Du Heng, Bai Bin, Qiu Yusheng, Yin Si, Bian Weiguo
Department of Orthopedics, The First Affiliated Hospital of Xi'an Jiaotong University Xi'an 710061, Shaanxi, China.
Int J Clin Exp Pathol. 2015 Jun 1;8(6):7415-20. eCollection 2015.
The aim of the present study was to investigate the association between tumor necrosis factor related apoptosis-inducing ligand (TRAIL) gene polymorphisms and the susceptibility and severity of lumbar disc degeneration (LDD) in the Chinese Han population.
A total of 153 patients with LDD and 131 healthy subjects were enrolled in the study. Four single-nucleotide polymorphisms (SNPs) in the 3' untranslated region (3'UTR) of TRAIL gene, including 1289 C/A, 1525 G/A, 1588 G/A and 1595 C/T, were genotyped with polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis.
The genotypes and alleles frequencies of TRAIL at 1525 and 1595 positions in all subjects were the same. There was a significant association between TRAIL 1525/1595 polymorphisms and the susceptibility of LDD. The frequencies of 1525 GG /1595 CC genotype, and 1525 G/1595 C allele were higher in the patients group than that in the control group. In addition, we found patients with the 1525 AA /1595 TT genotype, as well as 1525 A/1595 T allele exhibit significantly low frequency of high grades of disc degeneration. However, there were no significant differences in the genotype or allele distribution of TRAIL 1289 C/A or 1588 G/A between the patients and the control group.
TRAIL 1525/1595 polymorphisms were associated with the susceptibility and severity of LDD in the Chinese Han population.
本研究旨在探讨肿瘤坏死因子相关凋亡诱导配体(TRAIL)基因多态性与中国汉族人群腰椎间盘退变(LDD)易感性及严重程度之间的关联。
本研究共纳入153例LDD患者和131例健康受试者。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析对TRAIL基因3'非翻译区(3'UTR)的4个单核苷酸多态性(SNP),即1289 C/A、1525 G/A、1588 G/A和1595 C/T进行基因分型。
所有受试者中TRAIL基因1525和1595位点的基因型和等位基因频率相同。TRAIL基因1525/1595多态性与LDD易感性之间存在显著关联。患者组中1525 GG /1595 CC基因型及1525 G/1595 C等位基因的频率高于对照组。此外,我们发现1525 AA /1595 TT基因型以及1525 A/1595 T等位基因的患者,其椎间盘高度退变的频率显著较低。然而,患者组与对照组之间TRAIL基因1289 C/A或1588 G/A的基因型或等位基因分布无显著差异。
TRAIL基因1525/1595多态性与中国汉族人群LDD的易感性及严重程度相关。