DNA methylation status of the methylenetetrahydrofolate reductase gene promoter in peripheral blood of end-stage renal disease patients

被引:28
作者
Ghattas, Maivel [1 ]
El-shaarawy, Fatma [2 ]
Mesbah, Noha [3 ]
Abo-Elmatty, Dina [3 ]
机构
[1] Suez Canal Univ, Fac Med, Dept Med Biochem, Ismailia 41622, Egypt
[2] Sinai Univ, Fac Pharm & Pharmaceut Ind, Dept Pharmacol, North Sinai, Egypt
[3] Suez Canal Univ, Dept Biochem, Fac Pharm, Ismailia 41622, Egypt
关键词
End-stage renal disease; Methylenetetrahydrofolate reductase; DNA methylation; Epigenetics; DENSITY-LIPOPROTEIN CHOLESTEROL; GLOMERULAR-FILTRATION-RATE; TOTAL HOMOCYSTEINE; RISK-FACTOR; HYPERHOMOCYSTEINEMIA; PLASMA; KIDNEY; EPIGENETICS; HYPERMETHYLATION; POLYMORPHISM;
D O I
10.1007/s11033-013-2906-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
End-stage renal disease (ESRD) is one of the main causes of morbidity and mortality worldwide. DNA methylation is a major epigenetic modification of the genome that has the potential to silence gene expression. Methylenetetrahydrofolate reductase (MTHFR) gene inactivation was recognized as a predisposing factor of hyperhomocysteinemia in renal patients. The current study aimed to determine the methylation status within the MTHFR promoter region in DNA isolated from peripheral blood of ESRD patients and controls and the correlation of this methylation with the clinical and biochemical characteristics in ESRD patients. Ninety-six ESRD patients and 96 healthy ethnically, age and gender matched controls were included within the study. MTHFR promoter methylation was assessed using methylation specific polymerase chain reaction. The frequency of MTHFR methylation was significantly higher in ESRD patients than in controls (P = 0.003), additionally, MTHFR methylation was associated to a decrease in estimated glomerular filtration rate, serum high-density lipoprotein cholesterol level and an increase in both serum total cholesterol and low-density lipoprotein cholesterol levels. Data generated from this study suggest the possible involvement of MTHFR promoter methylation in the pathogenesis of ESRD and support a new dimension of MTHFR inactivation.
引用
收藏
页码:683 / 688
页数:6
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