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Acute respiratory distress syndrome: the Berlin Definition.急性呼吸窘迫综合征:柏林定义。
JAMA. 2012 Jun 20;307(23):2526-33. doi: 10.1001/jama.2012.5669.
2
Plasma sRAGE enables prediction of acute lung injury after cardiac surgery in children.血浆可溶性晚期糖基化终末产物受体能够预测儿童心脏手术后的急性肺损伤。
Crit Care. 2012 May 22;16(3):R91. doi: 10.1186/cc11354.
3
Plasma angiopoietin-2 in clinical acute lung injury: prognostic and pathogenetic significance.血浆血管生成素-2 在临床急性肺损伤中的作用:预后和发病机制意义。
Crit Care Med. 2012 Jun;40(6):1731-7. doi: 10.1097/CCM.0b013e3182451c87.
4
Biomarkers in acute lung injury--marking forward progress.急性肺损伤中的生物标志物——标志着向前发展。
Crit Care Clin. 2011 Jul;27(3):661-83. doi: 10.1016/j.ccc.2011.04.001.
5
Derivation and diagnostic accuracy of the surgical lung injury prediction model.手术性肺损伤预测模型的推导和诊断准确性。
Anesthesiology. 2011 Jul;115(1):117-28. doi: 10.1097/ALN.0b013e31821b5839.
6
Randomized, placebo-controlled clinical trial of an aerosolized β₂-agonist for treatment of acute lung injury.随机、安慰剂对照临床试验表明,雾化吸入β₂-激动剂可治疗急性肺损伤。
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Acute administration of recombinant Angiopoietin-1 ameliorates multiple-organ dysfunction syndrome and improves survival in murine sepsis.急性给予重组血管生成素-1可改善脓毒症小鼠多器官功能障碍综合征并提高存活率。
Cytokine. 2011 Aug;55(2):251-9. doi: 10.1016/j.cyto.2011.04.005. Epub 2011 Apr 30.
8
Use of risk reclassification with multiple biomarkers improves mortality prediction in acute lung injury.使用多种生物标志物进行风险再分类可提高急性肺损伤的死亡率预测。
Crit Care Med. 2011 Apr;39(4):711-7. doi: 10.1097/CCM.0b013e318207ec3c.
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ANGPT2 genetic variant is associated with trauma-associated acute lung injury and altered plasma angiopoietin-2 isoform ratio.ANGPT2 基因变异与创伤相关的急性肺损伤和血浆血管生成素-2 同工型比例改变有关。
Am J Respir Crit Care Med. 2011 May 15;183(10):1344-53. doi: 10.1164/rccm.201005-0701OC. Epub 2011 Jan 21.
10
Angiopoietin-1 and angiopoietin-2 as clinically informative prognostic biomarkers of morbidity and mortality in severe sepsis.血管生成素-1 和血管生成素-2 作为严重脓毒症发病率和死亡率的有临床意义的预后生物标志物。
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血浆血管生成素-2 可预测危重症患者急性肺损伤的发生。

Plasma angiopoietin-2 predicts the onset of acute lung injury in critically ill patients.

机构信息

School of Medicine, University of California-San Francisco, CA 94143, USA.

出版信息

Am J Respir Crit Care Med. 2013 Apr 1;187(7):736-42. doi: 10.1164/rccm.201208-1460OC.

DOI:10.1164/rccm.201208-1460OC
PMID:23328529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3678110/
Abstract

RATIONALE

Current clinical prediction scores for acute lung injury (ALI) have limited positive predictive value. No studies have evaluated predictive plasma biomarkers in a broad population of critically ill patients or as an adjunct to clinical prediction scores.

OBJECTIVES

To determine whether plasma angiopoietin-2 (Ang-2), von Willebrand factor (vWF), interleukin-8 (IL-8), and/or receptor for advanced glycation end products (sRAGE) predict ALI in critically ill patients.

METHODS

Plasma samples were drawn from critically ill patients (n = 230) identified in the emergency department. Patients who had ALI at baseline or in the subsequent 6 hours were excluded, and the remaining patients were followed for development of ALI.

MEASUREMENTS AND MAIN RESULTS

Nineteen patients developed ALI at least 6 hours after the sample draw. Higher levels of Ang-2 and IL-8 were significantly associated with increased development of ALI (P = 0.0008, 0.004, respectively). The association between Ang-2 and subsequent development of ALI was robust to adjustment for sepsis and vasopressor use. Ang-2 and the Lung Injury Prediction Score each independently discriminated well between those who developed ALI and those who did not (area under the receiver operating characteristic curve, 0.74 for each), and using the two together improved the area under the curve to 0.84 (vs. 0.74, P = 0.05). In contrast, plasma levels of sRAGE and vWF were not predictive of ALI.

CONCLUSIONS

Plasma biomarkers such as Ang-2 can improve clinical prediction scores and identify patients at high risk for ALI. In addition, the early rise of Ang-2 emphasizes the importance of endothelial injury in the early pathogenesis of ALI.

摘要

背景

目前,用于急性肺损伤(ALI)的临床预测评分的阳性预测值有限。尚无研究评估广泛危重病患者的预测性血浆生物标志物,或评估其是否可作为临床预测评分的辅助手段。

目的

确定血管生成素-2(Ang-2)、血管性血友病因子(vWF)、白细胞介素-8(IL-8)和/或晚期糖基化终产物受体(sRAGE)等血浆标志物是否可预测危重病患者的 ALI。

方法

从急诊科确定的危重病患者中抽取血浆样本(n=230)。排除基线或随后 6 小时内存在 ALI 的患者,随后对其余患者进行 ALI 发展的随访。

测量和主要结果

19 例患者在抽取样本至少 6 小时后发生 ALI。Ang-2 和 IL-8 水平较高与 ALI 发展的风险增加显著相关(分别为 P=0.0008 和 0.004)。Ang-2 与随后发生 ALI 的关联在调整脓毒症和血管加压剂使用后仍然稳健。Ang-2 和肺损伤预测评分均能很好地区分发生和未发生 ALI 的患者(接受者操作特征曲线下面积,分别为 0.74),两者结合可将曲线下面积提高至 0.84(与 0.74 相比,P=0.05)。相比之下,sRAGE 和 vWF 的血浆水平不能预测 ALI。

结论

Ang-2 等血浆生物标志物可改善临床预测评分,并识别出 ALI 风险较高的患者。此外,Ang-2 的早期升高强调了内皮损伤在 ALI 早期发病机制中的重要性。