Department of Sport and Exercise Sciences, Musculoskeletal Science and Sports Medicine Research Centre, Manchester Metropolitan University, Manchester, UK.
Department of Movement Sciences, Physical Activity, Sports & Health Research Group, KU Leuven, Leuven, Belgium.
Sci Rep. 2020 Feb 19;10(1):2913. doi: 10.1038/s41598-020-59722-9.
The prevalence of sarcopenia depends on the definition used. There are, however, consistent sarcopenic characteristics, including a low muscle mass and muscle strength. Few studies have investigated the relationship between sarcopenia and genotype. A cross-sectional study was conducted with 307 community-dwelling ≥60-year-old women in South Cheshire, UK. Handgrip strength was assessed with a handgrip dynamometer and skeletal muscle mass was estimated using bioelectrical impedance. DNA was extracted from saliva (∼38%) or blood (∼62%) and 24 single-nucleotide polymorphisms (SNPs) were genotyped. Three established sarcopenia definitions - %Skeletal Muscle Mass (%SMM), Skeletal Muscle Mass Index (SMI) and European Working Group on Sarcopenia in Older People (EWGSOP) - were used to assess sarcopenia prevalence. Binary logistic regression with age as covariate was used to identify SNPs associated with sarcopenia. The prevalence of sarcopenia was: %SMM 14.7%, SMI 60.6% and EWGSOP 1.3%. Four SNPs were associated with the %SMM and SMI definitions of sarcopenia; FTO rs9939609, ESR1 rs4870044, NOS3 rs1799983 and TRHR rs7832552. The first three were associated with the %SMM definition, and TRHR rs7832552 with the SMI definition, but none were common to both sarcopenia definitions. The gene variants associated with sarcopenia may help proper counselling and interventions to prevent individuals from developing sarcopenia.
肌少症的流行率取决于所使用的定义。然而,存在一致的肌少症特征,包括肌肉质量和肌肉力量低。很少有研究调查肌少症与基因型之间的关系。在英国南柴郡的 307 名 60 岁以上的社区居民中进行了一项横断面研究。使用握力计评估握力,使用生物电阻抗法估计骨骼肌质量。从唾液(约 38%)或血液(约 62%)中提取 DNA,并对 24 个单核苷酸多态性(SNP)进行基因分型。使用三种已建立的肌少症定义——骨骼肌质量百分比(%SMM)、骨骼肌质量指数(SMI)和欧洲老年人肌少症工作组(EWGSOP)——评估肌少症的流行率。使用包含年龄作为协变量的二元逻辑回归识别与肌少症相关的 SNP。肌少症的流行率为:%SMM 为 14.7%,SMI 为 60.6%,EWGSOP 为 1.3%。有 4 个 SNP 与 %SMM 和 SMI 定义的肌少症相关;FTO rs9939609、ESR1 rs4870044、NOS3 rs1799983 和 TRHR rs7832552。前三个与 %SMM 定义相关,而 TRHR rs7832552 与 SMI 定义相关,但都不是两种肌少症定义的共有 SNP。与肌少症相关的基因变异可能有助于进行适当的咨询和干预,以防止个体发展为肌少症。