<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu FQ</submitter><funding>Key Technologies Research and Development Program</funding><funding>Natural Science Foundation of Beijing Municipality</funding><funding>Department of Human Resources and Social Security of Jiangsu Province</funding><funding>Peking University Medicine</funding><funding>China Postdoctoral Science Foundation</funding><funding>National Natural Science Foundation of China</funding><funding>Capital Health Research and Development of Special Fund</funding><pagination>e2410417</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12165022</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(22)</volume><pubmed_abstract>Corticosteroids (CSs) are the initial therapy for immune thrombocytopenia (ITP); however, their efficacy is not adequately predicted. As a novel biomarker, the composition of the gut microbiota is non-invasively tested and altered in patients with ITP. This study aims to develop a predictive model that leverages gut microbiome data to predict the CS response in patients with ITP within the initial four weeks of treatment. Metagenomic sequencing is performed on fecal samples from 212 patients with ITP, 152 of whom underwent CS treatment and follow-up. Predictive models are trained using six machine-learning algorithms, integrating clinical indices and gut microbiome data. The support vector machine (SVM) algorithm-based model has the highest accuracy (AUC = 0.80). This model utilized a comp</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Correlation Between Fecal Microbiota and Corticosteroid Responsiveness in Primary Immune Thrombocytopenia: an Exploratory Study.</pubmed_title><pmcid>PMC12165022</pmcid><funding_grant_id>2024M761208</funding_grant_id><funding_grant_id>82350004</funding_grant_id><funding_grant_id>2022-1-4082</funding_grant_id><funding_grant_id>2023YFC2507803</funding_grant_id><funding_grant_id>2023ZB182</funding_grant_id><funding_grant_id>82430006</funding_grant_id><funding_grant_id>82300149</funding_grant_id><funding_grant_id>71003Y3035</funding_grant_id><funding_grant_id>82130008</funding_grant_id><funding_grant_id>7232188</funding_grant_id><funding_grant_id>7242154</funding_grant_id><funding_grant_id>82230004</funding_grant_id><pubmed_authors>Zhou JY</pubmed_authors><pubmed_authors>Yu L</pubmed_authors><pubmed_authors>Huang QS</pubmed_authors><pubmed_authors>Yu F</pubmed_authors><pubmed_authors>Wu YJ</pubmed_authors><pubmed_authors>Gao D</pubmed_authors><pubmed_authors>Zhang BS</pubmed_authors><pubmed_authors>Cooperative ITP Working Group</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Cui LJ</pubmed_authors><pubmed_authors>Zhu XY</pubmed_authors><pubmed_authors>Cheng YF</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhou HB</pubmed_authors><pubmed_authors>Wang LL</pubmed_authors><pubmed_authors>Li YY</pubmed_authors><pubmed_authors>Li ML</pubmed_authors><pubmed_authors>Liu FQ</pubmed_authors><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Chen YX</pubmed_authors><pubmed_authors>Jiang ZX</pubmed_authors><pubmed_authors>Ren JH</pubmed_authors><pubmed_authors>Li YH</pubmed_authors><pubmed_authors>Qu QY</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Fu HX</pubmed_authors><pubmed_authors>Zhang XH</pubmed_authors><pubmed_authors>Huang RB</pubmed_authors><pubmed_authors>Qiao JL</pubmed_authors><pubmed_authors>Zang MT</pubmed_authors><pubmed_authors>Wang QF</pubmed_authors><pubmed_authors>An ZY</pubmed_authors><pubmed_authors>Feng J</pubmed_authors><pubmed_authors>Huang XJ</pubmed_authors><pubmed_authors>Xiao MY</pubmed_authors><pubmed_authors>Liu ZG</pubmed_authors><pubmed_authors>Jing HM</pubmed_authors><pubmed_authors>Hu DH</pubmed_authors><pubmed_authors>Feng R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Correlation Between Fecal Microbiota and Corticosteroid Responsiveness in Primary Immune Thrombocytopenia: an Exploratory Study.</name><description>Corticosteroids (CSs) are the initial therapy for immune thrombocytopenia (ITP); however, their efficacy is not adequately predicted. As a novel biomarker, the composition of the gut microbiota is non-invasively tested and altered in patients with ITP. This study aims to develop a predictive model that leverages gut microbiome data to predict the CS response in patients with ITP within the initial four weeks of treatment. Metagenomic sequencing is performed on fecal samples from 212 patients with ITP, 152 of whom underwent CS treatment and follow-up. Predictive models are trained using six machine-learning algorithms, integrating clinical indices and gut microbiome data. The support vector machine (SVM) algorithm-based model has the highest accuracy (AUC = 0.80). This model utilized a comp</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2026-06-01T23:20:22.105Z</modification><creation>2026-05-23T03:08:09.083Z</creation></dates><accession>S-EPMC12165022</accession><cross_references><pubmed>40040609</pubmed><doi>10.1002/advs.202410417</doi></cross_references></HashMap>