细胞因子单核苷酸多态性(snp)与阿尔及利亚重症肌无力(MG)患者的关联:一个小群体的病例对照研究。

Mohamed Nadji Bouchtout, Fethi Meçabih, Chahrazad Boukadir, Elias Attal, Smail Daoudi, Halla Benkortbi, Chafia Touil-Boukoffa, Rachida Raache, Nabila Attal
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引用次数: 0

摘要

摘要重症肌无力(MG)是一种多因素病因的自身免疫性疾病,遗传因素和细胞因子似乎在其中起重要作用。本研究的目的是调查阿尔及利亚患者细胞因子单核苷酸多态性(snp)与MG的潜在关联。我们进行了一项病例对照研究,包括27名患者和74名健康受试者。细胞因子snp基因分型采用聚合酶链反应序列特异性引物(PCR-SSP)方法。结果显示,MG患者中TNF-α -308G/A (P < 0.005)和TGF-β1 +869T/T (P < 0.05)基因型发生率高于健康人群,TNF-α -308G/G (P < 0.0001)、TGF-β1 +869T/C (P < 0.05)和IFN-γ +874A/A (P < 0.05)基因型发生率低于健康人群。我们的结果还显示,IL-10和IL-6 snp在MG患者和健康个体之间的分布没有显着差异。我们的观察结果支持了MG中某些细胞因子遗传变异的假设。然而,我们的结果应该用更大的样本量来复制。此外,确切的基本过程仍有待澄清。重点:TNF-α -308G/A和TGF-β1 +869T/C基因型易患MG。IFN-γ +874A/A基因型对MG有保护作用。IL-6 -174C/G SNP与MG无关。
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Cytokines Single Nucleotide Polymorphisms (SNPs) Association With Myasthenia Gravis (MG) In Algerian Patients: A Case-Control Study On A Small Group.

Abstract: Myasthenia gravis (MG) is an autoimmune disease of multifactorial etiology in which genetic factors and cytokines seem to play an important role. The aim of this study was to investigate potential associations of cytokines single nucleotide polymorphisms (SNPs) and MG in Algerian patients. We performed a case-control study that included 27 patients and 74 healthy subjects. Cytokines SNPs genotyping was performed by the polymerase chain reaction sequence-specific primers (PCR-SSP) method. Our results showed that the TNF-α -308G/A (P < 0.005) and TGF-β1 +869T/T (P < 0.05) genotypes were more frequent among patients with MG compared with healthy individuals, whereas TNF-α -308G/G (P < 0.0001), TGF-β1 +869T/C (P < 0.05), and IFN-γ +874A/A (P < 0.05) were less frequent. Our results also showed that IL-10 and IL-6 SNPs did not show any significant difference in distribution between MG patients and healthy individuals. Our observations support the hypothesis that implicates genetic variants of certain cytokines in MG. However, ours results should be replicated with a larger sample size. In addition, the precise underlying processes remain to be clarified.

Highlights: TNF-α -308G/A and TGF-β1 +869T/C genotypes predispose to MG.IFN-γ +874A/A genotype protects against MG.IL-6 -174C/G SNP is not associated with MG.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
64
期刊介绍: Journal of Clinical Neuromuscular Disease provides original articles of interest to physicians who treat patients with neuromuscular diseases, including disorders of the motor neuron, peripheral nerves, neuromuscular junction, muscle, and autonomic nervous system. Each issue highlights the most advanced and successful approaches to diagnosis, functional assessment, surgical intervention, pharmacologic treatment, rehabilitation, and more.
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