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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.
Purpose:
To compare the risk of incident dementia in patients prescribed either an anticholinergic medication or mirabegron.
Materials And Methods:
This was a retrospective cohort study of patients treated for OAB with pharmacotherapy between the years 2012 and 2023, using data from the TrinetX Research Collaborative Network. Patients who were diagnosed with OAB who were prescribed Mirabegron, Oxybutynin, Tolterodine, Darifenacin, Trospium, Fesoterodine, or Solifenacin after 1/1/2012 were identified. Anticholinergic medications were stratified into high-risk (Oxybutynin, Tolterodine, and Solifenacin) and low-risk (Darifenacin, Trospium and Fesoterodine) Patients with OAB who were not prescribed medications were included as a control group. The primary outcome was incidence of dementia occurring after initiation of pharmacotherapy or entry into the study (for the control group). Using Cox proportional hazard analyses, and adjusting for age and sex and adjusting for Elixhauser comorbidity index, anticholinergic burden score, and the average treatment effect, the risk of each medication on incident dementia was determined.
Results:
A total of 941,402 met inclusion for the final analysis, with 83,550 prescribed any medication. With an average follow-up time of 4.3 years, the only medication not found to be associated with an increased risk of dementia in any group was fesoterodine, while mirabegron was found to have a significant association with dementia across all age groups for both sexes.
Conclusions:
Most anticholinergic medications and mirabegron are associated with an increased risk of dementia compared to untreated controls with OAB, while fesoterodine was not found to be associated with an increased risk in any group.
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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