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Increasing Extracellular Volume Fraction on Coronary CTA in Patients With Coronary Microvascular Dysfunction
Kodai Sayama1, Yoshihisa Kanaji1, Eisuke Usui1
1Department of Cardiovascular Medicine (K.S., Y.K., E.U., M. Hada, T.N., H.U., K.N., M.S., T.T., H.S., T.W., T. Sakamoto, R.S., T.M., M. Hoshino, T.K.), Tsuchiura Kyodo General Hospital, Japan.
Coronary computed tomography angiography (CCTA)-derived extracellular volume fraction (ECV) is linked to coronary microvascular dysfunction (CMD) in angina with nonobstructive coronary artery disease (ANOCA). Elevated ECV may help identify patients needing personalized management for chest pain.
Area of Science:
- Cardiology
- Radiology
- Medical Imaging
Background:
- Coronary microvascular dysfunction (CMD) is a key factor in chest pain, particularly in angina with nonobstructive coronary artery disease (ANOCA).
- Coronary computed tomography angiography (CCTA) can assess myocardial fibrosis via extracellular volume fraction (ECV), but its association with CMD in ANOCA is unclear.
Purpose of the Study:
- To investigate the relationship between CCTA-derived ECV and CMD in patients diagnosed with ANOCA.
Main Methods:
- A retrospective analysis of 57 ANOCA patients who underwent CCTA with ECV protocol and invasive functional testing.
- Exclusion criteria included significant epicardial stenosis, prior revascularization, myocardial infarction, or heart failure.
- CMD was defined by a coronary flow reserve <2.5; diastolic dysfunction (DD) was assessed via echocardiography.
Main Results:
- Of 57 patients, 26 (45.6%) had CMD. CMD correlated with age, NT-proBNP, calcium score, DD, and higher ECV.
- CCTA-derived ECV >31.9% was independently associated with CMD (OR, 10.50; P=0.002).
- Diastolic dysfunction (DD) was also an independent predictor (OR, 17.90; P=0.004), and adding ECV to a model with DD improved CMD discrimination (AUC, 0.854).
Conclusions:
- Patients with ANOCA and CMD exhibit significantly elevated ECV and a higher prevalence of DD.
- ECV and DD may serve as crucial biomarkers for tailoring management strategies in ANOCA patients with CMD.
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