Department of Orthopedics of the Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
The Engineering Research Center of Molecular Diagnosis and Cellular Treatment for Metabolic Bone Diseases of Jilin Province, Changchun, Jilin 130041, P.R. China.
Mol Med Rep. 2017 Nov;16(5):7145-7153. doi: 10.3892/mmr.2017.7473. Epub 2017 Sep 12.
Although lipid metabolism disorders have been recognized as a primary factor of osteonecrosis of the femoral head (ONFH), the molecular pathogenesis remains unclear. Sterol regulatory element‑binding protein 2 (SREBP2) specifically regulates cholesterol and fatty acid metabolism to maintain lipid homeostasis. To explore the roles of the SREBP2 gene in the development of ONFH, the authors analyzed the gene polymorphism and gene expression of three tag single nucleotide polymorphisms of the SREBP2 gene, the serum lipids levels, and their associations with ONFH development in 182 ONFH patients and 179 healthy controls. The results demonstrated that the stage IV proportions of ONFH patients carrying the rs2267439CT or CC genotype were significantly higher and lower than the stage III proportions of ONFH patients (P=0.039), respectively. The serum triglyceride, low‑density lipoprotein (LDL)‑c levels, and LDL‑C/high‑density lipoprotein (HDL)‑C ratio in the ONFH group were significantly increased compared to those in the control group (P=0.01, P=0.005, P=0.0001) while the HDL‑C level of ONFH group was remarkably lower than that of the control group (P=0.0001). Association analysis further revealed that the LDL‑c levels of the rs226744 GG and AG genotype carriers were statistically higher than that of the AA genotype carriers (P=0.039, P=0.05). These results demonstrated that the gene polymorphism of SREBP2 not only significantly associated with the clinical phenotypes of ONFH but also closely related to lipid metabolism disorder. The results indicated that SREBP2 gene polymorphism and function may play key roles in the development of ONFH.
尽管脂质代谢紊乱已被认为是股骨头坏死(ONFH)的主要因素,但分子发病机制仍不清楚。固醇调节元件结合蛋白 2(SREBP2)特异性调节胆固醇和脂肪酸代谢以维持脂质稳态。为了探讨 SREBP2 基因在 ONFH 发展中的作用,作者分析了 SREBP2 基因的三个标记单核苷酸多态性的基因多态性和基因表达、血清脂质水平及其与 182 例 ONFH 患者和 179 例健康对照者 ONFH 发展的相关性。结果表明,携带 rs2267439CT 或 CC 基因型的 ONFH 患者的 IV 期比例明显高于 III 期患者(P=0.039),而携带 rs2267439TT 基因型的 ONFH 患者的 III 期比例明显高于 IV 期患者(P=0.039)。ONFH 组的血清甘油三酯、低密度脂蛋白(LDL)-c 水平和 LDL-C/高密度脂蛋白(HDL)-C 比值明显高于对照组(P=0.01,P=0.005,P=0.0001),而 ONFH 组的 HDL-C 水平明显低于对照组(P=0.0001)。关联分析进一步表明,rs226744 GG 和 AG 基因型携带者的 LDL-c 水平明显高于 AA 基因型携带者(P=0.039,P=0.05)。这些结果表明,SREBP2 基因多态性不仅与 ONFH 的临床表型显著相关,而且与脂质代谢紊乱密切相关。研究结果表明,SREBP2 基因多态性和功能可能在 ONFH 的发展中起关键作用。