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Exercise genetics: seeking clarity from noise
  1. Craig Pickering1,2,
  2. John Kiely1
  1. 1 School of Sport and Wellbeing, Institute of Coaching and Performance, University of Central Lancashire, Preston, UK
  2. 2 Exercise and Nutritional Genomics Research Centre, DNAFit Ltd, London, UK
  1. Correspondence to Mr Craig Pickering; craig{at}dnafit.com

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The potential of recent advances in genetics research to supplement elite sport decision-making has potentially extensive implications, but remains highly controversial. One potential application is the use of genetic information to enhance exercise prescription, thereby positively influencing athletic performance and public health domains. Recent research suggests that this is both feasible and potentially beneficial.1 2 However, such an effective use of genetic information requires a clear understanding of the mechanism by which each reported single nucleotide polymorphism (SNP) mediates physical performance. In the absence of such a clear, mechanistic explanation, we are left with vague associations without causative roots. While uncovering gene associations is necessary, it is not sufficient to presume causation. Given the complex entangled routes through which genes and environment interact to express phenotype, superficial association-based logical inferences are likely to be misleading.

Association or causation?

As an example, within the HEalth, RIsk factors, exercise Training And GEnetics (HERITAGE) Family Study, variation in CREB1 (rs2253206) predicted heart rate (HR) response to exercise.3 Specifically, the A allele associated with a smaller reduction in HR during a submaximal exercise test following training, with the proposed mechanism relating to long-term cardiac memory. …

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