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The MicroRNA-based Liquid Biopsy Improves Early Assessment of Lethal Acetaminophen Poisoning: A Case Report

Patient: Female, 44-year-old Final Diagnosis: Acute liver failure Symptoms: APAP overdose Medication: Acetaminophen Clinical Procedure: — Specialty: Molecular Biology OBJECTIVE: Unusual clinical course BACKGROUND: Acetaminophen overdose is the most common cause of acute liver failure. Nevertheless,...

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Detalles Bibliográficos
Autores principales: Krauskopf, Julian, Gosink, Mark M., Schomaker, Shelli, Caiment, Florian, Warner, Roscoe, Johnson, Kent, Kleinjans, Jos, Aubrecht, Jiri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049075/
https://www.ncbi.nlm.nih.gov/pubmed/32086430
http://dx.doi.org/10.12659/AJCR.919289
Descripción
Sumario:Patient: Female, 44-year-old Final Diagnosis: Acute liver failure Symptoms: APAP overdose Medication: Acetaminophen Clinical Procedure: — Specialty: Molecular Biology OBJECTIVE: Unusual clinical course BACKGROUND: Acetaminophen overdose is the most common cause of acute liver failure. Nevertheless, new biomarker approaches enabling early prediction of the outcome of the acetaminophen overdose are needed. Recently, using next-generation sequencing analysis of serum from human study participants we uncovered injury-specific signatures of circulating microRNAs (miRNAs) that represented underlying molecular mechanisms of toxicity. This case study is first to show the application of miRNA profiling to assess prognosis of acetaminophen poisoning. CASE REPORT: The patient was admitted to the hospital following supra therapeutic acetaminophen ingestion. The patient showed elevated levels of biomarkers of hepatocellular injury alanine aminotransferase, aspartate transaminase, and glutamate dehydrogenase. Even though treatment with N-acetyl cysteine was initiated 24 hours post-ingestion, levels of alanine-aminotransferase and aspartate transaminase peaked at about 40 hours post ingestion of acetaminophen. We analyzed global circulating miRNA levels from 24 consecutive serum samples from this study participant covering the period from admission to time of death. CONCLUSIONS: The resulting global miRNA profiles were compared with profiles from study participants with non-lethal acetaminophen poisoning and healthy controls. At the admission, the miRNA profiles of both lethal and non-lethal acetaminophen poisoning showed induction of cellular stress and oxidative damage. Later, the miRNA profiles of the lethal poisoning featured fibrosis and coagulation pathways while profiles of non-lethal cases resembled those of healthy study participants. Although additional confirmatory studies are needed, our case study is first to indicate that global miRNA profiles to be used as liquid biopsies have potential to facilitate the assessment of acetaminophen poisoning.