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Relative contribution of afterload and interstitial tissue fibrosis to pre-operative longitudinal and circumferential function in patients with severe aortic stenosis

Authors :
Sophie Pierard
Anne-Catherine Pouleur
Julie Melchior
Clotilde Roy
Bernhard Gerber
Christophe Beauloye
Alisson Slimani
Amzulescu Mihaela
Jean-Louis Vanoverschelde
Agnes Pasquet
David Vancraeynest
Christophe De Mesteer
Source :
Archives of Cardiovascular Diseases Supplements. 10:217
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Background Previous studies have shown that, in patients with severe aortic stenosis (SAS), global longitudinal strain (GLS), as assessed by speckle tracking echocardiography (STE), is often reduced. The present study aimed to understand the mechanisms underlying this reduction by using stress-shortening relationships. Method Ninety-nine patients with isolated SAS (36% men, 69 ± 11 years) and 75 healthy volunteers (HV) underwent resting 2D-echo and STE to measure GLS, global circumferential strain (GCS), rate-corrected mean velocity of fiber shortening (Vcfc), and end-systolic wall stress (ESWS). Stress-GLS, GCS or Vcfc relationships were constructed using the HV data and fitted to a linear regression. The relative position of individual SAS patients on these relationships was calculated and used as a load-independent index of myocardial contractility (unloaded GLS,GCS or Vcfc). At the time of surgery, myocardial biopsy was obtained to quantify interstitial fibrosis. Results GLS and Vcfc were lower in SAS than HV (−17 ± 3 vs. −20 ± 2%, P 5.4%), a real gradient is draw between the groups. The more fibrosis they have, the worse the longitudinal and circumferential functions are altered for a given afterload ( Fig. 1 ). Conclusion In HV, longitudinal function is less afterload-dependent than circumferential function. In SAS, reduced longitudinal or circumferential function is a marker of interstitial fibrosis and LV remodeling.

Details

ISSN :
18786480
Volume :
10
Database :
OpenAIRE
Journal :
Archives of Cardiovascular Diseases Supplements
Accession number :
edsair.doi.dedup.....265b6ff9b2e08da9746187d80b035264
Full Text :
https://doi.org/10.1016/j.acvdsp.2018.02.090