MicroRNAs in biofluids are potential
biomarkers for detecting kidney and other organ
injuries. We profiled
microRNAs in urine samples from patients with Russell's viper envenoming or acute self-
poisoning following paraquat,
glyphosate, or
oxalic acid [with and without
acute kidney injury (AKI)] and on healthy controls. Discovery analysis profiled for 754
microRNAs using TaqMan OpenArray qPCR with three patients per group (12 samples in each toxic agent). From these, 53
microRNAs were selected and validated in a larger cohort of patients (Russell's viper envenoming = 53, paraquat = 51, glyphosate = 51, oxalic acid = 40) and 27 healthy controls. Urinary
microRNAs had significantly higher expression in patients poisoned/envenomed by different nephrotoxic agents in both discovery and validation cohorts. Seven
microRNAs discriminated severe AKI patients from no AKI for all four nephrotoxic agents. Four
microRNAs (miR-30a-3p, miR-30a-5p, miR-92a, and miR-204) had > 17 fold change (p < 0.0001) and receiver operator characteristics area-under-curve (ROC-AUC) > 0.72. Pathway analysis of target mRNAs of these differentially expressed
microRNAs showed association with the regulation of different nephrotoxic signaling pathways. In conclusion, human urinary
microRNAs could identify toxic AKI early after acute injury. These urinary
microRNAs have potential clinical application as early non-invasive diagnostic AKI
biomarkers.