» Articles » PMID: 36983336

Urinary Oxidative Stress Biomarker Levels Might Be Useful in Identifying Functional Bladder Disorders in Women with Frequency and Urgency Syndrome

Overview
Journal J Clin Med
Specialty General Medicine
Date 2023 Mar 29
PMID 36983336
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: lower urinary tract dysfunctions (LUTDs) are difficult to diagnose based on symptoms. This study used a cluster of urinary biomarkers, including inflammatory cytokines, neurogenic proteins, and oxidative stress biomarkers, to identify LUTDs in women with frequency and urgency symptoms.

Methods: in total, 253 women with video urodynamics (VUDS)- and cystoscopy-confirmed detrusor overactivity (DO), interstitial cystitis/bladder pain syndrome (IC/BPS), dysfunctional voiding (DV), and hypersensitive bladder (HSB), and normal controls were included. Before diagnosis and treatment, urine samples were collected for analysis of biomarkers. The urine levels of biomarkers were compared between groups with bladder dysfunctions and controls and were combined to test the sensitivity in identifying total pathological bladder diseases and specific bladder diseases.

Results: After video urodynamic study, VUDS, and urological examinations, bladder dysfunctions were classified into DO ( = 31), IC/BPS ( = 114), DV ( = 45), HSB ( = 29), and control ( = 34) groups. By using a cystomeric bladder capacity of ≤350 mL, 186/219 (84.9%) of the patients with DO, IC/BPS, DV, and HSB can be discriminated from the controls. Among these urine biomarkers, oxidative stress biomarkers 8-isoprostane, 8-hydroxydeoxyguanosine (8-OHdG), or total antioxidant capacity (TAC) are useful for identifying pathological bladder dysfunction (DO, IC/BPS, and DV) and HSB. With elevated IL-1β and lower IL-2, and elevated TNF-α levels, most patients with DV can be identified. Between DO and IC/BPS, a higher NGF level can identify 58.3% of IC/BPS cases, whereas a lower NGF level can identify 75.0% of DO cases.

Conclusion: by using a cluster of urine biomarkers, DO, IC/BPS, and DV cases can be identified based on elevated levels of urine oxidative stress biomarkers 8-isoprostane, TAC, or 8-OHdG, and HSB cases with a low TAC. These urine biomarkers are useful for identifying specific LUTDs in women with frequency and urgency symptoms.

Citing Articles

Integrating biomarker clustering for improved diagnosis of interstitial cystitis/bladder pain syndrome: a review.

Chen Y, Kuo H Int Urol Nephrol. 2025; .

PMID: 40088357 DOI: 10.1007/s11255-025-04452-y.


Using Urine Biomarkers to Differentiate Bladder Dysfunctions in Women with Sensory Bladder Disorders.

Chen Y, Jiang Y, Jhang J, Kuo H Int J Mol Sci. 2024; 25(17).

PMID: 39273307 PMC: 11395209. DOI: 10.3390/ijms25179359.


Urine biomarker could be a useful tool for differential diagnosis of a lower urinary tract dysfunction.

Yu W, Jiang Y, Jhang J, Kuo H Tzu Chi Med J. 2024; 36(2):110-119.

PMID: 38645782 PMC: 11025593. DOI: 10.4103/tcmj.tcmj_221_23.

References
1.
Pontari M, Hanno P, Ruggieri M . Comparison of bladder blood flow in patients with and without interstitial cystitis. J Urol. 1999; 162(2):330-4. View

2.
Wang H, Kuo H . Effects of different urodynamic characteristics on therapeutic outcomes of overactive bladder medication in a real-life clinical practice. Tzu Chi Med J. 2022; 34(4):441-447. PMC: 9791855. DOI: 10.4103/tcmj.tcmj_264_20. View

3.
Siddiqui N, Helfand B, Andreev V, Kowalski J, Bradley M, Lai H . Biomarkers Implicated in Lower Urinary Tract Symptoms: Systematic Review and Pathway Analyses. J Urol. 2019; 202(5):880-889. PMC: 6766427. DOI: 10.1097/JU.0000000000000257. View

4.
Speich J, Tarcan T, Hashitani H, Vahabi B, McCloskey K, Andersson K . Are oxidative stress and ischemia significant causes of bladder damage leading to lower urinary tract dysfunction? Report from the ICI-RS 2019. Neurourol Urodyn. 2020; 39 Suppl 3:S16-S22. PMC: 9794413. DOI: 10.1002/nau.24313. View

5.
Lin H, Lu J, Chuang S, Chueh K, Juan T, Liu Y . Urinary Biomarkers in Interstitial Cystitis/Bladder Pain Syndrome and Its Impact on Therapeutic Outcome. Diagnostics (Basel). 2022; 12(1). PMC: 8774507. DOI: 10.3390/diagnostics12010075. View