Literature DB >> 27605737

Methylenetetrahydrofolate Reductase C677T Polymorphism and Recurrent Pregnancy Loss Risk in Asian Population: A Meta-analysis.

Vandana Rai1.   

Abstract

The C677T polymorphism of the methylenetetrahydrofolate reductase (MTHFR) gene was implicated to be associated with thrombophilia due to its role in catalyzing the formation of 5-methylenetetrahydrofolate, a co-substrate for the conversion of homocysteine to methionine. Several case-control studies were investigated MTHFR C677T polymorphism as risk for recurrent pregnancy loss (RPL). These studies rendered contradictory results, some indicating that the polymorphism is associated with the risk of RPL whereas others concluded there is no association. To shed light on these inconclusive findings, a meta-analysis of all available studies published from Asian population relating the C677T polymorphism to the risk of RPL was conducted. The following electronic databases were searched without language restrictions: PubMed, Google Scholars, Elsevier and Springer Link up to December, 2015. Meta-analysis was performed using MetaAnalyst and Mix version 1.7. Meta-analysis results suggested that MTHFR C677T polymorphism contributed to the increased RPL risk in Asian population using all five genetic models (for T vs. C: OR 1.35, 95 % CI 1.09-1.68, p = 0.009; for TT + CT vs. CC: OR 1.44, 95 % CI 1.14-1.82, p = 0.006; for CT vs. CC: OR 1.39, 95 % CI 1.07-1.8, p = 0.01; for TT vs. CC: OR 1.79, 95 % CI 1.23.2.6, p = 0.007; for TT vs. CT + CC: OR 1.61, 95 % CI 1.02-2.56, p = 0.04). In conclusion, this meta-analysis demonstrates a strong association between the MTHFR C677T variant and RPL in Asian population and raising the importance of the use of folate in its treatment and prevention.

Entities:  

Keywords:  C677T; Folate; MTHFR; Meta-analysis; Recurrent pregnancy loss; Thrombophilic gene

Year:  2016        PMID: 27605737      PMCID: PMC4992492          DOI: 10.1007/s12291-016-0554-0

Source DB:  PubMed          Journal:  Indian J Clin Biochem        ISSN: 0970-1915


  74 in total

1.  Maternal homocysteine and chorionic vascularization in recurrent early pregnancy loss.

Authors:  W L Nelen; J Bulten; E A Steegers; H J Blom; A G Hanselaar; T K Eskes
Journal:  Hum Reprod       Date:  2000-04       Impact factor: 6.918

2.  A common mutation in the 5,10-methylenetetrahydrofolate reductase gene as a new risk factor for placental vasculopathy.

Authors:  E F van der Molen; G E Arends; W L Nelen; N J van der Put; S G Heil; T K Eskes; H J Blom
Journal:  Am J Obstet Gynecol       Date:  2000-05       Impact factor: 8.661

3.  Genetic thromobophilia in pregnancy: a case-control study among North Indian women.

Authors:  Lovejeet Kaur; Manju Puri; Shweta Kaushik; Mohinder Pal Sachdeva; Shubha Sagar Trivedi; Kallur Nava Saraswathy
Journal:  J Thromb Thrombolysis       Date:  2013-02       Impact factor: 2.300

Review 4.  Recurrent pregnancy loss.

Authors:  C L Cook; D D Pridham
Journal:  Curr Opin Obstet Gynecol       Date:  1995-10       Impact factor: 1.927

5.  Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations.

Authors:  Oztürk Ozdemir; Gonca Imir Yenicesu; Fatma Silan; Binnur Köksal; Sinem Atik; Filiz Ozen; Mert Göl; Ali Cetin
Journal:  Genet Test Mol Biomarkers       Date:  2011-11-02

6.  Methylenetetrahydrofolate reductase (MTHFR) polymorphism susceptibility to schizophrenia and bipolar disorder: an updated meta-analysis.

Authors:  Cai-Yun Hu; Zhen-Zhong Qian; Feng-Feng Gong; Shan-Shan Lu; Fang Feng; Yi-Le Wu; Hui-Yun Yang; Ye-Huan Sun
Journal:  J Neural Transm (Vienna)       Date:  2014-06-18       Impact factor: 3.575

7.  MTHFR C677T and factor V Leiden in recurrent pregnancy loss: a study among an endogamous group in North India.

Authors:  Rupak Mukhopadhyay; Kallur N Saraswathy; Pradeep K Ghosh
Journal:  Genet Test Mol Biomarkers       Date:  2009-12

8.  Polymorphisms in MTHFR, MTHFD, and PAI-1 and recurrent miscarriage among North Indian women.

Authors:  Farah Parveen; Moni Tuteja; Suraksha Agrawal
Journal:  Arch Gynecol Obstet       Date:  2013-05-18       Impact factor: 2.344

Review 9.  "Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis".

