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dc.contributor.authorHulme, Charlotte H.
dc.contributor.authorPeffers, Mandy J.
dc.contributor.authorHarrington, Gabriel M. B.
dc.contributor.authorWilson, Emma
dc.contributor.authorPerry, Jade
dc.contributor.authorRoberts, Sally
dc.contributor.authorGallacher, Pete
dc.contributor.authorJermin, Paul
dc.contributor.authorWright, Karina T.
dc.date.accessioned2025-10-07T08:56:15Z
dc.date.available2025-10-07T08:56:15Z
dc.date.issued2021-03-31
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/629655/Wilson%20-%20Identification%20of%20Candidate%20Synovial%20Fluid%20Biomarkers.pdf?sequence=2
dc.identifier.citationHulme, C. H., Peffers, M. J., Harrington, G. M. B., Wilson, E., Perry, J., Roberts, S., Gallacher, P., Jermin, P., & Wright, K. T. (2021). Identification of candidate synovial fluid biomarkers for the prediction of patient outcome after microfracture or osteotomy. The American Journal of Sports Medicine, 49(6), 1512-1523. https://doi.org/10.1177/0363546521995565en_US
dc.identifier.issn0363-5465en_US
dc.identifier.doi10.1177/0363546521995565en_US
dc.identifier.urihttp://hdl.handle.net/10034/629655
dc.description© 2021 The Author(s).en_US
dc.description.abstractBACKGROUND: Biomarkers are needed to predict clinical outcomes for microfracture and osteotomy surgeries to ensure patients can be better stratified to receive the most appropriate treatment. PURPOSE: To identify novel biomarker candidates and to investigate the potential of a panel of protein biomarkers for the prediction of clinical outcome after treatment with microfracture or osteotomy. STUDY DESIGN: Descriptive laboratory study. METHODS: To identify novel candidate biomarker proteins, we used label-free quantitation after liquid chromatography-tandem mass spectrometry of dynamic range-compressed synovial fluids (SFs) from individuals who responded excellently or poorly (based on change in Lysholm score) to microfracture (n = 6) or osteotomy (n = 7). Biomarkers that were identified in this proteomic analysis or that relate to osteoarthritis (OA) severity or have predictive value in another early OA therapy (autologous cell implantation) were measured in the SF of 19 and 13 patients before microfracture or osteotomy, respectively, using commercial immunoassays, and were normalized to urea. These were aggrecanase-1 (ADAMTS-4), cartilage oligomeric matrix protein (COMP), hyaluronan (HA), lymphatic vessel endothelial hyaluronan receptor 1 (LYVE-1), matrix metalloproteinase 1 and 3, soluble CD14, S100 calcium binding protein A13, and 14-3-3 protein theta (YWHAQ). Levels of COMP and HA were also measured in the plasma of these patients. To find predictors of postoperative function, multivariable regression analyses were performed. RESULTS: Proteomic analyses highlighted YWHAQ and LYVE-1 as being differentially abundant between the clinical responders/improvers and nonresponders after microfracture. A linear regression model after backward variable selection could relate preoperative concentrations of SF proteins (HA, YWHAQ, LYVE-1), activity of ADAMTS-4, and patient demographic characteristics (smoker status and sex) with Lysholm score 12 months after microfracture. Further, a generalized linear model with elastic net penalization indicated that lower preoperative activity of ADAMTS-4 in SF, being a nonsmoker, and being younger at the time of operation were indicative of a higher postoperative Lysholm score (improved joint function) after osteotomy surgery. CONCLUSION: We have identified biomarkers and generated regression models with the potential to predict clinical outcome in patients treated with microfracture or osteotomy of the knee. CLINICAL RELEVANCE: Candidate protein biomarkers identified in this study have the potential to help determine which patients will be best suited to treatment with microfracture or osteotomy.en_US
dc.description.sponsorshipResearch grant funds to perform the study were provided by Versus Arthritis (grant 20815, 21156); Wellcome Trust Intermediate Clinical Fellowship (107471/Z/15/Z); Versus Arthritis (grants 20815, 21156); Wellcome Trust Intermediate Clinical Fellowship (107471/Z/15/Z); Keele University Athena Swan Academic Returners Fund Granten_US
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherSAGE Publicationsen_US
dc.relation.urlhttps://journals.sagepub.com/doi/10.1177/0363546521995565en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.subjectEarly osteoarthritisen_US
dc.subjectKneeen_US
dc.subjectArthritisen_US
dc.subjectMicrofractureen_US
dc.subjectOsteotomyen_US
dc.subjectPredictive biomarkersen_US
dc.subjectSynovial fluiden_US
dc.subjectProteomicsen_US
dc.subjectImmunoassaysen_US
dc.subjectEnzyme activity assaysen_US
dc.titleIdentification of candidate synovial fluid biomarkers for the prediction of patient outcome after microfracture or osteotomyen_US
dc.typeArticleen_US
dc.identifier.eissn1552-3365en_US
dc.contributor.departmentKeele University; Robert Jones and Agnes Hunt Orthopaedic Hospital; University of Liverpool; University of Chesteren_US
dc.identifier.journalThe American Journal of Sports Medicineen_US
dc.date.updated2025-10-07T08:29:22Z
dc.identifier.volume49
dc.date.accepted2020-11-28
rioxxterms.identifier.projectn/aen_US
rioxxterms.versionAMen_US
rioxxterms.typeJournal Article/Review
dc.source.issue6
dc.source.beginpage1512-1523
dc.date.deposited2025-10-07en_US


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