The common marmoset as a translational model of age-related osteoarthritis

被引:0
|
作者
Dennis M. Minton
Aditya R. Ailiani
Michael D. K. Focht
Mariana E. Kersh
Angela J. Marolf
Kelly S. Santangelo
Adam B. Salmon
Adam R. Konopka
机构
[1] University of Wisconsin-Madison,Division of Geriatrics and Gerontology, Department of Medicine
[2] William S. Middleton Memorial Veterans Hospital,Geriatric Research Education and Clinical Center
[3] University of Illinois Urbana-Champaign,Department of Mechanical Science and Engineering
[4] University of Illinois Urbana-Champaign,Beckman Institute for Advanced Science and Technology
[5] Ohio State University,Department of Veterinary Clinical Sciences
[6] Colorado State University,Department of Microbiology, Immunology, and Pathology, College of Veterinary Medicine and Biomedical Sciences
[7] Barshop Institute for Longevity and Aging Studies,Department of Molecular Medicine
[8] University of Texas Health San Antonio,Geriatric Research, Education, and Clinical Center
[9] South Texas Veterans Healthcare System,undefined
来源
GeroScience | 2024年 / 46卷
关键词
Knee; Cartilage; Meniscus; Bone; Patella; Non-human primate; Naturally occurring osteoarthritis;
D O I
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中图分类号
学科分类号
摘要
Age-related osteoarthritis (OA) is a degenerative joint disease characterized by pathological changes in nearly every intra- and peri-articular tissue that contributes to disability in older adults. Studying the etiology of age-related OA in humans is difficult due to an unpredictable onset and insidious nature. A barrier in developing OA modifying therapies is the lack of translational models that replicate human joint anatomy and age-related OA progression. The purpose of this study was to determine whether the common marmoset is a faithful model of human age-related knee OA. Semi-quantitative microCT scoring revealed greater radiographic OA in geriatric versus adult marmosets, and the age-related increase in OA prevalence was similar between marmosets and humans. Quantitative assessments indicate greater medial tibial cortical and trabecular bone thickness and heterogeneity in geriatric versus adult marmosets which is consistent with an age-related increase in focal subchondral bone sclerosis. Additionally, marmosets displayed an age-associated increase in synovitis and calcification of the meniscus and patella. Histological OA pathology in the medial tibial plateau was greater in geriatric versus adult marmosets driven by articular cartilage damage, proteoglycan loss, and altered chondrocyte cellularity. The age-associated increase in medial tibial cartilage OA pathology and meniscal calcification was greater in female versus male geriatric marmosets. Overall, marmosets largely replicate human OA as evident by similar 1) cartilage and skeletal morphology, 2) age-related progression in OA pathology, and 3) sex differences in OA pathology with increasing age. Collectively, these data suggest that the common marmoset is a highly translatable model of the naturally occurring, age-related OA seen in humans.
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页码:2827 / 2847
页数:20
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