Literature DB >> 28215593

Influence of MTHFR C677T gene polymorphism in the development of cardiovascular disease in Egyptian patients with rheumatoid arthritis.

Tarek A Abd El-Aziz1, Rasha H Mohamed2.   

Abstract

OBJECTIVE: To investigate the association between increased carotid intima-media thickness (CIMT), homocysteine level, and MTHFR C677T (rs1801133) gene polymorphism in Egyptian people with rheumatoid arthritis (RA). SUBJECTS AND METHODS: 280 Egyptian women (160 RA patients and 120 controls) were included in the study. CIMT was measured using high resolution B-mode ultrasonography and homocysteine levels were measured using enzyme-linked immunosorbent assay. While, MTHFR C677T polymorphism was analyzed by polymerase chain reaction-restriction fragment length polymorphism.
RESULTS: We found that subjects who carried the TT genotype and T allele were significantly more likely to develop RA with 2.9 and 1.5 fold, respectively. RA patients carrying the T allele presented a statistically significant increased risk of developing atherosclerosis compared with those carrying the C allele. Moreover, MTHFR TT genotype was independent risk factor of thick CIMT.
CONCLUSIONS: C677T MTHFR gene polymorphism is associated with RA in Egyptians. MTHFR 677TT carriers had higher concentrations of serum Hcy than did subjects harboring the CC and CT genotypes. The presence of 677T allele increases the risk of atherosclerosis in patients with RA. This increased risk of atherosclerosis could be due to hyperhomocysteinemia.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Carotid intima-media thickness; Gene polymorphism; MTHFR; PCR–RFLP; RA

Mesh:

Substances:

Year:  2017        PMID: 28215593     DOI: 10.1016/j.gene.2017.02.015

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  9 in total

1.  Association of hyperhomocysteinemia with genetic variants in key enzymes of homocysteine metabolism and methotrexate toxicity in rheumatoid arthritis patients.

Authors:  Souhir Chaabane; Meriam Messedi; Rim Akrout; Mariem Ben Hamad; Mouna Turki; Sameh Marzouk; Leila Keskes; Zouheir Bahloul; Ahmed Rebai; Fatma Ayedi; Abdellatif Maalej
Journal:  Inflamm Res       Date:  2018-05-23       Impact factor: 4.575

2.  Prevalent genotypes of methylenetetrahydrofolate reductase (MTHFR) in recurrent miscarriage and recurrent implantation failure.

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Journal:  J Assist Reprod Genet       Date:  2018-05-21       Impact factor: 3.412

3.  Osteoprotegerin and MTHFR gene variations in rheumatoid arthritis: association with disease susceptibility and markers of subclinical atherosclerosis.

Authors:  Aikaterini Arida; Adrianos Nezos; Ioanna Papadaki; Petros P Sfikakis; Clio P Mavragani
Journal:  Sci Rep       Date:  2022-06-09       Impact factor: 4.996

4.  The interaction effect of angiogenesis and endothelial dysfunction-related gene variants increases the susceptibility of recurrent pregnancy loss.

Authors:  E A Trifonova; M G Swarovskaya; O A Ganzha; O V Voronkova; T V Gabidulina; V A Stepanov
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5.  C677T MTHFR Gene Polymorphism is Contributing Factor in Development of Renal Impairment in Young Hypertensive Patients.

Authors:  Hanaa H Elsaid; Khaled A El-Hefnawy; Saffaa M Elalawi
Journal:  Indian J Clin Biochem       Date:  2020-05-14

Review 6.  Mechanisms of vascular comorbidity in autoimmune diseases.

Authors:  György Nagy; Nóra Németh; Edit I Buzás
Journal:  Curr Opin Rheumatol       Date:  2018-03       Impact factor: 5.006

7.  Association of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of carotid atherosclerosis: a cross-sectional analysis of 730 Chinese Han adults in Chongqing.

Authors:  Xulei Peng; Yongli Zhou; Xiaoxing Wu; Xiaolin Wang; Huili Bai; Yongqiang Li; Zhichao Wang; Xuan Chen; Yonghong Wang
Journal:  BMC Cardiovasc Disord       Date:  2020-05-13       Impact factor: 2.298

8.  Recurrent Myocardial Infarction Despite Normal C-reactive Protein in a Patient with Behcet's Disease and Compound Heterozygous Methylenetetrahydrofolate Reductase (MTHFR) Mutations (C677T and A1298C).

Authors:  Muhammad Hamza Saad Shaukat; Aixa Toledo-Garcia; Mikhail Torosoff
Journal:  Cureus       Date:  2019-08-08

9.  Association of the methylenetetrahydrofolate reductase (MTHFR) gene variant C677T with serum homocysteine levels and the severity of ischaemic stroke: a case-control study in the southwest of China.

Authors:  Lu-Wen Huang; Lin-Lin Li; Juan Li; Xiao-Rong Chen; Ming Yu
Journal:  J Int Med Res       Date:  2022-02       Impact factor: 1.671

  9 in total

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