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Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis

BACKGROUND: Studies have shown psychological distress in patients with cirrhosis, yet no studies have evaluated the laboratory and physiologic correlates of psychological symptoms in cirrhosis. This study therefore measured both biochemistry data and heart rate variability (HRV) analyses, and aimed...

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Autores principales: Ko, Fang-Yuan, Yang, Albert C, Tsai, Shih-Jen, Zhou, Yang, Xu, Lie-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574854/
https://www.ncbi.nlm.nih.gov/pubmed/23339829
http://dx.doi.org/10.1186/1471-230X-13-18
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author Ko, Fang-Yuan
Yang, Albert C
Tsai, Shih-Jen
Zhou, Yang
Xu, Lie-Ming
author_facet Ko, Fang-Yuan
Yang, Albert C
Tsai, Shih-Jen
Zhou, Yang
Xu, Lie-Ming
author_sort Ko, Fang-Yuan
collection PubMed
description BACKGROUND: Studies have shown psychological distress in patients with cirrhosis, yet no studies have evaluated the laboratory and physiologic correlates of psychological symptoms in cirrhosis. This study therefore measured both biochemistry data and heart rate variability (HRV) analyses, and aimed to identify the physiologic correlates of depression, anxiety, and poor sleep in cirrhosis. METHODS: A total of 125 patients with cirrhosis and 55 healthy subjects were recruited. Each subject was assessed through routine biochemistry, 5-minutes ECG monitoring, and psychological ratings of depression, anxiety, and sleep. HRV analysis were used to evaluate autonomic functions. The relationship between depression, sleep, and physiologic correlates was assessed using a multiple regression analysis and stepwise method, controlling for age, duration of illness, and severity of cirrhosis. RESULTS: Reduced vagal-related HRV was found in patients with severe liver cirrhosis. Severity of cirrhosis measured by the Child-Pugh score was not correlated with depression or anxiety, and only had a weak correlation with poor sleep. The psychological distress in cirrhosis such as depression, anxiety, and insomnia were correlated specifically to increased levels of aspartate aminotransferase (AST), increased ratios of low frequency to high frequency power, or reduced nonlinear properties of HRV (α(1) exponent of detrended fluctuation analysis). CONCLUSIONS: Increased serum AST and abnormal autonomic nervous activities by HRV analysis were associated with psychological distress in cirrhosis. Because AST is an important mediator of inflammatory process, further research is needed to delineate the role of inflammation in the cirrhosis comorbid with depression.
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spelling pubmed-35748542013-02-18 Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis Ko, Fang-Yuan Yang, Albert C Tsai, Shih-Jen Zhou, Yang Xu, Lie-Ming BMC Gastroenterol Research Article BACKGROUND: Studies have shown psychological distress in patients with cirrhosis, yet no studies have evaluated the laboratory and physiologic correlates of psychological symptoms in cirrhosis. This study therefore measured both biochemistry data and heart rate variability (HRV) analyses, and aimed to identify the physiologic correlates of depression, anxiety, and poor sleep in cirrhosis. METHODS: A total of 125 patients with cirrhosis and 55 healthy subjects were recruited. Each subject was assessed through routine biochemistry, 5-minutes ECG monitoring, and psychological ratings of depression, anxiety, and sleep. HRV analysis were used to evaluate autonomic functions. The relationship between depression, sleep, and physiologic correlates was assessed using a multiple regression analysis and stepwise method, controlling for age, duration of illness, and severity of cirrhosis. RESULTS: Reduced vagal-related HRV was found in patients with severe liver cirrhosis. Severity of cirrhosis measured by the Child-Pugh score was not correlated with depression or anxiety, and only had a weak correlation with poor sleep. The psychological distress in cirrhosis such as depression, anxiety, and insomnia were correlated specifically to increased levels of aspartate aminotransferase (AST), increased ratios of low frequency to high frequency power, or reduced nonlinear properties of HRV (α(1) exponent of detrended fluctuation analysis). CONCLUSIONS: Increased serum AST and abnormal autonomic nervous activities by HRV analysis were associated with psychological distress in cirrhosis. Because AST is an important mediator of inflammatory process, further research is needed to delineate the role of inflammation in the cirrhosis comorbid with depression. BioMed Central 2013-01-22 /pmc/articles/PMC3574854/ /pubmed/23339829 http://dx.doi.org/10.1186/1471-230X-13-18 Text en Copyright ©2013 Ko et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ko, Fang-Yuan
Yang, Albert C
Tsai, Shih-Jen
Zhou, Yang
Xu, Lie-Ming
Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis
title Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis
title_full Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis
title_fullStr Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis
title_full_unstemmed Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis
title_short Physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis
title_sort physiologic and laboratory correlates of depression, anxiety, and poor sleep in liver cirrhosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574854/
https://www.ncbi.nlm.nih.gov/pubmed/23339829
http://dx.doi.org/10.1186/1471-230X-13-18
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