ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean Adults

Background. Little information is available about molecular markers for sarcopenia and osteoporosis in Asian populations. Objective. This study investigated the association of the ACTN3 polymorphism with sarcopenia and osteoporotic status in older Korean adults. Methods. Older Korean 62 men and 270...

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Main Authors: Jinkyung Cho, Inhwan Lee, Hyunsik Kang
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2017/4239648
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spelling doaj-f69f45c82f75467d86d57d1daa01e23c2020-11-24T22:51:54ZengHindawi LimitedBioMed Research International2314-61332314-61412017-01-01201710.1155/2017/42396484239648ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean AdultsJinkyung Cho0Inhwan Lee1Hyunsik Kang2College of Sport Science, Sungkyunkwan University, Suwon, Republic of KoreaCollege of Sport Science, Sungkyunkwan University, Suwon, Republic of KoreaCollege of Sport Science, Sungkyunkwan University, Suwon, Republic of KoreaBackground. Little information is available about molecular markers for sarcopenia and osteoporosis in Asian populations. Objective. This study investigated the association of the ACTN3 polymorphism with sarcopenia and osteoporotic status in older Korean adults. Methods. Older Korean 62 men and 270 women (mean age 73.7 ± 6.6 years) participated in this study. Body mass index, percent body fatness, appendicular skeletal muscle mass, and bone mineral density of the lumbar spine, femur, and total body were analyzed with dual-energy X-ray absorptiometry. ACTN3 R/X genotyping was determined using TaqMan probes. Results. Determination of odds ratios (ORs) and 95% confidence intervals (CIs) using binary logistic regression analyses showed that XX homozygotes were at a significantly higher risk of sarcopenia (OR=2.056, 95%  CI=1.024–4.127, p=0.043) and osteoporosis (OR=2.794, 95%  CI=1.208–5.461, p=0.016) than RR homozygotes (reference group, OR=1). The OR of XX homozygotes for having sarcopenia remained significant (OR=2.237, 95%  CI=1.044–4.836, p=0.038) after adjustments for age, gender, body fatness, and serum vitamin D. The OR of XX homozygotes for having osteoporosis was no longer significant (OR=2.682, 95%  CI=0.960–7.942, p=0.075) after adjustments for the covariates. Conclusion. Our findings suggest that the ACTN3 R577X genotype may influence decline in muscle and bone health phenotypes in older Korean adults.http://dx.doi.org/10.1155/2017/4239648
collection DOAJ
language English
format Article
sources DOAJ
author Jinkyung Cho
Inhwan Lee
Hyunsik Kang
spellingShingle Jinkyung Cho
Inhwan Lee
Hyunsik Kang
ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean Adults
BioMed Research International
author_facet Jinkyung Cho
Inhwan Lee
Hyunsik Kang
author_sort Jinkyung Cho
title ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean Adults
title_short ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean Adults
title_full ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean Adults
title_fullStr ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean Adults
title_full_unstemmed ACTN3 Gene and Susceptibility to Sarcopenia and Osteoporotic Status in Older Korean Adults
title_sort actn3 gene and susceptibility to sarcopenia and osteoporotic status in older korean adults
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2017-01-01
description Background. Little information is available about molecular markers for sarcopenia and osteoporosis in Asian populations. Objective. This study investigated the association of the ACTN3 polymorphism with sarcopenia and osteoporotic status in older Korean adults. Methods. Older Korean 62 men and 270 women (mean age 73.7 ± 6.6 years) participated in this study. Body mass index, percent body fatness, appendicular skeletal muscle mass, and bone mineral density of the lumbar spine, femur, and total body were analyzed with dual-energy X-ray absorptiometry. ACTN3 R/X genotyping was determined using TaqMan probes. Results. Determination of odds ratios (ORs) and 95% confidence intervals (CIs) using binary logistic regression analyses showed that XX homozygotes were at a significantly higher risk of sarcopenia (OR=2.056, 95%  CI=1.024–4.127, p=0.043) and osteoporosis (OR=2.794, 95%  CI=1.208–5.461, p=0.016) than RR homozygotes (reference group, OR=1). The OR of XX homozygotes for having sarcopenia remained significant (OR=2.237, 95%  CI=1.044–4.836, p=0.038) after adjustments for age, gender, body fatness, and serum vitamin D. The OR of XX homozygotes for having osteoporosis was no longer significant (OR=2.682, 95%  CI=0.960–7.942, p=0.075) after adjustments for the covariates. Conclusion. Our findings suggest that the ACTN3 R577X genotype may influence decline in muscle and bone health phenotypes in older Korean adults.
url http://dx.doi.org/10.1155/2017/4239648
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