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Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children

BACKGROUND: Chronic cadmium exposure has been associated with osteotoxicity in adults, but little is known concerning its effects on early growth, which has been shown to be impaired by cadmium. OBJECTIVES: Our objective was to assess the impact of early-life cadmium exposure on bone-related biomark...

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Autores principales: Malin Igra, Annachiara, Vahter, Marie, Raqib, Rubhana, Kippler, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Environmental Health Perspectives 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768315/
https://www.ncbi.nlm.nih.gov/pubmed/30848671
http://dx.doi.org/10.1289/EHP3655
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author Malin Igra, Annachiara
Vahter, Marie
Raqib, Rubhana
Kippler, Maria
author_facet Malin Igra, Annachiara
Vahter, Marie
Raqib, Rubhana
Kippler, Maria
author_sort Malin Igra, Annachiara
collection PubMed
description BACKGROUND: Chronic cadmium exposure has been associated with osteotoxicity in adults, but little is known concerning its effects on early growth, which has been shown to be impaired by cadmium. OBJECTIVES: Our objective was to assess the impact of early-life cadmium exposure on bone-related biomarkers and anthropometry at 9 y of age. METHODS: For 504 children in a mother–child cohort in Bangladesh, cadmium exposure was assessed by concentrations in urine (U-Cd, long-term exposure) and erythrocytes (Ery-Cd, ongoing exposure) at 9 and 4.5 y of age, and in their mothers during pregnancy. Biomarkers of bone remodeling [urinary deoxypyridinoline (DPD), urinary calcium, plasma parathyroid hormone, osteocalcin, vitamin D3, insulin-like growth factor (IGF) 1, IGF binding protein 3, thyroid stimulating hormone] were measured at 9 y of age. RESULTS: In multivariable-adjusted linear models, a doubling of concurrent U-Cd was associated with a mean increase in osteocalcin of [Formula: see text] (95% CI: 0.042, 5.9) and in urinary DPD of [Formula: see text] (95% CI: 12, 32). In a combined exposure model, a doubling of maternal Ery-Cd was associated with a mean increase in urinary DPD of [Formula: see text] (95% CI: [Formula: see text] , 30). Stratifying the osteocalcin model by gender ([Formula: see text] 0.001), a doubling of concurrent U-Cd was associated with a mean decrease in osteocalcin of [Formula: see text] (95% CI: [Formula: see text] , [Formula: see text]) in boys and a mean increase of [Formula: see text] (95% CI: 5.4, 13) in girls. The same pattern was seen with U-Cd at 4.5 y of age ([Formula: see text] 0.016). Children’s U-Cd and Ery-Cd, concurrent and at 4.5 y of age, were inversely associated with vitamin D3. CONCLUSIONS: Childhood cadmium exposure was associated with several bone-related biomarkers and some of the associations differed by gender. https://doi.org/10.1289/EHP3655
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spelling pubmed-67683152019-10-02 Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children Malin Igra, Annachiara Vahter, Marie Raqib, Rubhana Kippler, Maria Environ Health Perspect Research BACKGROUND: Chronic cadmium exposure has been associated with osteotoxicity in adults, but little is known concerning its effects on early growth, which has been shown to be impaired by cadmium. OBJECTIVES: Our objective was to assess the impact of early-life cadmium exposure on bone-related biomarkers and anthropometry at 9 y of age. METHODS: For 504 children in a mother–child cohort in Bangladesh, cadmium exposure was assessed by concentrations in urine (U-Cd, long-term exposure) and erythrocytes (Ery-Cd, ongoing exposure) at 9 and 4.5 y of age, and in their mothers during pregnancy. Biomarkers of bone remodeling [urinary deoxypyridinoline (DPD), urinary calcium, plasma parathyroid hormone, osteocalcin, vitamin D3, insulin-like growth factor (IGF) 1, IGF binding protein 3, thyroid stimulating hormone] were measured at 9 y of age. RESULTS: In multivariable-adjusted linear models, a doubling of concurrent U-Cd was associated with a mean increase in osteocalcin of [Formula: see text] (95% CI: 0.042, 5.9) and in urinary DPD of [Formula: see text] (95% CI: 12, 32). In a combined exposure model, a doubling of maternal Ery-Cd was associated with a mean increase in urinary DPD of [Formula: see text] (95% CI: [Formula: see text] , 30). Stratifying the osteocalcin model by gender ([Formula: see text] 0.001), a doubling of concurrent U-Cd was associated with a mean decrease in osteocalcin of [Formula: see text] (95% CI: [Formula: see text] , [Formula: see text]) in boys and a mean increase of [Formula: see text] (95% CI: 5.4, 13) in girls. The same pattern was seen with U-Cd at 4.5 y of age ([Formula: see text] 0.016). Children’s U-Cd and Ery-Cd, concurrent and at 4.5 y of age, were inversely associated with vitamin D3. CONCLUSIONS: Childhood cadmium exposure was associated with several bone-related biomarkers and some of the associations differed by gender. https://doi.org/10.1289/EHP3655 Environmental Health Perspectives 2019-03-08 /pmc/articles/PMC6768315/ /pubmed/30848671 http://dx.doi.org/10.1289/EHP3655 Text en EHP is an open-access journal published with support from the National Institute of Environmental Health Sciences, National Institutes of Health. All content is public domain unless otherwise noted.
spellingShingle Research
Malin Igra, Annachiara
Vahter, Marie
Raqib, Rubhana
Kippler, Maria
Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children
title Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children
title_full Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children
title_fullStr Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children
title_full_unstemmed Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children
title_short Early-Life Cadmium Exposure and Bone-Related Biomarkers: A Longitudinal Study in Children
title_sort early-life cadmium exposure and bone-related biomarkers: a longitudinal study in children
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768315/
https://www.ncbi.nlm.nih.gov/pubmed/30848671
http://dx.doi.org/10.1289/EHP3655
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