https://doi.org/10.1034/j.1600-0404.2003.00128.x ·
Journal: Acta Neurologica Scandinavica, 2003, №4, p.239-244
Publisher: Hindawi Limited
Authors:
- M. Baldereschi
- A. Di Carlo
- P. Vanni
- A. Ghetti
- P. Carbonin
- L. Amaducci
- D. Inzitari
- for the Italian Longitudinal Study on Aging Working Group
List of references
- Seidler, Possible environmental, occupational, and other etiologic factors for Parkinson's disease: a case control study in Germany, Neurology, № 46, с. 1275
https://doi.org/10.1212/WNL.46.5.1275 - Grandinetti, Prospective study of cigarette smoking and the risk of developing idiopathic Parkinson's disease, Am J Epidemiol, № 139, с. 1129
https://doi.org/10.1093/oxfordjournals.aje.a116960 - Mayeux, Smoking and Parkinson's disease, Mov Disord, № 9, с. 207
https://doi.org/10.1002/mds.870090215 - Tzourio, Smoking and Parkinson's disease. An age-dependent risk effect, Neurology, № 49, с. 1267
https://doi.org/10.1212/WNL.49.5.1267 - Liou, Environmental risk factors and Parkinson's disease: a case-control study in Taiwan, Neurology, № 48, с. 1583
https://doi.org/10.1212/WNL.48.6.1583 - Hubble, Risk factors for Parkinson's disease, Neurology, № 43, с. 1693
https://doi.org/10.1212/WNL.43.9.1693 - Semchuck, Parkinson's disease and exposure to agricultural work and pesticide chemicals, Neurology, № 42, с. 1328
https://doi.org/10.1212/WNL.42.7.1328 - Wood, Genes and parkinsonism, J Neurol Neurosurg Psychiatry, № 62, с. 305
https://doi.org/10.1136/jnnp.62.4.305 - Marder, Environmental risk factors for Parkinson's disease in an urban multiethnic community, Neurology, № 50, с. 279
https://doi.org/10.1212/WNL.50.1.279 - Maggi, The Italian Longitudinal Study on Aging (ILSA): design and methods, Aging Clin Exp Res, № 6, с. 464
https://doi.org/10.1007/BF03324279 - Fahn, Recent developments in Parkinson's disease, № 2, с. 153
- Norusis MJ SPSS for Windows. Base system user's guide and advanced statistics. Release 6.0 SPSS Inc. 1993
- Fratiglioni, Smoking and Parkinson's and Alzheimer's disease: review of the epidemiological studies, Behav Brain Res, № 113, с. 117
https://doi.org/10.1016/S0166-4328(00)00206-0 - Morens, Evidence against the operation of selective mortality in explaining the association between cigarette smoking and reduced occurrence of idiopathic Parkinson disease, Am J Epidemiol, № 144, с. 400
https://doi.org/10.1093/oxfordjournals.aje.a008941 - Diana, Tobacco smoking and nutrition, Ann NY Acad Sci, № 686, с. 1
https://doi.org/10.1111/j.1749-6632.1993.tb39147.x - Janson, Chronic nicotine treatment counteracts nigral cell loss induced by a partial mesodiencephalic hemitransection: an analysis of the total number and mean volume of neurons and glia in substantia nigra of the male rat, Neuroscience, № 57, с. 931
https://doi.org/10.1016/0306-4522(93)90039-I - James, Genetic and environmental aspects of the role of nicotinic receptors in neurodegenerative disorders: emphasis on Alzheimer's disease and Parkinson's disease, Behav Genet, № 25, с. 149
https://doi.org/10.1007/BF02196924 - Shahi, 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity: partial protection against striato-nigral dopamine depletion in C57BL/6J mice by cigarette smoke exposure and by beta-naphthoflavone-pretreatment, Neurosci Lett, № 127, с. 247
https://doi.org/10.1016/0304-3940(91)90804-3 - Chan, Genetic and environmental risk factors for Parkinson's disease in a Chinese population, J Neurol Neurosurg Psychiatry, № 65, с. 781
https://doi.org/10.1136/jnnp.65.5.781 - Fall, Nutritional and occupational factors influencing the risk of Parkinson's disease: a case-control study in southeastern Sweden, Mov Disord, № 14, с. 28
https://doi.org/10.1002/1531-8257(199901)14:1<28::AID-MDS1007>3.0.CO;2-O - Ritz, Parkinson's disease mortality and pesticide exposure in California 1984-1994, Int J Epidemiol, № 29, с. 323
https://doi.org/10.1093/ije/29.2.323 - Jimenez-Jimenez, Premorbid smoking, alcohol consumption, and coffee drinking habits in Parkinson's disease: a case-control study, Mov Disord, № 7, с. 339
https://doi.org/10.1002/mds.870070407 - Taylor, Environmental, medical, and family history risk factors for Parkinson's disease: a New England-based case control study, Am J Med Genet, № 88, с. 742
https://doi.org/10.1002/(SICI)1096-8628(19991215)88:6<742::AID-AJMG29>3.0.CO;2-# - Kuopio, Environmental risk factors in Parkinson's disease, Mov Disord, № 14, с. 928
https://doi.org/10.1002/1531-8257(199911)14:6<928::AID-MDS1004>3.0.CO;2-Z - Betarbet, Chronic systemic pesticide exposure reproduces features of Parkinson's disease, Nat Neurosci, № 3, с. 1301
https://doi.org/10.1038/81834 - Hart, Parkinson's disease and pesticides (Letter), Lancet, № 1, с. 38
https://doi.org/10.1016/S0140-6736(87)90721-5 - Perry, Cholinergic receptors in cognitive disorders, Can J Neurol Sci, № 13, с. 521
https://doi.org/10.1017/S0317167100037240 - Sanchez-Ramos, Paraquat and Parkinson's disease (Letter), Neurology, № 37, с. 728
https://doi.org/10.1212/WNL.37.4.728 - Le Couteur, Pesticides and Parkinson's disease, Biomed Pharmacother, № 53, с. 122
https://doi.org/10.1016/S0753-3322(99)80077-8 - Bhatt, Acute and reversible parkinsonism due to organophosphate pesticide intoxication: five cases, Neurology, № 52, с. 1467
https://doi.org/10.1212/WNL.52.7.1467 - Menegon, Parkinson's disease, pesticides, and glutathione transferase polymorphisms, Lancet, № 352, с. 1344
https://doi.org/10.1016/S0140-6736(98)03453-9 - Baldereschi, Parkinson's disease and parkinsonism in a longitudinal study. Two-fold higher incidence in men, Neurology, № 55, с. 1358
https://doi.org/10.1212/WNL.55.9.1358 - Sawada, Neuroprotective effects of estradiol in mesencephalic dopaminergic neurons, Neurosci Biobehav Rev, № 24, с. 143
https://doi.org/10.1016/S0149-7634(99)00059-7 - Miller, The impact of gender and estrogen on striatal dopaminergic neurotoxicity, Ann NY Acad Sci, № 844, с. 153
https://doi.org/10.1111/j.1749-6632.1998.tb08230.x - Green, Neuroprotective effects of estrogens: potential mechanisms of action, Int J Dev Neurosci, № 18, с. 347
https://doi.org/10.1016/S0736-5748(00)00017-4 - Sackett, Bias in analytic research, J Chronic Dis, № 32, с. 51
https://doi.org/10.1016/0021-9681(79)90012-2
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Number of citations | 43 |
Number of works in the list of references | 36 |
Journal indexed in Scopus | Yes |
Journal indexed in Web of Science | Yes |