Diastolic dysfunction in women with ischemia and no obstructive coronary artery disease: Mechanistic insight from magnetic resonance imaging

dc.contributor.authorSamuel, T. Jake
dc.contributor.authorWei, Janet
dc.contributor.authorSharif, Behzad
dc.contributor.authorTamarappoo, Balaji K.
dc.contributor.authorPattisapu, Varun
dc.contributor.authorMaughan, Jenna
dc.contributor.authorCipher, Daisha J.
dc.contributor.authorSuppogu, Nissi
dc.contributor.authorAldiwani, Haider
dc.contributor.authorThomson, Louise E. J.
dc.contributor.authorShufelt, Chrisandra
dc.contributor.authorBerman, Daniel S.
dc.contributor.authorLi, Debiao
dc.contributor.authorBairey Merz, C. Noel
dc.contributor.authorNelson, Michael D.
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-11-25T13:49:41Z
dc.date.available2024-11-25T13:49:41Z
dc.date.issued2021
dc.description.abstractBackground: Ischemia with no obstructive coronary artery disease (INOCA) is prevalent in women and is associated with increased risk of developing heart failure with preserved ejection fraction (HFpEF); however, the mechanism(s) contributing to this progression remains unclear. Given that diastolic dysfunction is common in women with INOCA, defining mechanisms related to diastolic dysfunction in INOCA could identify therapeutic targets to prevent HFpEF. Methods: Cardiac MRI was performed in 65 women with INOCA and 12 reference controls. Diastolic function was defined by left ventricular early diastolic circumferential strain rate (eCSRd). Contributors to diastolic dysfunction were chosen a priori as coronary vascular dysfunction (myocardial perfusion reserve index [MPRI]), diffuse myocardial fibrosis (extracellular volume [ECV]), and aortic stiffness (aortic pulse wave velocity [aPWV]). Results: Compared to controls, eCSRd was lower in INOCA (1.61 ± 0.33/s vs. 1.36 ± 0.31/s, P = 0.016); however, this difference was not exaggerated when the INOCA group was sub-divided by low and high MPRI (P > 0.05) nor was ECV elevated in INOCA (29.0 ± 1.9% vs. 28.0 ± 3.2%, control vs. INOCA; P = 0.38). However, aPWV was higher in INOCA vs. controls (8.1 ± 3.2 m/s vs. 6.1 ± 1.5 m/s; P = 0.045), and was associated with eCSRd (r = -0.50, P < 0.001). By multivariable linear regression analysis, aPWV was an independent predictor of decreased eCSRd (standardized β = -0.39, P = 0.003), as was having an elevated left ventricular mass index (standardized β = -0.25, P = 0.024) and lower ECV (standardized β = 0.30, P = 0.003). Conclusions: These data provide mechanistic insight into diastolic dysfunction in women with INOCA, identifying aortic stiffness and ventricular remodeling as putative therapeutic targets.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationSamuel TJ, Wei J, Sharif B, et al. Diastolic dysfunction in women with ischemia and no obstructive coronary artery disease: Mechanistic insight from magnetic resonance imaging. Int J Cardiol. 2021;331:1-7. doi:10.1016/j.ijcard.2021.01.064
dc.identifier.urihttps://hdl.handle.net/1805/44690
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.ijcard.2021.01.064
dc.relation.journalInternational Journal of Cardiology
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectAortic stiffness
dc.subjectCoronary vascular dysfunction
dc.subjectDiastolic function
dc.subjectMRI
dc.subjectMyocardial perfusion reserve
dc.subjectPulse wave velocity
dc.titleDiastolic dysfunction in women with ischemia and no obstructive coronary artery disease: Mechanistic insight from magnetic resonance imaging
dc.typeArticle
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