An exploratory analysis on gene-environment interactions for Parkinson disease

被引:38
作者
Gao, Jianjun [1 ]
Nalls, Michael A. [2 ]
Shi, Min [3 ]
Joubert, Bonnie R. [1 ]
Hernandez, Dena G. [2 ]
Huang, Xuemei [4 ]
Hollenbeck, Albert [5 ]
Singleton, Andrew B. [2 ]
Chen, Honglei [1 ]
机构
[1] NIEHS, Epidemiol Branch, Res Triangle Pk, NC 27709 USA
[2] NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
[3] NIEHS, Biostat Branch, Res Triangle Pk, NC 27709 USA
[4] Penn State Univ, Milton S Hershey Med Ctr, Dept Neurol, Hershey, PA 17033 USA
[5] Amer Assoc Retired Persons, Washington, DC USA
基金
美国国家卫生研究院;
关键词
Parkinson disease (PD); Gene-environment interactions; Genome-wide association study; GENOME-WIDE ASSOCIATION; RISK; VARIANTS;
D O I
10.1016/j.neurobiolaging.2012.06.007
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Little is known about gene-environment interactions in Parkinson disease (PD). We examined potential interactions of smoking and caffeine intake with 10 genome-wide association studies single nucleotide polymorphisms (SNPs) at or near the SNCA, MAPT, LRRK2, and HLA loci among 584 PD patients and 1571 controls. The main effects of these SNPs and environmental exposures were consistent with previous reports. Family history of PD was associated with PD risk (odds ratio = 2.71, 95% confidence interval, 1.97-3.74), which was little affected by further adjustment for these SNPs and environmental exposures. Overall, we did not find significant interactions of either smoking or caffeine intake with these SNPs. However, with a combined smoking and caffeine intake exposure, we found a significant interaction with rs2896905 at SLC2A13, near LRRK2 (p uncorrected = 0.0008). Each A allele was associated with a 35% higher PD risk among never smokers with low caffeine intake, but with a 32% lower risk among smokers with high caffeine intake. This study provides preliminary evidence of a potential gene-environment interaction for PD, which should be investigated in future studies. Published by Elsevier Inc.
引用
收藏
页码:2528.e1 / 2528.e6
页数:6
相关论文
共 50 条
[21]   Gene-Environment Interactions and Cardiovascular Risk Factors [J].
Ordovas, Jose M. .
REVISTA ESPANOLA DE CARDIOLOGIA, 2009, :39B-51B
[22]   Gene-Environment Interactions and Cardiovascular Risk Factors [J].
Ordovas, Jose M. .
REVISTA ESPANOLA DE CARDIOLOGIA, 2009, :39B-51B
[23]   Analysis of Gene-Environment Interactions Related to Developmental Disorders [J].
Nishimura, Yuhei ;
Kurosawa, Kenji .
FRONTIERS IN PHARMACOLOGY, 2022, 13
[24]   Gene-environment interactions in Alzheimer disease: the emerging role of epigenetics [J].
Migliore, Lucia ;
Coppede, Fabio .
NATURE REVIEWS NEUROLOGY, 2022, 18 (11) :643-660
[25]   An update on the rotenone models of Parkinson's disease: Their ability to reproduce the features of clinical disease and model gene-environment interactions [J].
Johnson, Michaela E. ;
Bobrovskaya, Larisa .
NEUROTOXICOLOGY, 2015, 46 :101-116
[26]   Identifying genes for primary hypertension: methodological limitations and gene-environment interactions [J].
Franks, P. W. .
JOURNAL OF HUMAN HYPERTENSION, 2009, 23 (04) :227-237
[27]   Conditional Inference Tree for Multiple Gene-Environment Interactions on Myocardial Infarction [J].
Wu, Zhijun ;
Su, Xiuxiu ;
Sheng, Haihui ;
Chen, Yanjia ;
Gao, Xiang ;
Bao, Le ;
Jin, Wei .
ARCHIVES OF MEDICAL RESEARCH, 2017, 48 (06) :546-552
[28]   Semiparametric Bayesian variable selection for gene-environment interactions [J].
Ren, Jie ;
Zhou, Fei ;
Li, Xiaoxi ;
Chen, Qi ;
Zhang, Hongmei ;
Ma, Shuangge ;
Jiang, Yu ;
Wu, Cen .
STATISTICS IN MEDICINE, 2020, 39 (05) :617-638
[29]   Gene-environment interactions in esophageal cancer [J].
Matejcic, Marco ;
Parker, M. Iqbal .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2015, 52 (05) :211-231
[30]   Gene-Environment Interactions on Growth Trajectories [J].
Wang, Shuang ;
Xiong, Wei ;
Ma, Weiping ;
Chanock, Stephen ;
Jedrychowski, Wieslaw ;
Wu, Rongling ;
Perera, Frederica P. .
GENETIC EPIDEMIOLOGY, 2012, 36 (03) :206-213