ACTN3, Morbidity, and Healthy Aging
As human longevity increases, recent research has focused on the maintenance of optimal health during old age. One such area of focus is that of muscle function in the elderly, with a loss of muscle mass increasing the risk of negative outcomes such as sarcopenia and a decrease in bone mineral densi...
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doaj-bdba0d41480a42f7952befc1d90a378a2020-11-24T23:55:23ZengFrontiers Media S.A.Frontiers in Genetics1664-80212018-01-01910.3389/fgene.2018.00015330390ACTN3, Morbidity, and Healthy AgingCraig Pickering0Craig Pickering1John Kiely2Institute of Coaching and Performance, School of Sport and Wellbeing, University of Central Lancashire, Preston, United KingdomExercise and Nutritional Genomics Research Centre, DNAFit Ltd., London, United KingdomInstitute of Coaching and Performance, School of Sport and Wellbeing, University of Central Lancashire, Preston, United KingdomAs human longevity increases, recent research has focused on the maintenance of optimal health during old age. One such area of focus is that of muscle function in the elderly, with a loss of muscle mass increasing the risk of negative outcomes such as sarcopenia and a decrease in bone mineral density. In this mini-review, we focus on the impact of a single nucleotide polymorphism in ACTN3, shown to impact muscle phenotype in elite athletes, on loss of muscle function, maintenance of bone mineral density, and metabolic disorder risk in an elderly population. From the surveyed research, this polymorphism has a clear and demonstrable impact on muscle phenotype and bone mineral density in this population, and acts as a potential modulator for metabolic disorders. As such, knowledge of an individual’s ACTN3 genotype may better inform the management of risk factors in the elderly, as well as driving innovations in exercise program design. Subsequently, such insights may contribute to the prolonged maintenance of health and function long into old age.http://journal.frontiersin.org/article/10.3389/fgene.2018.00015/fullACTN3geneticsagingsarcopeniabone mineral densitypersonalized |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Craig Pickering Craig Pickering John Kiely |
spellingShingle |
Craig Pickering Craig Pickering John Kiely ACTN3, Morbidity, and Healthy Aging Frontiers in Genetics ACTN3 genetics aging sarcopenia bone mineral density personalized |
author_facet |
Craig Pickering Craig Pickering John Kiely |
author_sort |
Craig Pickering |
title |
ACTN3, Morbidity, and Healthy Aging |
title_short |
ACTN3, Morbidity, and Healthy Aging |
title_full |
ACTN3, Morbidity, and Healthy Aging |
title_fullStr |
ACTN3, Morbidity, and Healthy Aging |
title_full_unstemmed |
ACTN3, Morbidity, and Healthy Aging |
title_sort |
actn3, morbidity, and healthy aging |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Genetics |
issn |
1664-8021 |
publishDate |
2018-01-01 |
description |
As human longevity increases, recent research has focused on the maintenance of optimal health during old age. One such area of focus is that of muscle function in the elderly, with a loss of muscle mass increasing the risk of negative outcomes such as sarcopenia and a decrease in bone mineral density. In this mini-review, we focus on the impact of a single nucleotide polymorphism in ACTN3, shown to impact muscle phenotype in elite athletes, on loss of muscle function, maintenance of bone mineral density, and metabolic disorder risk in an elderly population. From the surveyed research, this polymorphism has a clear and demonstrable impact on muscle phenotype and bone mineral density in this population, and acts as a potential modulator for metabolic disorders. As such, knowledge of an individual’s ACTN3 genotype may better inform the management of risk factors in the elderly, as well as driving innovations in exercise program design. Subsequently, such insights may contribute to the prolonged maintenance of health and function long into old age. |
topic |
ACTN3 genetics aging sarcopenia bone mineral density personalized |
url |
http://journal.frontiersin.org/article/10.3389/fgene.2018.00015/full |
work_keys_str_mv |
AT craigpickering actn3morbidityandhealthyaging AT craigpickering actn3morbidityandhealthyaging AT johnkiely actn3morbidityandhealthyaging |
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