胰高血糖素样肽-1是急性呼吸衰竭患者死亡率的预后因素。

IF 2.7 Q4 Medicine
Critical care explorations Pub Date : 2025-03-24 eCollection Date: 2025-04-01 DOI:10.1097/CCE.0000000000001247
Cole E Hansell, Hamam A Aneis, Georgios D Kitsios, William G Bain, Yanwu Zhao, Tomeka L Suber, John W Evankovich, Lokesh Sharma, Sadeesh K Ramakrishnan, Niall T Prendergast, Matthew K Hensley, Shehryar Malik, Nancy Petro, Jayshil J Patel, Seyed Mehdi Nouraie, Charles S Dela Cruz, Yingze Zhang, Bryan J McVerry, Faraaz A Shah
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引用次数: 0

摘要

目的:胰高血糖素样肽-1 (glucagon-like peptide-1, GLP-1)和葡萄糖依赖性胰岛素肽(glucose-dependent insulinotropic peptide, GIP)对糖尿病有治疗作用。先前的临床研究表明,肠促胰岛素是危重疾病不良结局的预后因素。我们研究了肠促胰岛素水平是否表明急性呼吸衰竭患者的疾病严重程度和临床结果,急性呼吸衰竭是危重疾病的常见原因。设计:回顾性队列研究。环境:宾夕法尼亚州西部UPMC卫生系统医院的icu。患者:297名患有急性呼吸衰竭的危重成人。干预措施:没有。测量和主要结果:我们测量了研究入组时收集的基线样本中的GLP-1和GIP水平。我们比较了不同疾病严重程度亚组的肠促肠素水平,并研究了肠促肠素与全身宿主反应和肠通透性标志物之间的关系。在我们的初步分析中,我们通过未调整分析和调整年龄、顺序器官衰竭评估评分和循环白细胞介素-6水平的分析,通过逻辑回归测试了每种肠促胰岛素水平与90天死亡率的关系。与气管插管保护患者相比,非幸存者和急性呼吸窘迫综合征患者或有急性呼吸窘迫综合征风险的患者GLP-1水平较高。GLP-1水平也与全身免疫反应生物标志物呈正相关,但与肠通透性标志物无关。未校正的GLP-1水平与死亡率呈正相关(优势比为1.99 [1.55-2.56];P < 0.01),调整后P < 2.02 [1.23-3.31];P < 0.01)分析。GIP水平与死亡率或宿主反应生物标志物无关。结论:GLP-1水平与急性呼吸衰竭危重患者全身炎症和死亡率呈正相关,而与GIP水平无关。升高的循环GLP-1水平可以作为预后生物标志物来识别可能有较差预后的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Glucagon-Like Peptide-1 Is Prognostic of Mortality in Acute Respiratory Failure.

Glucagon-Like Peptide-1 Is Prognostic of Mortality in Acute Respiratory Failure.

Glucagon-Like Peptide-1 Is Prognostic of Mortality in Acute Respiratory Failure.

Glucagon-Like Peptide-1 Is Prognostic of Mortality in Acute Respiratory Failure.

Objectives: The incretin hormones glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP) have therapeutic effects in diabetes mellitus. Prior clinical studies suggest incretins are prognostic of adverse outcomes in critical illness. We investigated whether incretin levels indicate disease severity and clinical outcomes in patients with acute respiratory failure, a common cause of critical illness.

Design: Retrospective cohort study.

Setting: ICUs in UPMC Health Systems hospitals within Western Pennsylvania.

Patients: Two hundred ninety-seven critically ill adults with acute respiratory failure.

Interventions: None.

Measurements and main results: We measured GLP-1 and GIP levels in baseline samples collected at the time of study enrollment. We compared incretin levels across subgroups differing by severity of illness and investigated associations between incretins and markers of systemic host responses and intestinal permeability. In our primary analysis, we tested the association of each incretin level with 90-day mortality by logistic regression in unadjusted analyses and in analyses adjusted for age, Sequential Organ Failure Assessment score, and circulating interleukin-6 levels. GLP-1 levels were higher in nonsurvivors and patients with or at-risk for acute respiratory distress syndrome compared to those intubated for airway protection. GLP-1 levels also positively correlated with systemic immune response biomarkers but not with markers of intestinal permeability. GLP-1 levels positively correlated with mortality in unadjusted (odds ratio, 1.99 [1.55-2.56]; p < 0.01) and adjusted (2.02 [1.23-3.31]; p < 0.01) analyses. GIP levels were not associated with mortality or with host response biomarkers.

Conclusions: GLP-1 but not GIP levels were positively associated with systemic inflammation and mortality in critically ill patients with acute respiratory failure. Increased circulating GLP-1 levels may serve as prognostic biomarkers to identify patients who are likely to have worse outcomes.

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