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血浆血管生成素-2 水平升高与人类感染性休克的液体超负荷、器官功能障碍和死亡相关。

Elevated Plasma Angiopoietin-2 Levels Are Associated With Fluid Overload, Organ Dysfunction, and Mortality in Human Septic Shock.

机构信息

1Centre for Heart Lung Innovation, St. Paul's Hospital and University of British Columbia, Vancouver, BC, Canada. 2Division of Critical Care Medicine, St. Paul's Hospital and University of British Columbia, Vancouver, BC, Canada.

出版信息

Crit Care Med. 2016 Nov;44(11):2018-2027. doi: 10.1097/CCM.0000000000001853.

Abstract

OBJECTIVES

Angiopoietins modulate endothelial permeability via endothelial cell junctions. Angiopoietin-2 blocks the angiopoietin-1/Tie-2 interaction that stabilizes these junctions, and elevated plasma angiopoietin-2 levels are associated with vascular leakage. We hypothesized that plasma angiopoietin-1 and angiopoietin-2 levels are associated with indirect markers of increased vascular permeability, organ dysfunction, mortality, and plasma proinflammatory cytokine levels in human septic shock.

DESIGN

Multicenter observational cohort study derived from a randomized controlled trial (Vasopressin and Septic Shock Trial of vasopressin versus norepinephrine in septic shock).

SETTING

ICUs of hospitals in Canada, Australia, and the United States.

PATIENTS

Three hundred forty-one patients in the randomized, controlled Vasopressin and Septic Shock Trial trial of vasopressin versus norepinephrine in septic shock.

INTERVENTIONS

None.

MEASUREMENT AND MAIN RESULTS

We measured plasma levels of angiopoietin-1 and angiopoietin-2 at study baseline and determined their association with percent fluid overload and acute organ dysfunction and generated a receiver operating characteristic curve for plasma angiopoietin-2 levels versus acute kidney injury. We also determined the association of angiopoietin-1 and angiopoietin-2 levels with hemodynamics, mortality, and plasma cytokine levels. Plasma angiopoietin-2 levels were directly associated with percent fluid overload at baseline (rs = 0.18; p = 0.0008) and at 6 hours (rs = 0.13; p = 0.023), but not at 24 hours (rs = 0.041; p = 0.46). Plasma angiopoietin-2 levels were associated with the development of hepatic (p < 0.0001) and coagulation (p < 0.0001) dysfunction and acute kidney injury (p < 0.0001). Receiver operating characteristic curve had an area under the curve of 0.73 for acute kidney injury. angiopoietin-2 levels were also inversely associated with days alive (r = -0.24; p = 0.010) and positively associated with increased 7-day (log-rank trend chi-square = 5.9; p = 0.015) and 28-day (log-rank chi square = 4.9; p = 0.027) mortality. A threshold of angiopoietin-2 levels above the first quartile (> 5,807 pg/mL) was observed to be associated with increased mortality risk, which aligns with prior studies. Plasma angiopoietin-2 levels were positively associated with plasma cytokine levels, including tumor necrosis factor-α and interleukin-6 at baseline (rs = 0.39; p < 0.0001 and rs = 0.51; p < 0.0001) and at 24 hours (rs = 0.29; p < 0.0001 and rs = 0.41; p < 0.0001).

CONCLUSIONS

Increased plasma angiopoietin-2 levels are associated with increased fluid overload, hepatic and coagulation dysfunction, acute kidney injury, mortality, and plasma cytokines in human septic shock. angiopoietin-2 activation may increase vascular leakage leading to increased fluid requirements, organ dysfunction, and death from septic shock.

摘要

目的

血管生成素通过血管内皮细胞连接调节内皮细胞通透性。血管生成素-2 阻断了稳定这些连接的血管生成素-1/Tie-2 相互作用,而升高的血浆血管生成素-2 水平与血管渗漏有关。我们假设,在人类感染性休克中,血浆血管生成素-1 和血管生成素-2 水平与间接标志物(血管通透性增加、器官功能障碍、死亡率和血浆前炎症细胞因子水平)相关。

设计

从血管加压素和感染性休克试验的随机对照试验(血管加压素与去甲肾上腺素治疗感染性休克的比较)中衍生的多中心观察队列研究。

地点

加拿大、澳大利亚和美国的医院 ICU。

患者

感染性休克中血管加压素与去甲肾上腺素试验的随机对照试验中的 341 例患者。

干预

无。

测量和主要结果

我们在基线研究时测量了血浆血管生成素-1 和血管生成素-2 水平,并确定它们与液体超负荷百分比和急性器官功能障碍之间的关系,并生成了血管生成素-2 水平对急性肾损伤的接收者操作特征曲线。我们还确定了血管生成素-1 和血管生成素-2 水平与血流动力学、死亡率和血浆细胞因子水平的关系。基线时(rs = 0.18;p = 0.0008)和 6 小时时(rs = 0.13;p = 0.023),血浆血管生成素-2 水平与液体超负荷百分比直接相关,但在 24 小时时不相关(rs = 0.041;p = 0.46)。血浆血管生成素-2 水平与肝(p < 0.0001)和凝血(p < 0.0001)功能障碍以及急性肾损伤(p < 0.0001)的发展相关。接受者操作特征曲线的曲线下面积为 0.73,用于急性肾损伤。血管生成素-2 水平也与存活天数呈负相关(r = -0.24;p = 0.010),与 7 天(对数秩检验卡方 = 5.9;p = 0.015)和 28 天(对数秩卡方 = 4.9;p = 0.027)死亡率增加呈正相关。观察到血管生成素-2 水平高于四分位数上限(> 5,807 pg/ml)与死亡率风险增加相关,这与先前的研究一致。基线时(rs = 0.39;p < 0.0001 和 rs = 0.51;p < 0.0001)和 24 小时时(rs = 0.29;p < 0.0001 和 rs = 0.41;p < 0.0001),血浆血管生成素-2 水平与血浆细胞因子水平(包括肿瘤坏死因子-α和白细胞介素-6)呈正相关。

结论

在人类感染性休克中,升高的血浆血管生成素-2 水平与液体超负荷、肝和凝血功能障碍、急性肾损伤、死亡率和血浆细胞因子相关。血管生成素-2 的激活可能会增加血管渗漏,导致液体需求增加、器官功能障碍和感染性休克死亡。

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