Metabolomic Profiles and Pathways in Osteoarthritic Human Cartilage: A Comparative Analysis with Healthy Cartilage.

cartilage mass spectrometry metabolomics osteoarthritis

Journal

Metabolites
ISSN: 2218-1989
Titre abrégé: Metabolites
Pays: Switzerland
ID NLM: 101578790

Informations de publication

Date de publication:
25 Mar 2024
Historique:
received: 09 02 2024
revised: 29 02 2024
accepted: 19 03 2024
medline: 26 4 2024
pubmed: 26 4 2024
entrez: 26 4 2024
Statut: epublish

Résumé

Osteoarthritis (OA) is a chronic joint disease with heterogenous metabolic pathology. To gain insight into OA-related metabolism, metabolite extracts from healthy (n = 11) and end-stage osteoarthritic cartilage (n = 35) were analyzed using liquid chromatography-mass spectrometry metabolomic profiling. Specific metabolites and metabolic pathways, including lipid and amino acid pathways, were differentially regulated in osteoarthritis-derived and healthy cartilage. The detected alterations in amino acids and lipids highlighted key differences in bioenergetic resources, matrix homeostasis, and mitochondrial alterations in OA-derived cartilage compared to healthy cartilage. Moreover, the metabolomic profiles of osteoarthritic cartilage separated into four distinct endotypes, highlighting the heterogenous nature of OA metabolism and the diverse landscape within the joint in patients. The results of this study demonstrate that human cartilage has distinct metabolomic profiles in healthy and end-stage OA patients. By taking a comprehensive approach to assess metabolic differences between healthy and osteoarthritic cartilage and within osteoarthritic cartilage alone, several metabolic pathways with distinct regulation patterns were detected. Additional investigation may lead to the identification of metabolites that may serve as valuable indicators of disease status or potential therapeutic targets.

Identifiants

pubmed: 38668311
pii: metabo14040183
doi: 10.3390/metabo14040183
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NIH HHS
ID : R01AR073964, R01AR081489
Pays : United States
Organisme : NASA
ID : 80NSSC20M0042
Pays : United States

Auteurs

Hope D Welhaven (HD)

Department of Chemistry & Biochemistry, Montana State University, Bozeman, MT 59717, USA.

Avery H Welfley (AH)

Department of Mechanical & Industrial Engineering, Montana State University, Bozeman, MT 59717, USA.

Priyanka Brahmachary (P)

Department of Mechanical & Industrial Engineering, Montana State University, Bozeman, MT 59717, USA.

Annika R Bergstrom (AR)

Department of Chemical & Biological Engineering, Villanova University, Villanova, PA 19085, USA.

Eden Houske (E)

Department of Biological and Environmental Sciences, Carroll College, Helena, MT 59625, USA.

Matthew Glimm (M)

Department of Biological and Environmental Sciences, Carroll College, Helena, MT 59625, USA.

Brian Bothner (B)

Department of Chemistry & Biochemistry, Montana State University, Bozeman, MT 59717, USA.

Alyssa K Hahn (AK)

Department of Biological and Environmental Sciences, Carroll College, Helena, MT 59625, USA.

Ronald K June (RK)

Department of Mechanical & Industrial Engineering, Montana State University, Bozeman, MT 59717, USA.

Classifications MeSH