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Early Environmental Origins of Neurodegenerative Disease in Later Life

Parkinson disease (PD) and Alzheimer disease (AD), the two most common neurodegenerative disorders in American adults, are of purely genetic origin in a minority of cases and appear in most instances to arise through interactions among genetic and environmental factors. In this article we hypothesiz...

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Autores principales: Landrigan, Philip J., Sonawane, Babasaheb, Butler, Robert N., Trasande, Leonardo, Callan, Richard, Droller, Daniel
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280407/
https://www.ncbi.nlm.nih.gov/pubmed/16140633
http://dx.doi.org/10.1289/ehp.7571
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author Landrigan, Philip J.
Sonawane, Babasaheb
Butler, Robert N.
Trasande, Leonardo
Callan, Richard
Droller, Daniel
author_facet Landrigan, Philip J.
Sonawane, Babasaheb
Butler, Robert N.
Trasande, Leonardo
Callan, Richard
Droller, Daniel
author_sort Landrigan, Philip J.
collection PubMed
description Parkinson disease (PD) and Alzheimer disease (AD), the two most common neurodegenerative disorders in American adults, are of purely genetic origin in a minority of cases and appear in most instances to arise through interactions among genetic and environmental factors. In this article we hypothesize that environmental exposures in early life may be of particular etiologic importance and review evidence for the early environmental origins of neurodegeneration. For PD the first recognized environmental cause, MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine), was identified in epidemiologic studies of drug abusers. Chemicals experimentally linked to PD include the insecticide rotenone and the herbicides paraquat and maneb; interaction has been observed between paraquat and maneb. In epidemiologic studies, manganese has been linked to parkinsonism. In dementia, lead is associated with increased risk in chronically exposed workers. Exposures of children in early life to lead, polychlorinated biphenyls, and methylmercury have been followed by persistent decrements in intelligence that may presage dementia. To discover new environmental causes of AD and PD, and to characterize relevant gene–environment interactions, we recommend that a large, prospective genetic and epidemiologic study be undertaken that will follow thousands of children from conception (or before) to old age. Additional approaches to etiologic discovery include establishing incidence registries for AD and PD, conducting targeted investigations in high-risk populations, and improving testing of the potential neurologic toxicity of chemicals.
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spelling pubmed-12804072005-11-30 Early Environmental Origins of Neurodegenerative Disease in Later Life Landrigan, Philip J. Sonawane, Babasaheb Butler, Robert N. Trasande, Leonardo Callan, Richard Droller, Daniel Environ Health Perspect Research Parkinson disease (PD) and Alzheimer disease (AD), the two most common neurodegenerative disorders in American adults, are of purely genetic origin in a minority of cases and appear in most instances to arise through interactions among genetic and environmental factors. In this article we hypothesize that environmental exposures in early life may be of particular etiologic importance and review evidence for the early environmental origins of neurodegeneration. For PD the first recognized environmental cause, MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine), was identified in epidemiologic studies of drug abusers. Chemicals experimentally linked to PD include the insecticide rotenone and the herbicides paraquat and maneb; interaction has been observed between paraquat and maneb. In epidemiologic studies, manganese has been linked to parkinsonism. In dementia, lead is associated with increased risk in chronically exposed workers. Exposures of children in early life to lead, polychlorinated biphenyls, and methylmercury have been followed by persistent decrements in intelligence that may presage dementia. To discover new environmental causes of AD and PD, and to characterize relevant gene–environment interactions, we recommend that a large, prospective genetic and epidemiologic study be undertaken that will follow thousands of children from conception (or before) to old age. Additional approaches to etiologic discovery include establishing incidence registries for AD and PD, conducting targeted investigations in high-risk populations, and improving testing of the potential neurologic toxicity of chemicals. National Institute of Environmental Health Sciences 2005-09 2005-05-26 /pmc/articles/PMC1280407/ /pubmed/16140633 http://dx.doi.org/10.1289/ehp.7571 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Landrigan, Philip J.
Sonawane, Babasaheb
Butler, Robert N.
Trasande, Leonardo
Callan, Richard
Droller, Daniel
Early Environmental Origins of Neurodegenerative Disease in Later Life
title Early Environmental Origins of Neurodegenerative Disease in Later Life
title_full Early Environmental Origins of Neurodegenerative Disease in Later Life
title_fullStr Early Environmental Origins of Neurodegenerative Disease in Later Life
title_full_unstemmed Early Environmental Origins of Neurodegenerative Disease in Later Life
title_short Early Environmental Origins of Neurodegenerative Disease in Later Life
title_sort early environmental origins of neurodegenerative disease in later life
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280407/
https://www.ncbi.nlm.nih.gov/pubmed/16140633
http://dx.doi.org/10.1289/ehp.7571
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