TY - JOUR A1 - El-Mashad, Ghada A1 - Khattab, Essam A1 - El-Mekkawy, Muhammad A1 - Saleh, Nagwan A1 - Abou El Yazed, Wafaa T1 - Interleukin-6 gene -572G>C polymorphism in Egyptian children with idiopathic nephrotic syndrome Y1 - 2021/1/1 JF - Menoufia Medical Journal JO - Menoufia Med J SP - 192 EP - 196 VL - 34 IS - 1 UR - http://www.mmj.eg.net/article.asp?issn=1110-2098;year=2021;volume=34;issue=1;spage=192;epage=196;aulast=El-Mashad DO - 10.4103/mmj.mmj_147_19 N2 - Objective To evaluate the association of -572G > C polymorphism with idiopathic nephrotic syndrome (INS) in children. Background Interleukin 6 (IL-6) gene promoter polymorphisms, including -572G > C polymorphism, have been implicated in INS. Patients and methods A total of 55 Egyptian children with INS were recruited along with 51 healthy controls. Genotyping for IL-6 gene -572G > C polymorphism was performed by PCR followed by restriction fragment length polymorphism. Results GC genotype was more prevalent among patients compared with controls [40 vs. 7.8%, odds ratio (OR)=5.5, P = 0.002], but there was no significant difference between patients and controls regarding CC genotype (9.1 vs. 2%, OR = 5, P = 0.14). Under the dominant model, the pooled GC + CC was more prevalent among patients compared with controls (OR = 5.4, P < 0.001). The distribution of C allele was significantly higher among patients compared with controls (29.1 vs. 5.9%, OR = 5.3, P < 0.001). No significant difference was found between patients and controls regarding the prevalence of any of the alleles or genotypes under codominant, recessive, or dominant models. Conclusion IL-6 gene -572G > C polymorphism confers susceptibility to INS among children, but it has no influence on the response to steroids. ER -