肌肉萎缩疾病在三维年龄- bmi - VO2峰值散点图上有两条不同的轨迹

Masamitsu Sugie, Kazumasa Harada, Tetsuya Takahashi, Marina Nara, Teruyuki Koyama, Hajime Fujimoto, Shunei Kyo, Hideki Ito
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引用次数: 4

摘要

目的虚弱和肌肉减少症是与年龄相关的病态状态,低体重指数(BMI)是虚弱和恶病质的一个特征。然而,没有一个共同的指标来评估这三种肌肉消耗状态,这使得很难理解它们之间的关系。峰值摄氧量(峰值VO2),一个预期寿命的指标,可能是一个有用的常用指标。因此,本研究旨在通过年龄、BMI和峰值VO2来探讨肌肉减少症、虚弱和恶病质之间的关系。方法与结果参与者为175名居住在日本社区的老年人(男性58人,女性117人;77.6年)。我们评估了生化、生理和物理因素,以及与虚弱和恶病质相关的症状。通过心肺运动试验评估峰值VO2。参与者被分为五组:健壮、体弱、体弱、肌肉减少症和恶病质。我们按年龄、BMI和峰值vo2与平均值和95%置信区间(ci)进行比较。17% (n=30)的参与者被分类为健壮,40% (n=70)为虚弱前期,12% (n=21)为肌肉减少症,25% (n=44)为虚弱,6% (n=10)为恶病质。年龄(健壮vs体弱,体弱前期vs体弱)、BMI(健壮vs病毒质、体弱vs病毒质、体弱vs病毒质)和峰值VO2(健壮vs体弱、体弱前期vs病毒质)的平均值和95% ci均存在显著差异。年龄、BMI和峰值VO2的三个维度揭示了肌肉萎缩疾病的两条轨迹(从强壮到虚弱,通过虚弱前期,从强壮到肌肉减少,通过恶病质)。结论本研究揭示了肌肉萎缩疾病的两条轨迹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Muscle wasting diseases has two distinct trajectories on the 3-dimensional age-BMI-peak VO2 scatterplot

Aims

Frailty and sarcopenia are age-related morbid states, and a low body mass index (BMI) is a characteristic of frailty and cachexia. However, no common index for assessing these three muscle wasting states is available, making it difficult to understand the relationship among them. Peak oxygen uptake (peak VO2), an index of life expectancy, may be a useful common index. Therefore, this study aimed to investigate the relationship among sarcopenia, frailty, and cachexia using age, BMI, and peak VO2.

Methods and Results

Participants were 175 Japanese community dwelling older adults (58 men, 117 women; 77.6 years). We assessed biochemical, physiological, and physical factors, and symptoms associated with frailty, and cachexia. Peak VO2 was assessed with a cardiopulmonary exercise test. Participants were classified into five groups: robust, pre-frail, frail, sarcopenia, and cachexia. We compared the groups by age, BMI, and peakVO2 with average values and 95% confidence intervals (CIs). 17% (n=30) of participants were classified as robust, 40% (n=70) as pre-frail, 12% (n=21) as sarcopenia, 25% (n=44) as frail, and 6% (n=10) as cachexia. Significant differences were found in age (robust vs. frail, pre-frail vs. frail), BMI (robust vs. cachexia, pre-frail vs. cachexia, frail vs. cachexia), and peak VO2 (robust vs. frail, robust vs. cachexia, pre-frail vs. cachexia) with average values and 95% CIs. Three dimensions among age, BMI and peak VO2 revealed two trajectories (from robust to frailty via pre-frailty, and from robust to cachexia via sarcopenia) among muscle wasting diseases.

Conclusions

This study revealed two trajectories among muscle wasting diseases.

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