Metabolomic profiles of cartilage and bone reflect tissue type, radiography-confirmed osteoarthritis, and spatial location within the joint

dc.contributor.authorWelhaven, Hope D.
dc.contributor.authorViles, Ethan
dc.contributor.authorStarke, Jenna
dc.contributor.authorWallace, Cameron
dc.contributor.authorBothner, Brian
dc.contributor.authorJune, Ronald K.
dc.contributor.authorHahn, Alyssa K.
dc.date.accessioned2024-07-18T18:02:38Z
dc.date.available2024-07-18T18:02:38Z
dc.date.issued2024-04
dc.description© This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.description.abstractOsteoarthritis 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.
dc.identifier.citationWelhaven, H. D., Viles, E., Starke, J., Wallace, C., Bothner, B., June, R. K., & Hahn, A. K. (2024). Metabolomic profiles of cartilage and bone reflect tissue type, radiography-confirmed osteoarthritis, and spatial location within the joint. Biochemical and Biophysical Research Communications, 703, 149683.
dc.identifier.doi10.1016/j.bbrc.2024.149683
dc.identifier.issn0006-291X
dc.identifier.urihttps://scholarworks.montana.edu/handle/1/18683
dc.language.isoen_US
dc.publisherElsevier BV
dc.rightscc-by-nc-nd
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectOsteoarthritis
dc.subjectarticular cartilage
dc.subjectbone
dc.subjecthip
dc.subjectmetabolism
dc.titleMetabolomic profiles of cartilage and bone reflect tissue type, radiography-confirmed osteoarthritis, and spatial location within the joint
dc.typeArticle
mus.citation.extentfirstpage1
mus.citation.extentlastpage31
mus.citation.journaltitleBiochemical and Biophysical Research Communications
mus.citation.volume703
mus.relation.collegeCollege of Letters & Science
mus.relation.departmentChemistry & Biochemistry
mus.relation.universityMontana State University - Bozeman

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