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基质金属蛋白酶8基因多态性与中国汉族人群股骨头坏死易感性相关。

MMP8 polymorphism is associated with susceptibility to osteonecrosis of the femoral head in a Chinese Han population.

作者信息

An Feimeng, Du Jieli, Cao Yuju, Shi Jianping, Guo Yongchang, Jin Tianbo, Li Jian, Chen Junyu, Li Ping, Dong Mei, Wang Guoqiang, Wang Jianzhong

机构信息

Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.

Department of Orthopedics and Traumatology, The Second Affiliated Hospital of Inner Mongolia University, Hohhot, Inner Mongolia, China.

出版信息

Oncotarget. 2017 Mar 28;8(13):21561-21566. doi: 10.18632/oncotarget.15371.

Abstract

Osteonecrosis of the femoral head (ONFH) is an orthopedic refractory disease that adversely affects quality of life. Matrix metalloproteinase-8 (MMP-8) produced by the bone marrow has been implicated in the degradation of collagen during bone development. We assessed whether MMP8 polymorphisms are associated with ONFH. In a case-control study, using χ2 tests and genetic model analyses, we genotyped 5 MMP8 single-nucleotide polymorphisms (SNPs) in 585 ONFH patients and 507 healthy control subjects in a Chinese Han population. The MMP8 rs11225394 SNP was associated with an increased risk of ONFH in an allele model (OR=1.34; 95% CI, 1.003-1.786, P=0.047). In addition, rs11225394 was associated with an increased risk of ONFH in a dominant model (OR =1.39, 95% CI, 1.02-1.89, P=0.036), over-dominant model (OR=1.39, 95% CI, 1.02-1.89, P=0.038), and log-additive model (OR =1.36, 95% CI, 1.01-1.84, P=0.039). After adjusting for age and gender, rs11225394 was associated with ONFH in a dominant (OR =1.44, 95% CI, 1.05-1.96, P=0.023), over-dominant (OR =1.44, 95% CI, 1.05-1.98, P=0.022), and log-additive model (OR =1.40, 95% CI, 1.04-1.90, P=0.027). These results provide the first evidence that MMP8 SNP at the rs11225394 locus is associated with the increased risk of ONFH in Chinese Han population.

摘要

股骨头坏死(ONFH)是一种影响生活质量的骨科难治性疾病。骨髓产生的基质金属蛋白酶-8(MMP-8)与骨骼发育过程中胶原蛋白的降解有关。我们评估了MMP8基因多态性是否与ONFH相关。在一项病例对照研究中,我们使用χ2检验和遗传模型分析,对585例ONFH患者和507名中国汉族健康对照者的5个MMP8单核苷酸多态性(SNP)进行了基因分型。MMP8 rs11225394 SNP在等位基因模型中与ONFH风险增加相关(OR=1.34;95%CI,1.003-1.786,P=0.047)。此外,rs11225394在显性模型(OR =1.39,95%CI,1.02-1.89,P=0.036)、超显性模型(OR=1.39,95%CI,1.02-1.89,P=0.038)和对数加性模型(OR =1.36,95%CI,1.01-1.84,P=0.039)中与ONFH风险增加相关。在调整年龄和性别后,rs11225394在显性模型(OR =1.44,95%CI,1.05-1.96,P=0.023)、超显性模型(OR =1.44,95%CI,1.05-1.98,P=0.022)和对数加性模型(OR =1.40,95%CI,1.04-1.90,P=0.027)中与ONFH相关。这些结果首次证明rs11225394位点的MMP8 SNP与中国汉族人群ONFH风险增加相关。

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