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Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil

✍ Scribed by Têmis Maria Félix; Sandra Leistner; Roberto Giugliani

Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
92 KB
Volume
70
Category
Article
ISSN
1542-0752

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✦ Synopsis

Abstract

BACKGROUND

The importance of metabolic factors in neural tube defects (NTDs) has been the focus of many investigations. Several authors have suggested that abnormalities in homocysteine metabolism, such as hyperhomocysteinemia, folate deficiency, and low vitamin B12, may be responsible for these malformations and that both nutritional factors and genetic abnormalities are associated with them.

METHODS

We conducted a case‐control study to investigate the influence of biochemical and genetic factors in NTDs in infants in southern Brazil. Levels of folate, vitamin B12, total homocysteine (t‐Hcy) and the 677C>T and 1298A>C polymorphisms of the MTHFR gene were analyzed in 41 NTD child–mother pairs and 44 normal child–mother control pairs.

RESULTS

Subjects in the case group had a higher mean blood folate level than those in the control group. The level of vitamin B12 was lower in mothers in the NTD group than in control mothers (p = 0.004). The level of t‐Hcy was not different in the two groups, but t‐Hcy and vitamin B12 were correlated (p = 0.002). There was no difference in the genotype distribution for 677C>T and 1298A>C polymorphisms of MTHFR in the case and control pairs. The level of t‐Hcy was correlated with 677TT.

CONCLUSIONS

Despite the small sample in this study, we suggest that low vitamin B12 and, consequently, hyperhomocysteinemia are important risk factors for NTDs in our population. Birth Defects Research (Part A), 2004. © 2004 Wiley‐Liss, Inc.

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