<it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California population

<p>Abstract</p> <p>Background</p> <p>Neural tube defects (NTDs) are among the most common of all human congenital defects. Over the last two decades, accumulating evidence has made it clear that periconceptional intake of folic acid can significantly reduce the risk of...

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Main Authors: Lammer Edward J, Shaw Gary M, Lu Wei, Yang Wei, Zhu Huiping, Enaw James, Finnell Richard H
Format: Article
Language:English
Published: BMC 2006-12-01
Series:BMC Medicine
Online Access:http://www.biomedcentral.com/1741-7015/4/36
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spelling doaj-15acf8961a5846db81a7043c540933ae2020-11-25T01:39:17ZengBMCBMC Medicine1741-70152006-12-01413610.1186/1741-7015-4-36<it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California populationLammer Edward JShaw Gary MLu WeiYang WeiZhu HuipingEnaw JamesFinnell Richard H<p>Abstract</p> <p>Background</p> <p>Neural tube defects (NTDs) are among the most common of all human congenital defects. Over the last two decades, accumulating evidence has made it clear that periconceptional intake of folic acid can significantly reduce the risk of NTD affected pregnancies. This beneficial effect may be related to the ability of folates to donate methyl groups for critical physiological reactions. Choline is an essential nutrient and it is also a methyl donor critical for the maintenance of cell membrane integrity and methyl metabolism. Perturbations in choline metabolism <it>in vitro </it>have been shown to induce NTDs in mouse embryos.</p> <p>Methods</p> <p>This study investigated whether single nucleotide polymorphisms (SNPs) in human choline kinase A (<it>CHKA</it>) gene and CTP:phosphocholine cytidylytransferase (<it>PCYT1A</it>) gene were risk factors for spina bifida. Fluorescence-based allelic discrimination analysis was performed for the two <it>CHKA </it>intronic SNPs hCV1562388 (rs7928739) and hCV1562393, and <it>PCYT1A </it>SNP rs939883 and rs3772109. The study population consisted of 103 infants with spina bifida and 338 non-malformed control infants who were born in selected California counties in the period 1989–1991.</p> <p>Results</p> <p>The <it>CHKA </it>SNP hCV1562388 genotypes with at least one C allele were associated with a reduced risk of spina bifida (odds ratio = 0.60, 95%CI = 0.38–0.94). The <it>PCYT1A </it>SNP rs939883 genotype AA was associated with a twofold increased risk of spina bifida (odds ratio = 1.89, 95% CI = 0.97–3.67). These gene-only effects were not substantially modified by analytic consideration to maternal periconceptional choline intake.</p> <p>Conclusion</p> <p>Our analyses showed genotype effects of <it>CHKA </it>and <it>PCYT1A </it>genes on spina bifida risk, but did not show evidence of gene-nutrient interactions. The underlying mechanisms are yet to be resolved.</p> http://www.biomedcentral.com/1741-7015/4/36
collection DOAJ
language English
format Article
sources DOAJ
author Lammer Edward J
Shaw Gary M
Lu Wei
Yang Wei
Zhu Huiping
Enaw James
Finnell Richard H
spellingShingle Lammer Edward J
Shaw Gary M
Lu Wei
Yang Wei
Zhu Huiping
Enaw James
Finnell Richard H
<it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California population
BMC Medicine
author_facet Lammer Edward J
Shaw Gary M
Lu Wei
Yang Wei
Zhu Huiping
Enaw James
Finnell Richard H
author_sort Lammer Edward J
title <it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California population
title_short <it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California population
title_full <it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California population
title_fullStr <it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California population
title_full_unstemmed <it>CHKA </it>and <it>PCYT1A </it>gene polymorphisms, choline intake and spina bifida risk in a California population
title_sort <it>chka </it>and <it>pcyt1a </it>gene polymorphisms, choline intake and spina bifida risk in a california population
publisher BMC
series BMC Medicine
issn 1741-7015
publishDate 2006-12-01
description <p>Abstract</p> <p>Background</p> <p>Neural tube defects (NTDs) are among the most common of all human congenital defects. Over the last two decades, accumulating evidence has made it clear that periconceptional intake of folic acid can significantly reduce the risk of NTD affected pregnancies. This beneficial effect may be related to the ability of folates to donate methyl groups for critical physiological reactions. Choline is an essential nutrient and it is also a methyl donor critical for the maintenance of cell membrane integrity and methyl metabolism. Perturbations in choline metabolism <it>in vitro </it>have been shown to induce NTDs in mouse embryos.</p> <p>Methods</p> <p>This study investigated whether single nucleotide polymorphisms (SNPs) in human choline kinase A (<it>CHKA</it>) gene and CTP:phosphocholine cytidylytransferase (<it>PCYT1A</it>) gene were risk factors for spina bifida. Fluorescence-based allelic discrimination analysis was performed for the two <it>CHKA </it>intronic SNPs hCV1562388 (rs7928739) and hCV1562393, and <it>PCYT1A </it>SNP rs939883 and rs3772109. The study population consisted of 103 infants with spina bifida and 338 non-malformed control infants who were born in selected California counties in the period 1989–1991.</p> <p>Results</p> <p>The <it>CHKA </it>SNP hCV1562388 genotypes with at least one C allele were associated with a reduced risk of spina bifida (odds ratio = 0.60, 95%CI = 0.38–0.94). The <it>PCYT1A </it>SNP rs939883 genotype AA was associated with a twofold increased risk of spina bifida (odds ratio = 1.89, 95% CI = 0.97–3.67). These gene-only effects were not substantially modified by analytic consideration to maternal periconceptional choline intake.</p> <p>Conclusion</p> <p>Our analyses showed genotype effects of <it>CHKA </it>and <it>PCYT1A </it>genes on spina bifida risk, but did not show evidence of gene-nutrient interactions. The underlying mechanisms are yet to be resolved.</p>
url http://www.biomedcentral.com/1741-7015/4/36
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