Coronary Microvascular Dysfunction in Rheumatoid Arthritis Compared to Diabetes Mellitus and Association With

Katherine P Liao1, Jie Huang1, Zeling He1

  • 1Brigham and Women's Hospital, Boston, Massachusetts.

Arthritis Care & Research
|November 10, 2019
PubMed

Insights

Coronary microvascular dysfunction (CMD) is prevalent in rheumatoid arthritis (RA) similar to diabetes mellitus (DM). CMD in RA patients is linked to increased all-cause mortality, suggesting a role in cardiovascular risk.

Area of Science:

  • Cardiology
  • Rheumatology
  • Vascular Biology

Background:

  • Coronary microvascular dysfunction (CMD) predicts cardiac death in diabetes mellitus (DM) independently of traditional risk factors.
  • Rheumatoid arthritis (RA) is linked to increased cardiovascular (CV) risk, with CMD hypothesized as a contributing factor, yet data are limited.
  • Limited data exist on CMD prevalence and its association with clinical outcomes in RA patients.

Purpose of the Study:

  • To compare the prevalence of CMD in RA patients versus DM patients.
  • To investigate the association between CMD and all-cause mortality in RA.
  • To explore the mechanistic link between inflammation and cardiovascular disease in RA.

Main Methods:

  • Retrospective cohort study utilizing stress myocardial perfusion positron emission tomography data (2006-2017).
  • Inclusion criterion: normal perfusion scan. Patients classified as RA or DM.
  • Coronary flow reserve (CFR) calculated; CMD defined as CFR <2.0. Mortality data linked.

Main Results:

  • Study included 73 RA patients and 441 DM patients.
  • CMD prevalence in RA was similar to DM among patients with normal perfusion scans (P=0.2).
  • CMD associated with increased all-cause mortality in RA (HR 2.4) and similar cardiac death rates as DM.

Conclusions:

  • CMD plays a significant role in the excess CV risk and mortality observed in RA.
  • Findings support CMD as a mechanistic link between inflammation and cardiovascular disease.
  • CMD is an important consideration for cardiovascular risk assessment in RA patients.
Abstract

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