Pharmacotherapy for overactive bladder syndrome and the risk of incident dementia

David Sheyn1, Jennifer Murphy2, Abhimanyu Mahajan3

  • 1Urology Institute, University Hospitals, Cleveland, OH, USA. David.d.sheyn@gmail.com.

PubMed
Abstract

Insights

Most anticholinergic drugs and mirabegron increase dementia risk in overactive bladder patients. Fesoterodine showed no increased dementia risk compared to untreated individuals.

Area of Science:

  • Gerontology
  • Pharmacology
  • Neurology

Background:

  • Overactive bladder (OAB) pharmacotherapy involves anticholinergic medications and mirabegron.
  • Concerns exist regarding the potential neurocognitive side effects of these OAB treatments.

Purpose of the Study:

  • To compare the risk of incident dementia in patients prescribed anticholinergic medications versus mirabegron.
  • To evaluate dementia risk associated with specific anticholinergic drugs stratified by risk level.

Main Methods:

  • Retrospective cohort study (2012-2023) using the TrinetX Research Collaborative Network.
  • Included patients treated for OAB with mirabegron, specific anticholinergics (high-risk: oxybutynin, tolterodine, solifenacin; low-risk: darifenacin, trospium, fesoterodine), or no medication (control).
  • Cox proportional hazard analyses adjusted for age, sex, Elixhauser comorbidity index, and anticholinergic burden score.

Main Results:

  • Analysis included 941,402 patients, with 83,550 on medication, followed for an average of 4.3 years.
  • Mirabegron was significantly associated with increased dementia risk across all demographics.
  • Fesoterodine was the only medication not associated with an increased dementia risk; most other anticholinergics also showed increased risk.

Conclusions:

  • Both mirabegron and most anticholinergic medications are linked to a higher incidence of dementia compared to untreated OAB patients.
  • Fesoterodine appears to be a safer alternative regarding dementia risk among OAB pharmacotherapies.
  • Further research into the long-term neurocognitive effects of OAB medications is warranted.

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