Coronary Vascular Function and Cardiomyocyte Injury

Author:

AlBadri Ahmed1,Wei Janet2,Quesada Odayme2,Mehta Puja K.1,Xiao Yi1ORCID,Ko Yi-An1,Anderson R. David3,Petersen John3,Azarbal Babak2,Samuels Bruce2,Henry Timothy D.2ORCID,Cook-Wiens Galen4ORCID,Handberg Eileen M.3,Van Eyk Jennifer2,Pepine Carl J.3ORCID,Bairey Merz C. Noel2ORCID

Affiliation:

1. Emory Clinical Cardiovascular Research Institute, Department of Medicine, Emory University School of Medicine, Atlanta, GA (A.A., P.K.M., Y.X., Y.-A.K.).

2. Barbra Streisand Women’s Heart Center, Cedars-Sinai Smidt Heart Institute, Los Angeles, CA (J.W., O.Q., B.A., B.S., T.D.H., J.V.E., C.N.B.M.).

3. Division of Cardiovascular Medicine, University of Florida College of Medicine, Gainesville (R.D.A., J.P., E.M.H., C.J.P.).

4. Biostatistics and Bioinformatics Research Center, Cedars-Sinai Medical Center, Los Angeles, CA (G.C.-W.).

Abstract

Objective: Women with symptoms or signs of myocardial ischemia but no obstructive coronary artery disease (INOCA) often have coronary vascular dysfunction and elevated risk for adverse cardiovascular events. We hypothesized that u-hscTnI (ultra-high–sensitivity cardiac troponin I), a sensitive indicator of ischemic cardiomyocyte injury, is associated with coronary vascular dysfunction in women with INOCA. Approach and Results: Women (N=263) with INOCA enrolled in the WISE-CVD study (Women’s Ischemic Syndrome Evaluation–Coronary Vascular Dysfunction) underwent invasive coronary vascular function testing and u-hscTnI measurements (Simoa HD-1 Analyzer; Quanterix Corporation, Lexington, MA). Logistic regression models, adjusted for traditional cardiovascular risk factors were used to evaluate associations between u-hscTnI and coronary vascular function. Women with coronary vascular dysfunction (microvascular constriction and limited coronary epicardial dilation) had higher plasma u-hscTnI levels (both P =0.001). u-hscTnI levels were associated with microvascular constriction (odds ratio, 1.38 per doubling of u-hscTnI [95% CI, 1.03–1.84]; P =0.033) and limited coronary epicardial dilation (odds ratio, 1.37 per doubling of u-hscTnI [95% CI, 1.04–1.81]; P =0.026). u-hscTnI levels were not associated with microvascular dilation or coronary epicardial constriction. Conclusions: Our findings indicate that higher u-hscTnI is associated with coronary vascular dysfunction in women with INOCA. This suggests that ischemic cardiomyocyte injury in the setting of coronary vascular dysfunction has the potential to contribute to adverse cardiovascular outcomes observed in these women. Additional studies are needed to confirm and investigate mechanisms underlying these findings in INOCA. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT00832702.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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