<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jangi S</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>NCATS NIH HHS</funding><funding>Tufts University School of Medicine</funding><funding>National Institutes of Health</funding><pagination>821-830.e7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10960711</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(4)</volume><pubmed_abstract>&lt;h4>Background &amp; aims&lt;/h4>Intestinal fungi have been implicated in the pathogenesis of ulcerative colitis (UC). However, it remains unclear if fungal composition is altered during active versus quiescent disease.&lt;h4>Methods&lt;/h4>We analyzed clinical and metagenomic data from the Study of a Prospective Adult Research Cohort with Inflammatory Bowel Disease (SPARC IBD), available via the IBD Plexus Program of the Crohn's &amp; Colitis Foundation. We evaluated the fungal composition of fecal samples from 421 patients with UC during clinical activity and remission. Within a longitudinal subcohort (n = 52), we assessed for dynamic taxonomic changes across alterations in clinical activity over time. We examined if fungal amplicon sequence variants and fungal-bacterial relationships were altered during activity versus remission. Finally, we classified activity in UC using a supervised machine learning random forest model trained on fungal abundance data.&lt;h4>Results&lt;/h4>During clinical activity, the relative abundance of genus Candida was increased 3.5-fold (P-adj &lt; 1 × 10&lt;sup>-4&lt;/sup>) compared with during remission. Patients with longitudinal reductions in clinical activity demonstrated parallel reductions in Candida relative abundance (P &lt; .05). Candida relative abundance correlated with Parabacteroides diastonis, Faecalibacterium prausnitzii, and Bacteroides dorei relative abundance (P &lt; .05) during remission; however, these correlations were disrupted during activity. Fungal abundance data successfully classified patients with active or quiescent UC (area under the curve ∼0.80), with Candida relative abundance critical to the success of the model.&lt;h4>Conclusions&lt;/h4>Clinical activity in UC is associated with an increased relative abundance of Candida, cross-sectionally and dynamically over time. The role of fecal Candida as a target for therapeutics in UC should be evaluated.</pubmed_abstract><journal>Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association</journal><pubmed_title>Dynamics of the Gut Mycobiome in Patients With Ulcerative Colitis.</pubmed_title><pmcid>PMC10960711</pmcid><funding_grant_id>KL2TR002545</funding_grant_id><funding_grant_id>KL2 TR002545</funding_grant_id><pubmed_authors>Friedman S</pubmed_authors><pubmed_authors>Zhao N</pubmed_authors><pubmed_authors>Michaud DS</pubmed_authors><pubmed_authors>Hsia K</pubmed_authors><pubmed_authors>Singh S</pubmed_authors><pubmed_authors>Jangi S</pubmed_authors><pubmed_authors>Kumamoto CA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dynamics of the Gut Mycobiome in Patients With Ulcerative Colitis.</name><description>&lt;h4>Background &amp; aims&lt;/h4>Intestinal fungi have been implicated in the pathogenesis of ulcerative colitis (UC). However, it remains unclear if fungal composition is altered during active versus quiescent disease.&lt;h4>Methods&lt;/h4>We analyzed clinical and metagenomic data from the Study of a Prospective Adult Research Cohort with Inflammatory Bowel Disease (SPARC IBD), available via the IBD Plexus Program of the Crohn's &amp; Colitis Foundation. We evaluated the fungal composition of fecal samples from 421 patients with UC during clinical activity and remission. Within a longitudinal subcohort (n = 52), we assessed for dynamic taxonomic changes across alterations in clinical activity over time. We examined if fungal amplicon sequence variants and fungal-bacterial relationships were altered during activity versus remission. Finally, we classified activity in UC using a supervised machine learning random forest model trained on fungal abundance data.&lt;h4>Results&lt;/h4>During clinical activity, the relative abundance of genus Candida was increased 3.5-fold (P-adj &lt; 1 × 10&lt;sup>-4&lt;/sup>) compared with during remission. Patients with longitudinal reductions in clinical activity demonstrated parallel reductions in Candida relative abundance (P &lt; .05). Candida relative abundance correlated with Parabacteroides diastonis, Faecalibacterium prausnitzii, and Bacteroides dorei relative abundance (P &lt; .05) during remission; however, these correlations were disrupted during activity. Fungal abundance data successfully classified patients with active or quiescent UC (area under the curve ∼0.80), with Candida relative abundance critical to the success of the model.&lt;h4>Conclusions&lt;/h4>Clinical activity in UC is associated with an increased relative abundance of Candida, cross-sectionally and dynamically over time. The role of fecal Candida as a target for therapeutics in UC should be evaluated.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-07-11T03:03:47.699Z</modification><creation>2025-07-11T03:03:47.699Z</creation></dates><accession>S-EPMC10960711</accession><cross_references><pubmed>37802272</pubmed><doi>10.1016/j.cgh.2023.09.023</doi></cross_references></HashMap>