ACTN3 genotype is associated with increases in muscle strength in response to resistance training in women

被引:218
作者
Clarkson, PM
Devaney, JM
Gordish-Dressman, H
Thompson, PD
Hubal, MJ
Urso, M
Price, TB
Angelopoulos, TJ
Gordon, PM
Moyna, NM
Pescatello, LS
Visich, PS
Zoeller, RF
Seip, RL
Hoffman, EP
机构
[1] Univ Massachusetts, Dept Exercise Sci, Amherst, MA 01003 USA
[2] Childrens Natl Med Ctr, Med Genet Res Ctr, Washington, DC 20010 USA
[3] Hartford Hosp, Henry Low Heart Ctr, Div Cardiol, Hartford, CT 06115 USA
[4] Yale Univ, Sch Med, Dept Diagnost Radiol, New Haven, CT 06510 USA
[5] Univ Cent Florida, Orlando, FL 32816 USA
[6] W Virginia Univ, Sch Med, Div Exercise Physiol, Morgantown, WV 26506 USA
[7] Dublin City Univ, Dept Hlth & Sport Sci, Dublin 9, Ireland
[8] Univ Connecticut, Sch Allied Hlth, Storrs, CT USA
[9] Cent Michigan Univ, Human Performance Lab, Mt Pleasant, MI 48859 USA
[10] Florida Atlantic Univ, Dept Exercise Sci & Hlth Promot, Davie, FL USA
关键词
quantitative trait loci; muscle genetics; alpha-actinin;
D O I
10.1152/japplphysiol.01139.2004
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The alpha-actinin 3 (ACTN3) gene encodes a protein of the Z disk of myofibers, and a polymorphism of ACTN3 results in complete loss of the protein. The ACTN3 genotype (R577X) has been found to be associated with performance in Australian elite athletes ( Yang N, MacArthur DG, Gulbin JP, Hahn AG, Beggs AH, Easteal S, and North K. Am J Hum Genet 73: 627 - 631, 2003). We studied associations between ACTN3 genotype and muscle size [cross-sectional area of the biceps brachii via magnetic resonance imaging (MRI)] and elbow flexor isometric (MVC) and dynamic [1-repetition maximum (1-RM)] strength in a large group of men ( N = 247) and women ( N = 355) enrolled in a 12-wk standardized elbow flexor/ extensor resistance training program of the nondominant arm at one of eight study centers. We found no association between ACTN3 R577X genotype and muscle phenotype in men. However, women homozygous for the ACTN3 577X allele (XX) had lower baseline MVC compared with heterozygotes ( P < 0.05) when adjusted for body mass and age. Women homozygous for the mutant allele ( 577X) demonstrated greater absolute and relative 1-RM gains compared with the homozygous wild type (RR) after resistance training when adjusted for body mass and age ( P < 0.05). There was a trend for a dose-response with genotype such that gains were greatest for XX and least for RR. Significant associations were validated in at least one ethnic subpopulation ( Caucasians, Asians) and were independent of training volume. About 2% of baseline MVC and of 1-RM strength gain after training were attributable to ACTN3 genotype ( likelihood-ratio test P value, P = 0.01), suggesting that ACTN3 is one of many genes contributing to genetic variation in muscle performance and adaptation to exercise.
引用
收藏
页码:154 / 163
页数:10
相关论文
共 31 条
[1]  
BAECHLE TR, 2000, ESSENTIALS STRENGTH, P407
[2]  
BEGGS AH, 1992, J BIOL CHEM, V267, P9281
[3]  
Clarkson PM, 2002, AM J PHYS MED REHAB, V81, pS52, DOI [10.1097/00002060-200211001-00007, 10.1097/01.PHM.0000029772.45258.43]
[4]   EFFECTS OF ECCENTRIC AND CONCENTRIC MUSCLE ACTIONS IN RESISTANCE TRAINING [J].
COLLIANDER, EB ;
TESCH, PA .
ACTA PHYSIOLOGICA SCANDINAVICA, 1990, 140 (01) :31-39
[5]   MUSCLE HYPERTROPHY IN MEN AND WOMEN [J].
CURETON, KJ ;
COLLINS, MA ;
HILL, DW ;
MCELHANNON, FM .
MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 1988, 20 (04) :338-344
[6]  
DUDLEY GA, 1991, AVIAT SPACE ENVIR MD, V62, P543
[7]   MYOFIBRILLAR DAMAGE FOLLOWING INTENSE ECCENTRIC EXERCISE IN MAN [J].
FRIDEN, J ;
SJOSTROM, M ;
EKBLOM, B .
INTERNATIONAL JOURNAL OF SPORTS MEDICINE, 1983, 4 (03) :170-176
[8]   The heat of shortening and the dynamic constants of muscle [J].
Hill, AV .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1938, 126 (843) :136-195
[9]   Effects of age, gender, and myostatin genotype on the hypertrophic response to heavy resistance strength training [J].
Ivey, FM ;
Roth, SM ;
Ferrell, RE ;
Tracy, BL ;
Lemmer, JT ;
Hurlbut, DE ;
Martel, GF ;
Siegel, EL ;
Fozard, JL ;
Metter, EJ ;
Fleg, JL ;
Hurley, BF .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2000, 55 (11) :M641-M648
[10]   Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis [J].
Kaplan, JM ;
Kim, SH ;
North, KN ;
Rennke, H ;
Correia, LA ;
Tong, HQ ;
Mathis, BJ ;
Rodríguez-Pérez, JC ;
Allen, PG ;
Beggs, AH ;
Pollak, MR .
NATURE GENETICS, 2000, 24 (03) :251-256