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Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease

In recent years, frailty has been increasingly recognized among researchers of distinct medical specialties worldwide. Frailty comprises a complex of multisystemic physiological decline, reduced physiologic reserve, and vulnerability to stressors. Frail people tend to have a shorter lifespan and gre...

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Autores principales: Karakousis, Nikolaos D., Chrysavgis, Lampros, Chatzigeorgiou, Antonios, Papatheodoridis, George, Cholongitas, Evangelos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hellenic Society of Gastroenterology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062844/
https://www.ncbi.nlm.nih.gov/pubmed/35599934
http://dx.doi.org/10.20524/aog.2022.0705
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author Karakousis, Nikolaos D.
Chrysavgis, Lampros
Chatzigeorgiou, Antonios
Papatheodoridis, George
Cholongitas, Evangelos
author_facet Karakousis, Nikolaos D.
Chrysavgis, Lampros
Chatzigeorgiou, Antonios
Papatheodoridis, George
Cholongitas, Evangelos
author_sort Karakousis, Nikolaos D.
collection PubMed
description In recent years, frailty has been increasingly recognized among researchers of distinct medical specialties worldwide. Frailty comprises a complex of multisystemic physiological decline, reduced physiologic reserve, and vulnerability to stressors. Frail people tend to have a shorter lifespan and greater disability, morbidity and mortality. In the field of hepatology, frailty is identified in nearly 50% of patients who have cirrhosis of any cause. The most predominant cause of chronic liver disease is nonalcoholic fatty liver disease (NAFLD), considered as the hepatic manifestation of the metabolic syndrome (MetS). Although it is viewed as a benign disease, it may progress to nonalcoholic steatohepatitis (NASH), characterized by the additional emergence of inflammation and hepatocyte ballooning, with or without fibrosis. During the progression of NAFLD to NASH and liver cirrhosis, NAFLD patients present sarcopenia along with lower skeletal muscle strength and function. Moreover, aging and the increased prevalence of comorbidities further exacerbate their physical performance. The aforementioned features are strongly associated with the frailty phenotype, implying that the latter could be associated with both MetS and NAFLD. Although it is a relatively new topic of research interest, in this review we aim to provide a synopsis of the current literature dealing with the interplay between frailty and MetS, and to shed more light on the association between NAFLD and frailty. Finally, we discuss the potential pathophysiological mechanisms linking the distinct features of MetS and NAFLD with aspects of the frailty phenotype.
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spelling pubmed-90628442022-05-19 Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease Karakousis, Nikolaos D. Chrysavgis, Lampros Chatzigeorgiou, Antonios Papatheodoridis, George Cholongitas, Evangelos Ann Gastroenterol Review Article In recent years, frailty has been increasingly recognized among researchers of distinct medical specialties worldwide. Frailty comprises a complex of multisystemic physiological decline, reduced physiologic reserve, and vulnerability to stressors. Frail people tend to have a shorter lifespan and greater disability, morbidity and mortality. In the field of hepatology, frailty is identified in nearly 50% of patients who have cirrhosis of any cause. The most predominant cause of chronic liver disease is nonalcoholic fatty liver disease (NAFLD), considered as the hepatic manifestation of the metabolic syndrome (MetS). Although it is viewed as a benign disease, it may progress to nonalcoholic steatohepatitis (NASH), characterized by the additional emergence of inflammation and hepatocyte ballooning, with or without fibrosis. During the progression of NAFLD to NASH and liver cirrhosis, NAFLD patients present sarcopenia along with lower skeletal muscle strength and function. Moreover, aging and the increased prevalence of comorbidities further exacerbate their physical performance. The aforementioned features are strongly associated with the frailty phenotype, implying that the latter could be associated with both MetS and NAFLD. Although it is a relatively new topic of research interest, in this review we aim to provide a synopsis of the current literature dealing with the interplay between frailty and MetS, and to shed more light on the association between NAFLD and frailty. Finally, we discuss the potential pathophysiological mechanisms linking the distinct features of MetS and NAFLD with aspects of the frailty phenotype. Hellenic Society of Gastroenterology 2022 2022-03-25 /pmc/articles/PMC9062844/ /pubmed/35599934 http://dx.doi.org/10.20524/aog.2022.0705 Text en Copyright: © Hellenic Society of Gastroenterology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Karakousis, Nikolaos D.
Chrysavgis, Lampros
Chatzigeorgiou, Antonios
Papatheodoridis, George
Cholongitas, Evangelos
Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease
title Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease
title_full Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease
title_fullStr Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease
title_full_unstemmed Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease
title_short Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease
title_sort frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062844/
https://www.ncbi.nlm.nih.gov/pubmed/35599934
http://dx.doi.org/10.20524/aog.2022.0705
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