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Published on: October 22, 2014
Bladder overactivity and post-void residual: Which relates more to systemic atherosclerotic markers?
Ayami Shimizu1, Ryuji Sakakibara2, Osamu Takahashi1
1Clinical Physiology Unit, Sakura Medical Center, Toho University, 564-1 Shimoshizu, Sakura 285-8741, Japan.
Detrusor overactivity, a type of lower urinary tract dysfunction (LUTD), is linked to systemic atherosclerosis. Post-void residual, another LUTD type, showed no such association in this study.
Area of Science:
- Urology
- Cardiology
- Geriatrics
Background:
- Lower urinary tract dysfunction (LUTD) and atherosclerosis share known associations.
- The specific LUTD type correlating with atherosclerosis remains unclear.
- This study investigates detrusor overactivity versus post-void residual in relation to atherosclerosis.
Purpose of the Study:
- To determine which LUTD subtype, detrusor overactivity or post-void residual, is more closely associated with atherosclerosis.
- To explore the relationship between urodynamic findings and systemic vascular health.
Main Methods:
- Standard urodynamic testing was performed on 183 patients (age > 60).
- Atherosclerosis was assessed using cardio-ankle vascular stiffness index (CAVI) and duplex carotid ultrasonography.
- Patients included 109 men and 74 women, with mean ages around 66.4 years.
Main Results:
- Detrusor overactivity showed a significant positive correlation with high CAVI values (p < 0.05).
- No significant association was found between detrusor overactivity and carotid intima-media thickness.
- Post-void residuals did not demonstrate a significant relationship with either CAVI or carotid intima-media thickness.
Conclusions:
- Urodynamic detrusor overactivity, potentially indicating central etiology, is positively linked to systemic atherosclerosis (measured by CAVI).
- Post-void residuals, possibly reflecting peripheral etiology, did not show a similar association with systemic atherosclerosis.
- Findings suggest detrusor overactivity may serve as a marker for systemic vascular disease in older adults.
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