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Oxybutynin-associated Cognitive Impairment: Evidence and Implications for Overactive Bladder Treatment
Michael B Chancellor1, Alvaro Lucioni2, David Staskin3
1Corewell Health Beaumont University Hospital, Oakland University William Beaumont School of Medicine, Royal Oak, MI.
Abstract:
Anticholinergic medications have long been a mainstay of overactive bladder (OAB) treatment. Oxybutynin, a first-generation anticholinergic, still accounts for more than half of all OAB medication prescriptions, despite associations with impaired memory and cognition, as well as mounting evidence that it may increase the risk of incident dementia. This review details the current literature regarding oxybutynin and cognition, including evidence from preclinical, clinical, and real-world studies that show that oxybutynin binds nonspecifically to muscarinic receptors in the brain and is associated with adverse cognitive outcomes. We also discuss society recommendations to reduce use of oxybutynin and other anticholinergics to treat OAB.
Insights
Oxybutynin, a common overactive bladder (OAB) medication, may negatively impact memory and increase dementia risk due to its brain receptor binding. Guidelines now suggest reducing its use for OAB treatment.
Area of Science:
- Pharmacology
- Gerontology
- Neurology
Background:
- Anticholinergic medications, particularly oxybutynin, are widely prescribed for overactive bladder (OAB).
- Oxybutynin, a first-generation anticholinergic, is associated with cognitive impairments and potential dementia risk.
- Concerns are rising regarding the long-term cognitive effects of oxybutynin in OAB patients.
Purpose of the Study:
- To review current literature on the relationship between oxybutynin and cognitive function.
- To examine evidence from preclinical, clinical, and real-world studies.
- To discuss updated recommendations for OAB treatment strategies.
Main Methods:
- Literature review of preclinical, clinical, and real-world studies on oxybutynin and cognition.
- Analysis of oxybutynin's mechanism of action on muscarinic receptors.
- Examination of epidemiological data and clinical trial outcomes.
Main Results:
- Oxybutynin binds non-specifically to muscarinic receptors in the brain.
- Evidence indicates a link between oxybutynin use and adverse cognitive outcomes.
- Studies suggest a potential increased risk of dementia with oxybutynin exposure.
Conclusions:
- Oxybutynin's anticholinergic properties are associated with negative cognitive effects.
- Reduced use of oxybutynin and similar anticholinergics for OAB is recommended.
- Further research into safer OAB treatment alternatives is warranted.
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