Wang Jiaqi, An Feimeng, Cao Yuju, Gao Hongyan, Sun Mingqi, Ma Chao, Wu Hao, Zhang Baoxin, Liu Wanlin, Wang Jianzhong
Inner Mongolia Medical University, Hohhot, China.
Zhengzhou Traditional Chinese Medicine Traumatology Hospital, Zhengzhou, China.
PeerJ. 2019 Jan 24;7:e6270. doi: 10.7717/peerj.6270. eCollection 2019.
In clinical treatment, the use of steroid hormones is an important etiological factor of non-traumatic osteonecrosis of the femoral head (ONFH) risk. As an endogenous inhibitor of matrix metalloproteinases (MMPs) in the extracellular matrix, the expression of tissue inhibitors of metalloprotease-4 (TIMP4) plays an essential role in cartilage and bone tissue damage and remodeling, vasculitis formation, intravascular thrombosis, and lipid metabolism.
This study aimed to detect the association between TIMP4 polymorphism and steroid-induced ONFH. We genotyped seven single-nucleotide polymorphisms (SNPs) in TIMP4 genes and analyzed the association with steroid-induced ONFH from 286 steroid-induced ONFH patients and 309 normal individuals.
We performed allelic model analysis and found that the minor alleles of five SNPs (rs99365, rs308952, rs3817004, rs2279750, and rs3755724) were associated with decreased steroid-induced ONFH ( = 0.02, = 0.03, = 0.04, = 0.01, = 0.04, respectively). rs2279750 showed a significant association with decreased risk of steroid-induced ONFH in the Dominant and Log-additive models ( = 0.042, = 0.028, respectively), and rs9935, rs30892, and rs3817004 were associated with decreased risk in the Log-additive model ( = 0.038, = 0.044, = 0.042, respectively). In further stratification analysis, TIMP4 gene variants showed a significant association with steroid-induced ONFH in gender under the genotypes. Haplotype analysis also revealed that "TCAGAC" and "CCGGAA" sequences have protective effect on steroid-induced ONFH.
Our results indicate that five TIMP4 SNPs (rs99365, rs308952, rs3817004 rs2279750, and rs3755724) are significantly associated with decreased risk of steroid-induced ONFH in the population of northern China.
在临床治疗中,使用类固醇激素是股骨头非创伤性骨坏死(ONFH)风险的一个重要病因。作为细胞外基质中基质金属蛋白酶(MMPs)的内源性抑制剂,金属蛋白酶组织抑制剂4(TIMP4)的表达在软骨和骨组织损伤与重塑、血管炎形成、血管内血栓形成以及脂质代谢中起着至关重要的作用。
本研究旨在检测TIMP4基因多态性与类固醇诱导的ONFH之间的关联。我们对TIMP4基因中的7个单核苷酸多态性(SNPs)进行基因分型,并分析了286例类固醇诱导的ONFH患者和309例正常个体与类固醇诱导的ONFH的关联。
我们进行了等位基因模型分析,发现5个SNPs(rs99365、rs308952、rs3817004、rs2279750和rs3755724)的次要等位基因与类固醇诱导的ONFH风险降低相关(分别为P = 0.02、P = 0.03、P = 0.04、P = 0.01、P = 0.04)。rs2279750在显性模型和对数加性模型中与类固醇诱导的ONFH风险降低显著相关(分别为P = 0.042、P = 0.028),rs9935、rs30892和rs3817004在对数加性模型中与风险降低相关(分别为P = 0.038、P = 0.044、P = 0.042)。在进一步的分层分析中,TIMP4基因变异在基因型下的性别中与类固醇诱导的ONFH显著相关。单倍型分析还显示,“TCAGAC”和“CCGGAA”序列对类固醇诱导的ONFH有保护作用。
我们的结果表明,在中国北方人群中,5个TIMP4 SNPs(rs99365、rs308952、rs3817004、rs2279750和rs3755724)与类固醇诱导的ONFH风险降低显著相关。