services/endothelial-function-testing.html.
Johnson T, et al. Methotrexate Is Associated with Reduced Cardiovascular Risk in Rheumatoid Arthritis Independent of Disease Activity Modification [abstract]. Arthritis & Rheumatology. 2019. https://acrabstracts.org/abstract/methotrexate-is-associated-with-reduced-cardiovascular-risk-in-rheumatoid-arthritis-independent-of-disease-activity-modification.
Ridker PM, et al. Low-Dose Methotrexate for the Prevention of Atherosclerotic Events. New England Journal of Medicine. 2019. doi: 10.1056/nejmoa1809798.
Westlake SL, et al. The effect of methotrexate on cardiovascular disease in patients with rheumatoid arthritis: a systematic literature review. Rheumatology. 2010. doi: 10.1093/rheumatology/kep366.