Abstract

IntroductionEvidence indicates that rheumatoid arthritis (RA) patients have increased susceptibility to myocardial ischaemia that contributes to myocardial infarction. The subendocardial viability ratio (SEVR) can be measured using pulse wave analysis and reflects myocardial oxygen supply and demand. The objective of the present study was to examine specific predictors of SEVR in RA patients, with a specific focus on inflammation and classical cardiovascular disease (CVD) risk factors.MethodsTwo patient cohorts were included in the study; a primary cohort consisting of 220 RA patients and a validation cohort of 127 RA patients. All patients underwent assessment of SEVR using pulse wave analysis. Thirty-one patients from the primary cohort who were about to start anti-inflammatory treatment were prospectively examined for SEVR at pretreatment baseline and 2 weeks, 3 months and 1 year following treatment. Systemic markers of disease activity and classical CVD risk factors were assessed in all patients.ResultsThe SEVR (mean ± standard deviation) for RA in the primary cohort was 148 ± 27 and in the validation cohort was 142 ± 25. Regression analyses revealed that all parameters of RA disease activity were associated with SEVR, along with gender, blood pressure and heart rate. These findings were the same in the validation cohort. Analysis of longitudinal data showed that C-reactive protein (P < 0.001), erythrocyte sedimentation rate (P < 0.005), Disease Activity Score in 28 joints (P < 0.001), mean blood pressure (P < 0.005) and augmentation index (P < 0.001) were significantly reduced after commencing anti-TNFα treatment. Increasing C-reactive protein was found to be associated with a reduction in SEVR (P = 0.02) and an increase in augmentation index (P = 0.001).ConclusionThe present findings reveal that the SEVR is associated with markers of disease activity as well as highly prevalent classical CVD risk factors in RA, such as high blood pressure and diabetes. Further prospective studies are required to determine whether the SEVR predicts future cardiac events in RA.

Highlights

  • Evidence indicates that rheumatoid arthritis (RA) patients have increased susceptibility to myocardial ischaemia that contributes to myocardial infarction

  • RA associates with an increased risk for cardiovascular disease (CVD) [1], which is only partially explained by traditional CVD risk factors [2]

  • Effects of medications on the subendocardial viability ratio Univariate analysis of variance showed that the SEVR did not differ between patients receiving or not receiving steroid treatment in both the primary and validation cohorts

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Summary

Introduction

Evidence indicates that rheumatoid arthritis (RA) patients have increased susceptibility to myocardial ischaemia that contributes to myocardial infarction. The objective of the present study was to examine specific predictors of SEVR in RA patients, with a specific focus on inflammation and classical cardiovascular disease (CVD) risk factors. A study in RA patients without overt coronary artery disease reported abnormalities in myocardial perfusion using contrast-enhanced magnetic resonance imaging (cMRI), and the degree of abnormality was related to the extent of RA disease-related inflammation [5]. RA patients undergoing coronary angiography had greater myocardial ischaemia than healthy controls who were matched for classical CVD risk factors, but had similar levels of ischaemia to agematched and sex-matched diabetic controls [6]. Myocardial ischaemia was evident despite the absence of obstructive coronary artery disease, suggesting a microvascular cause for the ischaemia [6]

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