학술논문

Neonatal folate, homocysteine, vitamin B12 levels and methylenetetrahydrofolate reductase variants in childhood asthma and eczema.
Document Type
Article
Source
Allergy. Jun2013, Vol. 68 Issue 6, p788-795. 8p. 5 Charts.
Subject
*FOLIC acid
*HOMOCYSTEINE
*VITAMIN B12
*METHYLENETETRAHYDROFOLATE reductase genetics
*ASTHMA in children
*ECZEMA in children
*NITRIC oxide
*LONGITUDINAL method
Language
ISSN
0105-4538
Abstract
Objectives To assess the associations of folate, homocysteine and vitamin B12 levels of children at birth and their methylenetetrahydrofolate reductase ( MTHFR) variants with asthma and eczema in childhood. Methods This study was embedded in a population-based prospective cohort study ( n = 2,001). Neonatal cord blood folate, homocysteine and vitamin B12 levels were measured, and MTHFR C677 T and A1298 C genotyped. Wheezing and physician-diagnosed eczema were annually obtained by questionnaire until 4 years. At 6 years, we collected information on physician-diagnosed asthma ever and self-reported eczema ever, measured fractional exhaled nitric oxide ( Fe NO), and interrupter resistance ( Rint). Data were analysed with generalized estimating equations or logistic regression: continuous outcomes with linear regression models. Results Folate, homocysteine and vitamin B12 levels of children at birth were not associated with wheezing or eczema until 4 years, asthma and eczema ever, or Fe NO or Rint at 6 years. In children carrying C677 T mutations in MTHFR, higher folate levels were associated with an increased risk of eczema (repeated eczema until 4 years: OR 1.40 (95% CI 1.09-1.80) ( SD change) P-interaction = 0.003, eczema ever at 6 years: OR 1.41 (0.97-2.03) P-interaction = 0.011). No interactions between MTHFR and child folate and homocysteine levels were observed for wheezing and asthma. Conclusions Folate, homocysteine and vitamin B12 levels of children at birth did not affect asthma- and eczema-related outcomes up to the age of 6 years. Further studies are warranted to establish the role of MTHFR variants in these associations. [ABSTRACT FROM AUTHOR]