首页> 外文期刊>The journals of gerontology.Series A. Biological sciences and medical sciences >An elevation of resting metabolic rate with declining health in nonagenarians may be associated with decreased muscle mass and function in women and men, respectively
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An elevation of resting metabolic rate with declining health in nonagenarians may be associated with decreased muscle mass and function in women and men, respectively

机译:非老年患者的静息代谢率升高和健康状况下降可能分别与女性和男性的肌肉量和功能下降有关

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摘要

Previously, we showed that FI34, a frailty index based on 34 health and function ability variables, is heritable and a reliable phenotypic indicator of healthy aging. We have now examined the relationship between major components of energy expenditure and the FI34 in participants of the Louisiana Healthy Aging Study. Resting metabolic rate was associated with FI34, even after adjustment for fat-free mass, fat mass, age, sex, thyroid hormones, and insulin-like growth factor 1 levels, in multiple regression analyses. In contrast, there was no association between total daily energy expenditure and FI34. Circulating creatine phosphokinase, a clinical marker of muscle damage, was also significantly associated with FI 34. However, these associations of resting metabolic rate with FI34 were restricted to the oldest old (≥90 years) and absent in younger age groups. In oldest old men, the association of FI34 with creatine phosphokinase persisted, whereas in the oldest old women, only the association with resting metabolic rate pertained with the appearance of an effect of body size and composition. These results point toward an increasing metabolic burden for the maintenance of homeodynamics as health declines in nonagenarians, and this has implications for contraction of metabolic reserve that may potentially accelerate the path to disability.
机译:以前,我们显示FI34是基于34个健康和功能能力变量的脆弱指数,是可遗传的并且是健康衰老的可靠表型指标。现在,我们已经研究了路易斯安那州健康老龄化研究参与者中能量消耗的主要成分与FI34之间的关系。在多次回归分析中,即使调整了无脂肪量,脂肪量,年龄,性别,甲状腺激素和胰岛素样生长因子1水平,静息代谢率也与FI34相关。相反,每日总能量消耗与FI34之间没有关联。循环肌酸磷酸激酶(一种肌肉损伤的临床标志物)也与FI 34显着相关。但是,静息代谢率与FI34的这些关联仅限于最老的年龄(≥90岁),而在较年轻的年龄组则不存在。在最老的老年男性中,FI34与肌酸磷酸激酶的关联持续存在,而在最老的老年女性中,仅与静止代谢率的关联与体型和组成的影响有关。这些结果表明,随着非agenarians的健康下降,维持体内动力学的新陈代谢负担将增加,这对代谢储备的收缩可能会加速致残途径的产生产生影响。

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