Ammonium quantification in human plasma by proton nuclear magnetic resonance for staging of liver fibrosis in alcohol-related liver disease and nonalcoholic fatty liver disease |
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Authors: | Marc Azagra Elisa Pose Francesco De Chiara Martina Perez Emma Avitabile Joan-Marc Servitja Laura Brugnara Javier Ramon-Azcón Irene Marco-Rius |
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Affiliation: | 1. Institute for Bioengineering of Catalonia, The Barcelona Institute of Science and Technology, Barcelona, Spain;2. Liver Unit, Hospital Clinic, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain;3. Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Barcelona, Spain;4. Institute for Bioengineering of Catalonia, The Barcelona Institute of Science and Technology, Barcelona, Spain ICREA-Institució Catalana de Recerca i Estudis Avançats, Barcelona, Spain |
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Abstract: | Liver fibrosis staging is a key element driving the prognosis of patients with chronic liver disease. Currently, biopsy is the only technique capable of diagnosing liver fibrosis in patients with alcohol-related liver disease (ArLD) and nonalcoholic fatty liver disease (NAFLD) unequivocally. Noninvasive (e.g. plasma-based) biomarker assays are attractive tools to diagnose and stage disease, yet must prove that they are reliable and sensitive to be used clinically. Here, we demonstrate proton nuclear magnetic resonance as a method to rapidly quantify the endogenous concentration of ammonium ions from human plasma extracts and show their ability to report upon early and advanced stages of ArLD and NAFLD. We show that, irrespective of the disease etiology, ammonium concentration is a more robust and informative marker of fibrosis stage than current clinically assessed blood hepatic biomarkers. Subject to validation in larger cohorts, the study indicates that the method can provide accurate and rapid staging of ArLD and NAFLD without the need for an invasive biopsy. |
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Keywords: | ammonium quantification blood biomarkers chronic liver disease disease biomarkers hepatic dysfunction NMR |
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