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The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis

BACKGROUND: The pathology of osteoarthritis (OA) is partly attributed to genetic factors; however, the role of ADAM12 polymorphism is still controversial. It is necessary to perform a meta-analysis to investigate this possible correlation. METHODS: Case–control studies on the association between OA...

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Autores principales: Wu, Zhen, Xu, Xin-Wei, Zhang, Xiao-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501635/
https://www.ncbi.nlm.nih.gov/pubmed/28721062
http://dx.doi.org/10.2147/TCRM.S134581
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author Wu, Zhen
Xu, Xin-Wei
Zhang, Xiao-Wen
author_facet Wu, Zhen
Xu, Xin-Wei
Zhang, Xiao-Wen
author_sort Wu, Zhen
collection PubMed
description BACKGROUND: The pathology of osteoarthritis (OA) is partly attributed to genetic factors; however, the role of ADAM12 polymorphism is still controversial. It is necessary to perform a meta-analysis to investigate this possible correlation. METHODS: Case–control studies on the association between OA susceptibility and ADAM12 polymorphism were comprehensively collected by searching PubMed, Embase, and Web of Science. Odds ratios (ORs) and 95% confidence intervals (CIs) were pooled to evaluate OA risk that was possibly conferred by ADAM12 variant. The analyses were performed not only among general population but also in male and female groups. RESULTS: A total of 8 studies with 10 populations were finally included in this meta-analysis. In the general population, 4 comparisons were carried out (C allele vs G allele, CC vs GG, GC + CC vs GG, and CC vs GC + GG) and found that ADAM12 rs3740199 polymorphism was not associated with increased OA vulnerability. On the other hand, the analyses stratified by gender made 5 comparisons (C allele vs G allele, CC vs GG, GC vs GG, GC + CC vs GG, and CC vs GC + GG). It was shown that rs3740199 polymorphism (GC + CC vs GG) was a risk factor for OA among male patients (OR =1.45, 95% CI =1.04–2.01). Sensitivity analysis indicated that it was an unstable outcome. No correlation was identified in women. Neither heterogeneity nor publication bias was detected in the analyses mentioned above. CONCLUSION: ADAM12 rs3740199 polymorphism is likely to be associated with OA susceptibility among male patients, other than the general population. More studies are needed to confirm this observation. The mechanism by which ADAM12 variant plays a role in OA pathogenesis is also warranted and important for interpreting this possible correlation.
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spelling pubmed-55016352017-07-18 The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis Wu, Zhen Xu, Xin-Wei Zhang, Xiao-Wen Ther Clin Risk Manag Original Research BACKGROUND: The pathology of osteoarthritis (OA) is partly attributed to genetic factors; however, the role of ADAM12 polymorphism is still controversial. It is necessary to perform a meta-analysis to investigate this possible correlation. METHODS: Case–control studies on the association between OA susceptibility and ADAM12 polymorphism were comprehensively collected by searching PubMed, Embase, and Web of Science. Odds ratios (ORs) and 95% confidence intervals (CIs) were pooled to evaluate OA risk that was possibly conferred by ADAM12 variant. The analyses were performed not only among general population but also in male and female groups. RESULTS: A total of 8 studies with 10 populations were finally included in this meta-analysis. In the general population, 4 comparisons were carried out (C allele vs G allele, CC vs GG, GC + CC vs GG, and CC vs GC + GG) and found that ADAM12 rs3740199 polymorphism was not associated with increased OA vulnerability. On the other hand, the analyses stratified by gender made 5 comparisons (C allele vs G allele, CC vs GG, GC vs GG, GC + CC vs GG, and CC vs GC + GG). It was shown that rs3740199 polymorphism (GC + CC vs GG) was a risk factor for OA among male patients (OR =1.45, 95% CI =1.04–2.01). Sensitivity analysis indicated that it was an unstable outcome. No correlation was identified in women. Neither heterogeneity nor publication bias was detected in the analyses mentioned above. CONCLUSION: ADAM12 rs3740199 polymorphism is likely to be associated with OA susceptibility among male patients, other than the general population. More studies are needed to confirm this observation. The mechanism by which ADAM12 variant plays a role in OA pathogenesis is also warranted and important for interpreting this possible correlation. Dove Medical Press 2017-06-30 /pmc/articles/PMC5501635/ /pubmed/28721062 http://dx.doi.org/10.2147/TCRM.S134581 Text en © 2017 Wu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wu, Zhen
Xu, Xin-Wei
Zhang, Xiao-Wen
The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis
title The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis
title_full The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis
title_fullStr The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis
title_full_unstemmed The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis
title_short The association of ADAM12 polymorphism with osteoarthritis susceptibility: a meta-analysis
title_sort association of adam12 polymorphism with osteoarthritis susceptibility: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501635/
https://www.ncbi.nlm.nih.gov/pubmed/28721062
http://dx.doi.org/10.2147/TCRM.S134581
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