Low myocardial energetic efficiency is associated with increased mortality in aortic stenosis.


Journal

Open heart
ISSN: 2053-3624
Titre abrégé: Open Heart
Pays: England
ID NLM: 101631219

Informations de publication

Date de publication:
08 2021
Historique:
received: 13 05 2021
accepted: 02 08 2021
entrez: 24 8 2021
pubmed: 25 8 2021
medline: 15 12 2021
Statut: ppublish

Résumé

In hypertension, low myocardial energetic efficiency (MEEi) has been documented as an integrated marker of metabolic and left ventricular (LV) myocardial dysfunction. We tested the predictive performance of MEEi in initially asymptomatic aortic stenosis (AS) patients free from diabetes and known cardiovascular disease. Data from 1703 patients with mostly moderate AS enrolled in the Simvastatin and Ezetimibe in Aortic Stenosis study followed for 4.3 years was used. MEE was calculated from Doppler stroke volume/([heart rate/60]) and indexed to LV mass (MEEi). The threshold value for MEEi associated with increased mortality was identified in generalised additive model with smoothing splines. Covariables of MEEi were identified in logistic regression analysis. Outcome was assessed in Cox regression analysis and reported as HR and 95% CI. MEEi <0.34 mL/s per gram was associated with increased cardiovascular mortality (n=80) (HR 2.53 (95% CI 1.50 to 4.28)) and all-cause mortality (n=155) (HR 1.74 (95% CI 1.20 to 2.52)) (both p<0.01). The association was independent of confounders of low MEEI (<0.34 mL/s per gram) identified in multivariable logistic regression analysis, including more severe AS, higher body mass index, lower LV midwall shortening and ejection fraction and presence of hypertension. Comparison of the Cox models with and without MEEi among the covariables demonstrated that MEEi significantly improved the prognostic yield (both p<0.01). In patients with initially asymptomatic AS, low MEEi was associated with clustering of cardiometabolic risk factors, lower LV myocardial function and subsequent increased mortality during 4.3 years follow-up, independent of known prognosticators. NCT00092677.

Identifiants

pubmed: 34426527
pii: openhrt-2021-001720
doi: 10.1136/openhrt-2021-001720
pmc: PMC8383869
pii:
doi:

Substances chimiques

Anticholesteremic Agents 0
Simvastatin AGG2FN16EV
Ezetimibe EOR26LQQ24

Banques de données

ClinicalTrials.gov
['NCT00092677']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Edda Bahlmann (E)

Department of Cardiology, Asklepios Kliniken St. Georg, Hamburg, Germany doc_edda@hotmail.com.

Eigir Einarsen (E)

Department of Clinical Science, University of Bergen Department of Medicine, Bergen, Norway.

Dana Cramariuc (D)

Department of Clinical Science, University of Bergen Department of Medicine, Bergen, Norway.
Department of Heart Disease, Haukeland University Hospital Department of Heart Disease, Bergen, Norway.

Helga Midtbø (H)

Department of Heart Disease, Haukeland University Hospital Department of Heart Disease, Bergen, Norway.

Costantino Mancusi (C)

Department of Advanced Biomedical Science and Hypertension Research Center, Federico II University of Naples, Naples, Italy.

Anne Rossebø (A)

Department of Cardiology, Oslo University Hospital Ullevaal, Oslo, Norway.

Stephan Willems (S)

Department of Cardiology, Asklepios Kliniken St. Georg, Hamburg, Germany.

Eva Gerdts (E)

Department of Clinical Science, University of Bergen Department of Medicine, Bergen, Norway.

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Classifications MeSH