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Detrusor underactivity is associated with metabolic syndrome in aged primates

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...

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Autores principales: Biscola, Natalia P., Bartmeyer, Petra M., Christe, Kari L., Colman, Ricki J., Havton, Leif A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130177/
https://www.ncbi.nlm.nih.gov/pubmed/37185781
http://dx.doi.org/10.1038/s41598-023-33112-3
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author Biscola, Natalia P.
Bartmeyer, Petra M.
Christe, Kari L.
Colman, Ricki J.
Havton, Leif A.
author_facet Biscola, Natalia P.
Bartmeyer, Petra M.
Christe, Kari L.
Colman, Ricki J.
Havton, Leif A.
author_sort Biscola, Natalia P.
collection PubMed
description 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.
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spelling pubmed-101301772023-04-27 Detrusor underactivity is associated with metabolic syndrome in aged primates Biscola, Natalia P. Bartmeyer, Petra M. Christe, Kari L. Colman, Ricki J. Havton, Leif A. Sci Rep Article 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. Nature Publishing Group UK 2023-04-25 /pmc/articles/PMC10130177/ /pubmed/37185781 http://dx.doi.org/10.1038/s41598-023-33112-3 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Biscola, Natalia P.
Bartmeyer, Petra M.
Christe, Kari L.
Colman, Ricki J.
Havton, Leif A.
Detrusor underactivity is associated with metabolic syndrome in aged primates
title Detrusor underactivity is associated with metabolic syndrome in aged primates
title_full Detrusor underactivity is associated with metabolic syndrome in aged primates
title_fullStr Detrusor underactivity is associated with metabolic syndrome in aged primates
title_full_unstemmed Detrusor underactivity is associated with metabolic syndrome in aged primates
title_short Detrusor underactivity is associated with metabolic syndrome in aged primates
title_sort detrusor underactivity is associated with metabolic syndrome in aged primates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130177/
https://www.ncbi.nlm.nih.gov/pubmed/37185781
http://dx.doi.org/10.1038/s41598-023-33112-3
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