Key result
18F-AlF-FAPI uptake inversely correlates with systolic LV wall thickening, detecting fibrosis and predicting mechanical dyssynchrony.
Why the study?
Myocardial fibrosis contributes to LV mechanical dyssynchrony, but the relationship between LVMD, myocardial fibrosis, and patterns of LV fibrosis distribution in CAD and DMVR participants using 18F-AlF-FAPI PET/MR required exploration.
Does 18F-AlF-FAPI PET/MR imaging detect myocardial fibrosis and predict left ventricular mechanical dyssynchrony in CAD and DMVR patients?
Observational (n=37)
No
Does 18F-AlF-FAPI PET/MR imaging detect myocardial fibrosis and predict left ventricular mechanical dyssynchrony in CAD and DMVR patients?
18F-AlF-FAPI PET/MR imaging can detect myocardial fibrosis, predict left ventricular mechanical dyssynchrony, and differentiate fibrosis patterns between CAD and DMVR patients.
Answers are grounded in this paper and cite their sources.
Supports noninvasive fibrosis detection in CAD/DMVR; leaves open clinical utility pending prospective validation.
• Uptake of 18 F-FAPI in the myocardium can detect fibrosis and predict LV dyssynchrony. • There are different distributions of FAPI-uptake in CAD and DMVR patients. • FAPI-uptake in the anterior, septal and inferior walls can detect cardiac dysfunction. • SUV mean of FAPI in the lateral wall can determine the progression of cardiac dysfunction. • FAPI-uptake in the basal inferospetal/basal inferior walls can assess the level of MR. Myocardial fibrosis contributes to LV mechanical dyssynchrony and fibroblast activation protein is considered as a specific biomarker related to tissue remodeling. The authors aimed to explore the relationship between LVMD and myocardial fibrosis, and patterns of LV fibrosis distribution in CAD and Degenerative Mitral Valve Regurgitant (DMVR) participants by the technique of 18 F-AlF-FAPI PET/MR. 37 CAD and DMVR participants with LVMD and normal ones underwent cardiac PET/MR imaging, the correlations between SUV mean of FAPI-uptakes and score/percentage of LV wall thickening, peak myocardial strains, and displacements were analyzed in PET/MR images, and ejection fractions and function parameters of mitral valve were compared. There was inverse correlation between SUV mean and score/percentage of LV wall thickening, peak circumferential and short-axial radial myocardial strains, and global peak myocardial strains and ejection fractions showed a decrease significantly in participants with heart diseases. In CAD participants, FAPI was distributed in the ischemic coronary arteries regions. Functions of myocardium in LAD and RCA regions were sensitive to fibrosis, however, those in LCX regions were resistant to fibrosis. In DMVR participants, high uptakes of FAPI were the locations of the valve annulus and papillary muscles, and SUV mean in the basal inferospetal/basal inferior segments were a positive correlation with function parameters of the mitral valve. Uptake of 18 F-AlF-FAPI in the myocardium could detect fibrosis and predict LVMD in CAD and DMVR participants. Moreover, there were different distributions of FAPI-uptake in those participants. In DMVR participants, SUV mean in the basal inferospetal/basal inferior segments could assess dysfunction of the mitral valve.
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Chen et al. (2025) conducted an observational in Coronary artery disease and degenerative mitral valve regurgitation with left ventricular mechanical dyssynchrony (n=37). 18F-AlF-FAPI PET/MR imaging vs. Healthy controls was evaluated on Correlation between SUVmean and score of systolic LV wall thickening on PET images (r = -0.260, p=<0.001). 18F-AlF-FAPI uptake in the myocardium inversely correlated with systolic left ventricular wall thickening (r = -0.260, p < 0.001), demonstrating its utility in detecting myocardial fibrosis and predicting mechanical dyssynchrony.
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