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

Author:

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

Abstract

Background Coronary 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 results We 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 (<20 mg/g). The group mean age was 54 ± 11 years, with a moderate cardiac risk factor burden including low diabetes prevalence, and a mean UACR of 12 ± 55 mg/g (range 9.5–322.7 mg/g). Overall, coronary endothelial-dependent variables (change in coronary blood flow and coronary diameter in response to cold pressor testing) had significant inverse correlations with log UACR (r = -0.17, p = 0.05; r = -0.18, p = 0.03, respectively). Conclusions Among 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 registration https://clinicaltrials.gov/ct2/show/NCT00832702.

Funder

National Heart, Lung and Blood Institutes

National Center for Research Resources

National Center for Advancing Translational Sciences

Gustavus and Louise Pfeiffer Research Foundation

The Women’s Guild of Cedars-Sinai Medical Center, Los Angeles, CA

Ladies Hospital Aid Society

QMED, Inc., Laurence Harbor, NJ

Edythe L. Broad and the Constance Austin Women’s Heart Research Fellowships, Cedars-Sinai Medical Center, Los Angeles, California

Barbra Streisand Women’s Cardiovascular Research and Education Program, Cedars-Sinai Medical Center, Los Angeles

The Society for Women’s Health Research (SWHR), Washington, D.C.

Linda Joy Pollin Women’s Heart Health Program, the Erika Glazer Women’s Heart Health Project

Adelson Family Foundation, Cedars-Sinai Medical Center, Los Angeles, California

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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