Educational attainment protects against epilepsy independent of cognitive function: A Mendelian randomization study

Epilepsia. 2021 Jun;62(6):1362-1368. doi: 10.1111/epi.16894. Epub 2021 Apr 5.

Abstract

Objective: Observational studies have suggested that increased levels of education and cognition are associated with a reduced risk of epilepsy. However, such associations are easily influenced by confounding or reverse causality. Hence, we conducted a two-sample univariable and multivariable Mendelian randomization (MR) to estimate the total and independent causal effects of educational attainment and cognition on epilepsy risk.

Methods: We performed MR estimates on International League Against Epilepsy (ILAE) Consortium genome-wide association study (GWAS) data (15 212 epilepsy cases and 29 677 controls). We then validated the results in FinnGen (3424 epilepsy cases and 110 963 controls) and applied meta-analysis to all the results.

Results: In the meta-analysis of the ILAE and FinnGen results, genetically determined increased educational attainment was associated with a reduced risk of epilepsy (odds ratio [OR] 0.84, 95% confidence interval [CI] 0.80-0.88; P < .001). Similarly, genetically determined increased cognitive function was associated with a reduced risk of epilepsy (OR 0.94, 95% CI 0.88-1.00, P = .043). When educational attainment and cognitive function were included in the same multivariable MR, only educational attainment was still associated with a reduced risk of epilepsy (OR 0.88, 95% CI 0.81-0.95, P = .002).

Significance: This MR study provides evidence to support that increased educational attainment can reduce the risk of developing epilepsy independent of cognitive function.

Keywords: Mendelian randomization; cognitive function; educational attainment; epilepsy.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Causality
  • Cognition*
  • Cohort Studies
  • Educational Status*
  • Epilepsy / genetics
  • Epilepsy / prevention & control*
  • Epilepsy / psychology*
  • Genome-Wide Association Study
  • Humans
  • Mendelian Randomization Analysis
  • Neuropsychological Tests
  • Polymorphism, Single Nucleotide
  • Risk Assessment
  • White People