Matrix Metalloproteinase (MMP)-9 Levels in Children on Hemodialysis: Association with MMP-9 C -1562 T Gene Polymorphism and Vitamin D Levels

Data concerning the concentration of matrix metalloproteinase-9 (MMP-9) and its functional polymorphisms in chronic kidney diseases (CKD) are conflicting. The present study aimed to evaluate the levels of MMP-9in children with end stage renal diseases (ESRD) on hemodialysis (HD) and to explore its a...

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Published inInternational journal of biomedical science Vol. 12; no. 3; p. 95
Main Authors Galal, Ashraf, Fadel, Fatina I, Mokhtar, Enas, Elshamaa, Manal F, Elghoroury, Eman A, Kamel, Solaf, Elsaeed, Gamila S M, Thabet, Eman H
Format Journal Article
LanguageEnglish
Published United States 01.09.2016
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Summary:Data concerning the concentration of matrix metalloproteinase-9 (MMP-9) and its functional polymorphisms in chronic kidney diseases (CKD) are conflicting. The present study aimed to evaluate the levels of MMP-9in children with end stage renal diseases (ESRD) on hemodialysis (HD) and to explore its association with MMP-9 polymorphism and vitamin D levels as an important risk factors for cardiovascular diseases (CVD). We studied 55 children with ESRD on hemodialysis and 18 healthy children served as controls. MMP-9 and vitamin D levels were measured by ELISA in serum of all patients and controls. Genotypes for MMP-9 polymorphism(C T) were determined by RFLP for only 28 of the patients and all the controls. There were insignificantly reduced MMP-9levels of patients vs. controls, however, there was significant increase in MMP-9 levels associated with CC genotypes for(C T) polymorphism compared with CT genotype ( =0.01). We found that at MMP-9 base position-1562, the frequencies of the genotypes CC and CT in Children on HD were 71.4% and 28.6% respectively while all our controls were of the CC genotype. The alleles frequencies of C and T in patients were 85.7% and 14.29% as compared to 100% and 0%, respectively in the controls. Significant decrease in vitamin D was observed in children on HD versus that in controls ( =0.008). Serum MMP9 levels and age were variables that were independently associated with CVD. MMP9 genetic polymorphism (C T) affects MMP9alterations in ESRD children on HD and vitamin D deficiency is common in our HD pediatric patients who require attention in accordance with current practice guidelines. They probably require supplementation with higher doses of cholecalciferol.
ISSN:1550-9702
1555-2810