Plasma metabolomics and incident major adverse cardiovascular events in patients with rheumatoid arthritis.

Authors

Christos P Kotanidis, Priyam Choksi, Pradeep Natarajan, Jessica Lasky-Su, Anand Rohatgi, Elizabeth Karlson, Katherine P Liao, Michael Garshick, Charalambos Antoniades, Ron Blankstein, Michael Honigberg, Leo Buckley, Brittany N Weber

Published in

Rheumatology (Oxford, England). Jul 31, 2026. Epub Jul 31, 2026.

Abstract

Patients with rheumatoid arthritis (RA) have excess cardiovascular risk beyond traditional factors. We evaluated associations between plasma metabolites and incident major adverse cardiovascular events (MACE) in RA and compared findings with matched controls.
We studied 1,271 Mass General Brigham Biobank participants with RA, without known cardiovascular disease, and no statin use at blood draw. 1H-NMR metabolomics quantified 168 metabolites spanning lipoprotein particles and contents, fatty acids, amino acids, and glycolysis. Incident MACE (myocardial infarction, stroke, transient ischemic attack, or death) was identified using ICD codes. Multivariable Cox models with false discovery rate correction assessed associations. Findings were compared with a 1:2 matched non-RA control cohort.
The mean age was 62 years, 80% were women, and 8% experienced incident MACE over a median follow-up of 7.8 years. Twenty-five plasma metabolites were significantly associated with MACE. Lower MACE risk was primarily associated with higher levels of small HDL particle concentration and lipid content, as well as circulating albumin and select amino acids. In contrast, higher MACE risk was strongly associated with triglyceride-rich and remnant-like lipoprotein measures. When compared with controls, several associations were unique to the RA patients, who demonstrated a distinct metabolomic risk profile, involving triglyceride-rich VLDL and HDL particles.
In this first metabolomic study in RA, we identified a distinct cardiovascular risk profile. Higher levels of large HDL particles were associated with increased risk, whereas small HDL particles were associated with lower risk, with potential implications for inflammation-targeted and HDL-modifying therapies.

PMID:
42538831
Bibliographic data and abstract were imported from PubMed on 01 Aug 2026.

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