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The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women
There is a scarcity of studies that have investigated the role of multiple single nucleotide polymorphisms (SNPs) on a range of muscle phenotypes in an elderly population. The present study investigated the possible association of 24 SNPs with skeletal muscle phenotypes in 307 elderly Caucasian wome...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762041/ https://www.ncbi.nlm.nih.gov/pubmed/33291384 http://dx.doi.org/10.3390/genes11121459 |
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author | Khanal, Praval He, Lingxiao Herbert, Adam J. Stebbings, Georgina K. Onambele-Pearson, Gladys L. Degens, Hans Morse, Christopher I. Thomis, Martine Williams, Alun G. |
author_facet | Khanal, Praval He, Lingxiao Herbert, Adam J. Stebbings, Georgina K. Onambele-Pearson, Gladys L. Degens, Hans Morse, Christopher I. Thomis, Martine Williams, Alun G. |
author_sort | Khanal, Praval |
collection | PubMed |
description | There is a scarcity of studies that have investigated the role of multiple single nucleotide polymorphisms (SNPs) on a range of muscle phenotypes in an elderly population. The present study investigated the possible association of 24 SNPs with skeletal muscle phenotypes in 307 elderly Caucasian women (aged 60–91 years, 66.3 ± 11.3 kg). Skeletal muscle phenotypes included biceps brachii thickness, vastus lateralis cross-sectional areas, maximal hand grip strength, isometric knee extension and elbow flexion torque. Genotyping for 24 SNPs, chosen on their skeletal muscle structural or functional links, was conducted on DNA extracted from blood or saliva. Of the 24 SNPs, 10 were associated with at least one skeletal muscle phenotype. HIF1A rs11549465 was associated with three skeletal muscle phenotypes and PTK2 rs7460 and ACVR1B rs10783485 were each associated with two phenotypes. PTK2 rs7843014, COL1A1 rs1800012, CNTF rs1800169, NOS3 rs1799983, MSTN rs1805086, TRHR rs7832552 and FTO rs9939609 were each associated with one. Elderly women possessing favourable genotypes were 3.6–13.2% stronger and had 4.6–14.7% larger muscle than those with less favourable genotypes. These associations, together with future work involving a broader range of SNPs, may help identify individuals at particular risk of an age-associated loss of independence. |
format | Online Article Text |
id | pubmed-7762041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77620412020-12-26 The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women Khanal, Praval He, Lingxiao Herbert, Adam J. Stebbings, Georgina K. Onambele-Pearson, Gladys L. Degens, Hans Morse, Christopher I. Thomis, Martine Williams, Alun G. Genes (Basel) Article There is a scarcity of studies that have investigated the role of multiple single nucleotide polymorphisms (SNPs) on a range of muscle phenotypes in an elderly population. The present study investigated the possible association of 24 SNPs with skeletal muscle phenotypes in 307 elderly Caucasian women (aged 60–91 years, 66.3 ± 11.3 kg). Skeletal muscle phenotypes included biceps brachii thickness, vastus lateralis cross-sectional areas, maximal hand grip strength, isometric knee extension and elbow flexion torque. Genotyping for 24 SNPs, chosen on their skeletal muscle structural or functional links, was conducted on DNA extracted from blood or saliva. Of the 24 SNPs, 10 were associated with at least one skeletal muscle phenotype. HIF1A rs11549465 was associated with three skeletal muscle phenotypes and PTK2 rs7460 and ACVR1B rs10783485 were each associated with two phenotypes. PTK2 rs7843014, COL1A1 rs1800012, CNTF rs1800169, NOS3 rs1799983, MSTN rs1805086, TRHR rs7832552 and FTO rs9939609 were each associated with one. Elderly women possessing favourable genotypes were 3.6–13.2% stronger and had 4.6–14.7% larger muscle than those with less favourable genotypes. These associations, together with future work involving a broader range of SNPs, may help identify individuals at particular risk of an age-associated loss of independence. MDPI 2020-12-05 /pmc/articles/PMC7762041/ /pubmed/33291384 http://dx.doi.org/10.3390/genes11121459 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Khanal, Praval He, Lingxiao Herbert, Adam J. Stebbings, Georgina K. Onambele-Pearson, Gladys L. Degens, Hans Morse, Christopher I. Thomis, Martine Williams, Alun G. The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women |
title | The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women |
title_full | The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women |
title_fullStr | The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women |
title_full_unstemmed | The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women |
title_short | The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women |
title_sort | association of multiple gene variants with ageing skeletal muscle phenotypes in elderly women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762041/ https://www.ncbi.nlm.nih.gov/pubmed/33291384 http://dx.doi.org/10.3390/genes11121459 |
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