Lee H-J, Choi S-J, Hong J M, Lee W K, Baek J-I, Kim S-Y, Park E K, Kim S-Y, Kim T-H, Kim U-K
Department of Biology, College of Natural Sciences, Kyungpook National University, Daegu 702-701, Republic of Korea.
Ann Hum Genet. 2009 Jan;73(1):34-41. doi: 10.1111/j.1469-1809.2008.00490.x. Epub 2008 Nov 25.
Reduction or disruption of the blood supply to the bone is involved in the pathogenesis of osteonecrosis of the femoral head (ONFH). An altered lipid metabolism is one of the major risk factors for ONFH. Sterol regulatory element binding protein, SREBF1 activates genes regulating lipid biosynthesis. The aim of this study was to examine the association between the polymorphisms of the SREBF1 gene and ONFH susceptibility in the Korean population. The SREBF1 gene in 24 unrelated Korean individuals was sequenced and two polymorphisms were detected. Two variants, IVS6 - 48 C > T and IVS7 + 117 A > G, were genotyped in 423 ONFH patients and 348 controls. The genotype frequency of IVS7 + 117 A > G in ONFH patients was significantly different from that of the control group with P value < 0.0001 (Adjusted OR; 6.88, 95% CI; 3.74-12.67). Moreover, the IVS7 + 117 A > G genotype showed an association with men, and further analysis stratified by etiological factors indicated that the genotype data was significantly associated with a high risk for patients with alcohol-induced ONFH (P < 0.0001). We found that the IVS7 + 117 A > G polymorphism of the SREBF1 gene is associated with an increased risk of ONFH in the Korean population.
股骨头缺血性坏死(ONFH)的发病机制涉及骨血供的减少或中断。脂质代谢改变是ONFH的主要危险因素之一。固醇调节元件结合蛋白SREBF1可激活调节脂质生物合成的基因。本研究旨在探讨韩国人群中SREBF1基因多态性与ONFH易感性之间的关联。对24名无亲缘关系的韩国个体的SREBF1基因进行测序,检测到两个多态性位点。在423例ONFH患者和348例对照中对两个变异体IVS6 - 48 C>T和IVS7 + 117 A>G进行基因分型。ONFH患者中IVS7 + 117 A>G的基因型频率与对照组有显著差异,P值<0.0001(校正OR;6.88,95%CI;3.74 - 12.67)。此外,IVS7 + 117 A>G基因型与男性相关,按病因因素分层的进一步分析表明,基因型数据与酒精性ONFH患者的高风险显著相关(P<0.0001)。我们发现SREBF1基因的IVS7 + 117 A>G多态性与韩国人群中ONFH风险增加相关。