Walkey Allan J, Demissie Serkalem, Shah Dilip, Romero Freddy, Puklin Leah, Summer Ross S
The Pulmonary Center, Boston University School of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Boston Medical Center, Boston, Massachusetts, United States of America.
Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, United States of America.
PLoS One. 2014 Sep 26;9(9):e108561. doi: 10.1371/journal.pone.0108561. eCollection 2014.
Adiponectin (APN) is an anti-inflammatory hormone derived from adipose tissue that attenuates acute lung injury in rodents. In this study, we investigated the association between circulating APN and outcomes among patients with acute respiratory distress syndrome (ARDS).
We performed a retrospective cohort study using data and plasma samples from participants in the multicenter ARDS Network Fluid and Catheter Treatment Trial.
Plasma APN concentrations were measured in 816 (81.6%) trial participants at baseline and in 568 (56.8%) subjects at both baseline and day 7 after enrollment. Clinical factors associated with baseline APN levels in multivariable-adjusted models included sex, body mass index, past medical history of cirrhosis, and central venous pressure (model R2 = 9.7%). We did not observe an association between baseline APN and either severity of illness (APACHE III) or extent of lung injury (Lung Injury Score). Among patients who received right heart catheterization (n = 384), baseline APN was inversely related to mean pulmonary artery pressure (β = -0.015, R2 1.5%, p = 0.02); however, this association did not persist in multivariable models (β = -0.009, R2 0.5%, p = 0.20). Neither baseline APN levels [HR per quartile1.04 (95% CI 0.91-1.18), p = 0.61], nor change in APN level from baseline to day 7 [HR 1.04 (95% CI 0.89-1.23), p = 0.62)] were associated with 60 day mortality in Cox proportional hazards regression models. However, subgroup analysis identified an association between APN and mortality among patients who developed ARDS from extra-pulmonary etiologies [HR per quartile 1.31 (95% CI 1.08-1.57)]. APN levels did not correlate with mortality among patients developing ARDS in association with direct pulmonary injury [HR 0.96 (95% CI 0.83-1.13)], pinteraction = 0.016.
Plasma APN levels did not correlate with disease severity or mortality in a large cohort of patients with ARDS. However, higher APN levels were associated with increased mortality among patients developing ARDS from extra-pulmonary etiologies.
脂联素(APN)是一种源自脂肪组织的抗炎激素,可减轻啮齿动物的急性肺损伤。在本研究中,我们调查了急性呼吸窘迫综合征(ARDS)患者循环中APN与预后之间的关联。
我们使用多中心ARDS网络液体与导管治疗试验参与者的数据和血浆样本进行了一项回顾性队列研究。
在基线时对816名(81.6%)试验参与者测量了血浆APN浓度,在入组时的基线和第7天对568名(56.8%)受试者进行了测量。多变量调整模型中与基线APN水平相关的临床因素包括性别、体重指数、既往肝硬化病史和中心静脉压(模型R2 = 9.7%)。我们未观察到基线APN与疾病严重程度(急性生理与慢性健康状况评分系统III)或肺损伤程度(肺损伤评分)之间存在关联。在接受右心导管检查的患者(n = 384)中,基线APN与平均肺动脉压呈负相关(β = -0.015,R2 1.5%,p = 0.02);然而,在多变量模型中这种关联未持续存在(β = -0.009,R2 0.5%,p = 0.20)。在Cox比例风险回归模型中,基线APN水平[每四分位数风险比1.04(95%置信区间0.91 - 1.18),p = 0.61]以及从基线到第7天APN水平的变化[风险比1.04(95%置信区间0.89 - 1.23),p = 0. = 0.62]均与60天死亡率无关。然而,亚组分析发现,因肺外病因发生ARDS的患者中,APN与死亡率之间存在关联[每四分位数风险比1.31(95%置信区间1.08 - 1.57)]。与直接肺损伤相关的ARDS患者中,APN水平与死亡率无相关性[风险比0.96(95%置信区间0.83 - 1.13)],p交互作用 = 0.016。
在一大群ARDS患者中,血浆APN水平与疾病严重程度或死亡率无关。然而,较高的APN水平与因肺外病因发生ARDS的患者死亡率增加相关。