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Published on: June 21, 2024
Urinary proteome analysis in congenital bilateral hydronephrosis.
Lene Stødkilde1, Mia Gebauer Madsen, Johan Palmfeldt
1The Water and Salt Research Center, Institute of Clinical Medicine, University of Aarhus, Aarhus, Denmark.
This study identified 33 urinary proteins related to congenital bilateral hydronephrosis. Five proteins were pinpointed as potential biomarkers for this congenital kidney disorder.
Area of Science:
- Biochemistry
- Nephrology
- Proteomics
Background:
- Congenital bilateral hydronephrosis involves abnormal kidney drainage in infants.
- Understanding pathophysiological processes is crucial for identifying biomarkers.
Purpose of the Study:
- To map urinary protein changes after relieving congenital bilateral hydronephrosis.
- To identify potential urinary biomarkers for congenital obstructive nephropathy.
Main Methods:
- Proteomics techniques and mass spectrometry were used to analyze urinary samples.
- Enzyme-linked immunosorbent assay (ELISA) validated changes in selected proteins.
Main Results:
- 33 proteins showed significantly altered urinary excretion post-obstruction relief.
- Fibrinogen, plasminogen, transthyretin, and transferrin levels decreased, while Tamm-Horsfall protein increased.
Conclusions:
- A proteomics strategy successfully identified proteins associated with congenital bilateral hydronephrosis.
- A panel of five proteins shows promise as urinary biomarkers for this condition.
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