Literature DB >> 21977149

Frequency of the Methylenetetrahydrofolate REDUCTASE 677CT and 1298AC mutations in an Iranian Turkish female population.

Morteza Bagheri1, Isa Abdi Rad.   

Abstract

INTRODUCTION: Gene-environmental interactions in the pathway of folate metabolism influence greatly the embryonic development. Individual specific MTHFR 677C/T and 1298A/C mutations are known as risk factors for predisposition to human disorders. Therefore, we studied the frequencies of the MTHFR 677CT and 1298AC mutations in a female general population from Iranian Azeri Turkish.
MATERIAL AND METHODS: We studied 108 unrelated women from Iranian Azeri Turkish general population. Genomic DNA was extracted using standard procedure. The MTHFR 677CT and 1298AC mutations determined by PCR-RFLP method. OUTCOMES: The frequencies (percent) at position 677 for C and T alleles were 159(74%), 57(26%), and for CC, CT, and TT genotypes were 59(54.6%), 41(38%), and 8(7.41%) respectively. The frequencies (percent) at position 1298 for A and C alleles were 136(63%), 80(37%), and for AA, AC, and CC genotypes were 43(39.8%), 50(46.3%), and 15(13.9%) respectively.
CONCLUSIONS: The frequency of MTHFR 677 C and T alleles were 0.74 and 0.26 while that of MTHFR 1298 A and C alleles were 0.63 and 0.37 in present study, respectively. This is the first report in its own kind in Iranian Azeri Turkish women.

Entities:  

Keywords:  A1298C; C677T; MTHFR; Turkish female

Year:  2010        PMID: 21977149      PMCID: PMC3177554     

Source DB:  PubMed          Journal:  Maedica (Buchar)        ISSN: 1841-9038


  59 in total

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Journal:  Clin Chem       Date:  2001-04       Impact factor: 8.327

2.  Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.

Authors:  Kelly A Volcik; Gary M Shaw; Edward J Lammer; Huiping Zhu; Richard H Finnell
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2003-03

3.  The C677T mutation in the methylenetetrahydrofolate reductase gene among the Indonesian Javanese population.

Authors:  Ahmad Hamim Sadewa; Retno Sutomo; Chiyo Hayashi; Myeong Jin Lee; Hitoshi Ayaki; Abdul Salam M Sofro; Masafumi Matsuo; Hisahide Nishio
Journal:  Kobe J Med Sci       Date:  2002-12

4.  Folate status, homocysteine metabolism, and methylene tetrahydrofolate reductase genotype in rural South African blacks with a history of pregnancy complicated by neural tube defects.

Authors:  J B Ubbink; A Christianson; M J Bester; M I Van Allen; P A Venter; R Delport; H J Blom; A van der Merwe; H Potgieter; W J Vermaak
Journal:  Metabolism       Date:  1999-02       Impact factor: 8.694

5.  Distribution of p53, GST, and MTHFR polymorphisms and risk of cervical intraepithelial lesions in sicily.

Authors:  Antonella Agodi; Martina Barchitta; Rosalba Cipresso; Rubina Marzagalli; Nadia La Rosa; Melania Caruso; Maria Grazia Castiglione; Salvatore Travali
Journal:  Int J Gynecol Cancer       Date:  2010-01       Impact factor: 3.437

6.  MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India.

Authors:  Cyrus Cyril; Padmalatha Rai; N Chandra; P M Gopinath; K Satyamoorthy
Journal:  Indian J Hum Genet       Date:  2009-05

7.  MTHFR promoter hypermethylation in testicular biopsies of patients with non-obstructive azoospermia: the role of epigenetics in male infertility.

Authors:  N Khazamipour; M Noruzinia; P Fatehmanesh; M Keyhanee; P Pujol
Journal:  Hum Reprod       Date:  2009-05-28       Impact factor: 6.918

8.  Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India.

Authors:  Shaik Mohammad Naushad; Akella Radha Rama Devi
Journal:  J Perinat Med       Date:  2010       Impact factor: 1.901

9.  Single nucleotide polymorphisms in homocysteine metabolism pathway genes: association of CHDH A119C and MTHFR C677T with hyperhomocysteinemia.

Authors:  Jitender Kumar; Gaurav Garg; Arun Kumar; Elayanambi Sundaramoorthy; Krishna Rao Sanapala; Saurabh Ghosh; Ganesan Karthikeyan; Lakshmy Ramakrishnan; Shantanu Sengupta
Journal:  Circ Cardiovasc Genet       Date:  2009-09-05

10.  Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring.

Authors:  Iris Scala; Barbara Granese; Maria Sellitto; Serena Salomè; Annalidia Sammartino; Antonio Pepe; Pierpaolo Mastroiacovo; Gianfranco Sebastio; Generoso Andria
Journal:  Genet Med       Date:  2006-07       Impact factor: 8.822

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  3 in total

1.  A Multiplex Allele Specific Polymerase Chain Reaction (MAS-PCR) for the Detection of Factor V Leiden and Prothrombin G20210A.

Authors:  Morteza Bagheri; Isa Abdi Rad
Journal:  Maedica (Buchar)       Date:  2011-01

2.  Distribution of MTHFR C677T Gene Polymorphism in Healthy North Indian Population and an Updated Meta-analysis.

Authors:  Upendra Yadav; Pradeep Kumar; Sanjay Gupta; Vandana Rai
Journal:  Indian J Clin Biochem       Date:  2016-10-11

3.  Effects of polymorphisms in the MTHFR gene on 5-FU hematological toxicity and efficacy in Thai colorectal cancer patients.

Authors:  Chalirmporn Atasilp; Rinradee Lenavat; Natchaya Vanwong; Phichai Chansriwong; Ekaphop Sirachainan; Thanyanan Reungwetwattana; Pimonpan Jinda; Somthawin Aiempradit; Suwannee Sirilerttrakul; Monpat Chamnanphon; Apichaya Puangpetch; Nipaporn Sankuntaw; Patompong Satapornpong; Chonlaphat Sukasem
Journal:  Front Oncol       Date:  2022-07-15       Impact factor: 5.738

  3 in total

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