Literature DB >> 10852844

Identifying critical windows of exposure for children's health.

S G Selevan1, C A Kimmel, P Mendola.   

Abstract

Several authors have considered the importance of exposure timing and how this affects the outcomes observed, but no one has systematically compiled preconceptional, prenatal, and postnatal developmental exposures and subsequent outcomes. Efforts were undertaken to examine the information available and to evaluate implications for risk assessment for several areas: a) respiratory and immune systems, b) reproductive system, c) nervous system, d) cardiovascular system, endocrine system, and general growth, and e) cancer. Major conclusions from a workshop on "Critical Windows of Exposure for Children's Health" included a) broad windows of sensitivity can be identified for many systems but detailed information is limited; b) cross-species comparisons of dose to target tissue and better data on the exposure-dose-outcome continuum are needed; c) increased interaction among scientific disciplines can further understanding by using laboratory animal results in designing epidemiological studies and human data to suggest specific laboratory studies on mechanisms and agent-target interactions; and d) thus far, only limited attention has been given to peripubertal/adolescent exposures, adult consequences of developmental exposures, and genome-environment interactions. More specific information on developmental windows will improve risk assessment by identifying the most sensitive window(s) for evaluation of dose-response relationships and exposure, evaluation of biological plausibility of research findings in humans, and comparison of data across species. In public health and risk management, information on critical windows may help identify especially susceptible subgroups for specific interventions.

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Year:  2000        PMID: 10852844      PMCID: PMC1637810          DOI: 10.1289/ehp.00108s3451

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  29 in total

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Review 2.  Workshop to identify critical windows of exposure for children's health: immune and respiratory systems work group summary.

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Journal:  Environ Health Perspect       Date:  2000-06       Impact factor: 9.031

Review 3.  Critical windows of exposure for children's health: the reproductive system in animals and humans.

Authors:  J L Pryor; C Hughes; W Foster; B F Hales; B Robaire
Journal:  Environ Health Perspect       Date:  2000-06       Impact factor: 9.031

Review 4.  Development of atopy and asthma: candidate environmental influences and important periods of exposure.

Authors:  D B Peden
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Review 5.  The mammalian respiratory system and critical windows of exposure for children's health.

Authors:  K E Pinkerton; J P Joad
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Review 6.  Workshop to identify critical windows of exposure for children's health: neurobehavioral work group summary.

Authors:  J Adams; S Barone; A LaMantia; R Philen; D C Rice; L Spear; E Susser
Journal:  Environ Health Perspect       Date:  2000-06       Impact factor: 9.031

Review 7.  Susceptible periods during embryogenesis of the heart and endocrine glands.

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Review 8.  Fetal, infant, and childhood growth are predictors of coronary heart disease, diabetes, and hypertension in adult men and women.

Authors:  C Osmond; D J Barker
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Review 9.  Workshop to identify critical windows of exposure for children's health: reproductive health in children and adolescents work group summary.

Authors:  G K Lemasters; S D Perreault; B F Hales; M Hatch; A N Hirshfield; C L Hughes; G L Kimmel; J C Lamb; J L Pryor; C Rubin; J G Seed
Journal:  Environ Health Perspect       Date:  2000-06       Impact factor: 9.031

Review 10.  Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.

Authors:  D Rice; S Barone
Journal:  Environ Health Perspect       Date:  2000-06       Impact factor: 9.031

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  155 in total

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7.  Prenatal bisphenol A exposure alters sex-specific estrogen receptor expression in the neonatal rat hypothalamus and amygdala.

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