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. 2023 Mar 3;14:1215. doi: 10.1038/s41467-023-36858-6

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Biomarkers cytoplasmic aconitate hydratase (ACO1), fructosebisphosphate aldolase B (ALDOB), argininosuccinate synthase (ASS1), liver carboxylesterase 1 (CES1), carbamoylphosphate synthase (CPS1), fructose-1,6-bisphosphatase 1 (FBP1), fumarylacetoacetase (FAH), glutathione S-transferase A1 (GSTA1), 4-hydroxyphenylpyruvate dioxygenase (HPD), leukocyte cell-derived chemotaxin-2 (LECT2), ornithine carbamoyltransferase (OTC) were identified using tandem mass tagging (TMT) mass spectrometry (MS) and subsequent ratio of light peptide/heavy isotopically labeled peptide or enzyme-linked immunosorbent assay (ELISA) in serum from healthy volunteers (HV), patients with nonalcoholic fatty liver disease (NAFLD), DILI or non-DILI, either at onset (DO or NDO, respectively) or at follow-up (DF or NDF).