<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu Q</submitter><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>6962</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12307705</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>Chronic kidney disease (CKD) is a global health challenge, but invasive renal biopsies, the gold standard for diagnosis and prognosis, are often clinically constrained. To address this, we developed the kidney intelligent diagnosis system (KIDS), a noninvasive model for renal biopsy prediction using 13,144 retinal images from 6773 participants. The KIDS achieves an area under the receiver operating characteristic curve (AUC) of 0.839-0.993 for CKD screening and accurately identifies the five most common pathological types (AUC: 0.790-0.932) in a multicenter and multi-ethnic validation, outperforming nephrologists by 26.98% in accuracy. Additionally, the KIDS further predicts disease progression based on pathological classification. Given its flexible strategy, the KIDS can be adapted to lo</pubmed_abstract><journal>Nature communications</journal><pubmed_title>A noninvasive model for chronic kidney disease screening and common pathological type identification from retinal images.</pubmed_title><pmcid>PMC12307705</pmcid><funding_grant_id>82371111</funding_grant_id><funding_grant_id>82370707</funding_grant_id><funding_grant_id>92368205</funding_grant_id><pubmed_authors>Fu R</pubmed_authors><pubmed_authors>Ma R</pubmed_authors><pubmed_authors>Jiang L</pubmed_authors><pubmed_authors>Wan P</pubmed_authors><pubmed_authors>Nur AH</pubmed_authors><pubmed_authors>Feng JJ</pubmed_authors><pubmed_authors>Wu Q</pubmed_authors><pubmed_authors>Huang N</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Dai Z</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Iao WC</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Ke Y</pubmed_authors><pubmed_authors>Zhao L</pubmed_authors><pubmed_authors>Wen J</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>Ting DSW</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Sabanayagam C</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Xie C</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Ling JOC</pubmed_authors><pubmed_authors>Hong H</pubmed_authors><pubmed_authors>Zhou S</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Rashid Hassan MH</pubmed_authors><pubmed_authors>Cheng KK</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Zhu M</pubmed_authors><pubmed_authors>Ye Q</pubmed_authors><pubmed_authors>Lin D</pubmed_authors><pubmed_authors>Lin H</pubmed_authors><pubmed_authors>Yin P</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Ye H</pubmed_authors><pubmed_authors>Kong Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>A noninvasive model for chronic kidney disease screening and common pathological type identification from retinal images.</name><description>Chronic kidney disease (CKD) is a global health challenge, but invasive renal biopsies, the gold standard for diagnosis and prognosis, are often clinically constrained. To address this, we developed the kidney intelligent diagnosis system (KIDS), a noninvasive model for renal biopsy prediction using 13,144 retinal images from 6773 participants. The KIDS achieves an area under the receiver operating characteristic curve (AUC) of 0.839-0.993 for CKD screening and accurately identifies the five most common pathological types (AUC: 0.790-0.932) in a multicenter and multi-ethnic validation, outperforming nephrologists by 26.98% in accuracy. Additionally, the KIDS further predicts disease progression based on pathological classification. Given its flexible strategy, the KIDS can be adapted to lo</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-07-15T09:48:43.906Z</modification><creation>2025-08-17T03:06:07.628Z</creation></dates><accession>S-EPMC12307705</accession><cross_references><pubmed>40730556</pubmed><doi>10.1038/s41467-025-62273-0</doi></cross_references></HashMap>