Skeletal Diseases Genome Research Center, Kyungpook National University Hospital, Daegu 700-412, Korea.
Exp Mol Med. 2010 May 31;42(5):376-85. doi: 10.3858/emm.2010.42.5.039.
Multiple factors have been implicated in the development of osteonecrosis of the femoral head (ONFH). In particular, non-traumatic ONFH is directly or indirectly related to injury of the vascular supply to the femoral head. Thus, hypoxia in the femoral head caused by impaired blood flow may be an important risk factor for ONFH. In this study, we investigated whether genetic variations of angiogenesis- and hypoxia-related genes contribute to an increased risk for the development of ONFH. Candidate genes were selected based on known hypoxia and angiogenesis pathways. An association study was performed using an Affymetrix Targeted Genotyping 3K Chip array with 460 ONFH patients and 300 control subjects. We showed that single nucleotide polymorphisms (SNPs) in the genes TF, VEGFC, IGFBP3, and ACE were associated with an increased risk of ONFH. On the other hand, SNPs in the KDR and NRP1 genes were associated with protection against ONFH. The most important finding was that one SNP (rs2453839) in the IGFBP3 gene was significantly associated with a higher risk of ONFH (P=0.0061, OR 7.74). In subgroup analysis, most candidate gene variations that were associated with ONFH occurred in the idiopathic subgroup. Among other SNPs, ACE SNPs were associated with steroid-induced ONFH (P=0.0018-0.0037, OR>3). Collectively, our findings suggest that genetic variations in angiogenesis- and hypoxia-related genes may help to identify susceptibility factors for the development of ONFH in the Korean population.
多种因素与股骨头坏死(ONFH)的发展有关。特别是,非创伤性 ONFH 直接或间接与股骨头血管供应损伤有关。因此,由于血流受损导致的股骨头缺氧可能是 ONFH 的一个重要危险因素。在这项研究中,我们研究了血管生成和缺氧相关基因的遗传变异是否会增加发生 ONFH 的风险。候选基因是基于已知的缺氧和血管生成途径选择的。使用 Affymetrix 靶向基因分型 3K 芯片阵列对 460 名 ONFH 患者和 300 名对照进行了关联研究。我们表明,TF、VEGFC、IGFBP3 和 ACE 基因中的单核苷酸多态性(SNP)与 ONFH 的风险增加相关。另一方面,KDR 和 NRP1 基因中的 SNP 与 ONFH 的保护作用相关。最重要的发现是,IGFBP3 基因中的一个 SNP(rs2453839)与 ONFH 的风险显著相关(P=0.0061,OR7.74)。在亚组分析中,与 ONFH 相关的大多数候选基因变异发生在特发性亚组中。在其他 SNP 中,ACE SNP 与激素诱导的 ONFH 相关(P=0.0018-0.0037,OR>3)。总之,我们的研究结果表明,血管生成和缺氧相关基因的遗传变异可能有助于鉴定韩国人群中发生 ONFH 的易感因素。