From the Division of Trauma, Critical Care, Emergency Surgery, and Burns, Department of Surgery (J.P., V.P., M.Z., N.K., M.H., K.H., E-R.Z., B.J.), College of Medicine, Section of Geriatrics, General Internal Medicine and Palliative Medicine (M.F.), and Department of Immunobiology College of Medicine (J.N-Z.), University of Arizona, Tucson, Arizona.
J Trauma Acute Care Surg. 2019 Jul;87(1):54-60. doi: 10.1097/TA.0000000000002229.
Frailty is a geriatric syndrome characterized by decreased physiological reserves, increased inflammation, and decreased anabolic-endocrine response. The biomarkers associated with frailty are poorly understood in trauma. The aim of this study was to analyze the association between frailty and immune: IL-1β, IL-6, IL-2Rα, tumor necrosis factor (TNF)-α, and endocrine biomarkers: insulin-like growth factor-1 and growth hormone in trauma patients.
We conducted a 1-year (2017-2018) prospective analysis of geriatric (≥65 years) trauma patients admitted to our Level I trauma center. Frailty was measured using the trauma-specific frailty index (TSFI) and blood samples were collected within 24 hours of admission. Patients were stratified into two groups: frail (TSFI > 0.25) and nonfrail (TSFI ≤ 0.25). We then measured the levels of immune and endocrine biomarkers by a colorimetric output that was read by a spectrophotometer (Quantikine ELISA). The outcome measures were the levels of the immune and endocrine markers in the two groups. Multivariable linear regression was performed.
A total of 100 geriatric trauma patients were consented and enrolled. The mean age was 77.1 ± 9.8 years and 34% were female. Thirty-nine (39%) patients were frail. Frail patients were more likely to present after falls (p = 0.01). There was no difference in age (p = 0.78), sex (p = 0.77), systolic blood pressure (p = 0.16), and heart rate (p = 0.24) between the two groups. Frail patients had higher levels of TNF-α (p = 0.01), IL-1β (p = 0.01), and IL-6(p = 0.01) but lower levels of growth hormone (p = 0.03) and insulin-like growth factor-1 (p < 0.04) compared with nonfrail patients. There was no difference in the level of IL-2Rα (p = 0.25). On regression analysis, frailty was positively correlated with the levels of proinflammatory biomarkers, that is, TNF- α, IL-1 β, and IL-6 and negatively correlated with endocrine biomarkers.
This study supports the association between frailty and immune and endocrine markers. Frailty acts synergistically with trauma in increasing the acute inflammatory response. Moreover, frail patients have lower levels of anabolic hormones. Understanding the inflammatory and endocrine response in frail trauma patients may result in better therapeutic strategies.
衰弱是一种以生理储备减少、炎症增加和合成代谢-内分泌反应减少为特征的老年综合征。与创伤相关的衰弱的生物标志物了解甚少。本研究的目的是分析创伤患者衰弱与免疫:白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-2 受体α(IL-2Rα)、肿瘤坏死因子(TNF)-α和内分泌生物标志物:胰岛素样生长因子-1(IGF-1)和生长激素之间的关系。
我们对我院 1 级创伤中心收治的老年(≥65 岁)创伤患者进行了为期 1 年(2017-2018 年)的前瞻性分析。使用创伤特异性衰弱指数(TSFI)测量衰弱程度,入院后 24 小时内采集血样。患者分为两组:衰弱组(TSFI>0.25)和非衰弱组(TSFI≤0.25)。然后通过分光光度计读取比色输出来测量免疫和内分泌生物标志物的水平(Quantikine ELISA)。主要观察指标为两组免疫和内分泌标志物的水平。采用多元线性回归分析。
共同意并纳入 100 例老年创伤患者。平均年龄为 77.1±9.8 岁,34%为女性。39 例(39%)患者衰弱。衰弱患者更有可能因跌倒而就诊(p=0.01)。两组之间在年龄(p=0.78)、性别(p=0.77)、收缩压(p=0.16)和心率(p=0.24)方面无差异。与非衰弱组相比,衰弱组 TNF-α(p=0.01)、IL-1β(p=0.01)和 IL-6(p=0.01)水平较高,但生长激素(p=0.03)和胰岛素样生长因子-1(p<0.04)水平较低。IL-2Rα水平无差异(p=0.25)。回归分析显示,衰弱与促炎生物标志物 TNF-α、IL-1β和 IL-6 呈正相关,与内分泌生物标志物呈负相关。
本研究支持衰弱与免疫和内分泌标志物之间的关联。衰弱与创伤协同作用,增加急性炎症反应。此外,衰弱患者的合成代谢激素水平较低。了解衰弱创伤患者的炎症和内分泌反应可能会产生更好的治疗策略。