Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet

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Standard

Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet. / Grandjean, Philippe; Weihe, Pal; Nielsen, Flemming; Heinzow, Birger; Debes, Frodi; Budtz-Jørgensen, Esben.

I: Neurotoxicology and Teratology, Bind 34, Nr. 4, 06.2012, s. 466-472.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Grandjean, P, Weihe, P, Nielsen, F, Heinzow, B, Debes, F & Budtz-Jørgensen, E 2012, 'Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet', Neurotoxicology and Teratology, bind 34, nr. 4, s. 466-472. https://doi.org/10.1016/j.ntt.2012.06.001

APA

Grandjean, P., Weihe, P., Nielsen, F., Heinzow, B., Debes, F., & Budtz-Jørgensen, E. (2012). Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet. Neurotoxicology and Teratology, 34(4), 466-472. https://doi.org/10.1016/j.ntt.2012.06.001

Vancouver

Grandjean P, Weihe P, Nielsen F, Heinzow B, Debes F, Budtz-Jørgensen E. Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet. Neurotoxicology and Teratology. 2012 jun.;34(4):466-472. https://doi.org/10.1016/j.ntt.2012.06.001

Author

Grandjean, Philippe ; Weihe, Pal ; Nielsen, Flemming ; Heinzow, Birger ; Debes, Frodi ; Budtz-Jørgensen, Esben. / Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet. I: Neurotoxicology and Teratology. 2012 ; Bind 34, Nr. 4. s. 466-472.

Bibtex

@article{b54264b901ff49efbbe3939095e5d95e,
title = "Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet",
abstract = "To determine the possible neurotoxic impact of prenatal exposure to polychlorinated biphenyls (PCBs), we analyzed banked cord blood from a Faroese birth cohort for PCBs. The subjects were born in 1986-1987, and 917 cohort members had completed a series of neuropsychological tests at age 7years. Major PCB congeners (118, 138, 153, and 180), the calculated total PCB concentration, and the PCB exposure estimated in a structural equation model showed weak associations with test deficits, with statistically significant negative associations only with the Boston Naming test. Likewise, neither hexachlorobenzene nor p,p'-dichlorodiphenyldichloroethylene showed clear links to neurobehavioral deficits. Thus, these associations were much weaker than those associated with the cord-blood mercury concentration, and adjustment for mercury substantially attenuated the regression coefficients for PCB exposure. When the outcomes were joined into motor and verbally mediated functions in a structural equation model, the PCB effects remained weak and virtually disappeared after adjustment for methylmercury exposure, while mercury remained statistically significant. Thus, in the presence of elevated methylmercury exposure, PCB neurotoxicity may be difficult to detect, and PCB exposure does not explain the methylmercury neurotoxicity previously reported in this cohort.",
author = "Philippe Grandjean and Pal Weihe and Flemming Nielsen and Birger Heinzow and Frodi Debes and Esben Budtz-J{\o}rgensen",
note = "Copyright {\textcopyright} 2012. Published by Elsevier Inc.",
year = "2012",
month = jun,
doi = "10.1016/j.ntt.2012.06.001",
language = "English",
volume = "34",
pages = "466--472",
journal = "Neurotoxicology and Teratology",
issn = "0892-0362",
publisher = "Elsevier",
number = "4",

}

RIS

TY - JOUR

T1 - Neurobehavioral deficits at age 7years associated with prenatal exposure to toxicants from maternal seafood diet

AU - Grandjean, Philippe

AU - Weihe, Pal

AU - Nielsen, Flemming

AU - Heinzow, Birger

AU - Debes, Frodi

AU - Budtz-Jørgensen, Esben

N1 - Copyright © 2012. Published by Elsevier Inc.

PY - 2012/6

Y1 - 2012/6

N2 - To determine the possible neurotoxic impact of prenatal exposure to polychlorinated biphenyls (PCBs), we analyzed banked cord blood from a Faroese birth cohort for PCBs. The subjects were born in 1986-1987, and 917 cohort members had completed a series of neuropsychological tests at age 7years. Major PCB congeners (118, 138, 153, and 180), the calculated total PCB concentration, and the PCB exposure estimated in a structural equation model showed weak associations with test deficits, with statistically significant negative associations only with the Boston Naming test. Likewise, neither hexachlorobenzene nor p,p'-dichlorodiphenyldichloroethylene showed clear links to neurobehavioral deficits. Thus, these associations were much weaker than those associated with the cord-blood mercury concentration, and adjustment for mercury substantially attenuated the regression coefficients for PCB exposure. When the outcomes were joined into motor and verbally mediated functions in a structural equation model, the PCB effects remained weak and virtually disappeared after adjustment for methylmercury exposure, while mercury remained statistically significant. Thus, in the presence of elevated methylmercury exposure, PCB neurotoxicity may be difficult to detect, and PCB exposure does not explain the methylmercury neurotoxicity previously reported in this cohort.

AB - To determine the possible neurotoxic impact of prenatal exposure to polychlorinated biphenyls (PCBs), we analyzed banked cord blood from a Faroese birth cohort for PCBs. The subjects were born in 1986-1987, and 917 cohort members had completed a series of neuropsychological tests at age 7years. Major PCB congeners (118, 138, 153, and 180), the calculated total PCB concentration, and the PCB exposure estimated in a structural equation model showed weak associations with test deficits, with statistically significant negative associations only with the Boston Naming test. Likewise, neither hexachlorobenzene nor p,p'-dichlorodiphenyldichloroethylene showed clear links to neurobehavioral deficits. Thus, these associations were much weaker than those associated with the cord-blood mercury concentration, and adjustment for mercury substantially attenuated the regression coefficients for PCB exposure. When the outcomes were joined into motor and verbally mediated functions in a structural equation model, the PCB effects remained weak and virtually disappeared after adjustment for methylmercury exposure, while mercury remained statistically significant. Thus, in the presence of elevated methylmercury exposure, PCB neurotoxicity may be difficult to detect, and PCB exposure does not explain the methylmercury neurotoxicity previously reported in this cohort.

U2 - 10.1016/j.ntt.2012.06.001

DO - 10.1016/j.ntt.2012.06.001

M3 - Journal article

C2 - 22705177

VL - 34

SP - 466

EP - 472

JO - Neurotoxicology and Teratology

JF - Neurotoxicology and Teratology

SN - 0892-0362

IS - 4

ER -

ID: 38410878