Skip to main content
Download PDF

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

Diabetology & Metabolic Syndrome volume 11, Article number: 4 (2019) Cite this article

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 < 0.05.

Results

Subjects with a hypermethylated profile and the 1298AA genotype showed the highest levels of blood glucose (p = 0.03), total cholesterol (p = 0.0001) and LDL cholesterol (p = 0.0006). The same profile was associated with higher levels of HbA1c (p = 0.025), glycemia (p = 0.04) and total cholesterol (0.004) in the control group and total cholesterol (p = 0.005) and LDL cholesterol (p = 0.002) in the complications group. Serum creatinine was higher in subjects in the hypermethylated group with the genotype 677CC only in the control group (p = 0.0020). The methylated profile in presence of 677CC + 1298AA and the 677CT/TT +1298AA haplotypes showed higher levels of total cholesterol (p = 0.0024; 0.0031) and LDL cholesterol (p = 0.0060; 0.0125) than 1298AC/CC carriers. The fasting glycemia was higher in hypermethylated profile in the presence of 677CC/1298AA haplotype (p = 0.0077).

Conclusion

The hypermethylated methylation profile associated with the 1298AA genotype appeared to be connected to higher values of glycemia, total cholesterol and LDL cholesterol.

Introduction

Diabetes mellitus (DM) is a multifactorial disease characterized by chronic hyperglycemia and represents an important public health demand because it causes significant impacts on the quality of life and health management costs of the patients, especially when chronic complications occur. Microvascular complications are common and are related to several factors, especially diabetes duration and poor glycemic control.

Methylenetetrahydrofolate reductase (MTHFR) is an enzyme involved in the re-methylation of homocysteine (Hcy) in methionine cycle and catalyzes the reduction reaction of 5,10-methylenetetrahydrofolate to 5-methylenetetrahydrofolate. Thus, MTHFR function is one of the factors involved in the control of plasma levels of homocysteine. Elevated plasma levels of Hcy have been related to insulin resistance and to chronic complications such as diabetic retinopathy (DR) and diabetic nephropathy (DN) [1,2,3]. MTHFR is involved in the synthesis of the primary universal donor of methyl groups, S-adenosylmethionine (SAM), which is formed from methionine [4]. SAM is a substrate for the DNA methylation process that consists of an epigenetic mechanism that regulates the transcription of several genes and generally inhibits gene expression.

A previous study showed the association between the methylation profile in the MTHFR gene with the occurrence of chronic complications in diabetic patients. Briefly, comparison of the methylation profile of the MTHFR gene was performed in individuals with type 2 diabetes (DM2) who have been diagnosed with DM for 5–10 years. While the unmethylated profile was not identified in the analyzed samples, the partially methylated pattern predominated (~ 60%). The hypermethylated profile was associated with diabetic retinopathy (DR), but not with diabetic nephropathy (DN). Higher levels of total cholesterol and LDL cholesterol were identified in the hypermethylated profile only in DR patients samples [5].

Similarly, other reports, although controversial, describe gene polymorphisms that seem to interfere with the enzymatic activity of MTHFR and predispose individuals to diabetic complications. Studies indicate that the C677T polymorphism in the MTHFR gene, which is associated or not with inadequate glycemic control, may be linked to the progression of diabetic retinopathy [6, 7]. In addition, studies point to a significant association between this genotype and the development of nephropathy in diabetic patients [8, 9]. The A1298C polymorphism (rs1801131) has also been linked to the development of DN or macroalbuminuria, either alone or in combination with other alleles of interest, including C677T [10, 11]. However, the parallel effect of methylation profile and MTHFR polymorphisms on metabolic aspects in diabetic patients has never been analyzed.

Based on these facts, the objective of this work is to investigate in an unprecedented way the simultaneous relationship between MTHFR methylation profile and the C677T and A1298C polymorphisms and metabolic, inflammatory and oxidative stress factors related to microvascular complications in patients with diabetes for 5 to 10 years.

Methodology

Recruitment of subjects

Patients with type 2 diabetes mellitus DM2 of both sexes, older than 40 years, with at least 5 and at most 10 years of diagnostic, were recruited at the endocrinology, ophthalmology and nephrology services of the Lauro Wanderley University Hospital of the Federal University of Paraíba (HULW/UFPB) from August 2013 to November 2016. The subjects were divided into two groups: control group—patients without complications and group with complications—patients with retinopathy (DR) and/or nephropathy (DN).

