Genetics Influence Neurocognitive Performance at Baseline but Not Concussion History in Collegiate Student-Athletes

Clin J Sport Med. 2018 Mar;28(2):125-129. doi: 10.1097/JSM.0000000000000443.

Abstract

Objective: This study investigates 4 single-nucleotide polymorphisms [Apolipoprotein E (APOE), APOE promoter, catechol-O-methyl transferase (COMT), and dopamine D2 receptor] that have been implicated in concussion susceptibility and/or cognitive ability in collegiate student-athletes.

Design: Cross-sectional study.

Setting: Neuroscience laboratory at Elon University.

Participants: Two hundred fifty division I collegiate student-athletes (66 women, 184 men) from various sports.

Intervention: All participants completed Immediate Postconcussion Assessment and Cognitive Testing (ImPACT) testing at baseline concussion testing and had a buccal swab taken for DNA for genotyping.

Main outcome measures: Self-reported history of concussions and neurocognitive performance were taken from ImPACT.

Results: Individuals carrying an ε4 allele in their APOE gene had a significantly slower reaction time (P = 0.001). Individuals homozygous for the Val allele of the COMT gene showed significantly worse impulse control scores (P = 0.014). None of the genotypes were able to predict self-reported concussion history in collegiate student-athletes.

Conclusions: These results indicate that certain genotypes may influence performance on cognitive testing at baseline and that the APOE genotypes may not influence concussion susceptibility as suggested by past studies.

MeSH terms

  • Adolescent
  • Apolipoproteins E / genetics*
  • Athletes
  • Brain Concussion / psychology*
  • Catechol O-Methyltransferase / genetics*
  • Cognition*
  • Cross-Sectional Studies
  • Female
  • Genotype
  • Humans
  • Male
  • Neuropsychological Tests
  • Polymorphism, Single Nucleotide*
  • Promoter Regions, Genetic
  • Reaction Time
  • Receptors, Dopamine D2 / genetics*
  • Self Report
  • Students
  • Young Adult

Substances

  • ApoE protein, human
  • Apolipoproteins E
  • DRD2 protein, human
  • Receptors, Dopamine D2
  • COMT protein, human
  • Catechol O-Methyltransferase