Rezaieyazdi Zahra, Delavar Payman, Rafatpanah Houshang, Ganjali Rashin, Sahebari Maryam, Tabaei Samira, Esmaeili Habibollah, Khodashahi Mandana
Rheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Mashhad University of Medical Sciences immunology Mashhad Iran.
Curr Rheumatol Rev. 2024 Aug 16. doi: 10.2174/0115733971304493240801094652.
Systemic lupus erythematosus (SLE) is an autoimmune disease of unknown etiology. Several studies have suggested that interleukin-18 (IL-18) is associated with SLE pathogenesis. The genotype distribution of IL-18 promoter polymorphisms differs among ethnic populations. The present study aimed to investigate the correlation between IL-18 polymorphisms at positions -137 and -607 in patients situated in Northeastern Iran.
This case-control study examined the prevalence of IL-18 -137C/G and -607C/A polymorphic variants among 95 SLE patients referred to the Department of Rheumatology, who were referred to the general clinics of Ghaem Hospital and Imam Reza Hospital in Mashhad, Iran, were included in the study. In addition, 100 healthy individuals were included in the control group. DNA from whole blood was extracted by the salting-out method using a commercial kit (Biogene, US). Allelic and genotypic frequencies of polymorphisms (-137G/C, -607C/A) in the IL-18 promoter gene were analyzed using a polymerase chain reaction (PCR)-based amplification refractory mutation system (ARMS) method.
The results of this study demonstrated that the frequency of SLE patients with the homozygous C/C genotype of the IL-18 promoter gene at position -137 was significantly higher than that of the homozygous G/G genotype (P < 0.001) in normal controls. Furthermore, the polymorphism analysis performed illustrated a significant association between (-137G/C) and (-607C/A) polymorphisms in the IL-18 promoter gene and SLE (P < 0.005).
These results indicated that the 607A/A and 137C/C polymorphisms are more prevalent in SLE. Further research involving larger sample sizes from various populations is necessary to elucidate the role of these polymorphisms and the distribution of alleles in SLE patients.
系统性红斑狼疮(SLE)是一种病因不明的自身免疫性疾病。多项研究表明,白细胞介素-18(IL-18)与SLE发病机制有关。IL-18启动子多态性的基因型分布在不同种族人群中有所不同。本研究旨在调查伊朗东北部患者中IL-18基因-137和-607位点多态性之间的相关性。
本病例对照研究检测了95例转诊至风湿病科的SLE患者中IL-18 -137C/G和-607C/A多态性变体的患病率,这些患者转诊至伊朗马什哈德的加姆医院和伊玛目礼萨医院的普通诊所,并纳入研究。此外,100名健康个体被纳入对照组。使用商业试剂盒(美国Biogene)通过盐析法从全血中提取DNA。采用基于聚合酶链反应(PCR)的扩增不应性突变系统(ARMS)方法分析IL-18启动子基因多态性(-137G/C,-607C/A)的等位基因和基因型频率。
本研究结果表明,IL-18启动子基因-137位点纯合C/C基因型的SLE患者频率显著高于正常对照组中的纯合G/G基因型(P < 0.001)。此外,进行的多态性分析表明,IL-18启动子基因中的(-137G/C)和(-607C/A)多态性与SLE之间存在显著关联(P < 0.005)。
这些结果表明,607A/A和137C/C多态性在SLE中更为普遍。有必要进行进一步研究,纳入来自不同人群的更大样本量,以阐明这些多态性的作用以及SLE患者中等位基因的分布情况。