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Vitamin D receptor Fok1 polymorphism and blood lead concentration in children.

Variation in blood lead concentration is caused by a complex interaction of environmental, social, nutritional, and genetic factors. We evaluated the association between blood lead concentration and a vitamin D receptor (VDR) gene polymorphism. Environmental samples and blood were analyzed for lead,...

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Autores principales: Haynes, Erin N, Kalkwarf, Heidi J, Hornung, Richard, Wenstrup, Richard, Dietrich, Kim, Lanphear, Bruce P
Formato: Texto
Lenguaje:English
Publicado: 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241691/
https://www.ncbi.nlm.nih.gov/pubmed/14527848
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author Haynes, Erin N
Kalkwarf, Heidi J
Hornung, Richard
Wenstrup, Richard
Dietrich, Kim
Lanphear, Bruce P
author_facet Haynes, Erin N
Kalkwarf, Heidi J
Hornung, Richard
Wenstrup, Richard
Dietrich, Kim
Lanphear, Bruce P
author_sort Haynes, Erin N
collection PubMed
description Variation in blood lead concentration is caused by a complex interaction of environmental, social, nutritional, and genetic factors. We evaluated the association between blood lead concentration and a vitamin D receptor (VDR) gene polymorphism. Environmental samples and blood were analyzed for lead, nutritional and behavioral factors were assessed, and VDR -Fok1 genotype was determined in 245 children. We found a significant interaction between floor dust lead and genotype on blood lead concentration. For every 1 microg/ft(2) increase in floor dust, children with VDR -FF genotype had a 1.1% increase in blood lead [95% confidence interval (CI), 0.69-1.5], VDR -Ff, 0.53% increase (95% CI, 0.1-0.92), and VDR -ff, 3.8% increase (95% CI, 1.2-6.3); however, at floor dust levels < 10 microg/ft(2), children with VDR -ff had the lowest blood lead concentrations. These data suggest that VDR -Fok1 is an effect modifier of the relationship of floor dust lead exposure and blood lead concentration.
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spelling pubmed-12416912005-11-08 Vitamin D receptor Fok1 polymorphism and blood lead concentration in children. Haynes, Erin N Kalkwarf, Heidi J Hornung, Richard Wenstrup, Richard Dietrich, Kim Lanphear, Bruce P Environ Health Perspect Research Article Variation in blood lead concentration is caused by a complex interaction of environmental, social, nutritional, and genetic factors. We evaluated the association between blood lead concentration and a vitamin D receptor (VDR) gene polymorphism. Environmental samples and blood were analyzed for lead, nutritional and behavioral factors were assessed, and VDR -Fok1 genotype was determined in 245 children. We found a significant interaction between floor dust lead and genotype on blood lead concentration. For every 1 microg/ft(2) increase in floor dust, children with VDR -FF genotype had a 1.1% increase in blood lead [95% confidence interval (CI), 0.69-1.5], VDR -Ff, 0.53% increase (95% CI, 0.1-0.92), and VDR -ff, 3.8% increase (95% CI, 1.2-6.3); however, at floor dust levels < 10 microg/ft(2), children with VDR -ff had the lowest blood lead concentrations. These data suggest that VDR -Fok1 is an effect modifier of the relationship of floor dust lead exposure and blood lead concentration. 2003-10 /pmc/articles/PMC1241691/ /pubmed/14527848 Text en
spellingShingle Research Article
Haynes, Erin N
Kalkwarf, Heidi J
Hornung, Richard
Wenstrup, Richard
Dietrich, Kim
Lanphear, Bruce P
Vitamin D receptor Fok1 polymorphism and blood lead concentration in children.
title Vitamin D receptor Fok1 polymorphism and blood lead concentration in children.
title_full Vitamin D receptor Fok1 polymorphism and blood lead concentration in children.
title_fullStr Vitamin D receptor Fok1 polymorphism and blood lead concentration in children.
title_full_unstemmed Vitamin D receptor Fok1 polymorphism and blood lead concentration in children.
title_short Vitamin D receptor Fok1 polymorphism and blood lead concentration in children.
title_sort vitamin d receptor fok1 polymorphism and blood lead concentration in children.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241691/
https://www.ncbi.nlm.nih.gov/pubmed/14527848
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