Ethical aspects

This project was approved by the Ethics Committee for Human Research of Federal University of Paraíba (Opinion No. 257.325; Report date: April 23, 2013). In addition, all procedures followed were in accordance with the institution’s ethical standards, conducted in compliance with Resolution 466/2012 of the National Health Council and the International Declaration of Helsinki.

Clinical categorization of patients

The funduscopy examination was used to identify DR and 24-h urine albumin determination for identification of DN, the patients were included in the following clinical groups: 47 patients with complications (13 patients had RD, 25 had ND and 9 had both RD and ND) and 60 patients without complications (control), for a total of 107 patients.

The diagnosis of DR was based on ophthalmoscopy after pupil dilation with tropicamide 0.5%. Images of the retina (macula and central disc) were captured at a 45° angle with a fundus camera. All analyzes included in this study were performed by the same ophthalmologist. The photographs were analyzed according to the standards and recommendations of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) and Early Treatment Diabetic Retinopathy Study (ETDRS). The presence of renal impairment was assessed by quantifying albumin in a 24-h urine sample. Microalbuminuria was defined as a urinary albumin concentration > 30 mg/L/24 h.

Clinical variables (age, date of diabetes diagnostic, glycemic control treatment, presence of hypertension, presence of dyslipidemia) were collected using an appropriate form.

Collection of biological samples

For determination of albuminuria, patients received an appropriate container and were instructed to collect all urine for 24 h. They should then take the container to the researchers, ending the 24 h with the last collection in the hospital, at the time of the start of the exam the day before.

The blood was collected by venipuncture and samples were placed in different containers. For biochemical analysis in general, in the presence of clot activator, for determination of HbA1C in the presence of anticoagulant and for determination of glucose in the presence of anticoagulant sodium fluoride. The samples were centrifuged at a speed of 3000 rpm for 10 min at room temperature for separation of serum or plasma and subjected to analysis within 2 h after collection, except the sample for HbA1C that was analyzed in hemolyzed whole blood.

For DNA extraction, blood collection was performed by venous puncture in sterile tubes containing 7.2 mg of K3 EDTA. Blood samples were stored for up to 20 days at − 20 °C until DNA extraction was performed.

Biochemical determinations

Determinations of fasting glucose (GLIC), serum creatinine (CREA-S), total cholesterol (TC), triglycerides (TRIG), HbA1C, C-reactive protein (CRP), alfa 1 acid glycoprotein (AGP), and high density lipoprotein cholesterol (HDL) were performed with commercial kits (Labtest®, Lagoa Santa, MG, Brazil) in automatic analyzer.

Light density lipoprotein cholesterol (LDL) concentration was determined using the Friedewald formula, where [LDL] = TC− [HDL] − [TRIG/5].

For determination of malondialdehyde (MDA), the method based on the reaction of thiobarbituric acid with hydroperoxides decomposition products was used. The total antioxidant capacity (TAC) of the serum was evaluated by the reduction of the 2,2-diphenyl-1-picryl-hydrazyl radical, which was measured by a colorimetric method in a spectrophotometer.

Urine was used to detect urinary albumin (M.ALB) using a commercial kit according to the guidelines recommended by the manufacturer (Labtest®, Lagoa Santa, MG, Brazil) in an automated analyzer. For the calculation of albumin excretion in 24 h, the value of the determination of albumin in the urine collected for 24 h (mg/dL) was multiplied by the total volume of urine collected in liters.

DNA extraction for molecular analyzes

Leukocyte DNA was isolated using an protocol adapted from Miller et al. [5, 12].

Determination of MTHFR genotypes C677T and A1298C

The presence of polymorphisms was determined using the restriction fragment length polymorphism (RFLP) technique by amplifying a fragment of the MTHFR gene by PCR using primers and temperature cycles described elsewhere [13, 14]. The 198 and 256 base pair fragments generated respectively by the amplification reaction of the polymorphisms C677T and A1298C were digested for 3 h with the endonucleases HinfI (C677) and MobII (A1298C) (Biolabs®) according to manufacturer’s guidelines. The RFLP profiles were generated by separation of DNA fragments in 15% polyacrylamide gel electrophoresis and observed by staining with silver nitrate or using the Gelred (Biotium®) intercalating dye followed by excitation by ultraviolet light in transilluminator. The genotypes 677 CC/CT/TT and 1298 AA/AC/CC were identified by the pattern of bands in the polyacrylamide gel according to the expected sizes described in the literature [13, 14].

