Use of data-independent acquisition mass spectrometry to identify an objective serum indicator of the need for osteoporotic therapeutic intervention.

Data-independent acquisition mass spectrometry (DIA-MS) Osteoporosis Proteomics Serum biomarker

Journal

Journal of proteomics
ISSN: 1876-7737
Titre abrégé: J Proteomics
Pays: Netherlands
ID NLM: 101475056

Informations de publication

Date de publication:
02 Apr 2024
Historique:
received: 07 09 2023
revised: 21 02 2024
accepted: 31 03 2024
medline: 5 4 2024
pubmed: 5 4 2024
entrez: 4 4 2024
Statut: aheadofprint

Résumé

Osteoporosis is characterized by weakened bone microstructure and loss of bone mass. Current diagnostic criteria for osteoporosis are based on the T-score, which is a measure of bone mineral density. However, osteoporotic fragility fractures can occur regardless of the T-score, underscoring the need for additional criteria for the early detection of patients at fracture risk. To identify indicators of reduced bone strength, we performed serum proteomic analysis using data-independent acquisition mass spectrometry with serum samples from two patient groups, one with osteoporosis but no fractures and the other with osteopenia and fragility fractures. Collective evaluation of the results identified six serum proteins that changed to a similar extent in both patient groups compared with controls. Of these, extracellular matrix protein 1 (ECM1), which contributes to bone formation, showed the most significant increase in serum levels in both patient groups. An ELISA-based assay suggested that ECM1 could serve as a serum indicator of the need for therapeutic intervention; however, further prospective studies with a larger sample size are necessary to confirm these results. The present findings may contribute to the provision of early and appropriate therapeutic strategies for patients at risk of osteoporotic fractures. SIGNIFICANCE: This study aimed to identify objective serum indicators of the need for therapeutic intervention in individuals at risk of osteoporotic fracture. Comprehensive proteome analyses of serum collected from patients with osteoporosis but no fractures, patients with osteopenia and fragility fractures, and controls were performed by data-independent acquisition mass spectrometry. Collective evaluation of the proteome analysis data and ELISA-based assays identified serum ECM1 as a potential objective marker of the risk of fragility fractures in patients with osteoporosis or osteopenia. The findings are an important step toward the development of appropriate bone health management methods to improve well-being and maintain quality of life.

Identifiants

pubmed: 38574990
pii: S1874-3919(24)00098-8
doi: 10.1016/j.jprot.2024.105166
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105166

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Auteurs

Yusuke Nakai (Y)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan.

Ken Kumagai (K)

Department of Orthopaedic Surgery, Yokohama City University, Yokohama 236-0004, Japan. Electronic address: kumagai@yokohama-cu.ac.jp.

Yoko Ino (Y)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan.

Tomoko Akiyama (T)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan.

Kayano Moriyama (K)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan.

Yuriko Takeda (Y)

Department of Biostatistics, Yokohama City University, Yokohama 236-0004, Japan.

Kenji Egashira (K)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan; R&D Headquarters, LION Corporation, Tokyo 132-0035, Japan.

Takashi Ohira (T)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan; Department of Physiology and Regenerative Medicine, Kindai University Faculty of Medicine, Osaka 589-8511, Japan.

Akihide Ryo (A)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan.

Tomoyuki Saito (T)

Yokohama Brain and Spine Center, Yokohama 235-0012, Japan.

Yutaka Inaba (Y)

Department of Orthopaedic Surgery, Yokohama City University, Yokohama 236-0004, Japan.

Hisashi Hirano (H)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan.

Yayoi Kimura (Y)

Advanced Medical Research Center, Yokohama City University, Yokohama 236-0004, Japan. Electronic address: ykimura@yokohama-cu.ac.jp.

Classifications MeSH