Abstract

Lower urinary tract (LUT) dysfunction is prevalent in the elderly population, and clinical manifestations include urinary retention, incontinence, and recurrent urinary tract infections. Age-associated LUT dysfunction is responsible for significant morbidity, compromised quality of life, and rising healthcare costs in older adults, but its pathophysiology is not well understood. We aimed to investigate the effects of aging on LUT function by urodynamic studies and metabolic markers in non-human primates. Adult (n = 27) and aged (n = 20) female rhesus macaques were evaluated by urodynamic and metabolic studies. Cystometry showed detrusor underactivity (DU) with increased bladder capacity and compliance in aged subjects. Metabolic syndrome indicators were present in the aged subjects, including increased weight, triglycerides, lactate dehydrogenase (LDH), alanine aminotransferase (ALT), and high sensitivity C-reactive protein (hsCRP), whereas aspartate aminotransferase (AST) was unaffected and the AST/ALT ratio reduced. Principal component analysis and paired correlations showed a strong association between DU and metabolic syndrome markers in aged primates with DU but not in aged primates without DU. The findings were unaffected by prior pregnancies, parity, and menopause. Our findings provide insights into possible mechanisms for age-associated DU and may guide new strategies to prevent and treat LUT dysfunction in older adults.

Details

Title
Detrusor underactivity is associated with metabolic syndrome in aged primates
Author
Biscola, Natalia P. 1 ; Bartmeyer, Petra M. 1 ; Christe, Kari L. 2 ; Colman, Ricki J. 3 ; Havton, Leif A. 4 

 Icahn School of Medicine at Mount Sinai, Department of Neurology, New York, USA (GRID:grid.59734.3c) (ISNI:0000 0001 0670 2351) 
 University of California at Davis, California National Primate Research Center, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684) 
 University of Wisconsin-Madison, Wisconsin National Primate Research Center, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675); University of Wisconsin-Madison, Department of Cell and Regenerative Biology, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675) 
 Icahn School of Medicine at Mount Sinai, Departments of Neurology and Neuroscience, New York, USA (GRID:grid.59734.3c) (ISNI:0000 0001 0670 2351); James J. Peters Veterans Affairs Medical Center, Bronx, USA (GRID:grid.274295.f) (ISNI:0000 0004 0420 1184) 
Pages
6716
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2805771831
Copyright
© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.