Kreitmaier, P. ; Suderman, M.* ; Southam, L. ; Coutinho de Almeida, R.* ; Hatzikotoulas, K. ; Meulenbelt, I.* ; Steinberg, J. ; Relton, C.L.* ; Wilkinson, J.M.* ; Zeggini, E.
An epigenome-wide view of osteoarthritis in primary tissues.
Am. J. Hum. Genet. 109, 1255-1271 (2022)
Osteoarthritis is a complex degenerative joint disease. Here, we investigate matched genotype and methylation profiles of primary chondrocytes from macroscopically intact (low-grade) and degraded (high-grade) osteoarthritis cartilage and from synoviocytes collected from 98 osteoarthritis-affected individuals undergoing knee replacement surgery. We perform an epigenome-wide association study of knee cartilage degeneration and report robustly replicating methylation markers, which reveal an etiologic mechanism linked to the migration of epithelial cells. Using machine learning, we derive methylation models of cartilage degeneration, which we validate with 82% accuracy in independent data. We report a genome-wide methylation quantitative trait locus (mQTL) map of articular cartilage and synovium and identify 18 disease-grade-specific mQTLs in osteoarthritis cartilage. We resolve osteoarthritis GWAS loci through causal inference and colocalization analyses and decipher the epigenetic mechanisms that mediate the effect of genotype on disease risk. Together, our findings provide enhanced insights into epigenetic mechanisms underlying osteoarthritis in primary tissues.
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Publication type
Article: Journal article
Document type
Scientific Article
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Keywords
Dna Methylation ; Ewas ; Cartilage ; Chondrocyte ; Machine Learning ; Methylation Qtl ; Osteoarthritis ; Synoviocyte ; Synovium
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Language
english
Publication Year
2022
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HGF-reported in Year
2022
ISSN (print) / ISBN
0002-9297
e-ISSN
1537-6605
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Volume: 109,
Issue: 7,
Pages: 1255-1271
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Elsevier
Publishing Place
New York, NY
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Peer reviewed
Institute(s)
Institute of Translational Genomics (ITG)
POF-Topic(s)
30205 - Bioengineering and Digital Health
Research field(s)
Genetics and Epidemiology
PSP Element(s)
G-506700-001
Grants
Wellcome Trust
Copyright
Erfassungsdatum
2022-07-08