<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li Z</submitter><funding>National Science Fund for Distinguished Young Scholars</funding><funding>National Natural Science Foundation of China</funding><funding>National Key Research and Development Program of China</funding><pagination>1965-1973</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10616486</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Chronic kidney disease (CKD) has emerged as a significant challenge to human health and economic stability in aging societies worldwide. Current clinical practice strategies remain insufficient for the early identification of kidney dysfunction, and the differential diagnosis of immunoglobulin A nephropathy (IgAN) predominantly relies on invasive kidney biopsy procedures.&lt;h4>Methods&lt;/h4>First, we assessed a case-control cohort to obtain urine samples from healthy controls and biopsy-confirmed CKD patients. Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry (MS) was applied to detect urinary peptide and then these urinary peptide profiles were used to construct diagnostic models to distinguish CKD patients from controls and identify I</pubmed_abstract><journal>Clinical kidney journal</journal><pubmed_title>Urinary peptidome analysis in CKD and IgA nephropathy.</pubmed_title><pmcid>PMC10616486</pmcid><funding_grant_id>2022YFA0806400</funding_grant_id><funding_grant_id>81 925 026</funding_grant_id><funding_grant_id>82 130 068</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Zeng N</pubmed_authors><pubmed_authors>Liang G</pubmed_authors><pubmed_authors>Lin X</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Zheng P</pubmed_authors><pubmed_authors>Zhou H</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors><pubmed_authors>Zheng D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Urinary peptidome analysis in CKD and IgA nephropathy.</name><description>&lt;h4>Background&lt;/h4>Chronic kidney disease (CKD) has emerged as a significant challenge to human health and economic stability in aging societies worldwide. Current clinical practice strategies remain insufficient for the early identification of kidney dysfunction, and the differential diagnosis of immunoglobulin A nephropathy (IgAN) predominantly relies on invasive kidney biopsy procedures.&lt;h4>Methods&lt;/h4>First, we assessed a case-control cohort to obtain urine samples from healthy controls and biopsy-confirmed CKD patients. Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry (MS) was applied to detect urinary peptide and then these urinary peptide profiles were used to construct diagnostic models to distinguish CKD patients from controls and identify I</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-04T14:36:00.987Z</modification><creation>2025-04-04T14:36:00.987Z</creation></dates><accession>S-EPMC10616486</accession><cross_references><pubmed>37915931</pubmed><doi>10.1093/ckj/sfad211</doi></cross_references></HashMap>