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The individual and combined influence of ACE and ACTN3 genotypes on muscle phenotypes before and after strength training

Authors

  • R. M. Erskine,

    Corresponding author
    1. Research Institute for Sport and Exercise Sciences, Liverpool John Moores University, Liverpool, UK
    2. Centre for Genomic Research into Exercise, Performance and Health, Manchester Metropolitan University, Crewe, UK
    • Corresponding author: Robert M. Erskine, PhD, School of Sport and Exercise Sciences, Liverpool John Moores University, Liverpool, L3 3AH, UK. E-mail:r.m.erskine@ljmu.ac.uk

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  • A. G. Williams,

    1. Centre for Genomic Research into Exercise, Performance and Health, Manchester Metropolitan University, Crewe, UK
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  • D. A. Jones,

    1. Institute for Biomedical Research into Human Movement and Health, Faculty of Science and Engineering, Manchester Metropolitan University, Manchester, UK
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  • C. E. Stewart,

    1. Research Institute for Sport and Exercise Sciences, Liverpool John Moores University, Liverpool, UK
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  • H. Degens

    1. Institute for Biomedical Research into Human Movement and Health, Faculty of Science and Engineering, Manchester Metropolitan University, Manchester, UK
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Abstract

Alternative measures of muscle size, strength, and power to those used in previous studies could help resolve the controversy surrounding associations between polymorphisms of the angiotensin-I converting enzyme (ACE) and α-actinin-3 (ACTN3) genes and skeletal muscle phenotypes, and the responses to resistance training (RT). To this end, we measured quadriceps femoris muscle volume (Vm), physiological cross-sectional area (PCSA), maximum isometric force (Ft), specific force (Ft per unit PCSA), maximum isoinertial strength (1-RM), and maximum power (Wmax; n = 40) before and after 9-week knee extension RT in 51 previously untrained young men, who were genotyped for the ACE I/D and ACTN3 R577X polymorphisms. ACTN3 R-allele carriers had greater Vm, 1-RM, and Wmax than XX homozygotes at baseline (all P < 0.05), but responses to RT were independent of ACTN3 genotype (all P > 0.05). Muscle phenotypes were independent of ACE genotype before (all P > 0.05) and after RT (all P > 0.01). However, people with the “optimal” ACE+ACTN3 genotype combination had greater baseline 1-RM and Wmax compared to those with the “suboptimal” profile (both P < 0.0125). We show for the first time that the ACTN3 R577X polymorphism is associated with human Vm and (independently and in combination with the ACE I/D polymorphism) influences 1-RM and Wmax.

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