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伊朗人群中白细胞介素 2、白细胞介素 12 和干扰素-γ 与椎间盘退变的关系。

Association of interleukin 2, interleukin 12, and interferon-γ with intervertebral disc degeneration in Iranian population.

机构信息

Molecular Immunology Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Dr Qarib St, Keshavarz Blvd, Tehran, 14194, Iran.

出版信息

BMC Med Genet. 2020 Jul 3;21(1):143. doi: 10.1186/s12881-020-01081-3.

Abstract

BACKGROUND

Intervertebral disc degeneration (IVDD) is an age-related degenerative disease, presenting with low back pain or radicular pain. The inflammatory changes would occur in discs in the process of IVDD. Therefore, the inflammatory and anti-inflammatory cytokines, as well as their respective genes, have been proposed to play roles in pathophysiology of disease. This study has been conducted to elucidate the role of IL-2, IL-12, and IFN-γ single nucleotide polymorphisms (SNP) in this disease.

METHOD

Seventy-six patients who were diagnosed with IVDD and 140 healthy controls who complied with eligibility criteria were included. A total volume of 5 cc peripheral blood was obtained from each participant to investigate the IL-2 + 166G/T, IL-2 -330G/T, IL-12 - 1188A/C, and IFN-γ +847A/T SNPs through PCR-SSP method.

RESULTS

The 'TG' and 'TT' genotypes of IL-2 - 330G/T polymorphism were significantly more common among patients and healthy controls respectively. The 'GT' and 'TT' haplotypes of IL-2 (comprised of -330G/T, and + 166G/T SNPs) were also more common among patients and controls respectively.

CONCLUSION

This study indicated the significant role of IL-2 genotypes and haplotypes in IVDD. These SNPs were differently distributed in patients and controls. Therefore, alteration in the structure of IL-2 gene could play an important role in pathophysiology of IVDD.

摘要

背景

椎间盘退行性病变(IVDD)是一种与年龄相关的退行性疾病,表现为腰痛或根性痛。在 IVDD 过程中,椎间盘会发生炎症变化。因此,炎症和抗炎细胞因子及其各自的基因被认为在疾病的病理生理学中发挥作用。本研究旨在阐明 IL-2、IL-12 和 IFN-γ 单核苷酸多态性(SNP)在这种疾病中的作用。

方法

纳入了 76 名确诊为 IVDD 的患者和 140 名符合入选标准的健康对照者。从每位参与者中抽取 5cc 外周血,通过 PCR-SSP 法检测 IL-2+166G/T、IL-2-330G/T、IL-12-1188A/C 和 IFN-γ+847A/T SNPs。

结果

IL-2-330G/T 多态性的“TG”和“TT”基因型在患者和健康对照者中分别更为常见。IL-2(由-330G/T 和+166G/T SNPs 组成)的“GT”和“TT”单倍型在患者和对照组中也更为常见。

结论

本研究表明 IL-2 基因型和单倍型在 IVDD 中具有重要作用。这些 SNP 在患者和对照者中的分布不同。因此,IL-2 基因结构的改变可能在 IVDD 的病理生理学中发挥重要作用。

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