Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study

Abstract Previous observational studies have identified correlations between Parkinson’s disease (PD) risk and lifestyle factors. However, whether or not those associations are causal remains unclear. To infer causality between PD risk and smoking or alcohol intake, we conducted a two-sample Mendeli...

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Main Authors: Carmen Domínguez-Baleón, Jue-Sheng Ong, Clemens R. Scherzer, Miguel E. Rentería, Xianjun Dong
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-93105-y
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spelling doaj-d5332b35691d4aecb36f96d210ba760a2021-07-11T11:28:51ZengNature Publishing GroupScientific Reports2045-23222021-07-0111111410.1038/s41598-021-93105-yUnderstanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization studyCarmen Domínguez-Baleón0Jue-Sheng Ong1Clemens R. Scherzer2Miguel E. Rentería3Xianjun Dong4Center for Advanced Parkinson Research and Precision Neurology Program, Brigham & Women’s Hospital, Harvard Medical SchoolDepartment of Genetics & Computational Biology, QIMR Berghofer Medical Research InstituteCenter for Advanced Parkinson Research and Precision Neurology Program, Brigham & Women’s Hospital, Harvard Medical SchoolCenter for Advanced Parkinson Research and Precision Neurology Program, Brigham & Women’s Hospital, Harvard Medical SchoolCenter for Advanced Parkinson Research and Precision Neurology Program, Brigham & Women’s Hospital, Harvard Medical SchoolAbstract Previous observational studies have identified correlations between Parkinson’s disease (PD) risk and lifestyle factors. However, whether or not those associations are causal remains unclear. To infer causality between PD risk and smoking or alcohol intake, we conducted a two-sample Mendelian randomization study using genome-wide association study summary statistics from the GWAS & Sequencing Consortium of Alcohol and Nicotine use study (1.2 million participants) and the latest meta-analysis from the International Parkinson’s Disease Genomics Consortium (37,688 PD cases and 18,618 proxy-cases). We performed sensitivity analyses, including testing for pleiotropy with MR-Egger and MR-PRESSO, and multivariable MR modeling to account for the genetic effects of competing substance use traits on PD risk. Our results revealed causal associations of alcohol intake (OR 0.79; 95% CI 0.65–0.96; p = 0.021) and smoking continuation (which compares current vs. former smokers) (OR 0.64; 95% CI 0.46–0.89; p = 0.008) with lower PD risk. Multivariable MR analyses showed that the causal association between drinks per week and PD is unlikely due to confounding by smoking behavior. Finally, frailty analyses suggested that the causal effects of both alcohol intake and smoking continuation on PD risk estimated from MR analysis are not explained by the presence of survival bias alone. Our findings support the role of smoking as a protective factor against PD, but only when comparing current vs. former smokers. Similarly, increased alcohol intake had a protective effect over PD risk, with the alcohol dehydrogenase 1B (ADH1B) locus as a potential candidate for further investigation of the mechanisms underlying this association.https://doi.org/10.1038/s41598-021-93105-y
collection DOAJ
language English
format Article
sources DOAJ
author Carmen Domínguez-Baleón
Jue-Sheng Ong
Clemens R. Scherzer
Miguel E. Rentería
Xianjun Dong
spellingShingle Carmen Domínguez-Baleón
Jue-Sheng Ong
Clemens R. Scherzer
Miguel E. Rentería
Xianjun Dong
Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study
Scientific Reports
author_facet Carmen Domínguez-Baleón
Jue-Sheng Ong
Clemens R. Scherzer
Miguel E. Rentería
Xianjun Dong
author_sort Carmen Domínguez-Baleón
title Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study
title_short Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study
title_full Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study
title_fullStr Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study
title_full_unstemmed Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study
title_sort understanding the effect of smoking and drinking behavior on parkinson's disease risk: a mendelian randomization study
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-07-01
description Abstract Previous observational studies have identified correlations between Parkinson’s disease (PD) risk and lifestyle factors. However, whether or not those associations are causal remains unclear. To infer causality between PD risk and smoking or alcohol intake, we conducted a two-sample Mendelian randomization study using genome-wide association study summary statistics from the GWAS & Sequencing Consortium of Alcohol and Nicotine use study (1.2 million participants) and the latest meta-analysis from the International Parkinson’s Disease Genomics Consortium (37,688 PD cases and 18,618 proxy-cases). We performed sensitivity analyses, including testing for pleiotropy with MR-Egger and MR-PRESSO, and multivariable MR modeling to account for the genetic effects of competing substance use traits on PD risk. Our results revealed causal associations of alcohol intake (OR 0.79; 95% CI 0.65–0.96; p = 0.021) and smoking continuation (which compares current vs. former smokers) (OR 0.64; 95% CI 0.46–0.89; p = 0.008) with lower PD risk. Multivariable MR analyses showed that the causal association between drinks per week and PD is unlikely due to confounding by smoking behavior. Finally, frailty analyses suggested that the causal effects of both alcohol intake and smoking continuation on PD risk estimated from MR analysis are not explained by the presence of survival bias alone. Our findings support the role of smoking as a protective factor against PD, but only when comparing current vs. former smokers. Similarly, increased alcohol intake had a protective effect over PD risk, with the alcohol dehydrogenase 1B (ADH1B) locus as a potential candidate for further investigation of the mechanisms underlying this association.
url https://doi.org/10.1038/s41598-021-93105-y
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