Department of Surgery, Sepsis and Critical Illness Research Center, College of Medicine, University of Florida, Gainesville, FL. Electronic address: https://www.twitter.com/ValeriePolcz.
Department of Surgery, Sepsis and Critical Illness Research Center, College of Medicine, University of Florida, Gainesville, FL.
Surgery. 2024 Nov;176(5):1516-1524. doi: 10.1016/j.surg.2024.07.031. Epub 2024 Aug 22.
Sarcopenia is a known risk factor for adverse outcomes across multiple disease states, including severe trauma. Factors such as age, hyperinflammation, prolonged immobilization, and critical illness may not only exacerbate progression of this disease but may also contribute to the development of induced sarcopenia, or sarcopenia secondary to hospitalization. This study seeks to (1) determine the effects of severe traumatic injury on changes in skeletal muscle mass in older adults; (2) test whether changes in skeletal muscle mass are associated with clinical frailty, physical performance, and health-related quality of life; and (3) examine trauma-induced frailty and temporal changes in myokine and chemokine profiles.
A prospective, longitudinal cohort study of 47 critically ill, older (≥45 years) adults presenting after severe blunt trauma was conducted. Repeated measures of computed tomography-based skeletal muscle index, frailty, and quality of life were obtained in addition to selected plasma biomarkers over 6 months.
Severe trauma was associated with significant losses in skeletal muscle mass and increased incidence of sarcopenia from 36% at baseline to 60% at 6 months. Severe trauma also was associated with a transient worsening of induced frailty and reduced quality of life irrespective of sarcopenia status, which returned to baseline by 6 months after injury. Admission biomarker levels were not associated with skeletal muscle index at the time points studied but demonstrated distinct temporal changes across our entire cohort.
Severe blunt trauma in older adults is associated with increased incidence of induced sarcopenia and reversible induced frailty. Despite muscle wasting, functional decline is transient, with a return to baseline by 6 months, suggesting a need for holistic definitions of sarcopenia and further investigation into long-term functional outcomes in this population.
肌少症是多种疾病状态(包括严重创伤)不良结局的已知危险因素。年龄、过度炎症、长时间固定不动和重症疾病等因素不仅可能使这种疾病恶化,而且还可能导致继发性肌少症(即因住院而导致的肌少症)的发生。本研究旨在:(1)确定严重创伤对老年患者骨骼肌质量变化的影响;(2)检验骨骼肌质量变化是否与临床虚弱、身体机能和健康相关的生活质量有关;(3)研究创伤诱导的虚弱和肌因子和趋化因子谱的时间变化。
对 47 名因严重钝性创伤住院的危重症老年(≥45 岁)患者进行前瞻性、纵向队列研究。除了选择在 6 个月内采集的血浆生物标志物外,还对 CT 扫描骨骼肌指数、虚弱和生活质量进行了重复测量。
严重创伤与骨骼肌质量的显著丢失以及肌少症的发生率从基线时的 36%增加到 6 个月时的 60%有关。严重创伤还与诱导性虚弱和生活质量的暂时性恶化有关,无论肌少症状态如何,在受伤后 6 个月时均恢复到基线水平。入院时的生物标志物水平与研究时的骨骼肌指数无关,但在整个队列中表现出明显的时间变化。
老年严重钝性创伤与继发性肌少症和可逆转的诱导性虚弱的发生率增加有关。尽管存在肌肉消耗,但功能下降是短暂的,在受伤后 6 个月时恢复到基线,这表明需要对肌少症进行全面定义,并进一步研究该人群的长期功能结局。