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首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >A controlled case study of the relationship between environmental risk factors and apoptotic gene polymorphism and lumbar disc herniation
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A controlled case study of the relationship between environmental risk factors and apoptotic gene polymorphism and lumbar disc herniation

机译:周围环境危险因素与凋亡基因多态性与腰椎间盘突出症关系的对照病例研究

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To explore the etiologic role of apoptosis-related genes, environmental risk factors, and their interaction in the occurrence of lumbar disk herniation (LDH), a controlled case study was performed with 128 LDH patients and 132 age- and sex-matched controls. Matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry assay was used to analyze the genotype of nine polymorphism sites in three genes, including Fas -1377G/A rs2234767, Fas -670G/A rs1800682, Fas rs2147420, Fas rs2296603, Fas rs7901656, Fas rs1571019, Fas ligand (FasL) -844C/T rs763110, caspase 9 (CASP9) -1263A>G rs4645978, and CASP9 -712C>T rs4645981. The patients and controls showed similar age and sex, but had significant differences in lumbar load, bed type, amateur sports, and leisure activities (P < 0.05). The correlation analysis revealed that polymorphism of FasL -844C/T (rs763110) and CASP9 -1263A>G (rs4645978) had a significant correlation with LDH, indicating that the genotypes of FasL -844C/T TT and CASP9 -1263A>G GG are probably high-risk genotypes for LDH. The results of environment-gene interaction analysis revealed that, in LDH, the interaction of the FasL -844TT genotype and level III to IV lumbar load was consistent with the ultramultiplying model, and the interaction of the CASP9 rs4645978 GG genotype and level III to IV lumbar load was consistent with the submultiplicative model. Therefore, the risk of LDH was determined by both environmental and genetic risk factors, and the mechanisms of interactions between different genotypes and environmental factors also differed. ? 2013 American Society for Investigative Pathology.
机译:为了探讨凋亡相关基因,环境危险因素及其在腰椎间盘突出症(LDH)发生中的相互作用的病因学作用,我们对128位LDH患者和132位年龄和性别匹配的对照进行了病例对照研究。使用基质辅助激光解吸/电离飞行时间质谱分析法分析了三个基因中的9个多态性位点的基因型,包括Fas -1377G / A rs2234767,Fas -670G / A rs1800682,Fas rs2147420,Fas rs2296603 ,Fas rs7901656,Fas rs1571019,Fas配体(FasL)-844C / T rs763110,胱天蛋白酶9(CASP9)-1263A> G rs4645978和CASP9 -712C> T rs4645981。患者和对照组的年龄和性别相似,但腰部负荷,床型,业余运动和休闲活动具有显着差异(P <0.05)。相关性分析显示,FasL -844C / T(rs763110)和CASP9 -1263A> G(rs4645978)的多态性与LDH显着相关,表明FasL -844C / T TT和CASP9 -1263A> G GG的基因型是可能是LDH的高风险基因型。环境-基因相互作用分析的结果表明,在LDH中,FasL -844TT基因型与III至IV级腰部负荷的相互作用与超乘模型一致,而CASP9 rs4645978 GG基因型与III至IV级的相互作用腰椎负荷与亚乘法模型一致。因此,LDH的风险由环境和遗传风险因素共同决定,不同基因型和环境因素之间相互作用的机制也不同。 ? 2013年美国调查病理学会。

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