Association of circulating hsa-miRNAs with sarcopenia: the SarcoPhAge study.

Circulating hsa-miRNAs Next generation sequencing Sarcopenia TaqMan qPCR

Journal

Aging clinical and experimental research
ISSN: 1720-8319
Titre abrégé: Aging Clin Exp Res
Pays: Germany
ID NLM: 101132995

Informations de publication

Date de publication:
14 Mar 2024
Historique:
received: 10 08 2023
accepted: 23 01 2024
medline: 18 3 2024
pubmed: 15 3 2024
entrez: 15 3 2024
Statut: epublish

Résumé

To identify a microRNA signature associated to sarcopenia in community-dwelling older adults form the SarcoPhAge cohort. In a screening phase by next generation sequencing (NGS), we compared the hsa-miRome expression of 18 subjects with sarcopenia (79.6 ± 6.8 years, 9 men) and 19 healthy subjects without sarcopenia (77.1 ± 6 years, 9 men) at baseline. Thereafter, we have selected eight candidate hsa-miRNAs according to the NGS results and after a critical assessment of previous literature. In a validation phase and by real-time qPCR, we then analyzed the expression levels of these 8 hsa-miRNAs at baseline selecting 92 healthy subjects (74.2 ± 10 years) and 92 subjects with sarcopenia (75.3 ± 6.8 years). For both steps, the groups were matched for age and sex. In the validation phase, serum has-miRNA-133a-3p and has-miRNA-200a-3p were significantly decreased in the group with sarcopenia vs controls [RQ: relative quantification; median (interquartile range)]: -0.16 (-1.26/+0.90) vs +0.34 (-0.73/+1.33) (p < 0.01) and -0.26 (-1.07/+0.68) vs +0.27 (-0.55/+1.10) (p < 0.01) respectively. Has-miRNA-744-5p was decreased and has-miRNA-151a-3p was increased in the group with sarcopenia vs controls, but this barely reached significance: +0.16 (-1.34/+0.79) vs +0.44 (-0.31/+1.00) (p = 0.050) and  +0.35 (-0.22/+0.90) vs  +0.03 (-0.68/+0.75) (p = 0.054). In subjects with sarcopenia, serum hsa-miRNA-133a-3p and hsa-miRNA-200a-3p expression were downregulated, consistent with their potential targets inhibiting muscle cells proliferation and differentiation.

Identifiants

pubmed: 38485856
doi: 10.1007/s40520-024-02711-z
pii: 10.1007/s40520-024-02711-z
pmc: PMC10940485
doi:

Substances chimiques

MicroRNAs 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

70

Informations de copyright

© 2024. The Author(s).

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Auteurs

Marjorie Millet (M)

INSERM 1033, Lyon, France.
PMO, Lyon, France.

Maxime Auroux (M)

INSERM 1033, Lyon, France.
Hôpital E. Herriot, Hospices Civils de Lyon, Lyon, France.

Charlotte Beaudart (C)

Clinical Pharmacology and Toxicology Research Unit (URPC), NARILIS, Department of Biomedical Sciences, Faculty of Medicine, University of Namur, Namur, Belgium.
WHO Collaborating Center for Epidemiology of Musculoskeletal Health and Aging, Division of Public Health, Epidemiology and Health Economics, University of Liège, Liege, Belgium.

Céline Demonceau (C)

WHO Collaborating Center for Epidemiology of Musculoskeletal Health and Aging, Division of Public Health, Epidemiology and Health Economics, University of Liège, Liege, Belgium.

Aurélie Ladang (A)

Department of Clinical Chemistry, CHU de Liège, University of Liège, Liege, Belgium.

Etienne Cavalier (E)

Department of Clinical Chemistry, CHU de Liège, University of Liège, Liege, Belgium.

Jean-Yves Reginster (JY)

WHO Collaborating Center for Epidemiology of Musculoskeletal Health and Aging, Division of Public Health, Epidemiology and Health Economics, University of Liège, Liege, Belgium.

Olivier Bruyère (O)

WHO Collaborating Center for Epidemiology of Musculoskeletal Health and Aging, Division of Public Health, Epidemiology and Health Economics, University of Liège, Liege, Belgium.

Roland Chapurlat (R)

INSERM 1033, Lyon, France.
PMO, Lyon, France.
Hôpital E. Herriot, Hospices Civils de Lyon, Lyon, France.
University of Lyon, Lyon, France.

Jean-Charles Rousseau (JC)

INSERM 1033, Lyon, France. jean-charles.rousseau@inserm.fr.
PMO, Lyon, France. jean-charles.rousseau@inserm.fr.

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