<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Roman-Saguillo S</submitter><funding>The Ministerio de Educación</funding><funding>Ministerio de Ciencia, Innovación y Universidades</funding><funding>Finance the Predoctoral Recruitment of Research Personnel by the Junta de Castilla y Leon</funding><funding>Junta de Castilla y León and the European Regional Development Fund</funding><funding>Ministerio de Ciencia e Innovación</funding><funding>Instituto de Salud Carlos III (ISCIII)</funding><pagination>6863</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11241776</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(13)</volume><pubmed_abstract>Several hepatic disorders are influenced by gut microbiota, but its role in idiosyncratic drug-induced liver injury (iDILI), whose main causative agent is amoxicillin-clavulanate, remains unknown. This pioneering study aims to unravel particular patterns of gut microbiota composition and associated metabolites in iDILI and iDILI patients by amoxicillin-clavulanate (iDILI-AC). Thus, serum and fecal samples from 46 patients were divided into three study groups: healthy controls (n = 10), non-iDILI acute hepatitis (n = 12) and iDILI patients (n = 24). To evaluate the amoxicillin-clavulanate effect, iDILI patients were separated into two subgroups: iDILI non-caused by amoxicillin-clavulanate (iDILI-nonAC) (n = 18) and iDILI-AC patients (n = 6). Gut microbiota composition and fecal metabolome p</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Idiosyncratic Drug-Induced Liver Injury and Amoxicillin-Clavulanate: Spotlight on Gut Microbiota, Fecal Metabolome and Bile Acid Profile in Patients.</pubmed_title><pmcid>PMC11241776</pmcid><funding_grant_id>GRS2126/A/2020</funding_grant_id><funding_grant_id>LE017-P20</funding_grant_id><funding_grant_id>FPU18/06257</funding_grant_id><funding_grant_id>PI20/00690</funding_grant_id><funding_grant_id>PID2020-120363RB-I00</funding_grant_id><pubmed_authors>Gonzalez-Gallego J</pubmed_authors><pubmed_authors>Robles-Diaz M</pubmed_authors><pubmed_authors>Garcia-Mediavilla MV</pubmed_authors><pubmed_authors>Stephens C</pubmed_authors><pubmed_authors>Juarez-Fernandez M</pubmed_authors><pubmed_authors>Jorquera Plaza F</pubmed_authors><pubmed_authors>Jover R</pubmed_authors><pubmed_authors>Sanchez-Campos S</pubmed_authors><pubmed_authors>Martinez-Florez S</pubmed_authors><pubmed_authors>Quinones Castro R</pubmed_authors><pubmed_authors>Nistal E</pubmed_authors><pubmed_authors>Soluyanova P</pubmed_authors><pubmed_authors>Roman-Saguillo S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Idiosyncratic Drug-Induced Liver Injury and Amoxicillin-Clavulanate: Spotlight on Gut Microbiota, Fecal Metabolome and Bile Acid Profile in Patients.</name><description>Several hepatic disorders are influenced by gut microbiota, but its role in idiosyncratic drug-induced liver injury (iDILI), whose main causative agent is amoxicillin-clavulanate, remains unknown. This pioneering study aims to unravel particular patterns of gut microbiota composition and associated metabolites in iDILI and iDILI patients by amoxicillin-clavulanate (iDILI-AC). Thus, serum and fecal samples from 46 patients were divided into three study groups: healthy controls (n = 10), non-iDILI acute hepatitis (n = 12) and iDILI patients (n = 24). To evaluate the amoxicillin-clavulanate effect, iDILI patients were separated into two subgroups: iDILI non-caused by amoxicillin-clavulanate (iDILI-nonAC) (n = 18) and iDILI-AC patients (n = 6). Gut microbiota composition and fecal metabolome p</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-07-09T11:09:35.752Z</modification><creation>2026-07-09T10:41:35.4Z</creation></dates><accession>S-EPMC11241776</accession><cross_references><pubmed>38999973</pubmed><doi>10.3390/ijms25136863</doi></cross_references></HashMap>