Analysis of the methylation profile in the MTHFR gene

Methylation analysis in the promoter of the MTHFR gene was performed using the methylation specific PCR (MSP) technique as previously described [5]. In short, the extracted leukocyte DNA was converted (500 ng) by sodium bisulfite protocol using EZ DNA Methylation ™ Kit (ZymoResearch) according to the manufacturer’s instructions. Methylation-specific PCR reactions were performed using 100 ng of bisulfite-transformed DNA, and specific pairs of primers for methylated and unmethylated targets in two separate amplification reactions. Methylated and unmethylated DNA (Cells-to-CpG ™ Methylated & Unmethylated DNA Control Kit, Life Technologies), which were modified as previously mentioned, and amplified by PCR, were analyzed together with the samples as a control for methylated and non-methylated conditions. Amplified PCR samples were loaded on 3% agarose gels with Gelred (Biotium®) and subjected to electrophoresis. The DNA bands were visualized with ultraviolet light. The samples were categorized as methylated (positive only for the methylated condition) or partially methylated (positive for methylated and non-methylated conditions). Non-methylated samples (positive only for the non-methylated condition) were not found in the population analyzed.

Statistical analysis

The data were compiled in an Excel® spreadsheet. Frequency was used for categorical variables and descriptive statistics for continuous variables. The Student’s t-test and Chi square test and, when necessary, the Mann–Whitney test and Fisher exact test were used in the program GraphPad, Instat, version 3.0. A post hoc test with total cholesterol results in the methylated profile was performed using the G* Power program 3.1.9.2. For all tests, p < 0.05 was used as the significance level.

Table 1 Demographic and clinical comparisons among the groups studied
Full size table

Results

A total of 107 diabetic patients, all with diabetes diagnosed within the previous 5 to 10 years, were included in the following two experimental groups: 47 patients with complications (DR and/or DN) and 60 patients without complications (control). Comparison of the clinical and demographic data of the control groups and patients with complications (Table 1) showed that there are differences in diagnosis time that is slightly higher in the group of patients with complications (p = 0.026). The main difference between the groups is in the pharmacological treatment of glycemic control. While in the control group the use of oral hypoglycemic agents predominates (p = 0.006), in the group of patients with complications, the use of insulin associated with oral hypoglycemic agents is significantly higher (p = 0.0002).

Initially, there was an association between the genotypes and the clinical condition after evaluating the simultaneous effect of methylation profile and polymorphism in the MTHFR gene in all studied patients, independent of the clinical condition. For this analysis, the patients were divided into two categories according to the methylation profile of the MTHFR promoter: methylated and partially methylated. From the 107 samples analyzed, none presented the unmethylated profile of the MTHFR gene promoter, so the unmethylated category was not included in this study. The relationship of polymorphisms together with the methylation profile and the clinical conditions of the patients were analyzed, taking into account the following four groups: methylated with complications, methylated without complications, partially methylated with complications and partially methylated without complications.

Influence of the methylation profile of MTHFR + polymorphism A1298C

Tables 2 and 3 describe relationships for the A1298C polymorphism. In Table 2, when all individuals were analyzed together, an association between the AA genotype and a hypermethylated promoter with higher glycemic values was identified (p = 0.03). A relationship between this same molecular profile and lipid profile was also observed, showing higher levels of TC (p = 0.0001) and LDL (p = 0.0006). A post hoc test with TC (methylated) was performed. At alpha significance level of 0.05, effect size and power (1-β err prob) were, respectively, 1.44 and 0.998. When the control and complication groups were analyzed separately (Table 3), it was observed that the effect of the genotype + hypermethylated profile appeared for glycemic control parameters fasting glycemia (p = 0.04) and HbA1C (p = 0.025) only in the control group. For the lipid profile parameters, while the relationship appeared in both groups for TC (p = 0.0049 and p = 0.0056, respectively), it remained only in the group with complications for LDL cholesterol (p = 0.002).

Table 2 Analysis of the association between the MTHF methylation profile and A1298C polymorphism of MTHFR and the biochemical, inflammatory and oxidative stress variables
Full size table
Table 3 Analysis of the relationship between the MTHFR methylation pattern and the A1298C polymorphism and biochemical, inflammatory and oxidative stress variables
Full size table

Influence of the methylation profile of MTHFR + C677T polymorphism

For the C677T polymorphism, the genotypic distribution was fairly balanced between the with complications and without complications phenotypic groups (data not show). For Table 4, analyzing all individuals (complicated + uncomplicated) there were no significant results. In Table 5, analyzing the methylation profile and clinical genotype, only the intersection between CC and TC + TT in the hypermethylated group for creatinine was significant (p = 0.0040). This trend continued when the division of the methylation profile was funneled between the with complications and control groups (p = 0.0020).

