<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Blesl A</submitter><funding>Austrian National Bank</funding><funding>Austrian Society of Gastroenterology and Hepatology</funding><pagination>9-19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10769779</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Corticosteroids are used for induction of remission in patients with moderately to severely active ulcerative colitis. However, up to one-third of patients fail to this therapy. We investigated if fecal microbial composition or its metabolic capacity are associated with response to systemic corticosteroids.&lt;h4>Methods&lt;/h4>In this prospective, multicenter study, patients with active ulcerative colitis (Lichtiger score ≥4) receiving systemic corticosteroids were eligible. Data were assessed and fecal samples collected before and after 4 weeks of treatment. Patients were divided into responders (decrease of Lichtiger Score ≥50%) and nonresponders. The fecal microbiome was assessed by the 16S rRNA gene marker and analyzed with QIIME 2. Microbial metabolic pathways were predi</pubmed_abstract><journal>Inflammatory bowel diseases</journal><pubmed_title>Prediction of Response to Systemic Corticosteroids in Active UC by Microbial Composition-A Prospective Multicenter Study.</pubmed_title><pmcid>PMC10769779</pmcid><funding_grant_id>DFG RU5042</funding_grant_id><funding_grant_id>01ZX1915A</funding_grant_id><funding_grant_id>17936</funding_grant_id><pubmed_authors>Reinisch W</pubmed_authors><pubmed_authors>Watschinger C</pubmed_authors><pubmed_authors>Kump P</pubmed_authors><pubmed_authors>Aden K</pubmed_authors><pubmed_authors>Mayer A</pubmed_authors><pubmed_authors>Hogenauer C</pubmed_authors><pubmed_authors>Tillinger W</pubmed_authors><pubmed_authors>Binder L</pubmed_authors><pubmed_authors>Ludwiczek O</pubmed_authors><pubmed_authors>Koch R</pubmed_authors><pubmed_authors>Reider S</pubmed_authors><pubmed_authors>Moschen A</pubmed_authors><pubmed_authors>Blesl A</pubmed_authors><pubmed_authors>Haas T</pubmed_authors><pubmed_authors>Grochenig HP</pubmed_authors><pubmed_authors>Novacek G</pubmed_authors><pubmed_authors>Furst S</pubmed_authors><pubmed_authors>Primas C</pubmed_authors><pubmed_authors>Reicht G</pubmed_authors><pubmed_authors>Waschina S</pubmed_authors><pubmed_authors>Kutschera M</pubmed_authors><pubmed_authors>Wurm P</pubmed_authors><pubmed_authors>Hennlich B</pubmed_authors><pubmed_authors>Gorkiewicz G</pubmed_authors><pubmed_authors>Miehsler W</pubmed_authors><pubmed_authors>Illiasch C</pubmed_authors><pubmed_authors>Steidl K</pubmed_authors><pubmed_authors>Steiner P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prediction of Response to Systemic Corticosteroids in Active UC by Microbial Composition-A Prospective Multicenter Study.</name><description>&lt;h4>Background&lt;/h4>Corticosteroids are used for induction of remission in patients with moderately to severely active ulcerative colitis. However, up to one-third of patients fail to this therapy. We investigated if fecal microbial composition or its metabolic capacity are associated with response to systemic corticosteroids.&lt;h4>Methods&lt;/h4>In this prospective, multicenter study, patients with active ulcerative colitis (Lichtiger score ≥4) receiving systemic corticosteroids were eligible. Data were assessed and fecal samples collected before and after 4 weeks of treatment. Patients were divided into responders (decrease of Lichtiger Score ≥50%) and nonresponders. The fecal microbiome was assessed by the 16S rRNA gene marker and analyzed with QIIME 2. Microbial metabolic pathways were predi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2026-06-01T21:51:14.804Z</modification><creation>2024-12-04T10:29:21.583Z</creation></dates><accession>S-EPMC10769779</accession><cross_references><pubmed>37463118</pubmed><doi>10.1093/ibd/izad126</doi></cross_references></HashMap>