<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu H</submitter><funding>Qingfeng Scientific Research Fund of the China Crohn's &amp; Colitis Foundation</funding><funding>Project 1010 of Sixth Affiliated Hospital of Sun Yat-Sen University</funding><funding>Project 5010 of Sun Yat-Sen University</funding><funding>National Natural Science Foundation of China</funding><funding>the program of Guangdong Provincial Clinical Research Center for Digestive Diseases</funding><funding>Guangzhou Science and Technology Fund</funding><pagination>190</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11761900</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>&lt;b>Background and Aims:&lt;/b> Inflammatory bowel disease (IBD) requires effective treatment options. Upadacitinib, a Janus kinase 1 (JAK1) inhibitor, has shown effectiveness in trials for Crohn's disease (CD) and ulcerative colitis (UC). This study evaluates its real-world effectiveness and safety. &lt;b>Methods:&lt;/b> We conducted a multicenter retrospective cohort study in tertiary care centers, involving patients treated with upadacitinib from January 2023 to September 2024. The study included adult patients aged 18 years or older, diagnosed with UC or CD, who received at least 8 weeks of upadacitinib therapy. Treatment outcomes were evaluated using established clinical, endoscopic, imaging, histological, and laboratory parameters. &lt;b>Results:&lt;/b> A total of 236 IBD patients received upadaciti</pubmed_abstract><journal>Biomedicines</journal><pubmed_title>An Analysis of the Effectiveness and Safety of Upadacitinib in the Treatment of Inflammatory Bowel Disease: A Multicenter Real-World Study.</pubmed_title><pmcid>PMC11761900</pmcid><funding_grant_id>1010PY(2020)-55</funding_grant_id><funding_grant_id>81900490 81670477 and 82270544</funding_grant_id><funding_grant_id>2020B1111170004</funding_grant_id><funding_grant_id>CCCF-QF-2022A53-2 and CCCF-QF-2022B43-14</funding_grant_id><funding_grant_id>2014008</funding_grant_id><funding_grant_id>2024A03J0791</funding_grant_id><pubmed_authors>Peng X</pubmed_authors><pubmed_authors>Xie T</pubmed_authors><pubmed_authors>Su T</pubmed_authors><pubmed_authors>Yao J</pubmed_authors><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Yu Q</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhi M</pubmed_authors><pubmed_authors>Wu H</pubmed_authors></additional><is_claimable>false</is_claimable><name>An Analysis of the Effectiveness and Safety of Upadacitinib in the Treatment of Inflammatory Bowel Disease: A Multicenter Real-World Study.</name><description>&lt;b>Background and Aims:&lt;/b> Inflammatory bowel disease (IBD) requires effective treatment options. Upadacitinib, a Janus kinase 1 (JAK1) inhibitor, has shown effectiveness in trials for Crohn's disease (CD) and ulcerative colitis (UC). This study evaluates its real-world effectiveness and safety. &lt;b>Methods:&lt;/b> We conducted a multicenter retrospective cohort study in tertiary care centers, involving patients treated with upadacitinib from January 2023 to September 2024. The study included adult patients aged 18 years or older, diagnosed with UC or CD, who received at least 8 weeks of upadacitinib therapy. Treatment outcomes were evaluated using established clinical, endoscopic, imaging, histological, and laboratory parameters. &lt;b>Results:&lt;/b> A total of 236 IBD patients received upadaciti</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-04T22:08:05.861Z</modification><creation>2025-04-04T22:08:05.861Z</creation></dates><accession>S-EPMC11761900</accession><cross_references><pubmed>39857773</pubmed><doi>10.3390/biomedicines13010190</doi></cross_references></HashMap>