Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2008-11-5
pubmed:abstractText
The R577X polymorphism in the alpha-actinin-3 encoding gene (ACTN3) has been associated with elite athletic performance, and recently with differences in isometric and dynamic muscle strength and power in the general population. In this study we sought to determine the association of ACTN3 R577X genotype with muscle strength and mass phenotypes in men and women across the adult age span. Eight hundred forty-eight (n = 848) adult volunteers (454 men and 394 women) aged 22-90 yr were genotyped for ACTN3 R577X. Knee extensor (KE) shortening and lengthening peak torque values were determined using isokinetic dynamometry and fat-free mass (FFM) by dual-energy X-ray absorptiometry. Women deficient in alpha-actinin-3 (X/X; n = 53) displayed lower KE shortening peak torque (30 degrees /s: 89.5 +/- 3.5 vs. 99.3 +/- 1.4 N.m, P = 0.011; 180 degrees /s: 60.3 +/- 2.6 vs. 67.0 +/- 1.0 N.m, P = 0.019) and KE lengthening peak torque (30 degrees /s: 122.8 +/- 5.7 vs. 137.0 +/- 2.2 N.m, P = 0.022; 180 degrees /s: 121.8 +/- 5.8 vs. 138.5 +/- 2.2 N.m, P = 0.008) compared with R/X + R/R women (n = 341). Women X/X homozygotes also displayed lower levels of both total body FFM (38.9 +/- 0.5 vs. 40.1 +/- 0.2 kg, P = 0.040) and lower limb FFM (11.9 +/- 0.2 vs. 12.5 +/- 0.1 kg, P = 0.044) compared with R/X + R/R women. No genotype-related differences were observed in men. In conclusion, our results indicate that the absence of alpha-actinin-3 protein (i.e., ACTN3 X/X genotype) influences KE peak torque and FFM in women but not men.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-10192379, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-11440986, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-11716195, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-12879365, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-15221860, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-15292341, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-15377647, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-15718405, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-15886711, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-16371478, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-17033684, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-17347381, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-17828264, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-17848603, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-17879893, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-18043716, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-18178581, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-18470530, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-18637739, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-18650267, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-2671039, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-8887951, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-8964743, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-9094325, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-9216968, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-9375323, http://linkedlifedata.com/resource/pubmed/commentcorrection/18756004-9887130
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
8750-7587
pubmed:author
pubmed:issnType
Print
pubmed:volume
105
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1486-91
pubmed:dateRevised
2011-1-26
pubmed:meshHeading
pubmed-meshheading:18756004-Absorptiometry, Photon, pubmed-meshheading:18756004-Actinin, pubmed-meshheading:18756004-Adult, pubmed-meshheading:18756004-Age Factors, pubmed-meshheading:18756004-Aged, pubmed-meshheading:18756004-Aged, 80 and over, pubmed-meshheading:18756004-Female, pubmed-meshheading:18756004-Humans, pubmed-meshheading:18756004-Knee, pubmed-meshheading:18756004-Longitudinal Studies, pubmed-meshheading:18756004-Male, pubmed-meshheading:18756004-Middle Aged, pubmed-meshheading:18756004-Muscle, Skeletal, pubmed-meshheading:18756004-Muscle Contraction, pubmed-meshheading:18756004-Muscle Strength, pubmed-meshheading:18756004-Muscle Strength Dynamometer, pubmed-meshheading:18756004-Phenotype, pubmed-meshheading:18756004-Polymorphism, Genetic, pubmed-meshheading:18756004-Sex Factors, pubmed-meshheading:18756004-Torque, pubmed-meshheading:18756004-Young Adult
pubmed:year
2008
pubmed:articleTitle
ACTN3 genotype is associated with muscle phenotypes in women across the adult age span.
pubmed:affiliation
Department of Kinesiology, School of Public Health, University of Maryland, College Park, MD 20742-2611, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural