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首页> 外文期刊>Connective tissue research >Caspase 9 gene polymorphism and susceptibility to lumbar disc disease in the Han population in northern China.
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Caspase 9 gene polymorphism and susceptibility to lumbar disc disease in the Han population in northern China.

机译:中国北方汉族人群Caspase 9基因多态性与腰椎间盘疾病的易感性。

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Many studies have demonstrated that apoptosis is involved in the development of disc degeneration. The initiator caspase 9 is activated through the apoptosome-driven intrinsic apoptotic pathway. The present study aimed to assess the potential association between the caspase 9 gene polymorphism and lumbar disc herniation (LDH) susceptibility, as well as severe grades of disc degeneration in the Han population in northern China. Genotyping was performed using the polymerase chain reaction and polymorphism was analyzed by restriction endonuclease cleavage in 387 patients with LDH and 412 control subjects. The allelic frequencies of caspase 9 Ex5+32 A were 0.483 and 0.391 in case patients and control subjects, respectively. Compared to those with the AA genotype, subjects with the GA/GG genotype have a higher risk to develop LDH (odds ratio 1.91; 95% confidence interval 1.29-2.81). Moreover, the GA/GG genotype was found to contribute to the risk of more severe grades of disc degeneration, as observed in magnetic resonance imaging scan. In conclusion, this study suggests that the single nucleotide polymorphism in the caspase 9 Ex5 + 32 G/A may be associated with LDH and disc degeneration in the Han population of northern China.
机译:许多研究表明,细胞凋亡与椎间盘退变的发展有关。起始胱天蛋白酶9通过凋亡小体驱动的固有凋亡途径被激活。本研究旨在评估中国北方汉族人群中半胱天冬酶9基因多态性与腰椎间盘突出症(LDH)敏感性以及严重程度的椎间盘退变之间的潜在关联。使用聚合酶链反应进行基因分型,并通过限制性内切核酸酶裂解技术分析了387例LDH患者和412例对照受试者的多态性。在病例患者和对照组中,胱天蛋白酶9 Ex5 + 32 A的等位基因频率分别为0.483和0.391。与具有AA基因型的受试者相比,具有GA / GG基因型的受试者发生LDH的风险更高(优势比为1.91; 95%置信区间为1.29-2.81)。此外,如在磁共振成像扫描中所观察到的,发现GA / GG基因型有助于更大程度的椎间盘退变。总之,这项研究表明,在中国北方汉族人群中,胱天蛋白酶9 Ex5 + 32 G / A的单核苷酸多态性可能与LDH和椎间盘退变有关。

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