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立陶宛多发性硬化症患者的基因多态性与白细胞介素-10血清水平

Gene Polymorphisms and IL-10 Serum Levels in Patients with Multiple Sclerosis in Lithuania.

作者信息

Masilionyte Ugne, Gedvilaite Greta, Kaikaryte Kriste, Vilkeviciute Alvita, Kriauciuniene Loresa, Glebauskiene Brigita, Balnyte Renata, Liutkeviciene Rasa

机构信息

Medical Academy, Lithuanian University of Health Sciences, Eiveniu Street 2, LT-50161 Kaunas, Lithuania.

Neuroscience Institute, Medical Academy, Lithuanian University of Health Sciences, Eiveniu Street 2, LT-50161 Kaunas, Lithuania.

出版信息

Brain Sci. 2022 Jun 18;12(6):800. doi: 10.3390/brainsci12060800.

Abstract

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system with features of demyelination and axonal degeneration at a young age. Genetic factors may play an important role in the development of multiple sclerosis. (1) Objective: To investigate IL-10 rs1800871, rs1800872, rs1800896, and IL-10 serum levels in patients with multiple sclerosis. (2) Methods: Our study included patients with multiple sclerosis (n = 127) and healthy volunteers (n = 195). The subjects’ DNA was extracted from peripheral blood leukocytes and genotyped by real-time polymerase chain reaction. The results were analyzed using the program “IBM SPSS Statistics 27.0”. (3) Results: The IL-10 SNPs were analyzed between the MS and control groups; however, no statistically significant results were found. The serum levels of IL-10 in the groups of MS and healthy subjects were not statistically significantly different (median (IQR): 0.828 (1.533) vs. 0.756 (0.528), p = 0.872). (4) Conclusions: IL-10 rs1800871, rs1800872, and rs1800896 and serum IL-10 levels are not likely to be associated with MS development. However, individuals carrying the rare haplotypes of rs1800871, rs1800872, and rs1800896 were associated with increased odds of MS (p = 0.006).

摘要

多发性硬化症(MS)是一种中枢神经系统的慢性炎症性疾病,在年轻时具有脱髓鞘和轴突变性的特征。遗传因素可能在多发性硬化症的发展中起重要作用。(1)目的:研究多发性硬化症患者中白细胞介素-10(IL-10)的rs1800871、rs1800872、rs1800896基因位点及IL-10血清水平。(2)方法:我们的研究纳入了多发性硬化症患者(n = 127)和健康志愿者(n = 195)。从外周血白细胞中提取受试者的DNA,并通过实时聚合酶链反应进行基因分型。使用“IBM SPSS Statistics 27.0”程序分析结果。(3)结果:对MS组和对照组之间的IL-10单核苷酸多态性(SNP)进行了分析;然而,未发现具有统计学意义的结果。MS组和健康受试者组的IL-10血清水平无统计学显著差异(中位数(四分位间距):0.828(1.533)对0.756(0.528),p = 0.872)。(4)结论:IL-10的rs1800871、rs1800872和rs1800896基因位点及血清IL-10水平不太可能与MS的发生相关。然而,携带rs1800871、rs1800872和rs1800896罕见单倍型的个体与MS发病几率增加相关(p = 0.006)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23fe/9221209/7b771fbbe17b/brainsci-12-00800-g001.jpg

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