Pathak Divya, Shrivastav Dharmsheel, Verma Amit K, Alsayegh Abdulrahman A, Yadav Prasant, Khan Nawaid Hussain, Al-Harbi Alhanouf I, Khan Mohammad Idreesh, Bihade Kapil, Singh Desh Deepak, Beg Mirza Masroor Ali
Central Drugs Standard Control Organisation, New Delhi, India.
Amity Institute of Biotechnology, Amity University, Rajasthan Jaipur, India.
J Diabetes Metab Disord. 2022 Feb 19;21(1):511-516. doi: 10.1007/s40200-022-01001-7. eCollection 2022 Jun.
Type 2 Diabetes is a glucose metabolic disorder occurred by insulin insensitivity in which folate metabolism plays an important role. it is believed that polymorphism of Methylenetetrahydrofolate reductase (MTHFR) C677T linked with type 2 diabetes mellitus. However, results are conflicted. therefore, in this study we re-examine the relationship between MTHFR C677T in type 2 diabetes mellitus patients.
Present research work included 100 newly diagnosed type 2 diabetic mellitus (T2DM) cases and 100 healthy individuals. After the blood sample collection all the biochemical parameters were evaluated among the T2DM cases and healthy individuals. DNA and RNA extraction from whole blood was done to study the MTHFR gene polymorphism by allele specific polymerase chain reaction method and its expression analysis was done by quantitative real time polymerase chain reaction method.
The significant difference was observed in genotype distribution among case and control group (=0.0002). Compared with wildtype CC genotype, CT heterozygous (OR=2.95, 95% Cl=1.62-5.38) and TT homozygous (OR=3.20, CI=1.79-5.73) suggest to have effect of MTHFR polymorphism on type 2 mellitus risk. Moreover, relative MTHFR mRNA expression was found for wild type CC genotype 3.02-fold, CT heterozygous genotype 2.57 fold and mutant TT homozygous genotype 0.50-fold which is down regulated (<0.0001).
Our results indicates that the polymorphism in MTHFR C677T plays significant role in type II diabetes risk. MTHFR CT heterozygous and mutant TT genotype showed reduced mRNA expression among the T2DM patients. However, large scale case-control studies are needed to strengthen such conclusion in the future.
2型糖尿病是一种因胰岛素不敏感而发生的葡萄糖代谢紊乱疾病,其中叶酸代谢起着重要作用。据信,亚甲基四氢叶酸还原酶(MTHFR)C677T基因多态性与2型糖尿病有关。然而,研究结果存在冲突。因此,在本研究中,我们重新审视2型糖尿病患者中MTHFR C677T之间的关系。
目前的研究工作包括100例新诊断的2型糖尿病(T2DM)病例和100名健康个体。采集血样后,对T2DM病例和健康个体的所有生化参数进行评估。通过等位基因特异性聚合酶链反应法从全血中提取DNA和RNA,以研究MTHFR基因多态性,并通过定量实时聚合酶链反应法进行其表达分析。
病例组和对照组的基因型分布存在显著差异(P=0.0002)。与野生型CC基因型相比,CT杂合子(OR=2.95,95%CI=1.62-5.38)和TT纯合子(OR=3.20,CI=1.79-5.73)表明MTHFR基因多态性对2型糖尿病风险有影响。此外,野生型CC基因型的相对MTHFR mRNA表达为3.02倍,CT杂合子基因型为2.57倍,突变型TT纯合子基因型为0.50倍,呈下调趋势(P<0.0001)。
我们的结果表明,MTHFR C677T基因多态性在II型糖尿病风险中起重要作用。MTHFR CT杂合子和突变型TT基因型在T2DM患者中显示出mRNA表达降低。然而,未来需要大规模的病例对照研究来加强这一结论。