University of Hertfordshire

Documents

  • M Antrobus
  • Jon Brazier
  • A Herbert
  • G Stebbings
  • S Day
  • S Heffernan
  • L Kilduff
  • Tom Cullen
  • Stuart Raleigh
  • R Erskine
  • A Williams
View graph of relations
Original languageEnglish
Publication statusPublished - 28 Oct 2020
Event25th Annual Congress of the European College of Sports Science -
Duration: 28 Oct 202030 Oct 2020

Conference

Conference25th Annual Congress of the European College of Sports Science
Period28/10/2030/10/20

Abstract

INTRODUCTION:
Incidence of and recovery from concussion have a substantial genetic component that probably involves the interaction of multiple genes. COMT (rs4680) AA carriers in youth and professional South African rugby athletes (RA) were ~3-fold more likely to have a history of concussion (Mc Fie et al., 2018). Similarly, BDNF-AS (rs6265) AA genotype has been associated with a higher risk of sustaining a concussion and associated with poorer outcomes post-concussion (Dretsch et al., 2016; Narayanan et al., 2016). Lower cerebral blood flow has been reported in NOS3 (rs2070744) C-allele carriers with traumatic brain injury, postulated to negatively affect a concussed individual during recovery (Robertson et al., 2011). As rugby has one of the highest incidences of concussion in sport (Williams et al., 2013), it was hypothesised that COMT AA, BDNF-AS AA and NOS3 CC genotypes would be less prevalent in elite rugby athletes because, previously associated with increased risk, they would be less compatible with achieving elite athlete status.
METHODS:
Participants were from the RugbyGene project, comprising elite Caucasian RA (648 men; mean (SD) height 1.85 (0.07) m, mass 101 (12) kg, age 28 (7) yr) competing at an elite level in rugby union (n = 550) and rugby league (n = 98) in the UK, Ireland, Italy and South Africa. Non-athlete participants (NA) were 803 Caucasian men and women (58% female, height 1.69 (0.10) m, mass 72 (14) kg, age 41 (23) yr). PCR of genomic DNA was used to determine genotypes using TaqMan probes, then groups were compared using χ2 and odds ratio (OR) statistics. Alpha was set at 0.05.
RESULTS:
All genotype data were in Hardy-Weinberg equilibrium. For COMT, the risk genotype (AA) was underrepresented in RA (25%) compared to NA (30%) and GG more common in RA (26%) than NA (22%) (χ2 = 6.129, P = .047; GG genotype frequency OR 2.43, 95% confidence intervals (CI) = 1.88-3.22). For BDNF-AS, there were no differences in genotype frequencies between RA and NA (4% AA genotype in both cohorts, χ2 = .311, P = .856). There were also no differences in NOS3 genotype frequencies (16% CC genotype in RA and 17% in NA, χ2 = 1.040, P = .595).
CONCLUSION:
The COMT AA genotype is 5% less common in elite rugby athletes than non-athletes. Therefore, carrying at least one rs4680 G allele, perhaps via a lower risk of experiencing concussion, a greater ability to recover from concussions or altered impulsivity and risk-taking behaviour, appears to increase the probability of reaching elite level in a sport with a high risk of concussion.

ID: 22879268