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伊朗人群中促炎细胞因子基因多态性与梅尼埃病的相关性研究。

Association of Pro-inflammatory Cytokine Gene Polymorphism with Meniere's Disease in an Iranian Sample.

机构信息

Otorhinolaryngology Research Center, Amir A'lam Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Otorhinolaryngology Research Center, Amir A'lam Hospital Complex, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Allergy Asthma Immunol. 2021 Dec 8;20(6):734-739. doi: 10.18502/ijaai.v20i6.8024.

Abstract

Meniere's disease (MD) is known as a rare chronic disorder of the inner ear with elevated serum levels of pro-inflammatory cytokines like tumor necrosis factor (TNF)-α, Interleukin (IL)-1, and IL-6. This study aims to evaluate genes polymorphism in some pro-inflammatory cytokines in a group of Iranian MD patients compared to the healthy controls. In this case-control study, 25 MD patients and 139 healthy controls were enrolled. DNA was extracted from blood samples, and single nucleotide polymorphisms were detected using polymerase chain reaction with sequence-specific primers assay. MD patients and controls were examined in terms of allele, genotype, and haplotype frequency of pro-inflammatory cytokine genes. Only the frequencies of alleles A/G at position -238 in the promoter of the TNF-α gene differed significantly between MD patients and healthy controls. G to A allele ratio was 23 and 3.6 in MD and controls, respectively. In individuals with MD, genotype GG was found to be significantly more prevalent at position -238 of the TNF-α gene promoter sequence. In addition, the heterozygote AG variant of -238 A/G TNF-α gene polymorphism was lower in MD patients than controls. Compared to the control group, the haplotype TNF- (-308, -238) AG was higher in MD patients, although not statistically significant. This is the first study that we know of that evaluates the frequencies of pro-inflammatory cytokine genes in an Iranian MD sample. This study shows the association between TNF-α and susceptibility to MD.

摘要

梅尼埃病(MD)是一种罕见的内耳慢性疾病,其血清中促炎细胞因子水平升高,如肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1 和 IL-6。本研究旨在评估一组伊朗 MD 患者与健康对照组之间某些促炎细胞因子基因的多态性。在这项病例对照研究中,共纳入 25 名 MD 患者和 139 名健康对照者。从血液样本中提取 DNA,采用聚合酶链反应与序列特异性引物法检测单核苷酸多态性。对 MD 患者和对照组进行促炎细胞因子基因的等位基因、基因型和单倍型频率检查。只有 TNF-α 基因启动子 -238 位的等位基因 A/G 的频率在 MD 患者和健康对照组之间有显著差异。MD 患者和对照组中 G 到 A 等位基因的比值分别为 23 和 3.6。在 MD 患者中,TNF-α 基因启动子序列 -238 位的 GG 基因型明显更为常见。此外,-238 A/G TNF-α 基因多态性的杂合子 AG 变体在 MD 患者中低于对照组。与对照组相比,MD 患者的 TNF-(-308,-238)AG 单倍型较高,但无统计学意义。这是我们所知的第一个评估伊朗 MD 样本中促炎细胞因子基因频率的研究。本研究表明 TNF-α 与 MD 的易感性有关。

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