Bakhshandeh Azam, Dolatabadi Alireza Kargar, Farazmanfar Touraj, Shahbazi Majid
Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences Gorgan, Iran.
Am J Clin Exp Immunol. 2024 Dec 25;13(6):278-284. doi: 10.62347/CMYA9839. eCollection 2024.
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, < 0.001). The average age was significantly lower in patients ( < 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.
遗传因素是多发性硬化症(MS)易感性的有效影响因素。先前的研究表明了热休克蛋白(HSP)基因多态性之间的关系。因此,HSP70单核苷酸多态性(SNP)被评估为MS的风险因素。在此,对包括伊朗MS患者和对照组的两组人群进行了HSP70基因多态性的DNA基因分型,这些多态性包括HSP70-1 +190 G>C、HSP70-1 -110 A>C、HSP70-1 +438 A>C和HSP70-hom +2437 A>G。采用标准的酚/氯仿法从外周血中分离DNA样本。使用序列特异性扩增(SSP)聚合酶链反应(PCR)对多态性进行基因分型。总体而言,共研究了76例(35.80%)MS患者和136例(65.10%)对照,平均年龄为36.0±8.0岁。患者的女性/男性比例显著高于对照组(4.43比0.10,P<0.001)。患者的平均年龄显著更低(P<0.001)。最常见的临床特征是复发缓解型(RR)MS;超过一半的人群来自法尔斯省。结果显示,HSP70-hom +2437 C>T的基因型与MS有显著关系(OR = 2.0,95%CI = 1.0 - 5.0,P = 0.03),HSP70-1 -110 A>C也是如此(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没有显著差异。HSP70-hom +2437 C>T和HSP70-1 -110 A>C可被视为我们人群中MS的风险因素。然而,未来应在更大规模的人群中研究其他HSP SNP。