Edinburgh Clinical Toxicology, Royal Infirmary of Edinburgh, Edinburgh, UK.
Department of Neuroscience, Psychiatry, Drug Area and Child Health (NEUROFARBA), Section of Pharmacology and Toxicology, University of Florence, Florence, Italy.
Mol Biol Rep. 2024 Apr 20;51(1):548. doi: 10.1007/s11033-024-09327-6.
Paracetamol (acetaminophen) overdose is a leading cause of acute liver failure in many Western countries. Diagnostic tools for this poisoning may be suboptimal in some cases and new biomarkers have been investigated. We investigated the role of capillary microRNA-122 (miR-122) as a prognostic biomarker of liver injury in the clinical management of patients with paracetamol overdose.
In a paracetamol overdose patient cohort, miR-122 was measured by quantitative polymerase chain reaction in a blood drop obtained by a finger prick at the end of an antidote cycle treatment with N-acetylcysteine treatment (12 h). Liver injury was defined as serum alanine aminotransferase (ALT) activity > 100 IU/L collected at 10 or 20 h after the start of treatment. Pearson's correlation analyses were performed.
In patients with paracetamol overdose, capillary miR-122 was positively correlated with ALT measured at 10 h and at 20 h (r = 0.83, P < 0.0001; r = 0.96, P < 0.0001, respectively).
This work supports the potential use of capillary miR-122 as a prognostic biomarker of liver injury throughout clinical management of patients with paracetamol overdose. Capillary miR-122 can be measured in a blood drop collected by a finger prick, a minimally invasive diagnostic test for patient stratification.
对乙酰氨基酚(扑热息痛)过量是许多西方国家急性肝衰竭的主要原因。这种中毒的诊断工具在某些情况下可能不够理想,已经研究了新的生物标志物。我们研究了毛细血管 microRNA-122(miR-122)作为乙酰半胱氨酸解毒治疗结束时指尖采血中检测到的预后生物标志物在扑热息痛过量患者临床管理中的作用。
在扑热息痛过量患者队列中,通过定量聚合酶链反应测量 N-乙酰半胱氨酸解毒治疗结束时指尖采血中的 miR-122(12 小时)。肝损伤定义为治疗开始后 10 或 20 小时采集的血清丙氨酸氨基转移酶(ALT)活性>100IU/L。进行 Pearson 相关分析。
在扑热息痛过量患者中,毛细血管 miR-122 与治疗 10 小时和 20 小时时测量的 ALT 呈正相关(r=0.83,P<0.0001;r=0.96,P<0.0001)。
这项工作支持毛细血管 miR-122 作为扑热息痛过量患者临床管理中肝损伤预后生物标志物的潜在用途。可以通过指尖采血测量毛细血管 miR-122,这是一种用于患者分层的微创诊断测试。