Authors:  Upendra Yadav; Pradeep Kumar; Sushil Kumar Yadav; Om Prakash Mishra; Vandana Rai
Journal:  Metab Brain Dis       Date:  2014-07-09       Impact factor: 3.584

10.  Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

Authors:  P F Jacques; A G Bostom; R R Williams; R C Ellison; J H Eckfeldt; I H Rosenberg; J Selhub; R Rozen
Journal:  Circulation       Date:  1996-01-01       Impact factor: 29.690

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  11 in total

1.  Evaluation of COMT Gene rs4680 Polymorphism as a Risk Factor for Endometrial Cancer.

Authors:  Pradeep Kumar; Garima Singh; Vandana Rai
Journal:  Indian J Clin Biochem       Date:  2018-12-04

2.  Polymorphisms of methalenetetrahydrofolate reductase in recurrent pregnancy loss: an overview of systematic reviews and meta-analyses.

Authors:  Boran Du; Xiangjun Shi; Chenghong Yin; Xin Feng
Journal:  J Assist Reprod Genet       Date:  2019-06-28       Impact factor: 3.412

3.  Methylenetetrahydrofolate reductase C677T polymorphism and susceptibility to epilepsy.

Authors:  Vandana Rai; Pradeep Kumar
Journal:  Neurol Sci       Date:  2018-09-28       Impact factor: 3.307

4.  Combined presence of coagulation factor XIII V34L and plasminogen activator inhibitor 1 4G/5G gene polymorphisms significantly contribute to recurrent pregnancy loss in Serbian population.

Authors:  Ivana Joksic; Zeljko Mikovic; Dejan Filimonovic; Jelena Munjas; Orlic Natasa Karadzov; Amira Egic; Gordana Joksic
Journal:  J Med Biochem       Date:  2020-01-23       Impact factor: 3.402

Review 5.  Relation Between Methylenetetrahydrofolate Reductase Polymorphisms (C677T and A1298C) and Migraine Susceptibility.

Authors:  Vandana Rai; Pradeep Kumar
Journal:  Indian J Clin Biochem       Date:  2021-09-20

Review 6.  Strong Association of C677T Polymorphism of Methylenetetrahydrofolate Reductase Gene With Nosyndromic Cleft Lip/Palate (nsCL/P).

Authors:  Vandana Rai
Journal:  Indian J Clin Biochem       Date:  2017-07-07

Review 7.  MTHFR 1298A>C Substitution is a Strong Candidate for Analysis in Recurrent Pregnancy Loss: Evidence from 14,289 Subjects.

Authors:  Poonam Mehta; Rahul Vishvkarma; Kiran Singh; Singh Rajender
Journal:  Reprod Sci       Date:  2021-03-19       Impact factor: 3.060

8.  Methylenetetrahydrofolate Reductase Polymorphisms and Risk of Recurrent Pregnancy Loss: a Case-Control Study.

Authors:  Kyu Ri Hwang; Young Min Choi; Jin Ju Kim; Sung Ki Lee; Kwang Moon Yang; Eun Chan Paik; Hyeon Jeong Jeong; Jong Kwan Jun; Sang Ho Yoon; Min A Hong
Journal:  J Korean Med Sci       Date:  2017-12       Impact factor: 2.153

9.  The methylenetetrahydrofolate reductase 677T-1298C haplotype is a risk factor for acute lymphoblastic leukemia in children.

Authors:  Ewelina Maria Kałużna; Ewa Strauss; Bogna Świątek-Kościelna; Olga Zając-Spychała; Ewelina Gowin; Jerzy S Nowak; Jolanta Rembowska; Danuta Januszkiewicz-Lewandowska
Journal:  Medicine (Baltimore)       Date:  2017-12       Impact factor: 1.817

10.  MTHFR 3'-untranslated region polymorphisms contribute to recurrent pregnancy loss risk and alterations in peripheral natural killer cell proportions.

Authors:  Eun Sun Kim; Jung Oh Kim; Hui Jeong An; Jung Hyun Sakong; Hyun Ah Lee; Ji Hyang Kim; Eun Hee Ahn; Young Ran Kim; Woo Sik Lee; Nam Keun Kim
Journal:  Clin Exp Reprod Med       Date:  2017-09-26
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