A Feasibility Study to Evaluate Changes in Urinary Metabolites after OnabotulinumtoxinA Injection for Refractory

Laura M Tellechea1, Samantha Freeman2, Ilir Agalliu2,3

  • 1Department of Obstetrics & Gynecology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Metabolites
|September 23, 2022
PubMed

Insights

Urinary metabolomics may predict overactive bladder (OAB) treatment success. Changes in specific metabolites like adenosine, N8-acetylspermidine, and guanidinoacetic acid correlate with symptom improvement after onabotulinumtoxinA (BTX-A) injections.

Area of Science:

  • Urology
  • Metabolomics
  • Biochemistry

Background:

  • Overactive bladder (OAB) is a common condition impacting quality of life.
  • Refractory OAB often requires advanced treatments like onabotulinumtoxinA (BTX-A) injections.
  • Predicting treatment response in OAB is crucial for personalized medicine.

Purpose of the Study:

  • To investigate the feasibility of using urinary metabolomics to predict treatment response in patients with refractory overactive bladder (OAB).
  • To correlate changes in the urinary metabolome with symptom improvement after intravesical onabotulinumtoxinA (BTX-A) injections.

Main Methods:

  • Feasibility study involving women with non-neurogenic refractory OAB.
  • Urine samples collected pre- and post-intravesical BTX-A (100 units) treatment.
  • CE-TOFMS metabolomics profiling and OAB-V8 questionnaire for symptom assessment.

Main Results:

  • Significant changes observed in 61 urinary metabolites post-BTX-A treatment.
  • Decreased adenosine levels and increased N8-acetylspermidine and guanidinoacetic acid levels correlated with OAB symptom improvement.
  • Statistical analysis included Kruskal-Wallis test and quantile regression.

Conclusions:

  • Intravesical BTX-A injection alters the urinary metabolome in patients with refractory OAB.
  • Specific urinary metabolites may serve as biomarkers for predicting treatment efficacy.
  • These findings offer insights into OAB pathophysiology and patient selection for chemodenervation therapy.

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