Research Papers:
Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head
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Abstract
Yuxin Qi1,2,*, Yong Zhu2,*, Yuju Cao3, Huiqiang Wu4, Mingqi Sun2, Hao Wu2, Linlin Pan2, Guoqiang Wang2 and Jianzhong Wang2
1Inner Mongolia Medical University, Hohhot, Inner Mongolia 010050, China
2Department of Orthopedics and Traumatology, The 2nd Affiliated Hospital of Inner Mongolia University, Hohhot, Inner Mongolia 010030, China
3Zhengzhou TCM Traumatology Hospital, Zhengzhou, Henan 450016, China
4Inner Mongolia Autonomous Region Hospital of Traditional Chinese Medicine, Hohhot, Inner Mongolia 010000, China
*These authors have contributed equally to this work and should be considered co-first authors
Correspondence to:
Guoqiang Wang, email: [email protected]
Jianzhong Wang, email: [email protected]
Keywords: case-control study; MMP3; single-nucleotide polymorphism; osteonecrosis of the femoral head
Received: May 02, 2017 Accepted: July 26, 2017 Published: November 06, 2017
ABSTRACT
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.
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