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The genetic contribution to severe post-traumatic osteoarthritis

OBJECTIVE: to compare the combined role of genetic variants loci associated with risk of knee or hip osteoarthritis (OA) in post-traumatic (PT) and non-traumatic (NT) cases of clinically severe OA leading to total joint replacement. METHODS: A total of 1590 controls, 2168 total knee replacement (TKR...

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Autores principales: Valdes, Ana M, Doherty, Sally A, Muir, Kenneth R, Wheeler, Margaret, Maciewicz, Rose A, Zhang, Weiya, Doherty, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786638/
https://www.ncbi.nlm.nih.gov/pubmed/23355107
http://dx.doi.org/10.1136/annrheumdis-2012-202562
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author Valdes, Ana M
Doherty, Sally A
Muir, Kenneth R
Wheeler, Margaret
Maciewicz, Rose A
Zhang, Weiya
Doherty, Michael
author_facet Valdes, Ana M
Doherty, Sally A
Muir, Kenneth R
Wheeler, Margaret
Maciewicz, Rose A
Zhang, Weiya
Doherty, Michael
author_sort Valdes, Ana M
collection PubMed
description OBJECTIVE: to compare the combined role of genetic variants loci associated with risk of knee or hip osteoarthritis (OA) in post-traumatic (PT) and non-traumatic (NT) cases of clinically severe OA leading to total joint replacement. METHODS: A total of 1590 controls, 2168 total knee replacement (TKR) cases (33.2% PT) and 1567 total hip replacement (THR) cases (8.7% PT) from 2 UK cohorts were genotyped for 12 variants previously reported to be reproducibly associated with risk of knee or hip OA. A genetic risk score was generated and the association with PT and NT TKR and THR was assessed adjusting for covariates. RESULTS: For THR, each additional genetic risk variant conferred lower risk among PT cases (OR=1.07, 95% CI 0.96 to 1.19; p=0.24) than NT cases (OR 1.11, 95% CI 1.06 to 1.17; p=1.55×10(−5)). In contrast, for TKR, each risk variant conferred slightly higher risk among PT cases (OR 1.12, 95% CI 1.07 to 1.19; p=1.82×10(−5)) than among NT cases (OR 1.08, 95% CI 1.03 to 1.1; p=0.00063). CONCLUSIONS: Based on the variants reported to date PT TKR cases have at least as high a genetic contribution as NT cases.
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spelling pubmed-37866382013-09-30 The genetic contribution to severe post-traumatic osteoarthritis Valdes, Ana M Doherty, Sally A Muir, Kenneth R Wheeler, Margaret Maciewicz, Rose A Zhang, Weiya Doherty, Michael Ann Rheum Dis Clinical and Epidemiological Research OBJECTIVE: to compare the combined role of genetic variants loci associated with risk of knee or hip osteoarthritis (OA) in post-traumatic (PT) and non-traumatic (NT) cases of clinically severe OA leading to total joint replacement. METHODS: A total of 1590 controls, 2168 total knee replacement (TKR) cases (33.2% PT) and 1567 total hip replacement (THR) cases (8.7% PT) from 2 UK cohorts were genotyped for 12 variants previously reported to be reproducibly associated with risk of knee or hip OA. A genetic risk score was generated and the association with PT and NT TKR and THR was assessed adjusting for covariates. RESULTS: For THR, each additional genetic risk variant conferred lower risk among PT cases (OR=1.07, 95% CI 0.96 to 1.19; p=0.24) than NT cases (OR 1.11, 95% CI 1.06 to 1.17; p=1.55×10(−5)). In contrast, for TKR, each risk variant conferred slightly higher risk among PT cases (OR 1.12, 95% CI 1.07 to 1.19; p=1.82×10(−5)) than among NT cases (OR 1.08, 95% CI 1.03 to 1.1; p=0.00063). CONCLUSIONS: Based on the variants reported to date PT TKR cases have at least as high a genetic contribution as NT cases. BMJ Publishing Group 2013-10 2013-01-26 /pmc/articles/PMC3786638/ /pubmed/23355107 http://dx.doi.org/10.1136/annrheumdis-2012-202562 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Clinical and Epidemiological Research
Valdes, Ana M
Doherty, Sally A
Muir, Kenneth R
Wheeler, Margaret
Maciewicz, Rose A
Zhang, Weiya
Doherty, Michael
The genetic contribution to severe post-traumatic osteoarthritis
title The genetic contribution to severe post-traumatic osteoarthritis
title_full The genetic contribution to severe post-traumatic osteoarthritis
title_fullStr The genetic contribution to severe post-traumatic osteoarthritis
title_full_unstemmed The genetic contribution to severe post-traumatic osteoarthritis
title_short The genetic contribution to severe post-traumatic osteoarthritis
title_sort genetic contribution to severe post-traumatic osteoarthritis
topic Clinical and Epidemiological Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786638/
https://www.ncbi.nlm.nih.gov/pubmed/23355107
http://dx.doi.org/10.1136/annrheumdis-2012-202562
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