Gene-Environment Interaction in Parkinson's Disease: Coffee, ADORA2A, and CYP1A2

被引:34
|
作者
Chuang, Yu-Hsuan [1 ]
Lill, Christina M. [6 ]
Lee, Pei-Chen [9 ]
Hansen, Johnni [10 ]
Lassen, Christina F. [10 ]
Bertram, Lars [7 ,8 ,11 ]
Greene, Naomi [1 ]
Sinsheimer, Janet S. [2 ,4 ]
Ritz, Beate [1 ,3 ,5 ]
机构
[1] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Dept Epidemiol, 650 Charles E Young Dr, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Dept Biostat, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Dept Environm Hlth Sci, Los Angeles, CA USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet & Biomathemat, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[6] Univ Lubeck, Inst Neurogenet, Genet & Mol Epidemiol Grp, Lubeck, Germany
[7] Univ Lubeck, Inst Neurogenet, Interdisciplinary Platform Genome Analyt LIGA, Lubeck, Germany
[8] Univ Lubeck, Inst Integrat & Expt Genom, Interdisciplinary Platform Genome Analyt LIGA, Lubeck, Germany
[9] Natl Taipei Univ Nursing Hlth Sci, Coll Healthcare Adm & Management, Dept Hlth Care Management, Taipei, Taiwan
[10] Danish Canc Soc, Res Ctr, Copenhagen, Denmark
[11] Imperial Coll Sci Technol & Med, Fac Med, Sch Publ Hlth, London, England
基金
美国国家卫生研究院;
关键词
Parkinson's disease; Caffeine; Adenosine A2A receptor (ADORA2A); Cytochrome P450 1A2 (CYP1A2); Meta-analysis; RECEPTOR INTERACTIONS; ADENOSINE RECEPTOR; CAFFEINE; RISK; ASSOCIATION; SMOKING; NEUROPROTECTION; POLYMORPHISMS; CONNECTION; MODEL;
D O I
10.1159/000450855
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background and Purpose: Drinking caffeinated coffee has been reported to provide protection against Parkinson's disease (PD). Caffeine is an adenosine A2A receptor (encoded by the gene ADORA2A) antagonist that increases dopaminergic neurotransmission and Cytochrome P450 1A2 (gene: CYP1A2) metabolizes caffeine; thus, gene polymorphisms in ADORA2A and CYP1A2 may influence the effect coffee consumption has on PD risk. Methods: In a population-based case-control study (PASIDA) in Denmark (1,556 PD patients and 1,606 birth year-and gender-matched controls), we assessed interactions between lifetime coffee consumption and 3 polymorphisms in ADORA2A and CYP1A2 for all subjects, and incident and prevalent PD cases separately using logistic regression models. We also conducted a meta-analysis combining our results with those from previous studies. Results: We estimated statistically significant interactions for ADORA2A rs5760423 and heavy vs. light coffee consumption in incident (OR interaction = 0.66 [95% CI 0.46-0.94], p = 0.02) but not prevalent PD. We did not observe interactions for CYP1A2 rs762551 and rs2472304 in incident or prevalent PD. In meta-analyses, PD associations with daily coffee consumption were strongest among carriers of variant alleles in both ADORA2A and CYP1A2. Conclusion: We corroborated results from a previous report that described interactions between ADORA2A and CYP1A2 polymorphisms and coffee consumption. Our results also suggest that survivor bias may affect results of studies that enroll prevalent PD cases. (C) 2017 S. Karger AG, Basel
引用
收藏
页码:192 / 200
页数:9
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