Table 4 Analysis of the relationship between the MTHFR methylation pattern and the C677T polymorphism of MTHFR and biochemical, inflammatory and oxidative stress variables
Full size table
Table 5 Analysis of the relationship between the MTHFR methylation pattern and the C677C polymorphism of MTHFR and biochemical, inflammatory and oxidative stress variables associated with clinical condition
Full size table

In the group with complications, the triglyceride values were higher in the partially methylated group profile in the presence of CT + TT (0.04) genotypes, while the TAC was higher in the same profile but in the presence of the CC genotype (p = 0.01). In addition, the lipid profile was also affected, with the partially methylated group presenting higher levels of HDL (p = 0.0273) in the control group in the presence of CT + TT genotypes.

Influence of the methylation profile of MTHFR + haplotype C677T/A1298C

Table 6 shows the results of intersections between the haplotypes C677T and A1298C, divided by the methylation profile (hypermethylated and partially methylated, respectively). For the hypermethylated group, glycemia was significant between 677CC/1298AA and 677CC/1298AC + CC (p = 0.0077), with values from the latter group (mean = 139.9 and median = 129.0) being significantly improved relative to the former (mean = 205.1 and median = 214.0). For total cholesterol (p = 0.0024) and LDL (p = 0.0060), the same trend was observed, with lower values for those with 677CC/1298AC + CC. In the relationship between the partially methylated individuals and the haplotype no significant difference was found.

Table 6 Analysis of the relationship between the MTHFR methylation pattern and the A1298C + C677T polymorphism of MTHFR and biochemical, inflammatory and oxidative stress variables
Full size table

Discussion

The main result of this work is the simultaneous effect of the hypermethylation and A1298C polymorphism of the MTHFR gene on lipid parameters and glycemic control in diabetic patients.

The MTHFR gene is located on the short arm of chromosome 1 (1p26.3), has 11 exons and is expressed through the production of three transcripts of different sizes in the human species, suggesting the involvement of complex gene regulation mechanisms [15]. Analysis of the promoter region by computational analysis revealed the presence of two CpG islands with potential binding sites for various transcription factors, suggesting that transcriptional control of the production of this enzyme may undergo methylation control [16].

Few studies have analyzed the effects of the methylation profile of MTHFR and the occurrence of complications in diabetes. A recent study in which samples of healthy, diabetic, early-stage and advanced-stage DN patients were analyzed an association between MTHFR demethylation and DN morbidity was identified in diabetic patients. While the healthy control group did not have demethylated specimens, the diabetic group and the group with early DN showed a higher level of demethylated samples, and the clinical DN group did not present methylated samples [17]. In addition, these results showed an association between increasing levels of homocysteine (Hcy) and demethylation of MTHFR. This effect of the concentration of HCY on the methylation profile of MTHFR has already been demonstrated in in vitro experiments with human muscle cells, which revealed an even higher production of transcripts in the demethylated MTHFR pattern [18]. The authors argue that there may be a compensatory effect causing MTHFR demethylation when HCY is elevated to increase the expression of the enzyme and consequently the conversion of Hcy to methionine. This effect would be evident in the samples of patients with clinical DN, who had high levels of HCY and demethylated profiles [17]. Another study that analysed the relationship between MTHFR methylation and end-stage renal disease, not specifically in DN, has been reported an association between methylation and higher levels of total cholesterol and LDL cholesterol [19]. Diabetic retinopathy and higher levels of total cholesterol and LDL cholesterol has also been associated with the hypermethylated MTHFR pattern in patients with a diagnosis time of diabetes of 5 to 10 years [5], although the relationship has not been identified in samples from patients with DN.

In this work the objective was to simultaneously analyze the effect of the methylation profile and polymorphisms in the MTHFR gene on biochemical variables taking into consideration the clinical condition of the diabetic patient.

Two polymorphisms in MTHFR, C677T and A1298C, have been most studied because they affect enzymatic activity. The C677T polymorphism, which causes an alanine substitution by valine (Ala222Val), occurs in exon 4 of the MTHFR gene and results in enzyme thermolability and decreased activity. It has been shown that 677TT homozygotes and 677CT heterozygotes have approximately 70% and 35% reduced MTHFR activity, respectively [13, 20]. The 677TT genotype is associated with global hypomethylation in the healthy cell genome of cancer patients [21].

The A1298C polymorphism results in the substitution of glutamic acid for alanine (Glu429Ala), and although the homozygote showed a slight reduction in enzymatic activity, it had no effect on Hcy concentration [14]. This polymorphism is located in the regulatory domain of the enzyme responsible for binding to NADPH and S-adenosylmethionine [22].

