Profile of urinary exosomal microRNAs and their contribution to diabetic kidney disease through a predictive classification model
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Aim: Evaluate the expression of exomiRs-126, -146, and -155 in urinary exosomes of patients with T2DM and diabetic kidney disease to establish a predictive classification model with exomiRs and clinical variables in order to determine their contribution to DKD. Methods: The study group included 92 subjects: 64 patients diagnosed with T2DM subclassified into two groups with albuminuria (T2DM with albuminuria, n = 30) and without albuminuria (TD2M, n = 34) as well as 28 healthy, non-diabetic participants. Exosomes were isolated from urine and identified by TEM and flow cytometry. Profile expression of exomiRs-126, -146 and -155 was evaluated by RT-qPCR. Data were analysed by permutational multivariate analysis of variance (PERMANOVA), similarity percentage (SIMPER), principal coordinate analysis (PCO), and canonical analysis of principal coordinates (CAP). Results: T2DM patients with and without albuminuria showed higher levels of miR-155 and miR-146 compared with controls. In addition, T2DM patients with albuminuria presented a significant increase in miR-126 contrasted to controls and patients without albuminuria. PCO analysis explained 34.6%25 of the total variability of the data (PERMANOVA; p <.0001). Subsequently, SIMPER analysis showed that miR-146, miR-155, and miR-126 together, with some clinical parameters, contributed to 50%25 of the between-group significance. Finally, the CAP analysis developed showed a correct classification of 89.01%25 with the analysed parameters. Conclusion: A platform using a combination of clinical variables and exomiRs could be used to classify individuals with T2D as risk for developing DKD. © 2022 Asian Pacific Society of Nephrology.
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diabetic kidney disease; early biomarkers; microRNAs; type 2 diabetes mellitus; urinary exosomes microRNA; microRNA 126; microRNA 146; microRNA 155; unclassified drug; biological marker; microRNA; adult; albuminuria; Article; controlled study; diabetic nephropathy; disease classification; exosome; human; major clinical study; non insulin dependent diabetes mellitus; predictive value; urine level; albuminuria; complication; diabetic nephropathy; female; genetics; male; metabolism; non insulin dependent diabetes mellitus; Albuminuria; Biomarkers; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Female; Humans; Male; MicroRNAs
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