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dc.creatorStout, Alina C.
dc.creatorBarbe, Mary
dc.creatorEaton, Charles B.
dc.creatorAmin, Mamta
dc.creatorAl-Eid, Fatimah
dc.creatorPrice, Lori Lyn
dc.creatorLu, Bing
dc.creatorLo, Grace H.
dc.creatorZhang, Ming
dc.creatorPang, Jincheng
dc.creatorMcAlindon, Timothy E.
dc.creatorDriban, Jeffrey B.
dc.date.accessioned2023-03-07T20:01:13Z
dc.date.available2023-03-07T20:01:13Z
dc.date.issued2018-01-05
dc.identifier.citationStout, A.C., Barbe, M.F., Eaton, C.B. et al. Inflammation and glucose homeostasis are associated with specific structural features among adults without knee osteoarthritis: a cross-sectional study from the osteoarthritis initiative. BMC Musculoskelet Disord 19, 1 (2018). https://doi.org/10.1186/s12891-017-1921-6
dc.identifier.issn1471-2474
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/8344
dc.identifier.urihttp://hdl.handle.net/20.500.12613/8377
dc.description.abstractBackground: Greater age and body mass index are strong risk factors for osteoarthritis (OA). Older and overweight individuals may be more susceptible to OA because these factors alter tissue turnover in menisci, articular cartilage, and bone via altered glucose homeostasis and inflammation. Understanding the role of inflammation and glucose homeostasis on structural features of early-stage OA may help identify therapeutic targets to delay or prevent the onset of OA among subsets of adults with these features. We examined if serum concentrations of glucose homeostasis (glucose, glycated serum protein [GSP]) or inflammation (C-reactive protein [CRP]) were associated with prevalent knee bone marrow lesions (BMLs) or effusion among adults without knee OA. Methods: We conducted a cross-sectional study using baseline data from the Osteoarthritis Initiative. We selected participants who had no radiographic knee OA but were at high risk for knee OA. Blinded staff conducted assays for CRP, GSP, and glucose. Readers segmented BML volume and effusion using semi-automated programs. Our outcomes were prevalent BML (knee with a BML volume > 1 cm3) and effusion (knee with an effusion volume > 7.5 cm3). We used logistic regression models with CRP, GSP, or glucose concentrations as the predictors. We adjusted for age, sex, body mass index (BMI), and Physical Activity Scale for the Elderly (PASE) scores. Results: We included 343 participants: mean age = 59 ± 9 years, BMI = 27.9 ± 4.5 kg/m2, PASE score = 171 ± 82, and 64% female. Only CRP was associated with BML prevalence (odds ratio [OR] = 1.43, 95% confidence interval [CI] = 1.09 to 1.87). For effusion, we found an interaction between BMI and CRP: only among adults with a BMI <25 kg/m2 was there a significant trend towards a positive association between CRP and effusion (OR = 1.40, 95% CI = 1.00 to 1.97). We detected a U-shaped relationship between GSP and effusion prevalence. Fasting glucose levels were not significantly associated with the presence of baseline effusion or BML. Conclusions: Among individuals without knee OA, CRP may be related to the presence of BMLs and effusion among normal weight individuals. Abnormal GSP may be associated with effusion. Future studies should explore whether inflammation and glucose homeostasis are predictive of symptomatic knee OA.
dc.format.extent9 pages
dc.languageEnglish
dc.language.isoeng
dc.relation.ispartofFaculty/ Researcher Works
dc.relation.haspartBMC Musculoskeletal Disorders, Vol. 19, No. 1
dc.relation.isreferencedbyBMC
dc.rightsAttribution CC BY
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectBone marrow lesions
dc.subjectEffusion
dc.subjectMagnetic resonance imaging
dc.subjectOsteoarthritis
dc.titleInflammation and glucose homeostasis are associated with specific structural features among adults without knee osteoarthritis: a cross-sectional study from the osteoarthritis initiative
dc.typeText
dc.type.genreJournal article
dc.description.departmentAnatomy and Cell Biology
dc.relation.doihttps://doi.org/10.1186/s12891-017-1921-6
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.schoolcollegeLewis Katz School of Medicine
dc.creator.orcidBarbe|0000-0002-5235-9803
dc.temple.creatorBarbe, Mary F.
dc.temple.creatorAmin, Mamta
refterms.dateFOA2023-03-07T20:01:13Z


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