<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Latosinska A</submitter><funding>Bundesministerium für Bildung und Forschung</funding><funding>FIS/Fondos FEDER</funding><funding>Comunidad de Madrid en Biomedicina</funding><funding>Austrian Science Fund FWF</funding><funding>Instituto de Salud Carlos III</funding><funding>Agence Nationale de la Recherche</funding><funding>Horizon 2020 Framework Programme</funding><funding>Bundesministerium für Wirtschaft und Klimaschutz</funding><funding>European Health and Digital Executive Agency</funding><funding>European Cooperation in Science and Technology</funding><funding>HORIZON EUROPE Marie Sklodowska- Curie Actions</funding><funding>HORIZON EUROPE Marie Sklodowska-Curie Actions</funding><pagination>943</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12372250</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>Chronic kidney disease (CKD) contributes to global morbidity and mortality. Early, targeted intervention can help mitigate its impact. CK273 is a urinary peptide classifier previously validated in a prospective clinical trial for the early detection of nephropathy. We hypothesized that drug-induced molecular changes in the urinary peptidome could be predicted in silico and guide selecting interventions for individual patients. The efficacy of the urinary peptidomic classifier CKD273 in predicting major adverse kidney events (≥ 40% decline in estimated glomerular filtration rate or kidney failure -median follow-up: 1.50 (95%CI 0.35, 5.0) years), was confirmed in a retrospective cohort of 935 participants. In silico prediction of treatment effects from four drug-based interventions (Mineralo</pubmed_abstract><journal>Journal of translational medicine</journal><pubmed_title>In silico prediction of optimal multifactorial intervention in chronic kidney disease.</pubmed_title><pmcid>PMC12372250</pmcid><funding_grant_id>P2022/BMD-7223</funding_grant_id><funding_grant_id>ANR-22-PERM-0002-06</funding_grant_id><funding_grant_id>AC22/00027</funding_grant_id><funding_grant_id>Grant-DOI 10.55776/I6464</funding_grant_id><funding_grant_id>SPACKDc PMP21/00109</funding_grant_id><funding_grant_id>101168626</funding_grant_id><funding_grant_id>RICORS program to RICORS2040 (RD21/0005/0001)</funding_grant_id><funding_grant_id>101101220</funding_grant_id><funding_grant_id>CIFRACOR-CM</funding_grant_id><funding_grant_id>101072828</funding_grant_id><funding_grant_id>ZIMKK5560002AP3</funding_grant_id><funding_grant_id>848011</funding_grant_id><funding_grant_id>CA21165</funding_grant_id><funding_grant_id>01EK2105C</funding_grant_id><funding_grant_id>01EK2105B</funding_grant_id><funding_grant_id>01EK2105A</funding_grant_id><funding_grant_id>01KU2307</funding_grant_id><funding_grant_id>I 6464</funding_grant_id><pubmed_authors>Delles C</pubmed_authors><pubmed_authors>Golovko I</pubmed_authors><pubmed_authors>Beige J</pubmed_authors><pubmed_authors>Siwy J</pubmed_authors><pubmed_authors>Rossing P</pubmed_authors><pubmed_authors>Nguyen TMN</pubmed_authors><pubmed_authors>Mayer G</pubmed_authors><pubmed_authors>Persson F</pubmed_authors><pubmed_authors>Peter K</pubmed_authors><pubmed_authors>Latosinska A</pubmed_authors><pubmed_authors>Ortiz A</pubmed_authors><pubmed_authors>Rupprecht H</pubmed_authors><pubmed_authors>Schanstra JP</pubmed_authors><pubmed_authors>Mina IK</pubmed_authors><pubmed_authors>Staessen JA</pubmed_authors><pubmed_authors>Rychlik I</pubmed_authors><pubmed_authors>Keller F</pubmed_authors><pubmed_authors>Glorieux G</pubmed_authors><pubmed_authors>Clark AL</pubmed_authors><pubmed_authors>Campbell A</pubmed_authors><pubmed_authors>Mischak H</pubmed_authors><pubmed_authors>Vlahou A</pubmed_authors></additional><is_claimable>false</is_claimable><name>In silico prediction of optimal multifactorial intervention in chronic kidney disease.</name><description>Chronic kidney disease (CKD) contributes to global morbidity and mortality. Early, targeted intervention can help mitigate its impact. CK273 is a urinary peptide classifier previously validated in a prospective clinical trial for the early detection of nephropathy. We hypothesized that drug-induced molecular changes in the urinary peptidome could be predicted in silico and guide selecting interventions for individual patients. The efficacy of the urinary peptidomic classifier CKD273 in predicting major adverse kidney events (≥ 40% decline in estimated glomerular filtration rate or kidney failure -median follow-up: 1.50 (95%CI 0.35, 5.0) years), was confirmed in a retrospective cohort of 935 participants. In silico prediction of treatment effects from four drug-based interventions (Mineralo</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-08T10:50:51.036Z</modification><creation>2026-05-03T03:05:54.901Z</creation></dates><accession>S-EPMC12372250</accession><cross_references><pubmed>40842026</pubmed><doi>10.1186/s12967-025-06977-3</doi></cross_references></HashMap>