LAUSR

Abstract Introduction Primary nephrotic syndrome (NS) is a common glomerular disease in children. We assessed the genotypes and frequency of the rs5370 allelic variant of the EDN1 gene in children with primary NS. Patients and methods We conducted a case-control study in Mansoura University Children's Hospital, Egypt between December 2015 and January 2018. We recruited 50 patients with steroid-sensitive NS (SSNS) and 50 patients with steroid-resistant NS (SRNS) in addition to 100 healthy controls. The patients underwent clinical evaluations and tests including measurement of serum albumin, cholesterol, creatinine and urea levels and a 24 -h urinary protein test. We used polymerase chain reaction methods to assess the genotypes of rs5370 variants of the EDN1 gene (GG, GT and TT) and alleles (T and G) in the groups under study. Results The most frequent genotype of the EDN1 gene at the locus of interest in the control group was the GT genotype (88%; P = .001) while the GG genotype was more frequent in the NS group compared to the control group (P = .02). We did not find statistically significant differences between the NS and control groups in regard to the EDN1 rs5370 alleles (P = .69). The GG genotype was more frequent in the SSNS group compared to the SRNS and control groups (P = .03). When we compared allele frequencies between the control, SSNS and SRNS groups, we did not find significant differences (P = .89). The GT genotype was associated with normal blood pressure in children with NS (P = .007), while the GG genotype was associated with hypertension (P  Conclusions The GG genotype at the rs5370 locus of the EDN1 gene may be associated with an increased risk of primary NS and a better response to steroid therapy.