In this study, while the C677T polymorphism did not appear to affect the distribution of the patients in the with complications and without complications groups, the 1298C allele genotypes (AC + CC) appeared in a higher percentage in the group without complications in diabetes, although without statistical significance, suggesting a protective effect of the C allele. This is the allele that appears to have a minor impact on MTHFR activity, although studies have shown that individuals with the 677CC/1298CC haplotype have lower homocysteine levels than do those with the 677CC/1298AA haplotype [23]. However, the allele 1298C has appeared as a protective factor for other medical conditions, such as congenital heart defects [24]. A possible explanation for this fact, noted by the authors of the cited articles, is the present linkage disequilibrium between the 677T allele, which causes significant reduction in the enzymatic activity and the allele in question, 1298C, which would result in a false protection effect of the mutant allele 1298C. The study further proposes that the 1298C allele may appear in linkage disequilibrium with another yet unrecognized polymorphism of MTHFR. In addition, the 1298C allele was cited as a protective factor for folate deficiency and related to higher levels of this nutrient in comparison with the 1298AA genotype [20, 25]. A possible explanation for these findings is related to the location of the polymorphism, which affects the binding site for the negative allosteric effector S-adenosylmethionine, which could therefore interfere with the inhibitory effect of the enzymatic activity [22]. However, there is controversy about these data, and other studies have identified lower levels of folate in carriers of the 1298C allele [26].

In a previous study by our group, a relationship was found between higher levels of total cholesterol and LDL cholesterol in the MTHFR hypermethylated samples of patients with DR [5]. The proposed mechanism for these findings is related to the reduction of MTHFR expression in the hypermethylated profile [18] that could result in higher concentrations of homocysteine, which in turn stimulates hepatic cholesterol synthesis [27].

In the present study, it was demonstrated that individuals with the hypermethylated profile and AA genotype of the A1298C polymorphism had higher levels of TC and LDL and also glycemia and HbA1C than did those with the genotype containing the C allele. Regarding glycemic control, evidenced through fasting glycemia and HbA1C analysis, the results were significantly higher in the AA group only in control group, whereas for the lipid parameters, the relationship occurred in both groups for total cholesterol and only in complication group for LDL cholesterol.

Haplotype analysis revealed that increased levels of total cholesterol and LDL were elevated in patients with a hypermethylated profile and 1298AA genotype independent of the C677T genotype, ruling out the possibility of the result being related to the haplotype or being a consequence of a cross-effect. On the other hand, the effect on glycemic control parameters was only observed in the 677CC/1298AA haplotype.

As demonstrated in this and other studies, the DNA methylation profile, whether global or in specific genes, seems to be related to the pathophysiology of diabetes and its chronic complications [28]. The most likely hypothesis, as previously described, is that hypermethylation reduces the production of messenger RNA of the MTHFR gene. At the same time, the level of MTHFR activity, mediated by the A1298C and C677T polymorphisms, may impact the metabolic pathway of the enzyme, affecting the formation and availability of SAM and consequently impacting the methylation profile of the carriers. However, the results of this study suggest that this appears to be true only when the promoter of the gene is hypermethylated, thereby reducing expression and strengthening the biological effect of the A1298C polymorphism. Surprisingly, no biologically important relationships were found in the analyses of the C677T polymorphism, which is precisely what has the most significant impacts on the enzymatic activity.

Both glycemic control and dyslipidemia are important biochemical factors related to diabetes complications. The results presented here demonstrate for the first time, to our knowledge, that the methylation profile associated with common genotypes of MTHFR are very significantly related to levels of HbA1C, glycemia, total cholesterol and LDL cholesterol. This work refines previously published data relating the hypermethylated profile to the occurrence of chronic complications in diabetes, especially diabetic retinopathy. In addition to genotypic distribution and biochemical analysis, considering the methylation profile and genotype, we can suggest that patients with genotype 1298AA and a hypermethylated profile present a worse metabolic situation.

Interestingly, epigenetic marker profiles are reversible. This has already been demonstrated in cultured human cells for the MTHFR gene [18]. Thus, studies such as these that show unfavorable metabolic conditions in certain profiles can define groups of patients who need observation and differential treatment, in addition to allowing the monitoring of the effectiveness of therapeutic interventions.

