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Kao, C.-C.

Publications and source records attributed to Kao, C.-C..

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Integrated Proteo-Metabolomics of Urinary Extracellular Vesicles Reveals Early Molecular Divergence and Temporal Pathogenesis of Sepsis-Associated AKI

BackgroundSepsis-associated acute kidney injury (S-AKI) is a major contributor to morbidity and mortality in critically ill patients. However, the molecular mechanisms underlying its temporal progression remain poorly understood because conventional biomarkers primarily reflect renal dysfunction rather than disease pathogenesis. Urinary extracellular vesicles (uEVs), which carry kidney-derived molecular cargo, provide a promising platform for monitoring renal-specific biological alterations during disease progression. MethodsWe conducted a longitudinal multi-omics study of uEVs collected from 81 patients with sepsis, including 48 patients with S-AKI and 33 sepsis-only controls. Patients were randomly assigned to a discovery cohort (n = 52) and an independent validation cohort (n = 29). Urine samples were collected at Day 1, Day 4, and Day 8 after AKI diagnosis. High-resolution proteomic and metabolomic profiling was performed to characterize temporal molecular alterations. Enriched pathways identified in the discovery cohort were evaluated in the validation cohort using pathway-level concordance analysis. ResultsComparative analysis between S-AKI and sepsis-only patients identified distinct stage-specific molecular alterations throughout disease progression. At the early stage (Day 1), validated pathways included complement and coagulation cascades, ferroptosis, HIF-1 signaling, sphingolipid metabolism, and arachidonic acid metabolism, highlighting coordinated inflammatory, hypoxic, and lipid metabolic responses. During the mid-stage (Day 4), persistent activation of complement and coagulation cascades, ferroptosis, and HIF-1 signaling was accompanied by metabolic reprogramming involving alanine, aspartate and glutamate metabolism and tyrosine metabolism. Although limited sample availability reduced statistical power at Day 8, phenylalanine metabolism remained validated in the metabolomic analysis, suggesting persistent metabolic dysregulation during late-stage disease progression. ConclusionsThis study provides the first longitudinal, independently validated multi-omics characterization of human uEVs in S-AKI. By integrating proteomic and metabolomic profiling, we reveal the temporal evolution of renal-specific molecular pathways from early inflammatory and hypoxic responses to subsequent metabolic reprogramming. These findings establish uEV-based multi-omics as a promising strategy for molecular phenotyping of S-AKI beyond conventional clinical biomarkers and provide a valuable resource for future biomarker discovery and therapeutic target identification.

biochemistry↗

Multi-Omics Characterization of Plasma and Urine Extracellular Vesicles Identifies Non-Invasive Biomarkers for IgA Nephropathy

BackgroundIgA nephropathy (IgAN) is increasingly recognized as a systemic immune-mediated disease characterized by aberrant IgA1 glycosylation, circulating immune complex formation, complement activation, and emerging metabolic perturbations. However, clinical diagnosis still relies on invasive renal biopsy, and non-invasive biomarkers capable of capturing both systemic immune activation and kidney-specific alterations remain lacking. Extracellular vesicles (EVs), as biologically active carriers of proteins and metabolites, provide a unique opportunity to interrogate compartment-specific molecular signatures underlying IgAN pathophysiology. MethodsWe performed an integrated, untargeted multi-omics analysis of plasma- and urine-derived EVs from 60 individuals (24 IgAN, 21 chronic kidney disease [CKD], and 15 controls). Differentially expressed proteins (DEPs) and metabolite features (DEFs) discriminating IgAN from CKD and controls were identified using Venn diagram analysis, followed by pathway enrichment and receiver operating characteristic (ROC) evaluation. ResultsVenn analysis identified 22 and 3 candidate DEPs in plasma EVs (pEVs) and urinary EVs (uEVs), respectively, revealing broader systemic proteomic alterations relative to renal EV cargo. Notably, complement and coagulation regulators, including C4b-binding protein alpha chain (C4BPA) and vitamin K-dependent protein S (PROS1), demonstrated strong discriminatory performance between IgAN and CKD (AUC = 0.826 and 0.795), suggesting EV-associated complement-coagulation crosstalk in IgAN. Metabolomic profiling revealed 1,006 and 540 candidate DEFs in pEVs and uEVs, respectively. Enrichment analyses highlighted steroid biosynthesis and fatty acid metabolism pathways in both compartments, indicating immune-metabolic reprogramming. Three metabolite features (C27H44O, C30H50O, and C28H46O) distinguished IgAN from CKD with high accuracy (AUC = 0.942-0.877). ConclusionsThis study provides the first compartment-resolved, plasma- and urine-derived EV multi-omics landscape of IgAN. Our findings suggest that EV cargo reflects coordinated complement dysregulation and metabolic alterations, extending current understanding of IgAN beyond glomerular immune complex deposition. These EV-associated proteins and metabolites offer a mechanistically informed framework for non-invasive biomarker development and for exploring immune-metabolic pathways involved in IgAN progression.

biochemistry↗