Gene-toxin interaction as a putative risk factor for Parkinson's disease with dementia

被引:33
作者
Hubble, JP
Kurth, JH
Glatt, SL
Kurth, MC
Schellenberg, GD
Hassanein, RES
Lieberman, A
Koller, WC
机构
[1] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66103 USA
[2] Univ Kansas, Med Ctr, Dept Biometry, Kansas City, KS 66103 USA
[3] Barrow Neurol Inst, Dept Neurol, Phoenix, AZ 85013 USA
[4] Vet Affairs Puget Sound Hlth Care Syst, Ctr Geriatr Res Educ & Clin, Seattle, WA USA
关键词
Parkinson's disease; dementia; cytochrome P-450; pesticides;
D O I
10.1159/000026159
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
We had previously examined environmental, sociodemographic and clinical variables as predictors for Parkinson's disease with dementia (PD + D) and found that lower educational attainment, greater motor impairment and advanced age at disease onset were more common in PD + D than in subjects with Parkinson's disease without dementia (PD - D), We now explore the hypothesis that genetic traits coupled with nongenetic factors may raise the risk of development of PD + D, The study cohort of 43 PD + D and 51 PD - D subjects was analyzed examining environmental, sociodemographic and clinical variables along with 3 candidate gene markers: poor debrisoquine metabolizer allele (CYP 2D6 29B+), monoamine oxidase B allele 1, and apolipoprotein E epsilon 4 allele, Variables were initially entered into a multivariate model singly. Again lower education, age at onset and motor impairment appeared as predictors of PD + D while other variables (including allele status) failed to emerge as significant individual risk factors for dementia, We then examined environmental and genetic variables analyzed in tandem to look for potential variable interactions. Subjects who had pesticide exposure and at least I copy of the CYP 2D6 29B+ allele had 83 % predicted probability of PD + D (stepwise logistic regression model: p = 0.0491), This case-control study provides preliminary evidence that a gene-toxin interaction may play an etiological role in PD + D, Further assessment of the role of these putative risk factors in incident dementia in PD is indicated.
引用
收藏
页码:96 / 104
页数:9
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