This study has some methodological weaknesses that need to be taken into account. Although the population analyzed was recruited on the basis of strict exclusion criteria, restricted to only patients with diabetes time between 5 and 10 years, the experimental number is small. The plasma homocysteine variable, not analyzed in this study, could help to confirm some assumptions made in the discussion of the results. The promoter methylation analysis technique does not assess the integrity of the CpG islands of the gene promoter. Finally, the absence of unmethylated samples in the studied sample impairs the understanding of the relationship between the methylation profile and the studied genotypes.

Conclusion

The hypermethylated methylation profile associated with the 1298AA genotype appeared to be connected to higher values of glycemia, total cholesterol and LDL cholesterol.

Abbreviations

AGP:

alpha 1 acid glycoprotein

TAC:

total antioxidant capacity

COL T:

total cholesterol

CpG:

cytosine/phosphodiester-linked guanine

CREA-S:

serum creatinine

EDTA:

ethylenediaminetetraacetic acid

BG:

blood glucose

HbA1c:

glycated hemoglobin

Hcy:

homocysteine

HDL:

high-density lipoprotein

LDL:

low-density lipoprotein

M. ALB:

microalbuminuria

MDA:

malondialdehyde

MTHFR:

5,10-methylenetetrahydrofolate reductase

DN:

diabetic nephropathy

CRP:

C-reactive protein

DR:

diabetic retinopathy

SAMe:

S-adenosylmethionine

TRIG:

triglycerides

References

  1. Satyanarayana A, Balakrishna N, Pitla S, et al. Status of B-vitamins and homocysteine in diabetic retinopathy: association with vitamin-B12 deficiency and hyperhomocysteinemia. PLoS ONE. 2011;6(11):e26747.

    Article  CAS  Google Scholar 

  2. Li Y, Zhang H, Jiang C, et al. Hyperhomocysteinemia promotes insulin resistance by inducing endoplasmic reticulum stress in adipose tissue. J Biol Chem. 2013;288(14):9583–92.

    Article  CAS  Google Scholar 

  3. Buysschaert M, Dramais AS, Wallemacq PE, Hermans MP. Hyperhomocysteinemia in type 2 diabetes: relationship to macroangiopathy, nephropathy, and insulin resistance. Diabetes Care. 2000;23(12):1816–22.

    Article  CAS  Google Scholar 

  4. Hoffman DR, Cornatzer WE, Duerre JA. Relationship between tissue levels of S-adenosylmethionine, S-adenylhomocysteine, and transmethylation reactions. Can J Biochem. 1979;57(1):56–65.

    Article  CAS  Google Scholar 

  5. Dos Santos Nunes MK, Silva AS, Queiroga IW, et al. Hypermethylation in the promoter of the MTHFR gene is associated with diabetic complications and biochemical indicators. Diabetol Metab Syndr. 2017;9:84.

    Article  Google Scholar 

  6. Maeda M, Yamamoto I, Fukuda M, et al. MTHFR gene polymorphism is susceptible to diabetic retinopathy but not to diabetic nephropathy in Japanese type 2 diabetic patients. J Diab Compli. 2008;22(2):119–25.

    Article  Google Scholar 

  7. Settin A, El-Baz R, Ismaeel A, Tolba W, Alá WA. Association of ACE and MTHFR genetic polymorphisms with type 2 diabetes mellitus: susceptibility and complications. J Renin Angiot Aldosterone. 2015;16(4):838–43.

    Article  CAS  Google Scholar 

  8. Cui WP, Du B, Jia Y, et al. Is C677T polymorphism in methylenetetrahydrofolate reductase gene a risk factor for diabeticnephropathy or diabetes mellitus in a Chinese population? Arch Med Res. 2012;43(1):42–50.

    Article  CAS  Google Scholar 

  9. Yang S, Zhang J, Feng C, Huang L. MTHFR 677T variant contributes to diabetic nephropathy risk in Caucasian individuals with type 2 diabetes: a meta-analysis. Metabolism. 2013;62(4):586–94.

    Article  CAS  Google Scholar 

  10. Jafari Y, Rahimi Z, Vaisi- Raygani A, Rezaei M. Interaction of eNOS polymorphism with MTHFR variants increase the risk of diabetic nephropathy and its progression in type 2 diabetes mellitus patients. Mol Cell Biochem. 2011;353(1–2):23–34.

    Article  CAS  Google Scholar 

  11. El- Baz R, Settin A, Ismaeel A, et al. MTHFR C677T, A1298C and ACE I/D polymorphisms as risk factors for diabetic nephropathy among type 2 diabetic patients. J Renin Angiotensin Aldosterone Syst. 2012;13(4):472–7.

    Article  Google Scholar 

  12. Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16(3):1215.

