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Association of interleukin-1 receptor antagonist gene polymorphism with response to conservative treatment of lumbar herniated nucleus pulposus.

机译:白介素1受体拮抗剂基因多态性与对腰椎间盘突出髓核的保守治疗的反应相关。

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STUDY DESIGN: A case-control study. OBJECTIVE: To evaluate the relationship between gene polymorphism in interleukin 1 receptor antagonist (IL1RN) and response to conservative treatment of lumbar herniated nucleus pulposus (HNP). SUMMARY OF BACKGROUND DATA: There had been several studies on IL1RN polymorphism related with incidence of disc degeneration or back pain but, there had been no report on clinical features of lumbar HNP. METHODS: We analyzed the variable number tandem repeat polymorphism of IL1RN genes in 54 single level subligamentous extruded lumbar HNP patients and compared allele frequency and incidence of heterozygote with 227 healthy adult controls. Within HNP group, we compared 2 groups; surgery group and conservative treatment group according to response to conservative treatment. RESULTS: The prevalence of A1 (odd ratio = 0.45, P = 0.0009) and A3 (odd ratio = 3.86, P = 0.0006) was significantly higher in HNP group than control group. The allele frequency of A1, A2, A3, A4, and A5 were 84.2:84.6, 7.3:15.4, 8.5:0, 0:0, 0:0, respectively, in surgical and conservative treatment group. The allele frequency for A3 was found significantly higher in the surgery group than in the conservative treatment group. CONCLUSION: These results suggest that a high allele prevalence of A3 contribute to the clinical progression and the response to conservative treatment for lumbar HNP. IL1RN gene polymorphism may affect the clinical course of lumbar HNP.
机译:研究设计:病例对照研究。目的:探讨白细胞介素1受体拮抗剂(IL1RN)基因多态性与腰椎间盘突出髓核(HNP)保守治疗反应的关系。背景资料摘要:已有关于椎间盘退变或腰痛发生率相关的IL1RN多态性的研究,但尚无关于腰椎HNP临床特征的报道。方法:我们分析了54例单水平亚韧带挤压性腰椎HNP患者IL1RN基因的可变数目串联重复多态性,并与227例健康成人对照者比较了等位基因频率和杂合子发生率。在HNP组中,我们比较了2个组。手术组和保守治疗组根据对保守治疗的反应。结果:HNP组的A1(奇数比= 0.45,P = 0.0009)和A3(奇数比= 3.86,P = 0.0006)的患病率明显高于对照组。在外科和保守治疗组中,A1,A2,A3,A4和A5的等位基因频率分别为84.2:84.6、7.3:15.4、8.5:0、0:0、0:0。在手术组中发现A3的等位基因频率显着高于保守治疗组。结论:这些结果表明,A3的高等位基因患病率有助于腰椎HNP的临床进展和对保守治疗的反应。 IL1RN基因多态性可能影响腰椎HNP的临床过程。

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