Association of ACTN3 R577X but not ACE I/D gene variants with elite rugby union player status and playing position.

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

Fersiynau electronig

Dangosydd eitem ddigidol (DOI)

  • Shane M. Heffernan
    MMU
  • Liam P. Kilduff
    Swansea University
  • Robert M. Erskine
    Centre for Public Health, Liverpool John Moores University
  • Stephen H. Day
    MMU
  • Jamie S. McPhee
    MMU
  • Gerald Eugene McMahon
    MMU
  • Georgina Kate Stebbings
    MMU
  • Joshua P.H. Neale
    MMU
  • Sarah J. Lockey
    MMU
  • William J. Ribbans
    University of Northampton
  • Christian Cook
  • Beth Vance
    Institute of Health and Wellbeing, University of Glasgow, Glasgow, Scotland
  • Stuart M. Raleigh
    University of Northampton
  • Craig Roberts
    South African Rugby Union
  • Mark A. Bennett
    Swansea University
  • Guan Wang
    University of Brighton
  • Mark Collins
    University of Cape Town
  • Yannis P. Pitsiladis
    University of Brighton
  • Alun G. Williams
    MMU
We aimed to quantify the ACE I/D and ACTN3 R577X (rs1815739) genetic variants in elite rugby athletes (rugby union and league), compare genotype frequencies to controls and between playing positions. The rugby athlete cohort consisted of 507 Caucasian men, including 431 rugby union athletes that for some analyses were divided into backs and forwards and into specific positional groups: front five, back row, half backs, centers and back three. Controls were 710 Caucasian men and women. Real-time PCR of genomic DNA was used to determine genotypes using TaqMan probes and groups were compared using Chi-square and odds ratio (OR) statistics. Correction of p-values for multiple comparisons was according to Benjamini-Hochberg. There was no difference in ACE I/D genotype between groups. ACTN3 XX genotype tended to be underrepresented in rugby union backs (15.7%) compared to forwards (24.8%; P=0.06). Interestingly, the 69 back three players (wings and full backs) in rugby union included only six XX genotype individuals (8.7%), with the R allele more common in the back three (68.8%) than controls (58.0%; χ2=6.672, P=0.04; OR=1.60) and forwards (47.5%; χ2=11.768, P=0.01; OR=2.00). Association of ACTN3 R577X with playing position in elite rugby union athletes suggests inherited fatigue resistance is more prevalent in forwards while inherited sprint ability is more prevalent in backs, especially wings and full backs. These results also demonstrate the advantage of focusing genetic studies on a large cohort within a single sport, especially when intra-sport positional differences exist, instead of combining several sports with varied demands and athlete characteristics
Iaith wreiddiolSaesneg
Tudalennau (o-i)196-201
CyfnodolynPhysical Genomics
Cyfrol48
Rhif y cyfnodolyn3
Dyddiad ar-lein cynnar12 Ion 2016
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - 1 Maw 2016
Gweld graff cysylltiadau