Progression of Hypertrophy and Myocardial Fibrosis in Aortic Stenosis A Multicenter Cardiac Magnetic Resonance Study
Author(s)
Type
Journal Article
Abstract
Background:
Aortic stenosis is accompanied by progressive left ventricular hypertrophy and fibrosis. We investigated the natural history of these processes in asymptomatic patients and their potential reversal post-aortic valve replacement (AVR).
Methods:
Asymptomatic and symptomatic patients with aortic stenosis underwent repeat echocardiography and magnetic resonance imaging. Changes in peak aortic-jet velocity, left ventricular mass index, diffuse fibrosis (indexed extracellular volume), and replacement fibrosis (late gadolinium enhancement [LGE]) were quantified.
RESULTS:
In 61 asymptomatic patients (43% mild, 34% moderate, and 23% severe aortic stenosis), significant increases in peak aortic-jet velocity, left ventricular mass index, indexed extracellular volume, and LGE mass were observed after 2.1±0.7 years, with the most rapid progression observed in patients with most severe stenosis. Patients with baseline midwall LGE (n=16 [26%]; LGE mass, 2.5 g [0.8–4.8 g]) demonstrated particularly rapid increases in scar burden (78% [50%–158%] increase in LGE mass per year). In 38 symptomatic patients (age, 66±8 years; 76% men) who underwent AVR, there was a 19% (11%–25%) reduction in left ventricular mass index (P<0.0001) and an 11% (4%–16%) reduction in indexed extracellular volume (P=0.003) 0.9±0.3 years after surgery. By contrast midwall LGE (n=10 [26%]; mass, 3.3 g [2.6–8.0 g]) did not change post-AVR (n=10; 3.5 g [2.1–8.0 g]; P=0.23), with no evidence of regression even out to 2 years.
Conclusions:
In patients with aortic stenosis, cellular hypertrophy and diffuse fibrosis progress in a rapid and balanced manner but are reversible after AVR. Once established, midwall LGE also accumulates rapidly but is irreversible post valve replacement. Given its adverse long-term prognosis, prompt AVR when midwall LGE is first identified may improve clinical outcomes.
Aortic stenosis is accompanied by progressive left ventricular hypertrophy and fibrosis. We investigated the natural history of these processes in asymptomatic patients and their potential reversal post-aortic valve replacement (AVR).
Methods:
Asymptomatic and symptomatic patients with aortic stenosis underwent repeat echocardiography and magnetic resonance imaging. Changes in peak aortic-jet velocity, left ventricular mass index, diffuse fibrosis (indexed extracellular volume), and replacement fibrosis (late gadolinium enhancement [LGE]) were quantified.
RESULTS:
In 61 asymptomatic patients (43% mild, 34% moderate, and 23% severe aortic stenosis), significant increases in peak aortic-jet velocity, left ventricular mass index, indexed extracellular volume, and LGE mass were observed after 2.1±0.7 years, with the most rapid progression observed in patients with most severe stenosis. Patients with baseline midwall LGE (n=16 [26%]; LGE mass, 2.5 g [0.8–4.8 g]) demonstrated particularly rapid increases in scar burden (78% [50%–158%] increase in LGE mass per year). In 38 symptomatic patients (age, 66±8 years; 76% men) who underwent AVR, there was a 19% (11%–25%) reduction in left ventricular mass index (P<0.0001) and an 11% (4%–16%) reduction in indexed extracellular volume (P=0.003) 0.9±0.3 years after surgery. By contrast midwall LGE (n=10 [26%]; mass, 3.3 g [2.6–8.0 g]) did not change post-AVR (n=10; 3.5 g [2.1–8.0 g]; P=0.23), with no evidence of regression even out to 2 years.
Conclusions:
In patients with aortic stenosis, cellular hypertrophy and diffuse fibrosis progress in a rapid and balanced manner but are reversible after AVR. Once established, midwall LGE also accumulates rapidly but is irreversible post valve replacement. Given its adverse long-term prognosis, prompt AVR when midwall LGE is first identified may improve clinical outcomes.
Date Issued
2018-06-01
Date Acceptance
2018-04-23
Citation
CIRCULATION-CARDIOVASCULAR IMAGING, 2018, 11 (6)
ISSN
1941-9651
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Journal / Book Title
CIRCULATION-CARDIOVASCULAR IMAGING
Volume
11
Issue
6
Copyright Statement
© 2018 The Authors.
Circulation:
Cardiovascular Imaging
is published
on behalf of the American Heart
Association, Inc., by Wolters Kluwer
Health, Inc. This is an open access
article under the terms of the
Creative
Commons Attribution
License (https://creativecommons.org/licenses/by/4.0/),
which permits use, distribution, and
reproduction in any medium, provided
that the original work is properly cited.
Circulation:
Cardiovascular Imaging
is published
on behalf of the American Heart
Association, Inc., by Wolters Kluwer
Health, Inc. This is an open access
article under the terms of the
Creative
Commons Attribution
License (https://creativecommons.org/licenses/by/4.0/),
which permits use, distribution, and
reproduction in any medium, provided
that the original work is properly cited.
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000435564000005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Radiology, Nuclear Medicine & Medical Imaging
Cardiovascular System & Cardiology
aortic valve stenosis
fibrosis
gadolinium
hypertrophy
magnetic resonance imaging
LATE GADOLINIUM ENHANCEMENT
VALVE-REPLACEMENT
PROGNOSTIC-SIGNIFICANCE
MIDWALL FIBROSIS
DISEASE
HEART
T1
QUANTIFICATION
OPTIMIZATION
VALIDATION
Publication Status
Published
Article Number
ARTN e007451
Date Publish Online
2018-06-18