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Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head
Many potential causative factors are related to the initiation and progression of osteonecrosis of the femoral head (ONFH). The matrix metalloproteinase/tissue inhibitor of metalloproteinases (MMPs/TIMPs) system was found to play a significant role in the development of ONFH. The aim of this study i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752487/ https://www.ncbi.nlm.nih.gov/pubmed/29312574 http://dx.doi.org/10.18632/oncotarget.22313 |
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author | Qi, Yuxin Zhu, Yong Cao, Yuju Wu, Huiqiang Sun, Mingqi Wu, Hao Pan, Linlin Wang, Guoqiang Wang, Jianzhong |
author_facet | Qi, Yuxin Zhu, Yong Cao, Yuju Wu, Huiqiang Sun, Mingqi Wu, Hao Pan, Linlin Wang, Guoqiang Wang, Jianzhong |
author_sort | Qi, Yuxin |
collection | PubMed |
description | Many potential causative factors are related to the initiation and progression of osteonecrosis of the femoral head (ONFH). The matrix metalloproteinase/tissue inhibitor of metalloproteinases (MMPs/TIMPs) system was found to play a significant role in the development of ONFH. The aim of this study is to investigate the association between polymorphisms of MMP-3 and ONFH in the Chinese population. We selected 8 single-nucleotide polymorphisms (SNPs) in 2 genes selected from the MMPs/TIMPs system in a case–control study with 585 cases of ONFH and 507 healthy controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using the chi-squared test, genetic model analysis, haplotype analysis, and stratification analysis. We found that the minor allele of rs650108 and rs522616 (p<0.05) was assumed a risk allele compared to the wild-type allele. In the genetic model analysis, We observed two susceptibility SNPs additionally: rs650108, dominant model analyses (with adjustment: OR=0.73; 95%CI 0.56-0.95; p=0.017) and additive model analyses (with adjustment: OR=0.83; 95%CI 0.70-0.99; p=0.044); and rs522616 recessive model analyses (with adjustment: OR=1.52; 95%CI 1.07-2.14; p=0.018) and additive model analyses (with adjustment: OR=1.21; 95% CI 1.02-1.44; p=0.033). Our results verify that genetic variants of MMP3 contribute to ONFH susceptibility in the population of northern China. In addition, we found that gender differences might interact with MMP3 polymorphisms to contribute to the overall susceptibility to ONFH. |
format | Online Article Text |
id | pubmed-5752487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57524872018-01-08 Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head Qi, Yuxin Zhu, Yong Cao, Yuju Wu, Huiqiang Sun, Mingqi Wu, Hao Pan, Linlin Wang, Guoqiang Wang, Jianzhong Oncotarget Research Paper Many potential causative factors are related to the initiation and progression of osteonecrosis of the femoral head (ONFH). The matrix metalloproteinase/tissue inhibitor of metalloproteinases (MMPs/TIMPs) system was found to play a significant role in the development of ONFH. The aim of this study is to investigate the association between polymorphisms of MMP-3 and ONFH in the Chinese population. We selected 8 single-nucleotide polymorphisms (SNPs) in 2 genes selected from the MMPs/TIMPs system in a case–control study with 585 cases of ONFH and 507 healthy controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using the chi-squared test, genetic model analysis, haplotype analysis, and stratification analysis. We found that the minor allele of rs650108 and rs522616 (p<0.05) was assumed a risk allele compared to the wild-type allele. In the genetic model analysis, We observed two susceptibility SNPs additionally: rs650108, dominant model analyses (with adjustment: OR=0.73; 95%CI 0.56-0.95; p=0.017) and additive model analyses (with adjustment: OR=0.83; 95%CI 0.70-0.99; p=0.044); and rs522616 recessive model analyses (with adjustment: OR=1.52; 95%CI 1.07-2.14; p=0.018) and additive model analyses (with adjustment: OR=1.21; 95% CI 1.02-1.44; p=0.033). Our results verify that genetic variants of MMP3 contribute to ONFH susceptibility in the population of northern China. In addition, we found that gender differences might interact with MMP3 polymorphisms to contribute to the overall susceptibility to ONFH. Impact Journals LLC 2017-11-06 /pmc/articles/PMC5752487/ /pubmed/29312574 http://dx.doi.org/10.18632/oncotarget.22313 Text en Copyright: © 2017 Qi et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Qi, Yuxin Zhu, Yong Cao, Yuju Wu, Huiqiang Sun, Mingqi Wu, Hao Pan, Linlin Wang, Guoqiang Wang, Jianzhong Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head |
title | Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head |
title_full | Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head |
title_fullStr | Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head |
title_full_unstemmed | Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head |
title_short | Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head |
title_sort | association between mmp-3 polymorphisms among chinese patients with osteonecrosis of the femoral head |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752487/ https://www.ncbi.nlm.nih.gov/pubmed/29312574 http://dx.doi.org/10.18632/oncotarget.22313 |
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