Causal relationship between addictive behaviors and epilepsy risk: A mendelian randomization study.


Journal

Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858

Informations de publication

Date de publication:
10 2023
Historique:
received: 02 06 2023
revised: 27 08 2023
accepted: 05 09 2023
medline: 13 10 2023
pubmed: 20 9 2023
entrez: 20 9 2023
Statut: ppublish

Résumé

Previous studies have reported inconsistent results regarding the potential relationships between addictive behaviors and the risk of epilepsy. To assess whether genetically predicted addictive behaviors are causally associated with the risk of epilepsy outcomes. The causation between five addictive behaviors (including cigarettes per day, alcoholic drinks per week, tea intake, coffee intake, and lifetime cannabis use) and epilepsy was evaluated by using a two-sample Mendelian Randomization (MR) analysis. The inverse-variance weighted (IVW) method was used as the primary outcome. The other MR analysis methods (MR Egger, weighted median, simulation extrapolation corrected MR-Egger, and Mendelian Randomization Pleiotropy Residual Sum and Outlier (MR-PRESSO)) were performed to complement IVW. In addition, the robustness of the MR analysis results was assessed by leave-one-out analysis. The IVW analysis method indicated an approximately 20% increased risk of epilepsy per standard deviation increase in lifetime cannabis use (odds ratio [OR], 1.20; 95% confidence interval [CI]), 1.02-1.42, P = 0.028). However, there is no causal association between the other four addictive behaviors and the risk of epilepsy (cigarettes per day: OR, 1.04; 95% CI, 0.92-1.18, P = 0.53; alcoholic drinks per week: OR, 1.31; 95% CI, 0.93-1.84, P = 0.13; tea intake: OR, 1.15; 95% CI, 0.84-1.56, P = 0.39; coffee intake: OR, 0.86; 95% CI, 0.59-1.23, P = 0.41). The other MR analysis methods and further leave-one-out sensitivity analysis suggested the results were robust. This MR study indicated a potential genetically predicted causal association between lifetime cannabis use and higher risk of epilepsy. As for the other four addictive behaviors, no evidence of a causal relationship with the risk of epilepsy was found in this study.

Sections du résumé

BACKGROUND
Previous studies have reported inconsistent results regarding the potential relationships between addictive behaviors and the risk of epilepsy.
OBJECTIVE
To assess whether genetically predicted addictive behaviors are causally associated with the risk of epilepsy outcomes.
METHODS
The causation between five addictive behaviors (including cigarettes per day, alcoholic drinks per week, tea intake, coffee intake, and lifetime cannabis use) and epilepsy was evaluated by using a two-sample Mendelian Randomization (MR) analysis. The inverse-variance weighted (IVW) method was used as the primary outcome. The other MR analysis methods (MR Egger, weighted median, simulation extrapolation corrected MR-Egger, and Mendelian Randomization Pleiotropy Residual Sum and Outlier (MR-PRESSO)) were performed to complement IVW. In addition, the robustness of the MR analysis results was assessed by leave-one-out analysis.
RESULTS
The IVW analysis method indicated an approximately 20% increased risk of epilepsy per standard deviation increase in lifetime cannabis use (odds ratio [OR], 1.20; 95% confidence interval [CI]), 1.02-1.42, P = 0.028). However, there is no causal association between the other four addictive behaviors and the risk of epilepsy (cigarettes per day: OR, 1.04; 95% CI, 0.92-1.18, P = 0.53; alcoholic drinks per week: OR, 1.31; 95% CI, 0.93-1.84, P = 0.13; tea intake: OR, 1.15; 95% CI, 0.84-1.56, P = 0.39; coffee intake: OR, 0.86; 95% CI, 0.59-1.23, P = 0.41). The other MR analysis methods and further leave-one-out sensitivity analysis suggested the results were robust.
CONCLUSION
This MR study indicated a potential genetically predicted causal association between lifetime cannabis use and higher risk of epilepsy. As for the other four addictive behaviors, no evidence of a causal relationship with the risk of epilepsy was found in this study.

Identifiants

pubmed: 37729683
pii: S1525-5050(23)00362-1
doi: 10.1016/j.yebeh.2023.109443
pii:
doi:

Substances chimiques

Coffee 0
Cannabinoid Receptor Agonists 0
Tea 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

109443

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Zhen Liang (Z)

Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China.

Lin Qiu (L)

Department of South Lake Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China.

Yingyue Lou (Y)

Department of Rehabilitation, The Second Hospital of Jilin University, Changchun, Jilin Province, China.

Zhaoshi Zheng (Z)

Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China.

Qi Guo (Q)

Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China.

Qing Zhao (Q)

Department of South Lake Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China. Electronic address: zhaoqing@jlu.edu.cn.

Songyan Liu (S)

Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China. Electronic address: liu_sy@jlu.edu.cn.

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Classifications MeSH