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    Evaluation of a 7-gene genetic profile for athletic endurance phenotype in ironman championship triathletes

    Access Status
    Open access via publisher
    Authors
    Grealy, R.
    Herruer, J.
    Smith, C.
    Hiller, D.
    Haseler, Luke
    Griffiths, L.
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Grealy, R. and Herruer, J. and Smith, C. and Hiller, D. and Haseler, L. and Griffiths, L. 2015. Evaluation of a 7-gene genetic profile for athletic endurance phenotype in ironman championship triathletes. PLoS ONE. 10 (12).
    Source Title
    PLoS ONE
    DOI
    10.1371/journal.pone.0145171
    ISSN
    1932-6203
    School
    School of Physiotherapy and Exercise Science
    URI
    http://hdl.handle.net/20.500.11937/58296
    Collection
    • Curtin Research Publications
    Abstract

    © 2015 Grealy et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Polygenic profiling has been proposed for elite endurance performance, using an additive model determining the proportion of optimal alleles in endurance athletes. To investigate this model's utility for elite triathletes, we genotyped seven polymorphisms previously associated with an endurance polygenic profile (ACE Ins/Del, ACTN3 Arg577Ter, AMPD1 Gln12Ter, CKMM 1170bp/985+185bp, HFEHis63Asp, GDF8 Lys153Arg and PPARGC1A Gly482Ser) in a cohort of 196 elite athletes who participated in the 2008 Kona Ironman championship triathlon. Mean performance time (PT) was not significantly different in individual marker analysis. Age, sex, and continent of origin had a significant influence on PT and were adjusted for. Only the AMPD1 endurance-optimal Gln allele was found to be significantly associated with an improvement in PT (model p = 5.79 × 10- 17 , AMPD1 genotype p = 0.01). Individual genotypes were combined into a total genotype score (TGS);TGS distribution ranged from 28.6 to 92.9, concordant with prior studies in endurance athletes (mean±SD: 60.75±12.95). TGS distribution was shifted toward higher TGS in the top 10% of athletes, though the mean TGS was not significantly different (p = 0.164) and not significantly associated with PT even when adjusted for age, sex, and origin. Receiver operating characteristic curve analysis determined that TGS alone could not significantly predict athlete finishing time with discriminating sensitivity and specificity for three outcomes (less than median PT, less than mean PT, or in the top 10%), though models with the age, sex, continent of origin, and either TGS orAMPD1 genotype could. These results suggest three things: that more sophisticated genetic models may be necessary to accurately predict athlete finishing time in endurance events; that non-genetic factors such as training are hugely influential and should be included in genetic analyses to prevent confounding; and that large collaborations may be necessary to obtain sufficient sample sizes for powerful and complex analyses of endurance performance.

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