Prior Steven J, Ryan Alice S, Blumenthal Jacob B, Watson Jonathan M, Katzel Leslie I, Goldberg Andrew P
Division of Gerontology and Geriatric Medicine, Department of Medicine, University of Maryland School of Medicine, Baltimore. Baltimore Veterans Affairs Geriatric Research, Education and Clinical Center, and Research and Development Service, Baltimore, Maryland.
J Gerontol A Biol Sci Med Sci. 2016 Aug;71(8):1096-101. doi: 10.1093/gerona/glw017. Epub 2016 Feb 17.
Skeletal muscle capillary rarefaction limits the transcapillary transport of nutrients and oxygen to muscle and may contribute to sarcopenia and functional impairment in older adults. We tested the hypothesis that skeletal muscle capillarization and exercise capacity (VO2max) are lower in sarcopenic than in nonsarcopenic older adults and that the degree of sarcopenia is related to lower skeletal muscle capillarization.
Body composition, VO2max, and vastus lateralis capillarization were determined in 76 middle-aged and older men and women (age = 61±1 years, body mass index [BMI] = 30.7±0.5kg/m(2) [mean ± SEM]). Participants were classified as sarcopenic if appendicular lean mass divided by BMI (ALMBMI) was less than 0.789 for men or less than 0.512 for women.
Sarcopenic subjects (ALMBMI = 0.65±0.04, n = 16) had 20% lower capillary-to-fiber ratio, as well as 13% and 15% lower VO2max expressed as mL/kg/min or L/min, respectively, compared with sex-, race-, and age-matched participants without sarcopenia (ALMBMI = 0.81±0.05, n = 16; p < .05). In all 76 subjects, ALMBMI, thigh muscle cross-sectional area, and VO2max correlated directly with capillarization (r = .30-.37, p ≤ .05), after accounting for age, sex, and race.
These findings suggest that low skeletal muscle capillarization is one factor that may contribute to sarcopenia and reduced exercise capacity in older adults by limiting diffusion of substrates, oxygen, hormones, and nutrients. Strategies to prevent the aging-related decline in skeletal muscle capillarization may help to prevent or slow the progression of sarcopenia and its associated functional declines in generally healthy older adults.
骨骼肌毛细血管稀疏限制了营养物质和氧气向肌肉的跨毛细血管转运,并可能导致老年人肌肉减少症和功能障碍。我们检验了以下假设:与非肌肉减少症的老年人相比,肌肉减少症患者的骨骼肌毛细血管化和运动能力(最大摄氧量)更低,且肌肉减少症的程度与较低的骨骼肌毛细血管化有关。
对76名中老年男性和女性(年龄=61±1岁,体重指数[BMI]=30.7±0.5kg/m²[平均值±标准误])的身体成分、最大摄氧量和股外侧肌毛细血管化进行了测定。如果男性的四肢瘦体重除以BMI(ALMBMI)小于0.789,或女性小于0.512,则将参与者分类为肌肉减少症患者。
与无肌肉减少症的性别、种族和年龄匹配的参与者(ALMBMI=0.81±0.05,n=16;p<.05)相比,肌肉减少症患者(ALMBMI=0.65±0.04,n=16)的毛细血管与纤维比率低20%,以mL/kg/min或L/min表示的最大摄氧量分别低13%和15%。在所有76名受试者中,在考虑年龄、性别和种族后,ALMBMI、大腿肌肉横截面积和最大摄氧量与毛细血管化直接相关(r=0.30-0.37,p≤.05)。
这些发现表明,低骨骼肌毛细血管化是一个可能通过限制底物、氧气、激素和营养物质的扩散而导致老年人肌肉减少症和运动能力下降的因素。预防与衰老相关的骨骼肌毛细血管化下降的策略可能有助于预防或减缓一般健康老年人肌肉减少症及其相关功能下降的进展。