PLoS ONE (Jan 2021)

Coronary endothelial dysfunction appears to be a manifestation of a systemic process: A report from the Women's Ischemia Syndrome Evaluation - Coronary Vascular Dysfunction (WISE-CVD) study.

  • Sawan Jalnapurkar,
  • Sofy Landes,
  • Janet Wei,
  • Puja K Mehta,
  • Chrisandra Shufelt,
  • Margo Minissian,
  • Carl J Pepine,
  • Eileen Handberg,
  • Galen Cook-Wiens,
  • George Sopko,
  • C Noel Bairey Merz

DOI
https://doi.org/10.1371/journal.pone.0257184
Journal volume & issue
Vol. 16, no. 9
p. e0257184

Abstract

Read online

BackgroundCoronary microvascular dysfunction (CMD) is prevalent in symptomatic women with ischemia but no obstructive coronary artery disease (INOCA). Urine albumin-creatinine ratio (UACR) is a measure of renal microvascular endothelial dysfunction. Both are predictors of adverse cardiovascular events. It is unknown if CMD could be a manifestation of a systemic process. We evaluated the relationship between renal microvascular dysfunction and CMD as measured by invasive coronary function testing (CFT).Methods and resultsWe measured urine albumin and creatinine to provide UACR in 152 women enrolled in the Women's Ischemia Syndrome Evaluation-Coronary Vascular Dysfunction (WISE-CVD) study (2008-2015) with suspected INOCA who underwent CFT. Invasive CFT measures of endothelial and non-endothelial dependent coronary microvascular function were obtained. Subjects were divided into those with detectable (≥20 mg/g) and undetectable urine albumin (ConclusionsAmong women with INOCA and relatively low risk factor including diabetes burden, renal microvascular dysfunction, measured by UACR, is related to coronary endothelial-dependent CMD. These results suggest that coronary endothelial-dependent function may be a manifestation of a systemic process. Enhancing efferent arteriolar vasodilatation in both coronary endothelial-dependent function and renal microvascular dysfunction pose potential targets for investigation and treatment.Clinical trial registrationhttps://clinicaltrials.gov/ct2/show/NCT00832702.