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Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies

Metabolic syndrome (MetS) is defined by a group of cardiovascular risk factors, including impaired glucose tolerance, central obesity, hypertension, and dyslipidemia. Overactive bladder (OAB) syndrome consists of symptoms such as urinary urgency, frequency, and nocturia with or without urge incontin...

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Autores principales: Hsu, Lin-Nei, Hu, Ju-Chuan, Chen, Po-Yen, Lee, Wei-Chia, Chuang, Yao-Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405560/
https://www.ncbi.nlm.nih.gov/pubmed/36009505
http://dx.doi.org/10.3390/biomedicines10081957
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author Hsu, Lin-Nei
Hu, Ju-Chuan
Chen, Po-Yen
Lee, Wei-Chia
Chuang, Yao-Chi
author_facet Hsu, Lin-Nei
Hu, Ju-Chuan
Chen, Po-Yen
Lee, Wei-Chia
Chuang, Yao-Chi
author_sort Hsu, Lin-Nei
collection PubMed
description Metabolic syndrome (MetS) is defined by a group of cardiovascular risk factors, including impaired glucose tolerance, central obesity, hypertension, and dyslipidemia. Overactive bladder (OAB) syndrome consists of symptoms such as urinary urgency, frequency, and nocturia with or without urge incontinence. The high prevalences of metabolic syndrome (MetS) and overactive bladder (OAB) worldwide affect quality of life and cause profound negative impacts on the social economy. Accumulated evidence suggests that MetS might contribute to the underlying mechanisms for developing OAB, and MetS-associated OAB could be a subtype of OAB. However, how could these two syndromes interact with each other? Based on results of animal studies and observations in epidemiological studies, we summarized the common pathophysiologies existing between MetS and OAB, including autonomic and peripheral neuropathies, chronic ischemia, proinflammatory status, dysregulation of nutrient-sensing pathways (e.g., insulin resistance at the bladder mucosa and excessive succinate intake), and the probable role of dysbiosis. Since the MetS-associated OAB is a subtype of OAB with distinctive pathophysiologies, the regular and non-specific medications, such as antimuscarinics, beta-3 agonist, and botulinum toxin injection, might lead to unsatisfying results. Understanding the pathophysiologies of MetS-associated OAB might benefit future studies exploring novel biomarkers for diagnosis and therapeutic targets on both MetS and OAB.
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spelling pubmed-94055602022-08-26 Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies Hsu, Lin-Nei Hu, Ju-Chuan Chen, Po-Yen Lee, Wei-Chia Chuang, Yao-Chi Biomedicines Review Metabolic syndrome (MetS) is defined by a group of cardiovascular risk factors, including impaired glucose tolerance, central obesity, hypertension, and dyslipidemia. Overactive bladder (OAB) syndrome consists of symptoms such as urinary urgency, frequency, and nocturia with or without urge incontinence. The high prevalences of metabolic syndrome (MetS) and overactive bladder (OAB) worldwide affect quality of life and cause profound negative impacts on the social economy. Accumulated evidence suggests that MetS might contribute to the underlying mechanisms for developing OAB, and MetS-associated OAB could be a subtype of OAB. However, how could these two syndromes interact with each other? Based on results of animal studies and observations in epidemiological studies, we summarized the common pathophysiologies existing between MetS and OAB, including autonomic and peripheral neuropathies, chronic ischemia, proinflammatory status, dysregulation of nutrient-sensing pathways (e.g., insulin resistance at the bladder mucosa and excessive succinate intake), and the probable role of dysbiosis. Since the MetS-associated OAB is a subtype of OAB with distinctive pathophysiologies, the regular and non-specific medications, such as antimuscarinics, beta-3 agonist, and botulinum toxin injection, might lead to unsatisfying results. Understanding the pathophysiologies of MetS-associated OAB might benefit future studies exploring novel biomarkers for diagnosis and therapeutic targets on both MetS and OAB. MDPI 2022-08-12 /pmc/articles/PMC9405560/ /pubmed/36009505 http://dx.doi.org/10.3390/biomedicines10081957 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hsu, Lin-Nei
Hu, Ju-Chuan
Chen, Po-Yen
Lee, Wei-Chia
Chuang, Yao-Chi
Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies
title Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies
title_full Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies
title_fullStr Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies
title_full_unstemmed Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies
title_short Metabolic Syndrome and Overactive Bladder Syndrome May Share Common Pathophysiologies
title_sort metabolic syndrome and overactive bladder syndrome may share common pathophysiologies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405560/
https://www.ncbi.nlm.nih.gov/pubmed/36009505
http://dx.doi.org/10.3390/biomedicines10081957
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