巨噬细胞迁移抑制因子作为对乙酰氨基酚过量的潜在生物标志物:一项初步研究。

Joshua Bloom, Teddy Uzamere, Yasmin Hurd, Alex F Manini
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引用次数: 0

摘要

在美国,对乙酰氨基酚过量是导致肝功能衰竭的主要原因。巨噬细胞迁移抑制因子(MIF)是一种早期释放的细胞因子,在临床前模型中促进对乙酰氨基酚的毒性。这种细胞因子可能被证明是急诊科(ED)患者在急性对乙酰氨基酚过量后的一个有用的生物标志物。方法:我们从疑似急性用药过量的ED患者前瞻性连续队列中选择了13例患者作为方便样本。研究人员收集用于MIF分析的废弃标本,这些标本在用于临床护理后仍然存在。我们的研究小组将确诊的对乙酰氨基酚过量患者(n=9)与未暴露或肝损伤的患者(n=3)和未检测到对乙酰氨基酚的肝损伤患者(n=1)进行了比较。结果:在我们的对乙酰氨基酚组,所有9例患者都有可测量的对乙酰氨基酚浓度。过量组中位MIF血清浓度为16.08 ng/mL (IQR为2.06,91.40),对照组中位MIF血清浓度为0.19 ng/mL (IQR为0.05,0.32)(p = 0.0091)。结论:在这项初步研究中,MIF在ED药物过量队列的标本中是可行的,并且与没有肝损伤的非对乙酰氨基酚组相比,对乙酰氨基酚组的MIF显著升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Macrophage Migration Inhibitory Factor as a Potential Biomarker in Acetaminophen Overdose: A Pilot Study.

Macrophage Migration Inhibitory Factor as a Potential Biomarker in Acetaminophen Overdose: A Pilot Study.

Macrophage Migration Inhibitory Factor as a Potential Biomarker in Acetaminophen Overdose: A Pilot Study.

Introduction: Acetaminophen overdose is a leading cause of liver failure in the United States. Macrophage migration inhibitory factor (MIF) is a cytokine that is released early and promotes acetaminophen toxicity in preclinical models. This cytokine could prove a useful biomarker in emergency department (ED) patients immediately following an acute acetaminophen overdose.

Methods: We selected a convenience sample of thirteen patients from a prospective consecutive cohort of ED patients with suspected acute overdose. Research associates collected waste specimens for MIF analysis that remained after use for clinical care. Our team compared patients with confirmed acetaminophen overdose (n=9) to patients without acetaminophen exposure or liver injury (n=3) and a patient with liver injury in the absence of detectable acetaminophen (n=1).

Results: In our acetaminophen group, all nine patients had measurable acetaminophen concentrations. Median MIF serum concentrations were 16.08 ng/mL (IQR 2.06, 91.40) in the overdose group compared with the control group serum concentrations of 0.19 ng/mL (IQR 0.05, 0.32) (p = 0.0091).

Conclusion: In this pilot study, MIF was feasible to measure in specimens from an ED drug overdose cohort, and was significantly elevated in the acetaminophen group compared to non-acetaminophen controls without liver injury.

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