Literature DB >> 15719048

[Study of serum Hcy and polymorphisms of Hcy metabolic enzymes in 192 families affected by congenital heart disease].

Yong Li1, Jun Cheng, Wen-li Zhu, Jing-jing Dao, Li-ying Yan, Meng-yi Li, Shu-qin Li.   

Abstract

OBJECTIVE: To explore genotype distributions at MTHFR C677T, MS A2756G, MTHFD G1958A and CBS 844 ins68bp loci in healthy Chinese living in northern area, and to assess the association of single or combined gene mutations with folic acid, Vit.B(12), Hcy levels and CHD.
METHODS: 192 patients having CHD and their biological parents in Liaoning province registered as birth defects were included in this study as case group, and 124 healthy subjects (age and gender matched) and their biological parents were simultaneously selected from the same geographic area as control. To all subjects, the gene polymorphism at MTHFR C677T, MS A2756G, MTHFD G1958A and CBS 844 ins68bp loci was examined with PCR-RFLP. The serum folic acid and homocysteine (Hcy) level were analyzed with Radioimmunoassay or fluorescence polarization immunoassay (FPIA).
RESULTS: In healthy Chinese living in northern China, the mutant allele frequencies of these four loci were MTHFR 51.18%, MS 7.58%, MTHFD 24.32%, and CBS insertion 2.36%, respectively. The heterozygosity of CBS 844 ins68bp was more prevalent in case than in control (12.57% vs 2.97% in children, 10.88% vs 3.09% in father and 11.54% vs 1.02% in mother, respectively), and yielded an odds ratio (OR) of 4.70 (95% CI 1.34-25.15) in children, 3.83 (95% CI 1.05-20.98) in fathers and 12.65 (95% CI 1.92-532.47) in mothers. There is no existed significant difference at the other three loci. The percents of mothers with MTHFR, CBS and MTHFD gene polymorphisms, of mothers with MTHFR and CBS being polymorphisms (OR=8.44, 95aCI 1.23-362.26), of mothers with MTHFD and CBS being polymorphisms in case were higher than those in control. Serum folic acid levels of mothers and fathers in case were significantly higher than those of counterparts in control. Serum Hcy level of mothers in case was higher than that of counterparts in control without significant difference. Homozygous mutation at MTHFR and MTHFD loci made serum folic acid and Vit.B(12) levels slightly decreased and serum Hcy level increased.
CONCLUSION: The study showed presence of ethnic and district difference of gene polymorphisms at these four loci. 68 bp insertion at exon 8 of CBS gene base 844 could be a risk factor for CHD, and the insertion in parents (especially in mothers) could increase CHD risk in offspring.

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Year:  2005        PMID: 15719048

Source DB:  PubMed          Journal:  Beijing Da Xue Xue Bao Yi Xue Ban        ISSN: 1671-167X


  13 in total

Review 1.  Association between MTHFR C677T polymorphism and congenital heart disease. A family-based meta-analysis.

Authors:  Z Li; Y Jun; R Zhong-Bao; L Jie; L Jian-Ming
Journal:  Herz       Date:  2014-09-27       Impact factor: 1.443

2.  MTHFD1 gene polymorphisms as risk factors involved in orofacial cleft: an independent case-control study and a meta-analysis.

Authors:  Jun Wu; Yafei Chen; Jun Pei; Jian Pan
Journal:  Int J Clin Exp Med       Date:  2015-05-15

3.  Association of genetic and epigenetic variants in one-carbon metabolism gene with folate treatment response in hyperhomocysteinaemia.

Authors:  Dankang Li; Qinglin Zhao; Xiaowen Huang; Chengda Zhang; Opolot Godfrey; Weidong Zhang
Journal:  Eur J Clin Nutr       Date:  2020-03-20       Impact factor: 4.016

4.  Variants of folate metabolism genes and the risk of conotruncal cardiac defects.

Authors:  Elizabeth Goldmuntz; Stacy Woyciechowski; Daniel Renstrom; Philip J Lupo; Laura E Mitchell
Journal:  Circ Cardiovasc Genet       Date:  2008-12-09

5.  Polymorphisms in MTHFR, MS and CBS genes and homocysteine levels in a Pakistani population.

Authors:  Mohsin Yakub; Naushad Moti; Siddiqa Parveen; Bushra Chaudhry; Iqbal Azam; Mohammad Perwaiz Iqbal
Journal:  PLoS One       Date:  2012-03-21       Impact factor: 3.240

6.  Cystathionine beta-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children.

Authors:  Samikshan Dutta; Swagata Sinha; Anindita Chattopadhyay; Prasanta Kumar Gangopadhyay; Jotideb Mukhopadhyay; Manoranjan Singh; Kanchan Mukhopadhyay
Journal:  Behav Brain Funct       Date:  2005-12-26       Impact factor: 3.759

7.  Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls.

Authors:  Chao Xuan; Hui Li; Jin-Xia Zhao; Hong-Wei Wang; Yi Wang; Chun-Ping Ning; Zhen Liu; Bei-Bei Zhang; Guo-Wei He; Li-Min Lun
Journal:  Sci Rep       Date:  2014-12-04       Impact factor: 4.379

8.  Association between 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and congenital heart disease: A meta-analysis.

Authors:  Wenju Wang; Zongliu Hou; Chunhui Wang; Chuanyu Wei; Yaxiong Li; Lihong Jiang
Journal:  Meta Gene       Date:  2013-10-28

Review 9.  Genetic polymorphism of methylenetetrahydrofolate reductase as a potential risk factor for congenital heart disease: A meta-analysis in Chinese pediatric population.

Authors:  Ye Yuan; Xia Yu; Fenglan Niu; Na Lu
Journal:  Medicine (Baltimore)       Date:  2017-06       Impact factor: 1.889

10.  MTHFR C677T polymorphism and risk of congenital heart defects: evidence from 29 case-control and TDT studies.

Authors:  Wei Wang; Yujia Wang; Fangqi Gong; Weihua Zhu; Songling Fu
Journal:  PLoS One       Date:  2013-03-11       Impact factor: 3.240

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