Tumor necrosis factor alpha gene polymorphism affects the pattern of idiopathic nephrotic syndrome in Kuwaiti Arab children

• Published in: Journal of tropical pediatrics (1980) Vol. 70; no. 1
• Main Authors: Al-Eisa, MD, Amal A, Al Rushood, Maysoun, Kashyap, Sumedha, Haider, Mohammad Z
• Format: Journal Article
• Language: English
• Published: England 06.12.2023
• Subjects: Arabs - genetics; Child; Genotype; Humans; Kuwait - epidemiology; Nephrotic Syndrome - diagnosis; Nephrotic Syndrome - drug therapy; Nephrotic Syndrome - genetics; Polymorphism, Genetic; Steroids - therapeutic use; Tumor Necrosis Factor-alpha - genetics; Kuwait; tumor necrosis factor alpha; gene polymorphism; nephrotic syndrome
• ISSN: 1465-3664
• DOI: 10.1093/tropej/fmad047

TNF-α is a pro-inflammatory cytokine that has been implicated in many inflammatory diseases, but its association with idiopathic nephrotic syndrome (INS) is poorly understood. This study looked for an association of TNF-α gene polymorphisms with INS, as well as its effect on steroid responsiveness among Kuwaiti Arab children. Genotypes of the TNF-a gene polymorphisms were analyzed using polymerase chain reaction-restriction fragment length polymorphism in 151 INS Kuwaiti Arab patients and 64 age and sex-matched controls. Clinical data of all subjects were reviewed. The heterozygous AG genotype was detected in 8.6% of INS patients compared 23.4% of the controls (p < 0.01). Comparing steroid responsiveness, AA genotype was significantly more common in steroid-sensitive nephrotic syndrome (SSNS) cases than steroid-resistant nephrotic syndrome (SRNS) patients (p = 0.001). However, AG genotype was significantly more common in SRNS patients compared to the SSNS cases (p = 0.001). No difference was found between these two subgroups in the GG genotype frequency. AG genotype of TNF-a gene polymorphisms may be considered a suitable marker for INS disease among Kuwaiti children. Both AA and AG genotypes may be useful in predicting steroid responsiveness among these cases of Arab ethnicity. The findings might open the era for the use of genetic markers in the early treatment of NS.