    Article  CAS  Google Scholar 

  13. Frosst P, Blom HJ, Milos R, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet. 1995;10(1):111–3.

    Article  CAS  Google Scholar 

  14. Van der Put NM, Gabreëls F, Stevens EM, et al. A second common mutation in the methylenetetrahydrofolatereductase gene: an additional risk factor for neural-tube defects? Am J Hum Genet. 1998;62(5):1044–51.

    Article  Google Scholar 

  15. Gaughan DJ, Barbaux S, Kluijtmans LA, Whitehead AS. The human and mouse methylenetetrahydrofolatereductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene. Gene. 2000;257(2):279–89.

    Article  CAS  Google Scholar 

  16. Wei K, Sutherland H, Camilleri E, Haupt LM, Griffiths LR, Gan SH. Computational epigenetic profiling of CpG islets in MTHFR. Mol Biol Rep. 2014;41(12):8285–92.

    Article  CAS  Google Scholar 

  17. Yang XH, Cao RF, Yu Y, et al. A study on the correlation between MTHFR promoter methylation and diabetic nephropathy. Am J Transl Res. 2016;8(11):4960–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Wang L, Zhang J, Wang S. Demethylation in the promoter region of MTHFR gene and its mRNA expression in cultured human vascular smooth muscle cells induced by homocysteine. Wei Sheng Yan Jiu. 2007;36(3):291–4.

    PubMed  Google Scholar 

  19. Ghattas M, El-Shaarawy F, Mesbah N, Abo-Elmatty D. DNA methylation status of the methylenetetrahydrofolate reductase gene promoter in peripheral blood of end-stage renal disease patients. Mol Biol Rep. 2014;41(2):683–8.

    Article  CAS  Google Scholar 

  20. Li WX, Dai SX, Zheng JJ, Liu JQ, Huang JF. Homocysteine metabolism gene polymorphisms (MTHFR C677T, MTHFR A1298C, MTR A2756G and MTRR A66G) jointly elevate the risk of folate deficiency. Nutrients. 2015;7(8):6670–87.

    Article  CAS  Google Scholar 

  21. Paz MF, Avila S, Fraga MF, et al. Germ-line variants in methyl-group metabolism genes and susceptibility to DNA methylation in normal tissues and human primary tumors. Can Res. 2002;62:4519–24.

    CAS  Google Scholar 

  22. Shahzad K, Hai A, Ahmed A, Kizilbash N, Alruwaili J. A structured-based model for the decreased activity of Ala222Val and Glu429Ala methylenetetrahydrofolatereductase (MTHFR) mutants. Bioinformation. 2013;9:929–36.

    Article  Google Scholar 

  23. Friedman G, Goldschmidt N, Yechiel F. A common mutation A1298C in human methylenetetrahydrofolatereductase gene: association with plasma total homocysteine and folate concentrations. J Nutr. 1999;119(9):1656–61.

    Article  Google Scholar 

  24. Hobbs CA, James SJ, et al. Congenital heart defects and genetic variants in the methylenetetrahydroflatereductase gene. J Med Genet. 2006;43:162–6.

    Article  CAS  Google Scholar 

  25. Biselli PM, Guerzoni AR, de Godoy MF. Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease. J Thromb Thrombolysis. 2010;29(1):32–40.

    Article  CAS  Google Scholar 

  26. Safarinejad MR, Shafiei N, Safarinejad S. Methylenetetrahydrofolatereductase (MTHFR) gene C677T, A1298C and G1793A polymorphisms: association with risk for clear cell renal cell carcinoma and tumourbehaviour in men. ClinOncol. 2012;24(4):269–81.

    CAS  Google Scholar 

  27. Karmin O, Lynn EG, Chung YH, Siow YL, Man RYK, Choy PC. Homocysteine stimulates the production and secretion of cholesterol in hepatic cells. BBA. 1998;1393:317–24.

    Google Scholar 

  28. Zheng J, Cheng J, Zhang Q, Xiao X. Novel insights into DNA methylation and its critical implications in diabetic vascular complications. Biosci Rep. 2017;37(2):2016061.

    Google Scholar 

Download references

Authors’ contributions

HSB: performed statistical analysis, interpretation of the results and writing of the manuscript. CSA: collaborated in writing the manuscript. MKSN: participated in data collection, biochemical analysis and molecular biology experiments. IWQE: participated in data collection and performed ophthalmological consultation in individuals. JMF: participated in data collection and performed endocrinological consultation in individuals. CNAPG: participated in data collection and held individual consultations. RAFN: performed experiments in molecular biology. RCPL: participated in the writing of the manuscript. MJCC: participated in the drafting of the manuscript. NFPO: participated in molecular biology experiments and writing of the manuscript. DCP: participated in all stages of the research (study design and logistics, data collection, molecular biology experiments, interpretation of results, statistical analysis and writing of the manuscript). All authors read and approved the final manuscript.

