Sex Differences in Skeletal Muscle Pathology in Patients With Heart Failure and Reduced Ejection Fraction.

atrophy capillaries exercise muscles sarcopenia women

Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
09 Oct 2024
Historique:
medline: 9 10 2024
pubmed: 9 10 2024
entrez: 9 10 2024
Statut: aheadofprint

Résumé

Women with heart failure and reduced ejection fraction (HFrEF) have greater symptoms and a lower quality of life compared with men; however, the role of noncardiac mechanisms remains poorly resolved. We hypothesized that differences in skeletal muscle pathology between men and women with HFrEF may explain clinical heterogeneity. Muscle biopsies from both men (n=22) and women (n=16) with moderate HFrEF (New York Heart Association classes I-III) and age- and sex-matched controls (n=18 and n=16, respectively) underwent transcriptomics (RNA-sequencing), myofiber structural imaging (histology), and molecular signaling analysis (gene/protein expression), with serum inflammatory profiles analyzed (enzyme-linked immunosorbent assay). Two-way ANOVA was conducted (interaction sex and condition). RNA-sequencing identified 5629 differentially expressed genes between men and women with HFrEF, with upregulated terms for catabolism and downregulated terms for mitochondria in men. mRNA expression confirmed an effect of sex ( Sex differences in muscle pathology in HFrEF exist, with men showing greater abnormalities compared with women related to the transcriptome, fiber phenotype, capillarity, and circulating factors. These preliminary data question whether muscle pathology is a primary mechanism contributing to greater symptoms in women with HFrEF and highlight the need for further investigation.

Sections du résumé

BACKGROUND UNASSIGNED
Women with heart failure and reduced ejection fraction (HFrEF) have greater symptoms and a lower quality of life compared with men; however, the role of noncardiac mechanisms remains poorly resolved. We hypothesized that differences in skeletal muscle pathology between men and women with HFrEF may explain clinical heterogeneity.
METHODS UNASSIGNED
Muscle biopsies from both men (n=22) and women (n=16) with moderate HFrEF (New York Heart Association classes I-III) and age- and sex-matched controls (n=18 and n=16, respectively) underwent transcriptomics (RNA-sequencing), myofiber structural imaging (histology), and molecular signaling analysis (gene/protein expression), with serum inflammatory profiles analyzed (enzyme-linked immunosorbent assay). Two-way ANOVA was conducted (interaction sex and condition).
RESULTS UNASSIGNED
RNA-sequencing identified 5629 differentially expressed genes between men and women with HFrEF, with upregulated terms for catabolism and downregulated terms for mitochondria in men. mRNA expression confirmed an effect of sex (
CONCLUSIONS UNASSIGNED
Sex differences in muscle pathology in HFrEF exist, with men showing greater abnormalities compared with women related to the transcriptome, fiber phenotype, capillarity, and circulating factors. These preliminary data question whether muscle pathology is a primary mechanism contributing to greater symptoms in women with HFrEF and highlight the need for further investigation.

Identifiants

pubmed: 39381880
doi: 10.1161/CIRCHEARTFAILURE.123.011471
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e011471

Auteurs

Nathanael Wood (N)

Faculty of Biological Sciences, School of Biomedical Sciences (N.W., A.C., M.G.P., S.E., T.S.B.).

Annabel Critchlow (A)

Faculty of Biological Sciences, School of Biomedical Sciences (N.W., A.C., M.G.P., S.E., T.S.B.).

Chew W Cheng (CW)

Leeds Institute of Cardiovascular and Metabolic Medicine (C.W.C., S.S., S.B.W., K.K.W., L.D.R.).

Sam Straw (S)

Leeds Institute of Cardiovascular and Metabolic Medicine (C.W.C., S.S., S.B.W., K.K.W., L.D.R.).

Paul W Hendrickse (PW)

University of Leeds, United Kingdom. Medical Faculty, Lancaster University, United Kingdom (P.W.H.).

Marcelo G Pereira (MG)

Faculty of Biological Sciences, School of Biomedical Sciences (N.W., A.C., M.G.P., S.E., T.S.B.).

Stephen B Wheatcroft (SB)

Leeds Institute of Cardiovascular and Metabolic Medicine (C.W.C., S.S., S.B.W., K.K.W., L.D.R.).

Stuart Egginton (S)

Faculty of Biological Sciences, School of Biomedical Sciences (N.W., A.C., M.G.P., S.E., T.S.B.).

Klaus K Witte (KK)

Leeds Institute of Cardiovascular and Metabolic Medicine (C.W.C., S.S., S.B.W., K.K.W., L.D.R.).
Clinic for Cardiology, Angiology and Internal Intensive Care Medicine, RWTH Aachen University, Germany (K.K.W.).

Lee D Roberts (LD)

Leeds Institute of Cardiovascular and Metabolic Medicine (C.W.C., S.S., S.B.W., K.K.W., L.D.R.).

T Scott Bowen (TS)

Faculty of Biological Sciences, School of Biomedical Sciences (N.W., A.C., M.G.P., S.E., T.S.B.).

Classifications MeSH