Exercise capacity as a predictor of coronary microvascular dysfunction

European Heart Journal

3 October 2022
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ESC Journals

Abstract

AbstractIntroduction

Exercise capacity (EC) is an important prognostic test in patients with coronary artery disease (CAD). Positron-emission tomography (PET) is an important risk-stratifying tool to tailor management of patients with coronary artery disease.

Purpose

We aimed to assess EC in predicting positron emission tomography (PET) myocardial perfusion imaging (MPI) derived coronary flow reserve (CFR).

Methods

Consecutive patients who had clinically indicated PET MPI and EC were included. EC was defined based on peak metabolic equivalents (METS) achieved during exercise stress test. Myocardial blood flow (MBF) in ml/gm/min was obtained from dynamic PET MPI images at rest and peak hyperemia. The coronary flow reserve (CFR) was calculated as the ratio of stress to rest MBF of the left ventricle.

Results

The study population consisted of 511 patients who underwent PET MPI and EC testing (mean age 56 (±11), 71% male). Cardiovascular risk factors were prevalent (75% hypertensive, 82% dyslipidemic, 43% diabetics, 27% known CAD). Peak METS >6 was achieved in 81% of patients, and the CFR <2 was present in 27%. In multivariable logistic regression models adjusted for age, sex, cardiovascular risk factors (hypertension, diabetes, dyslipidemia) and medication use (angiotensin converting enzyme inhibitor/angiotensin receptor blocker, statins, beta-blockers), patients with peak METS >6 had a statistically significant lower odds of microvascular dysfunction (CFR <2: OR 0.43, 95% CI 0.26–0.71, p=0.001). Assessment of discrimination showed the model with CFR <2 had an incremental improvement of Harrell's C statistic over clinical variables (0.65 vs 0.69, p=0.02).

Conclusion

Our findings showed exercise capacity was a good predictor of CFR and microvascular coronary health over and above clinical variables. Further studies are needed to assess the prognostic interplay between EC and CFR.

Funding Acknowledgement

Type of funding sources: None.

Contributors