Sex differences in left ventricular remodelling, myocardial fibrosis and mortality after aortic valve replacement.


Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
12 2019
Historique:
received: 28 02 2019
revised: 07 06 2019
accepted: 08 06 2019
pubmed: 31 8 2019
medline: 12 6 2020
entrez: 31 8 2019
Statut: ppublish

Résumé

To investigate sex differences in left ventricular remodelling and outcome in patients undergoing surgical or transcatheter aortic valve replacement (SAVR/TAVR). In this multicentre, observational, outcome study with imaging core-lab analysis, patients with severe aortic stenosis (AS) listed for intervention at one of six UK centres were prospectively recruited and underwent cardiovascular magnetic resonance imaging. The primary endpoint was all-cause mortality and secondary endpoint was cardiovascular mortality. 674 patients (425 men, 249 women, age 75±14 years) were included: 399 SAVR, 275 TAVR. Women were older, had higher surgical risk scores and underwent TAVR more frequently (53% vs 33.6%, p<0.001). More men had bicuspid aortic valves (BAVs) (26.7% vs 14.9%, p<0.001) and demonstrated more advanced remodelling than women. During a median follow-up of 3.6 years, 145 (21.5%) patients died, with no significant sex difference in all-cause mortality (23.3% vs 20.5%, p=0.114), but higher cardiovascular mortality in women (13.7% vs 8.5%, p=0.012). There were no significant sex-related differences in outcome in the SAVR or TAVR subgroups, or after excluding those with BAV. Factors independently associated with all-cause mortality were age, left ventricular ejection fraction (LVEF), BAV (better) and myocardial fibrosis detected with late gadolinium enhancement (LGE) in men, and age, LVEF and LGE in women. Age and LGE were independently associated with cardiovascular mortality in both sexes. Men demonstrate more advanced remodelling in response to a similar severity of AS. The higher cardiovascular mortality observed in women following AVR is accounted for by women having less BAV and higher risk scores resulting in more TAVR. LGE is associated with a worse prognosis in both sexes.

Identifiants

pubmed: 31467152
pii: heartjnl-2019-314987
doi: 10.1136/heartjnl-2019-314987
pmc: PMC6900227
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1818-1824

Subventions

Organisme : British Heart Foundation
ID : FS/10/015/28104
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/11/126/29321
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/17/34/32901
Pays : United Kingdom
Organisme : Department of Health
ID : PDF-2011-04-051
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/10/026/28209
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/08/028/24767
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/07/068/2334
Pays : United Kingdom
Organisme : Department of Health
ID : RP-2017-08-ST2-007
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/10/40/28260
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/14/78/31020
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/10/026
Pays : United Kingdom
Organisme : Department of Health
ID : DRF-2013-06-102
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/16/31/32185
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Anvesha Singh (A)

Cardiovascular Sciences, University of Leicester and the NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.

Tarique Al Musa (TA)

Cardiovascular Sciences, Multidisciplinary Cardiovascular Research Centre and The Division of Biomedical Imaging, Leeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Thomas A Treibel (TA)

Cardiovascular Sciences, Barts Health NHS Trust and University College London, London, UK.

Vassiliou S Vassiliou (VS)

Cardiovascular Sciences, Imperial College London, Royal Brompton Hospital, London, UK.
University of East Anglia and Norfolk and Norwich University Hospitals, Norwich, Norfolk, United Kingdom.

Gabriella Captur (G)

Cardiovascular Sciences, Barts Health NHS Trust and University College London, London, UK.

Calvin Chin (C)

Cardiovascular Medicine, National Heart Center Singapore, Singapore, Singapore.

Laura E Dobson (LE)

Cardiovascular Sciences, Multidisciplinary Cardiovascular Research Centre and The Division of Biomedical Imaging, Leeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Silvia Pica (S)

Cardiovascular Sciences, Barts Health NHS Trust and University College London, London, UK.

Margaret Loudon (M)

Cardiovascular Sciences, University of Oxford Centre for Clinical Magnetic Resonance Research, Oxford, UK.

Tamir Malley (T)

Cardiovascular Sciences, Imperial College London, Royal Brompton Hospital, London, UK.

Marzia Rigolli (M)

Cardiovascular Sciences, University of Oxford Centre for Clinical Magnetic Resonance Research, Oxford, UK.

James Robert John Foley (JRJ)

Cardiovascular Sciences, Multidisciplinary Cardiovascular Research Centre and The Division of Biomedical Imaging, Leeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Petra Bijsterveld (P)

Cardiovascular Sciences, Multidisciplinary Cardiovascular Research Centre and The Division of Biomedical Imaging, Leeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Graham R Law (GR)

Medical Statistics, School of Health and Social Care, University of Lincoln and Multidisciplinary Cardiovascular Research Centre and The Division of Biomedical Imaging, Leeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds, Lincoln and Leeds, UK.

Marc Richard Dweck (MR)

Cardiovascular Sciences, Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK marcdweck@hotmail.com.

Saul G Myerson (SG)

Cardiovascular Sciences, University of Oxford Centre for Clinical Magnetic Resonance Research, Oxford, UK.

Sanjay K Prasad (SK)

Cardiology, Royal Brompton Hospital, London, UK.

James C Moon (JC)

Cardiovascular Sciences, Barts Health NHS Trust and University College London, London, UK.

John P Greenwood (JP)

Cardiovascular Sciences, Multidisciplinary Cardiovascular Research Centre and The Division of Biomedical Imaging, Leeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Gerry P McCann (GP)

Cardiovascular Sciences, University of Leicester and the NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.

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Classifications MeSH