Genetic susceptibility loci, environmental exposures, and Parkinson's disease: A case-control study of gene-environment interactions

被引:21
作者
Chung, Sun Ju [1 ,2 ]
Armasu, Sebastian M. [3 ]
Anderson, Kari J. [3 ]
Biernacka, Joanna M. [3 ]
Lesnick, Timothy G. [3 ]
Rider, David N. [3 ]
Cunningham, Julie M. [4 ]
Ahlskog, J. Eric [2 ]
Frigerio, Roberta [5 ]
Maraganore, Demetrius M. [6 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul, South Korea
[2] Mayo Clin, Dept Neurol, Rochester, MN USA
[3] Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
[4] Mayo Clin, Dept Lab Med, Rochester, MN USA
[5] NorthShore Univ HealthSyst, Res Inst, Evanston, IL 60201 USA
[6] NorthShore Univ HealthSyst, Neurol Inst, Dept Neurol, Evanston, IL 60201 USA
关键词
Parkinson's disease; Genes; Environment; Interactions; ALPHA-SYNUCLEIN GENE; LRRK2; MUTATIONS; ALCOHOL; COFFEE; CONSUMPTION; PATHOLOGY; DEMENTIA; SMOKING; MAPT;
D O I
10.1016/j.parkreldis.2013.02.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Prior studies causally linked mutations in SNCA, MAPT, and LRRK2 genes with familial Parkinsonism. Genome-wide association studies have demonstrated association of single nucleotide polymorphisms (SNPs) in those three genes with sporadic Parkinson's disease (PD) susceptibility worldwide. Here we investigated the interactions between SNPs in those three susceptibility genes and environmental exposures (pesticides application, tobacco smoking, coffee drinking, and alcohol drinking) also associated with PD susceptibility. Methods: Pairwise interactions between environmental exposures and 18 variants (16 SNPs and two variable number tandem repeats, or "VNTRs") in SNCA, MAPT and LRRK2, were investigated using data from 1098 PD cases from the upper Midwest, USA and 1098 matched controls. Environmental exposures were assessed using a validated telephone interview script. Results: Five pairwise interactions had uncorrected P-values < 0.05. These included pairings of pesticides x SNCA rs3775423 or MAPT rs4792891, coffee drinking x MAPT H1/H2 haplotype or MAPT rs16940806, and alcohol drinking x MAPT rs2435211. None of these interactions remained significant after Bonferroni correction. Secondary analyses in strata defined by type of control (sibling or unrelated), sex, or age at onset of the case also did not identify significant interactions after Bonferroni correction. Conclusions: This study documented limited pairwise interactions between established genetic and environmental risk factors for PD; however, the associations were not significant after correction for multiple testing. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:595 / 599
页数:5
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