Coronary Microvascular Dysfunction in Rheumatoid Arthritis Compared to Diabetes Mellitus and Association With All-Cause Mortality.
Aged
Arthritis, Rheumatoid
/ diagnosis
Cause of Death
Coronary Artery Disease
/ diagnostic imaging
Coronary Circulation
Coronary Vessels
/ diagnostic imaging
Diabetes Mellitus
/ diagnosis
Female
Heart Disease Risk Factors
Humans
Male
Microcirculation
Middle Aged
Prevalence
Prognosis
Registries
Retrospective Studies
Risk Assessment
Journal
Arthritis care & research
ISSN: 2151-4658
Titre abrégé: Arthritis Care Res (Hoboken)
Pays: United States
ID NLM: 101518086
Informations de publication
Date de publication:
02 2021
02 2021
Historique:
received:
02
02
2019
accepted:
05
11
2019
pubmed:
11
11
2019
medline:
24
2
2021
entrez:
10
11
2019
Statut:
ppublish
Résumé
Coronary microvascular dysfunction (CMD) is a predictor of cardiac death in diabetes mellitus (DM) independent of traditional cardiovascular (CV) risk factors. Rheumatoid arthritis (RA) is a chronic inflammatory condition, with excess CV risk compared to the general population, in which CMD is hypothesized to play a role; however, there are limited data on CMD in RA and any association with clinical outcomes. The objective of this study was to compare the prevalence of CMD in RA to that in DM and to test the association with all-cause mortality. We performed a retrospective cohort study using data from a registry of all patients undergoing stress myocardial perfusion positron emission tomography as part of routine clinical care from 2006 to 2017. The inclusion criterion was a normal perfusion scan. Patients with RA or DM were classified using previously published approaches. Coronary flow reserve (CFR) was calculated for all patients in the registry and linked with mortality data. CMD was defined as CFR <2.0. We studied 73 patients with RA and 441 patients with DM. Among patients with a normal perfusion scan, the prevalence of CMD in RA was similar to that in DM (P = 0.2). CMD was associated with increased risk for all-cause mortality in RA (hazard ratio 2.4 [95% confidence interval 1.4-4.2]) as well as increased risk for cardiac-related death at rates similar to those in DM. These findings suggest an important role for CMD as a potential contributor to excess CV risk and mortality in RA, as previously observed in DM, as well as evidence for a mechanistic link between inflammation and cardiovascular disease.
Identifiants
pubmed: 31705724
doi: 10.1002/acr.24108
pmc: PMC7210065
mid: NIHMS1058575
doi:
Types de publication
Comparative Study
Journal Article
Observational Study
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
159-165Subventions
Organisme : NIAMS NIH HHS
ID : P30 AR072577
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL127118
Pays : United States
Informations de copyright
© 2019, American College of Rheumatology.
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