Heat shock protein 70 gene polymorphisms in Iranian patients with Multiple sclerosis.

IF 1.4 Q4 IMMUNOLOGY American journal of clinical and experimental immunology Pub Date : 2024-12-25 eCollection Date: 2024-01-01 DOI:10.62347/CMYA9839
Azam Bakhshandeh, Alireza Kargar Dolatabadi, Touraj Farazmanfar, Majid Shahbazi
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Abstract

Genetic factors are effective reagents in susceptibility to multiple sclerosis (MS). Previous studies have shown the relationship between heat shock protein (HSP) gene polymorphisms. So, HSP70 single nucleotide polymorphisms (SNPs) were evaluated as MS risk factors. Here, DNA genotyping was done for HSP70 gene polymorphisms, including HSP70-1 +190 G>C, HSP70-1 -110 A>C, HSP70-1 +438 A>C, and HSP70-hom +2437 A>G in two groups including Iranian MS patients and controls. A standard phenol/chloroform method isolated DNA samples from peripheral blood. Sequence-specific amplification (SSP) polymerase chain reaction (PCR) was used for genotyping polymorphisms. Overall, 76 (35.80%) MS patients and 136 (65.10%) controls were studied with an age mean of 36.0 ± 8.0 years. Female/male was significantly higher in patients than in controls (4.43 vs. 0.10, P < 0.001). The average age was significantly lower in patients (P < 0.001). The most common clinical feature was relapsing-remitting (RR) MS; more than half of the population was Fars. Results showed that genotypes of HSP70-hom +2437 C>T had a significant relation with MS (OR = 2.0, 95% CI = 1.0-5.0, P = 0.03) and the same applies to HSP70-1 -110 A>C (OR = 0.0, 95% CI = 0.0-1.0, P < 0.001). Allele and genotype frequency of two other HSP70 SNPs (HSP70-1 +190 G>C, HSP70-1 +438 A>C) showed no significant differences between patients and controls. HSP70-hom +2437 C>T and HSP70-1 -110 A>C can be considered as risk factors for MS in our population. However, other HSP SNPs should be studied in a larger population in the future.

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伊朗多发性硬化症患者热休克蛋白70基因多态性
遗传因素是影响多发性硬化症易感性的有效因素。以往的研究已经证实了热休克蛋白(HSP)基因多态性之间的关系。因此,HSP70单核苷酸多态性(snp)被评价为MS的危险因素。在伊朗MS患者和对照组中,对HSP70基因多态性进行了DNA基因分型,包括HSP70-1 +190 G>C、HSP70-1 -110 A>C、HSP70-1 +438 A>C和HSP70- home +2437 A>G。标准的苯酚/氯仿法从外周血中分离DNA样本。序列特异性扩增(SSP)聚合酶链反应(PCR)用于基因分型多态性。总的来说,76例(35.80%)MS患者和136例(65.10%)对照者被研究,平均年龄为36.0±8.0岁。患者中女性/男性比例显著高于对照组(4.43 vs. 0.10, P < 0.001)。患者的平均年龄明显降低(P < 0.001)。最常见的临床特征是复发缓解型(RR) MS;一半以上的人口是法尔人。结果表明,HSP70-hom +2437 C>T基因型与MS有显著相关性(OR = 2.0, 95% CI = 1.0 ~ 5.0, P = 0.03), HSP70-1 -110 a >C基因型与MS有显著相关性(OR = 0.0, 95% CI = 0.0 ~ 1.0, P < 0.001)。另外两个HSP70 snp (HSP70-1 +190 G>C, HSP70-1 +438 A>C)的等位基因和基因型频率在患者和对照组之间无显著差异。hsp70 - hsp70 +2437℃和HSP70-1 -110℃可被认为是我们人群中多发性硬化症的危险因素。然而,其他的HSP snp需要在未来更大的人群中进行研究。
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