Evidence map›Paper›PMID 42625985›Full record

ArticleWorld journal of nephrology2026

Potential diagnostic role of urinary exosomal microRNAs in immunoglobulin A nephropathy: A case-control study.

Mythri Shankar, Manju Moorthy, Aditya Shetty, Sreedhara C Gurusiddaiah

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Article in World journal of nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Mythri ShankarDepartment of Nephrology, Institute of Nephrourology, Bengaluru 560102, Karnataka, India. mythri.nish@gmail.com.
Manju MoorthyDepartment of Bioinformatics, Theraques, Bangalore 560102, Karnātaka, India.
Aditya ShettyDepartment of Nephrology, AJ Institute of Medical Sciences and Research Centre, Mangalore 575008, Karnātaka, India.
Sreedhara C GurusiddaiahDepartment of Nephrology, Institute of Nephrourology, Bengaluru 560102, Karnataka, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe most common type of primary glomerulonephritis is immunoglobulin A nephropathy (IgAN), which can eventually cause end-stage kidney disease among individuals. A kidney biopsy, which is invasive and has risks of mortality or morbidity, is currently the "gold standard" for diagnosis. Urinary exosomes contain abundant, well-preserved microRNAs (miRNAs), which are small, non-coding endogenous RNAs that may be used as non-invasive biomarkers. Studies on urinary exosomal miRNA profiles for the diagnosis of IgAN are rare.

aimTo examine the profile of urinary exosomal miRNAs in Indian individuals diagnosed with IgAN.

methodsOver a period of 4 years (2020-2024), fifty biopsy-confirmed IgAN patients, fifty healthy controls, and fifty disease controls (DC) were recruited. Urinary exosomes were first discovered and then utilized for miRNA extraction. The nCounter

resultsThe average age of patients diagnosed with IgAN was 36.32 years, with a standard deviation of 3.07 years. The average proteinuria was 2.69 ± 0.64 g/day, and the average creatinine level was 2.26 ± 0.318 mg/dL. Nine candidate miRNAs - hsa-miR-4532, hsa-miR-4488, hsa-miR-3158-3p, hsa-miR-151b, hsa-miR-3195, hsa-miR-1289, hsa-miR-20a-5p, hsa-miR-20b-5p, hsa-miR-32-5p, and hsa-miR-525-3p - successfully differentiate IgAN cases from both healthy and DC, exhibiting under the curve values of 0.7, 1, and 0.8 for healthy controls, DC, and IgAN cases, respectively. When compared to healthy and DC, a combination of just two miRNAs - hsa-miR-4532 and hsa-miR-548a-3p - was found to be sufficiently effective for detecting IgAN, with an area under the curve > 0.8.

conclusionOur investigation involving Indian participants revealed a marked alteration in the urinary exosomal miRNA patterns among individuals with IgAN compared to both healthy subjects and those with other kidney diseases, demonstrating the effectiveness of miRNAs in the non-invasive diagnosis of IgAN.

Indexed as

GlomerulonephritisImmunoglobulin A nephropathyIndian cohortKidney biopsyNon-invasive biomarkerUrinary exosomal microRNA

Identifiers

PMID42625985
PMCPMC13491225

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