A Pilot Study on Circulating, Cellular, and Tissue Biomarkers in Osteosarcopenic Patients.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
28 May 2024
Historique:
received: 30 04 2024
revised: 23 05 2024
accepted: 25 05 2024
medline: 19 6 2024
pubmed: 19 6 2024
entrez: 19 6 2024
Statut: epublish

Résumé

Aging comes with the loss of muscle and bone mass, leading to a condition known as osteosarcopenia. Circulating, cellular, and tissue biomarkers research for osteosarcopenia is relatively scarce and, currently, no established biomarkers exist. Here we find that osteosarcopenic patients exhibited elevated basophils and TNFα levels, along with decreased aPPT, PT/INR, IL15, alpha-Klotho, DHEA-S, and FGF-2 expression and distinctive bone and muscle tissue micro-architecture and biomarker expressions. They also displayed an increase in osteoclast precursors with a concomitant imbalance towards spontaneous osteoclastogenesis. Similarities were noted with osteopenic and sarcopenic patients, including a lower neutrophil percentage and altered cytokine expression. A linear discriminant analysis (LDA) on models based on selected biomarkers showed a classification accuracy in the range of 61-78%. Collectively, our data provide compelling evidence for novel biomarkers for osteosarcopenia that may hold potential as diagnostic tools to promote healthy aging.

Identifiants

pubmed: 38892069
pii: ijms25115879
doi: 10.3390/ijms25115879
pii:
doi:

Substances chimiques

Biomarkers 0
Cytokines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : This research was funded by PROGETTO RETE AGING - REALIZZAZIONE DEL PROGETTO DEL PIANO ESECUTIVO RETE AGING RCR-2022, Network Medicine: per migliorare la stratificazione prognostica di pazienti anziani con multimorbilità, fragilità e disabilità.
ID : CUP: D33C22001520001.

Auteurs

Francesca Salamanna (F)

Surgical Sciences and Technologies, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.

Cesare Faldini (C)

1st Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.
Department of Biomedical and Neuromotor Science (DIBINEM), University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.

Francesca Veronesi (F)

Surgical Sciences and Technologies, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.

Veronica Borsari (V)

Surgical Sciences and Technologies, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.

Alberto Ruffilli (A)

1st Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.
Department of Biomedical and Neuromotor Science (DIBINEM), University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.

Marco Manzetti (M)

1st Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.
Department of Biomedical and Neuromotor Science (DIBINEM), University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.

Giovanni Viroli (G)

1st Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.
Department of Biomedical and Neuromotor Science (DIBINEM), University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.

Matteo Traversari (M)

1st Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.

Laura Marchese (L)

Surgical Sciences and Technologies, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.

Milena Fini (M)

Scientific Direction, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.

Gianluca Giavaresi (G)

Surgical Sciences and Technologies, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.

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Classifications MeSH