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The MTHFR promoter hypermethylation pattern associated with the A1298C polymorphism influences lipid parameters and glycemic control in diabetic patients

Authors :
Herlanny Santana Bezerra
Caroline Severo de Assis
Mayara Karla dos Santos Nunes
Isabella Wanderley de Queiroga Evangelista
João Modesto Filho
Cecília Neta Alves Pegado Gomes
Rayner Anderson Ferreira do Nascimento
Rafaella Cristhine Pordeus Luna
Maria José de Carvalho Costa
Naila Francis Paulo de Oliveira
Darlene Camati Persuhn
Source :
Diabetology & Metabolic Syndrome, Vol 11, Iss 1, Pp 1-15 (2019)
Publication Year :
2019
Publisher :
BMC, 2019.

Abstract

Abstract Background Polymorphisms in the gene encoding methylenetetrahydrofolate reductase (MTHFR) have been investigated as risk factors for microvascular complications of diabetes; however, simultaneous analysis of these polymorphisms and the methylation pattern of the gene has never been conducted. The objective of the present study was to evaluate the simultaneous relationship between MTHFR methylation and MTHFR C6TT7 and A1298C polymorphisms with metabolic, inflammatory and oxidative stress parameters related to microvascular complications, diabetic retinopathy (DR) and diabetic nephropathy (DN) in diabetic patients. Methods A total of 107 patients who were diagnosed in the previous 5 to 10 years were recruited and divided into groups with complications (DR and/or DN) or without complications. Methylation analysis of the gene promoter was conducted using the MSP technique, and analysis of the A1298C and C677T polymorphisms was conducted using the restriction fragment length polymorphism (RFLP) assay. Microalbuminuria was determined using urine samples, and other analytes of interest were determined in blood samples using commercial kits. The Mann–Whitney and Chi square statistical tests were used with significance considered at p

Details

Language :
English
ISSN :
17585996
Volume :
11
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Diabetology & Metabolic Syndrome
Publication Type :
Academic Journal
Accession number :
edsdoj.338abb6677474b7b920412536f874484
Document Type :
article
Full Text :
https://doi.org/10.1186/s13098-019-0399-9