Abstract | OBJECTIVES: METHODS: RESULTS: Prevalence of the 2 heterozygous polymorphisms of the thermolabile MTHFR gene (CT and AC) was encountered more commonly in patients with diabetes mellitus than in the healthy controls (p<10-3). Subjects with diabetes had significantly higher homocysteine (Hcy) levels than the control subjects; however, there was no statistical difference in plasma Hcy values between carriers of mutant genotypes (CT/TT for C677T and AC/CC for A1298C) and wild types (CC and AA) in patients with diabetes. Retinopathy was found to be a vascular complication in patients with either the 677CT or the 1298(AC+CC) genotype more commonly than in those with the wild-type genotypes (p=0.003; OR=3.2, 95% CI, 1.4 to 7.4; p<10-3; OR=5.9, 95% CI, 2.7 to 13). Only patients who carry the A1298C mutation (AC+CC) are at risk for at least 1 complication (p=0.002). Double heterozygous mutants were at the greatest risk for retinopathy and for suffering at least 1 complication (p<10-3). CONCLUSIONS: Studies involving a larger study population and various ethnic groups are required before ruling out the role of MTHFR gene in type 2 diabetes mellitus and in vascular complications.
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Authors | Najiba Fekih-Mrissa, Meriem Mrad, Hazard Ibrahim, Imen Akremi, Aicha Sayeh, Amel Jaidane, Haroun Ouertani, Borni Zidi, Nasreddine Gritli |
Journal | Canadian journal of diabetes
(Can J Diabetes)
Vol. 41
Issue 4
Pg. 366-371
(Aug 2017)
ISSN: 2352-3840 [Electronic] Canada |
PMID | 28341195
(Publication Type: Journal Article)
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Copyright | Copyright © 2017 Diabetes Canada. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- MTHFR protein, human
- Methylenetetrahydrofolate Reductase (NADPH2)
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Topics |
- Adult
- Diabetes Mellitus, Type 2
(epidemiology, genetics)
- Diabetic Retinopathy
(epidemiology, genetics)
- Female
- Humans
- Hypertension
(epidemiology, genetics)
- Male
- Methylenetetrahydrofolate Reductase (NADPH2)
(genetics)
- Middle Aged
- Polymorphism, Single Nucleotide
(genetics)
- Vascular Diseases
(epidemiology, genetics)
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