Acknowledgements

We thank the University Hospital Lauro Wanderley of the Federal University of Paraíba and all participants in the study for accepting and allowing the collection of blood samples and the financial support institutions, Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, Brasilia, Brazil), the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES, Brasília, Brazil) and the Fundação de Apoio à Pesquisa do Estado da Paraíba (FAPESQ, Paraíba, Brazil).

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Consent for publication

Not applicable.

Ethical approval and consent to participate

The study was approved by the Human Research Ethics Committee of the Lauro Wanderley University Hospital, Federal University of Paraíba (Opinion: 257.325/2013). The informed consent of all participants was requested in writing.

Funding

This study was funded by the Fundação de Apoio à Pesquisa do Estado da Paraíba (FAPESQ, Paraíba, Brazil). The Brazilian National Council for Scientific and Technological Development (CNPq, Brasilia, Brazil) Project 057/13, public notice 001/2013 FAPESQ/Ministry of Health/CNPq under the agreement SINCOV 774379/2012 FAPESQ/Ministry of Health/CNPq in the PPSUS program for the acquisition of inputs, reagents and materials necessary for the development of the research. This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior-Basil (CAPES)—Finance Code 001. Herlanny Santana Bezerra was a fellow of the Institutional Program of Scientific Initiation of the Federal University of Paraiba/National Council for Scientific and Technological Development (CNPq, Brasília, Brazil).

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Author information

Authors and Affiliations

  1. Scientific Initiation Program, Federal University of Paraiba, Joao Pessoa, Brazil

    Herlanny Santana Bezerra

  2. Nutrition Sciences, Federal University of Paraiba, Joao Pessoa, Brazil

    Caroline Severo de Assis

  3. Development and Technological Innovation of Medicines, Federal University of Paraiba, João Pessoa, Brazil

    Mayara Karla dos Santos Nunes

  4. Unidade da Visão, Hospital Universitário Lauro Wanderley, Federal University of Paraíba, Joao Pessoa, Brazil

    Isabella Wanderley de Queiroga Evangelista

  5. Department of Internal Medicine, Federal University of Paraiba, Joao Pessoa, Brazil

    João Modesto Filho

  6. Nephrology Clinic, Lauro Wanderley University Hospital, Federal University of Paraiba, Joao Pessoa, Brazil

    Cecília Neta Alves Pegado Gomes

  7. Faculty Mauricio of Nassau, Joao Pessoa, Brazil

    Rayner Anderson Ferreira do Nascimento

  8. Post-Graduate Program in Nutrition Science, Federal University of Paraiba, Joao Pessoa, Brazil

    Rafaella Cristhine Pordeus Luna

  9. Nutrition Science Department and Post-Graduate Program in Nutrition Science, Federal University of Paraiba, Joao Pessoa, Brazil

    Maria José de Carvalho Costa

  10. Department of Molecular Biology, Federal University of Paraiba, Joao Pessoa, Brazil

    Naila Francis Paulo de Oliveira

  11. Department of Molecular Biology and Post-Graduate Program in Nutrition Science, Federal University of Paraiba, João Pessoa, PB, CEP 58051-900, Brazil

    Darlene Camati Persuhn

Authors
  1. Herlanny Santana Bezerra
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Caroline Severo de Assis
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Mayara Karla dos Santos Nunes
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Isabella Wanderley de Queiroga Evangelista
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. João Modesto Filho
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Cecília Neta Alves Pegado Gomes
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Rayner Anderson Ferreira do Nascimento
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Rafaella Cristhine Pordeus Luna
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Maria José de Carvalho Costa
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Naila Francis Paulo de Oliveira
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Darlene Camati Persuhn
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Darlene Camati Persuhn.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Santana Bezerra, H., Severo de Assis, C., dos Santos Nunes, M.K. et al. The MTHFR promoter hypermethylation pattern associated with the A1298C polymorphism influences lipid parameters and glycemic control in diabetic patients. Diabetol Metab Syndr 11, 4 (2019). https://doi.org/10.1186/s13098-019-0399-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13098-019-0399-9

Keywords

Diabetology & Metabolic Syndrome

ISSN: 1758-5996

Contact us