The Natural History of Bone Marrow Lesions and Cysts in the Dunkin-Hartley Guinea Pig Knee Osteoarthritis Model

dc.contributor.advisorManske, Sarah Lynn
dc.contributor.authorFrancis, Destiny
dc.contributor.committeememberMatyas, John Robert
dc.contributor.committeememberDunn, Jeff F.
dc.date2020-11
dc.date.accessioned2020-10-15T15:47:37Z
dc.date.available2020-10-15T15:47:37Z
dc.date.issued2020-10-14
dc.description.abstractIdiopathic knee osteoarthritis (OA) is a disease with unknown etiology, where age is described as a major risk factor. There is a need to document OA's natural history to gain insight into its etiology. Therefore, an animal model like the Dunkin-Hartley (DH) guinea pig that spontaneously develops a knee OA phenotype similar to idiopathic OA observed in humans can be used to study the disease-related bony degeneration. This phenotype includes osteophyte formation, sclerosis, bone marrow lesions (BMLs), and cysts within a relatively short period. This thesis employs advanced magnetic resonance imaging (MRI), micro-computed tomography (μCT), and histological techniques to assess knee joint degeneration in DH guinea pigs at ages 2, 4, 6, 12, and 24 months. The results from this project show evidence of cartilage degradation and bone cyst formation in the 6-month age group, which becomes more apparent in the 12 and 24-month age groups. When present, cysts were primarily located in the central compartment of the bone and often accompanied by osteophytes and sclerosis. Joint degeneration was most severe in the 24-month age group with the largest cysts as well as the greatest osteophyte size and number. Bone microarchitecture was also significantly affected in this age group. Overall femoral and tibial trabecular number (Tb.N) was lowest in the 24-month age group, and it had the highest medial femoral subchondral bone plate thickness (Sbp.Th), femoral and tibial subchondral bone plate porosity (Sbp.Po), femoral trabecular separation (Tb.Sp), and medial tibial trabecular thickness (Tb.Th). The medial compartment also revealed greater joint degeneration, as demonstrated by greater femoral and tibial Sbp.Th and femoral Sbp.Po in the 12 and 24-month age groups compared with the lateral compartment. This project demonstrates that age-related joint degeneration occurs in the DH guinea pig spontaneous knee OA model with evidence of osteophytes, cysts, and bone microarchitecture alterations in older age groups. Although histology revealed abnormalities in the bone that have been associated with MRI-defined BMLs, I am unable to conclude whether or not BMLs occur in this model as a further investigation with MRI is still required.en_US
dc.identifier.citationFrancis, D. (2020). The Natural History of Bone Marrow Lesions and Cysts in the Dunkin-Hartley Guinea Pig Knee Osteoarthritis Model (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca.en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/38335
dc.identifier.urihttp://hdl.handle.net/1880/112686
dc.language.isoengen_US
dc.publisher.facultyCumming School of Medicineen_US
dc.publisher.institutionUniversity of Calgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.en_US
dc.subjectOsteoarthritisen_US
dc.subjectMagnetic resonance imagingen_US
dc.subjectMicro-computed tomographyen_US
dc.subjectHistologyen_US
dc.subjectGuinea pigen_US
dc.subjectCysten_US
dc.subjectBone marrow lesionen_US
dc.subjectBone microarchitectureen_US
dc.subject.classificationPathologyen_US
dc.subject.classificationRadiologyen_US
dc.subject.classificationEngineering--Biomedicalen_US
dc.titleThe Natural History of Bone Marrow Lesions and Cysts in the Dunkin-Hartley Guinea Pig Knee Osteoarthritis Modelen_US
dc.typemaster thesisen_US
thesis.degree.disciplineEngineering – Biomedicalen_US
thesis.degree.grantorUniversity of Calgaryen_US
thesis.degree.nameMaster of Science (MSc)en_US
ucalgary.item.requestcopytrueen_US
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