Genetic polymorphism of ACE and the angiotensin II type1 receptor genes in children with chronic kidney disease

• Published in: Journal of inflammation (London, England) Vol. 8; no. 1; p. 20
• Main Authors: Elshamaa, Manal F, Sabry, Samar M, Bazaraa, Hafez M, Koura, Hala M, Elghoroury, Eman A, Kantoush, Nagwa A, Thabet, Eman H, Abd-El Haleem, Dalia A
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 23.08.2011; BioMed Central; BMC
• Subjects: Angiotensin converting enzyme; angiotensin II type one receptor; Care and treatment; Diagnosis; DNA polymorphisms; end-stage renal disease, Children; Genetic aspects; Genetic polymorphisms; Kidney diseases; Physiological aspects; Egypt
• ISSN: 1476-9255; 1476-9255
• DOI: 10.1186/1476-9255-8-20

We investigated the association between polymorphisms of the angiotensin converting enzyme-1 (ACE-1) and angiotensin II type one receptor (AT1RA1166C) genes and the causation of renal disease in 76 advanced chronic kidney disease (CKD) pediatric patients undergoing maintenance hemodialysis (MHD) or conservative treatment (CT). Serum ACE activity and creatine kinase-MB fraction (CK-MB) were measured in all groups. Left ventricular mass index (LVMI) was calculated according to echocardiographic measurements. Seventy healthy controls were also genotyped. The differences of D allele and DI genotype of ACE were found significant between MHD group and the controls (p = 0.0001). ACE-activity and LVMI were higher in MHD, while CK-MB was higher in CT patients than in all other groups. The combined genotype DD v/s ID+II comparison validated that DD genotype was a high risk genotype for hypertension .~89% of the DD CKD patients were found hypertensive in comparison to ~ 61% of patients of non DD genotype(p = 0.02). The MHD group showed an increased frequency of the C allele and CC genotype of the AT1RA1166C polymorphism (P = 0.0001). On multiple linear regression analysis, C-allele was independently associated with hypertension (P = 0.04). ACE DD and AT1R A/C genotypes implicated possible roles in the hypertensive state and in renal damage among children with ESRD. This result might be useful in planning therapeutic strategies for individual patients.