Ontology highlight
ABSTRACT: Background
Cardiorenal syndrome (CRS) reflects bidirectional heart-kidney injury whose mechanisms extend far beyond hemodynamics. High-throughput genomics and multi-omics now illuminate the molecular circuits that couple cardiac and renal dysfunction.Methods
We narratively synthesize animal and human studies leveraging transcriptomics, proteomics, peptidomics, metabolomics, and non-coding RNA profiling to map convergent pathways in CRS and to highlight biomarker and therapeutic implications.Results
Across acute and chronic CRS models, omics consistently converge on extracellular matrix (ECM) remodeling and fibrosis (e.g., FN1, POSTN, collagens), immune-inflammatory activation (IL-6 axis, macrophage/complement signatures), renin-angiotensin-aldosterone system hyperac
SUBMITTER: Ang SP
PROVIDER: S-EPMC12652397 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature