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Epicardial fat volume is associated with primary coronary slow-flow phenomenon in patients with severe aortic stenosis undergoing transcatheter valve implantation.

Authors :
Weferling M
Rolf A
Treiber J
Fischer-Rasokat U
Liebetrau C
Hamm CW
Dey D
Kim WK
Source :
BMC cardiovascular disorders [BMC Cardiovasc Disord] 2024 May 16; Vol. 24 (1), pp. 253. Date of Electronic Publication: 2024 May 16.
Publication Year :
2024

Abstract

Background: Primary coronary slow flow (CSF) is defined as delayed opacification of the distal epicardial vasculature during coronary angiography in the absence of relevant coronary artery stenoses. Microvascular disease is thought to be the underlying cause of this pathology. Epicardial fat tissue (EFT) is an active endocrine organ directly surrounding the coronary arteries that provides pro-inflammatory factors to the adjacent tissue by paracrine and vasocrine mechanisms. The aim of the present study was to investigate a potential association between EFT and primary CSF and whether EFT can predict the presence of primary CSF.<br />Methods: Between 2016 and 2017, n = 88 patients with high-grade aortic stenosis who were planned for transcatheter aortic valve implantation (TAVI) were included in this retrospective study. EFT volume was measured by pre-TAVI computed tomography (CT) using dedicated software. The presence of primary CSF was defined based on the TIMI frame count from the pre-TAVI coronary angiograms.<br />Results: Thirty-nine of 88 TAVI patients had CSF (44.3%). EFT volume was markedly higher in patients with CSF (142 ml [IQR 107-180] vs. 113 ml [IQR 89-147]; p = 0.009) and was strongly associated with the presence of CSF (OR 1.012 [95%CI 1.002-1.021]; p = 0.014). After adjustment, EFT volume was still an independent predictor of CSF (OR 1.016 [95%CI 1.004-1.026]; p = 0.009).<br />Conclusion: Primary CSF was independently associated with increased EFT volume. Further studies are needed to validate this finding and elucidate whether a causal relationship exists.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1471-2261
Volume :
24
Issue :
1
Database :
MEDLINE
Journal :
BMC cardiovascular disorders
Publication Type :
Academic Journal
Accession number :
38750455
Full Text :
https://doi.org/10.1186/s12872-024-03927-7