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Metabolomic profiles of cartilage and bone reflect tissue type, radiography-confirmed osteoarthritis, and spatial location within the joint.
Welhaven, Hope D; Viles, Ethan; Starke, Jenna; Wallace, Cameron; Bothner, Brian; June, Ronald K; Hahn, Alyssa K.
Afiliação
  • Welhaven HD; Department of Chemistry & Biochemistry, Montana State University, Bozeman, MT, 59717, United States. Electronic address: hopewelhaven@msu.montana.edu.
  • Viles E; Department of Mechanical & Industrial Engineering, Montana State University, Bozeman, MT, 59717, United States. Electronic address: ethan.viles@montana.edu.
  • Starke J; Montana WWAMI, University of Washington School of Medicine, Seattle, WA, 98195, United States. Electronic address: jennamstarke@gmail.com.
  • Wallace C; Department of Orthopaedic Surgery, University of Utah Health, Salt Lake City, UT, 84103, United States. Electronic address: c33wallace@gmail.com.
  • Bothner B; Department of Chemistry & Biochemistry, Montana State University, Bozeman, MT, 59717, United States. Electronic address: bbothner@montana.edu.
  • June RK; Department of Mechanical & Industrial Engineering, Montana State University, Bozeman, MT, 59717, United States. Electronic address: rjune@montana.edu.
  • Hahn AK; Department of Biological and Environmental Sciences, Carroll College, Helena, MT, 59625, United States. Electronic address: alyssahahn19@gmail.com.
Biochem Biophys Res Commun ; 703: 149683, 2024 Apr 09.
Article em En | MEDLINE | ID: mdl-38373382
ABSTRACT
Osteoarthritis is the most common chronic joint disease, characterized by the abnormal remodeling of joint tissues including articular cartilage and subchondral bone. However, there are currently no therapeutic drug targets to slow the progression of disease because disease pathogenesis is largely unknown. Thus, the goals of this study were to identify metabolic differences between articular cartilage and subchondral bone, compare the metabolic shifts in osteoarthritic grade III and IV tissues, and spatially map metabolic shifts across regions of osteoarthritic hip joints. Articular cartilage and subchondral bone from 9 human femoral heads were obtained after total joint arthroplasty, homogenized and metabolites were extracted for liquid chromatography-mass spectrometry analysis. Metabolomic profiling revealed that distinct metabolic endotypes exist between osteoarthritic tissues, late-stage grades, and regions of the diseased joint. The pathways that contributed the most to these differences between tissues were associated with lipid and amino acid metabolism. Differences between grades were associated with nucleotide, lipid, and sugar metabolism. Specific metabolic pathways such as glycosaminoglycan degradation and amino acid metabolism, were spatially constrained to more superior regions of the femoral head. These results suggest that radiography-confirmed grades III and IV osteoarthritis are associated with distinct global metabolic and that metabolic shifts are not uniform across the joint. The results of this study enhance our understanding of osteoarthritis pathogenesis and may lead to potential drug targets to slow, halt, or reverse tissue damage in late stages of osteoarthritis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoartrite / Cartilagem Articular Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoartrite / Cartilagem Articular Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article