4.6 Article

ACE genotype and the muscle hypertrophic and strength responses to strength training

Journal

MEDICINE AND SCIENCE IN SPORTS AND EXERCISE
Volume 40, Issue 4, Pages 677-683

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1249/MSS.0b013e318161eab9

Keywords

angiotensin-converting enzyme; genetics; muscle mass; muscle size; skeletal muscle

Categories

Funding

  1. NIA NIH HHS [T32-AG000268, T32 AG000268-12, K01 AG022791-05, AG042148, K01 AG022791, R01 AG021500, AG021500, R01 AG021500-03, R01 AG018336, AG018336, AG022791, R01 AG018336-05, T32 AG000268] Funding Source: Medline

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Purpose: Previous studies have linked an insertion/deletion polymorphism in the angiotensin-converting enzyme (ACE) gene with variability in muscle strength responses to strength training (ST), though conclusions have been inconsistent across investigations. Moreover, most previous studies have not investigated the influence of sex on the association of ACE I/D genotype with muscle phenotypes. The purpose of this study was to investigate the association of ACE genotype with muscle phenotypes before and after ST in older men and women. Methods: Eighty-six inactive men and 139 inactive women, ages 50-85 yr (mean: 62 yr), were studied before and after 10 wk of unilateral knee extensor ST. The one-repetition maximum (1 RM) test was used to assess knee extensor muscle strength, and computed tomography was used to measure quadriceps muscle volume (MV). Differences were compared among ACE genotype groups (11 vs ID vs DD). Results: Across the entire cohort at baseline, ACE genotype was significantly associated with total lean mass and body weight, with higher values in DD genotype carriers (both P < 0.05). At baseline, DD genotype carriers exhibited significantly greater MV compared with 11 genotype carriers for both the trained leg (men: 1828 44 vs 1629 70; women: 1299 34 vs 1233 +/- 49; P = 0.02) and untrained leg (men: 1801 +/- 46 vs 1559 +/- 72; women: 1268 +/- 36 vs 1189 +/- 51; P = 0.01), with no significant genotype x sex interaction. No ACE genotype associations were observed for the I RM or MV adaptations to ST in either men or women. Conclusions: In the present study, ACE genotype was associated with baseline differences in muscle volume, but it was not associated with the muscle hypertrophic response to ST.

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