Handgrip strength to screen early-onset sarcopenia in heart failure.


Journal

Clinical nutrition ESPEN
ISSN: 2405-4577
Titre abrégé: Clin Nutr ESPEN
Pays: England
ID NLM: 101654592

Informations de publication

Date de publication:
08 2022
Historique:
received: 16 12 2021
revised: 09 05 2022
accepted: 26 05 2022
entrez: 25 7 2022
pubmed: 26 7 2022
medline: 27 7 2022
Statut: ppublish

Résumé

Sarcopenia in heart failure (HF) is associated with severe outcomes, increased mortality, and high healthcare cost burden. Systematic muscle screening in patients with chronic HF would improve quality and appropriateness of care. Here we tested handgrip strength (HGS) as a screening tool for sarcopenia in patients with chronic HF, using the EWGSOP 2010 and 2019 reference-standard definitions of sarcopenia. HF inpatients, aged 65 years old or above, were prospectively included between November 2014 and September 2018, and relevant sociodemographic, anthropometric and HF characterization data was collected. The accuracy of HGS as a screening test for sarcopenia was assessed by gender using area under the receiver operating characteristic (ROC) curves (AUC). The population consisted of 118 older patients (age: 78.9 yrs; BMI: 26.6 kg/m HGS can be used as a valid tool to screen for sarcopenia in older (≥65 yrs) patients with chronic HF. NCT03153774.

Sections du résumé

BACKGROUND & AIMS
Sarcopenia in heart failure (HF) is associated with severe outcomes, increased mortality, and high healthcare cost burden. Systematic muscle screening in patients with chronic HF would improve quality and appropriateness of care. Here we tested handgrip strength (HGS) as a screening tool for sarcopenia in patients with chronic HF, using the EWGSOP 2010 and 2019 reference-standard definitions of sarcopenia.
METHODS
HF inpatients, aged 65 years old or above, were prospectively included between November 2014 and September 2018, and relevant sociodemographic, anthropometric and HF characterization data was collected. The accuracy of HGS as a screening test for sarcopenia was assessed by gender using area under the receiver operating characteristic (ROC) curves (AUC).
RESULTS
The population consisted of 118 older patients (age: 78.9 yrs; BMI: 26.6 kg/m
CONCLUSIONS
HGS can be used as a valid tool to screen for sarcopenia in older (≥65 yrs) patients with chronic HF.
CLINICAL TRIAL REGISTRATION
NCT03153774.

Identifiants

pubmed: 35871922
pii: S2405-4577(22)00284-4
doi: 10.1016/j.clnesp.2022.05.019
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT03153774']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

183-190

Informations de copyright

Copyright © 2022 European Society for Clinical Nutrition and Metabolism. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no conflicts of interest.

Auteurs

Marie Blanquet (M)

Department of Medicine, Mauriac Hospital Centre, 15200 Mauriac, France; Department of Public Health, Clermont-Ferrand University Hospital, Clermont-Ferrand, France; Université Clermont Auvergne, Clermont-Ferrand University Hospital, CNRS, SIGMA Clermont, Institut Pascal, 63000 Clermont-Ferrand, France. Electronic address: mblanquet@chu-clermontferrand.fr.

Grégoire Massoulié (G)

Department of Cardiology, Clermont-Ferrand University Hospital, France.

Yves Boirie (Y)

Clinical Nutrition Department, Clermont-Ferrand University Hospital, France; Université Clermont Auvergne, Nutritional Health Unit, INRAE, CRNH Auvergne, 63000, Clermont-Ferrand, France.

Candy Guiguet-Auclair (C)

Department of Public Health, Clermont-Ferrand University Hospital, Clermont-Ferrand, France; Université Clermont Auvergne, Clermont-Ferrand University Hospital, CNRS, SIGMA Clermont, Institut Pascal, 63000 Clermont-Ferrand, France.

Aurélien Mulliez (A)

Biostatistics Unit (Clinical Research and Innovation Division), Clermont-Ferrand University Hospital, Clermont-Ferrand, France.

Stefan Anker (S)

Department of Cardiology (CVK), Berlin Institute of Health Center for Regenerative Therapies (BCRT), German Centre for Cardiovascular Research 5dzhk° Partner Site Berlin, Charité Universitätsmedizin Berlin, Germany.

Marie-Claire d'Agrosa Boiteux (MD)

Durtol, Cardiac Rehabilitation Centre, Durtol, France.

Frédéric Jean (F)

Department of Cardiology, Clermont-Ferrand University Hospital, France.

Nicolas Combaret (N)

Department of Cardiology, Clermont-Ferrand University Hospital, France.

Géraud Souteyrand (G)

Department of Cardiology, Clermont-Ferrand University Hospital, France.

Clément Riocreux (C)

Department of Cardiology, Clermont-Ferrand University Hospital, France.

Bruno Pereira (B)

Biostatistics Unit (Clinical Research and Innovation Division), Clermont-Ferrand University Hospital, Clermont-Ferrand, France.

Pascal Motreff (P)

Department of Cardiology, Clermont-Ferrand University Hospital, France.

Patrick Rossignol (P)

Lorraine Université, France; INSERM, Clinical Investigation Centre CIC-P 1433, Nancy Regiona University Hospital, 54000, Nancy, France; INSERM U1116, Nancy, France; F-CRIN, INI-CRCT, Nancy, France.

Guillaume Clerfond (G)

Department of Cardiology, Clermont-Ferrand University Hospital, France.

Romain Eschalier (R)

Université Clermont Auvergne, Clermont-Ferrand University Hospital, CNRS, SIGMA Clermont, Institut Pascal, 63000 Clermont-Ferrand, France; Department of Cardiology, Clermont-Ferrand University Hospital, France; INSERM U1116, Nancy, France.

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