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Neural tube defects and maternal biomarkers of folate, homocysteine, and glutathione metabolism

✍ Scribed by Weizhi Zhao; Bridget S. Mosley; Mario A. Cleves; Stepan Melnyk; S. Jill James; Charlotte A. Hobbs


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
102 KB
Volume
76
Category
Article
ISSN
1542-0752

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✦ Synopsis


Abstract

BACKGROUND

Alterations in maternal folate and homocysteine metabolism are associated with neural tube defects (NTDs). The role played by specific micronutrients and metabolites in the causal pathway leading to NTDs is not fully understood.

METHODS

We conducted a case‐control study to investigate the association between NTDs and maternal alterations in plasma micronutrients and metabolites in two metabolic pathways: methionine remethylation and glutathione transsulfuration. Biomarkers were measured in a population‐based sample of women who had NTD‐affected pregnancies (n = 43) and a control group of women who had a pregnancy unaffected by a birth defect (n = 160). We compared plasma concentrations of folate, vitamin B~12~, vitamin B~6~, methionine, S‐adenosylmethionine (SAM), s‐adenosylhomocysteine (SAH), adenosine, homocysteine, cysteine, and reduced and oxidized glutathione between cases and controls after adjusting for lifestyle and sociodemographic factors.

RESULTS

Women with NTD‐affected pregnancies had significantly higher plasma concentrations of SAH (29.12 vs. 23.13 nmol/liter, P = .0011), adenosine (0.323 vs. 0.255 μmol/liter; P = .0269), homocysteine (9.40 vs. 7.56 μmol/liter; P < .001), and oxidized glutathione (0.379 vs. 0.262 μmol/liter; P = .0001), but lower plasma SAM concentrations (78.99 vs. 83.16 nmol/liter; P = .0172) than controls. This metabolic profile is consistent with reduced methylation capacity and increased oxidative stress in women with affected pregnancies.

CONCLUSIONS

Increased maternal oxidative stress and decreased methylation capacity may contribute to the occurrence of NTDs. Further analysis of relevant genetic and environmental factors is required to define the basis for these observed alterations. Birth Defects Research (Part A), 2006. © 2006 Wiley‐Liss, Inc.


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