The Association of Multiple Gene Variants with Ageing Skeletal Muscle Phenotypes in Elderly Women

被引:16
作者
Khanal, Praval [1 ,2 ]
He, Lingxiao [1 ,2 ]
Herbert, Adam J. [3 ]
Stebbings, Georgina K. [1 ]
Onambele-Pearson, Gladys L. [1 ]
Degens, Hans [4 ,5 ,6 ]
Morse, Christopher, I [1 ]
Thomis, Martine [2 ]
Williams, Alun G. [1 ,7 ]
机构
[1] Manchester Metropolitan Univ, Musculoskeletal Sci & Sports Med Res Ctr, Dept Sport & Exercise Sci, Manchester M15 6BH, Lancs, England
[2] Katholieke Univ Leuven, Dept Movement Sci, Phys Act Sports & Hlth Res Grp, B-3001 Leuven, Belgium
[3] Birmingham City Univ, Dept Sport & Exercise, Birmingham B5 5JU, W Midlands, England
[4] Manchester Metropolitan Univ, Dept Life Sci, Manchester M15 6BH, Lancs, England
[5] Lithuanian Sports Univ, Inst Sport Sci & Innovat, LT-44221 Kaunsas, Lithuania
[6] Univ Med, Pharm Targu Mures, Targu Mures 540142, Romania
[7] UCL, Inst Sport Exercise & Hlth, London W1T 7HA, England
关键词
single nucleotide polymorphisms; neuromuscular; elderly; genotyping; CILIARY NEUROTROPHIC FACTOR; SP1; BINDING-SITE; NITRIC-OXIDE SYNTHASE; BONE-MINERAL DENSITY; SINGLE-NUCLEOTIDE POLYMORPHISMS; MUSCULAR STRENGTH; BODY-COMPOSITION; OSTEOPOROTIC FRACTURE; PROTEIN-DEGRADATION; HANDGRIP STRENGTH;
D O I
10.3390/genes11121459
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:1 / 18
页数:18
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