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OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study

Background/aims: Studies have demonstrated that osteopontin (OPN) was associated with the severity and development of knee osteoarthritis (OA). Methods: The purpose of this case–control study was to investigate the association between OPN gene rs11730582 polymorphism and knee OA risk in a Chinese po...

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Detalles Bibliográficos
Autores principales: Shang, Houlai, Hao, Yuedong, Hu, Wenhao, Hu, Xiaohui, Jin, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393225/
https://www.ncbi.nlm.nih.gov/pubmed/30777930
http://dx.doi.org/10.1042/BSR20182023
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author Shang, Houlai
Hao, Yuedong
Hu, Wenhao
Hu, Xiaohui
Jin, Qing
author_facet Shang, Houlai
Hao, Yuedong
Hu, Wenhao
Hu, Xiaohui
Jin, Qing
author_sort Shang, Houlai
collection PubMed
description Background/aims: Studies have demonstrated that osteopontin (OPN) was associated with the severity and development of knee osteoarthritis (OA). Methods: The purpose of this case–control study was to investigate the association between OPN gene rs11730582 polymorphism and knee OA risk in a Chinese population. Genotyping was analyzed using standard PCR and restriction fragment length polymorphism (PCR-RFLP). Results: The present study found that C allele or CC genotype of OPN gene rs11730582 polymorphism was related to decreased risk for knee OA. Furthermore, positive associations were obtained amongst the females, and body mass index (BMI) < 25 kg/m(2) groups. Conclusions: To sum up, the present study reveals that OPN gene rs11730582 polymorphism decreases the risk of knee OA in Chinese Han population.
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spelling pubmed-63932252019-03-06 OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study Shang, Houlai Hao, Yuedong Hu, Wenhao Hu, Xiaohui Jin, Qing Biosci Rep Research Articles Background/aims: Studies have demonstrated that osteopontin (OPN) was associated with the severity and development of knee osteoarthritis (OA). Methods: The purpose of this case–control study was to investigate the association between OPN gene rs11730582 polymorphism and knee OA risk in a Chinese population. Genotyping was analyzed using standard PCR and restriction fragment length polymorphism (PCR-RFLP). Results: The present study found that C allele or CC genotype of OPN gene rs11730582 polymorphism was related to decreased risk for knee OA. Furthermore, positive associations were obtained amongst the females, and body mass index (BMI) < 25 kg/m(2) groups. Conclusions: To sum up, the present study reveals that OPN gene rs11730582 polymorphism decreases the risk of knee OA in Chinese Han population. Portland Press Ltd. 2019-02-27 /pmc/articles/PMC6393225/ /pubmed/30777930 http://dx.doi.org/10.1042/BSR20182023 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Shang, Houlai
Hao, Yuedong
Hu, Wenhao
Hu, Xiaohui
Jin, Qing
OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study
title OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study
title_full OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study
title_fullStr OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study
title_full_unstemmed OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study
title_short OPN gene locus is associated with the risk of knee osteoarthritis: a case–control study
title_sort opn gene locus is associated with the risk of knee osteoarthritis: a case–control study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393225/
https://www.ncbi.nlm.nih.gov/pubmed/30777930
http://dx.doi.org/10.1042/BSR20182023
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