Yu Yan, Xie Zhilan, Wang Jihan, Chen Chu, Du Shuli, Chen Peng, Li Bin, Jin Tianbo, Zhao Heping
Clinical Laboratory of Hong-Hui Hospital, Xi'an Jiaotong University College of Medicine Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), Ministry of Education, College of Life Sciences, Northwest University Xi'an Tiangen Precision Medical Institute Institution of Basic Medical Science, Xi'an Medical University, Xi'an, Shaanxi Province, China.
Medicine (Baltimore). 2016 Dec;95(49):e5407. doi: 10.1097/MD.0000000000005407.
The proportion of alcohol-induced osteonecrosis of the femoral head (ONFH) in all ONFH patients was 30.7%, with males prevailing among the ONFH patients in mainland China (70.1%). Matrix metalloproteinase 2 (MMP2), a member of the MMP gene family, encodes the enzyme MMP2, which can promote osteoclast migration, attachment, and bone matrix degradation. In this case-control study, we aimed to investigate the association between MMP2 and the alcohol-induced ONFH in Chinese males.In total, 299 patients with alcohol-induced ONFH and 396 healthy controls were recruited for a case-control association study. Five single-nucleotide polymorphisms within the MMP2 locus were genotyped and examined for their correlation with the risk of alcohol-induced ONFH and treatment response using Pearson χ test and unconditional logistic regression analysis. We identified 3 risk alleles for carriers: the allele "T" of rs243849 increased the risk of alcohol-induced ONFH in the allele model, the log-additive model without adjustment, and the log-additive model with adjustment for age. Conversely, the genotypes "CC" in rs7201 and "CC" in rs243832 decreased the risk of alcohol-induced ONFH, as revealed by the recessive model. After the Bonferroni multiple adjustment, no significant association was found. Furthermore, the haplotype analysis showed that the "TT" haplotype of MMP2 was more frequent among patients with alcohol-induced ONFH by unconditional logistic regression analysis adjusted for age.In conclusion, there may be an association between MMP2 and the risk of alcohol-induced ONFH in North-Chinese males. However, studies on larger populations are needed to confirm this hypothesis; these data may provide a theoretical foundation for future studies.
在所有股骨头坏死(ONFH)患者中,酒精性股骨头坏死所占比例为30.7%,在中国大陆的ONFH患者中男性占主导(70.1%)。基质金属蛋白酶2(MMP2)是MMP基因家族的成员之一,编码MMP2酶,该酶可促进破骨细胞迁移、附着及骨基质降解。在本病例对照研究中,我们旨在探讨MMP2与中国男性酒精性ONFH之间的关联。
总共招募了299例酒精性ONFH患者和396例健康对照进行病例对照关联研究。对MMP2基因座内的5个单核苷酸多态性进行基因分型,并使用Pearson χ检验和无条件逻辑回归分析检查它们与酒精性ONFH风险及治疗反应的相关性。我们确定了携带者的3个风险等位基因:rs243849的等位基因“T”在等位基因模型、未调整的对数加性模型以及调整年龄后的对数加性模型中增加了酒精性ONFH的风险。相反,rs7201中的基因型“CC”和rs243832中的基因型“CC”在隐性模型中降低了酒精性ONFH的风险。经过Bonferroni多重校正后,未发现显著关联。此外,单倍型分析显示,经年龄调整的无条件逻辑回归分析表明,MMP2的“TT”单倍型在酒精性ONFH患者中更为常见。
总之,MMP2与中国北方男性酒精性ONFH风险之间可能存在关联。然而,需要对更大规模人群进行研究以证实这一假设;这些数据可为未来研究提供理论基础。