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Urine miRNA in nephrotic syndrome
1Department of Medicine & Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
Urinary microRNAs (miRNAs) show promise as biomarkers for diagnosing and monitoring nephrotic syndrome, offering a less invasive alternative to kidney biopsies. Further research is needed to validate these findings.
Area of Science:
- Nephrology
- Molecular Biology
- Biomarker Discovery
Background:
- Nephrotic syndrome is a significant clinical nephrology issue, typically indicating glomerular disease with diverse causes.
- Kidney biopsy, the current standard for histological classification and monitoring, is invasive and carries risks.
- MicroRNAs (miRNAs) are regulatory molecules with altered urinary levels observed in nephrotic syndrome.
Purpose of the Study:
- To explore the potential of urinary miRNAs as non-invasive biomarkers for nephrotic syndrome diagnosis and monitoring.
- To review current evidence on specific urinary miRNA alterations in various nephrotic conditions.
Main Methods:
- Analysis of existing literature on urinary miRNA levels in nephrotic syndrome.
- Comparison of miRNA profiles across different etiological subtypes of nephrotic syndrome.
Main Results:
- Urinary miR-192 levels are lower in diabetic nephropathy.
- Urinary miR-200c levels are elevated in minimal change nephropathy and focal glomerulosclerosis.
- Elevated urinary miR-21, miR-216a, and miR-494 may predict renal function decline.
- Urinary miRNA targets show potential in lupus nephritis assessment.
Conclusions:
- Urinary miRNAs are stable and quantifiable, presenting a potential non-invasive diagnostic and monitoring tool for nephrotic syndrome.
- Current evidence is based on small-scale studies, necessitating larger research efforts for clinical validation.
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