Diabetes mellitus is an independent prognostic factor for major liver‐related outcomes in patients with cirrhosis and chronic hepatitis C

In patients with chronic hepatitis C (CHC), cirrhosis is associated with age, gender, diabetes, alcohol abuse, and coinfection with human immunodeficiency virus (HIV) or hepatitis B virus (HBV). The effect of these factors on the outcome of cirrhosis is unknown. This study in CHC patients with cirrh...

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Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2014-09, Vol.60 (3), p.823-831
Hauptverfasser: Elkrief, Laure, Chouinard, Pascale, Bendersky, Noelle, Hajage, David, Larroque, Béatrice, Babany, Gérard, Kutala, Blaise, Francoz, Claire, Boyer, Nathalie, Moreau, Richard, Durand, François, Marcellin, Patrick, Rautou, Pierre‐Emmanuel, Valla, Dominique
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container_title Hepatology (Baltimore, Md.)
container_volume 60
creator Elkrief, Laure
Chouinard, Pascale
Bendersky, Noelle
Hajage, David
Larroque, Béatrice
Babany, Gérard
Kutala, Blaise
Francoz, Claire
Boyer, Nathalie
Moreau, Richard
Durand, François
Marcellin, Patrick
Rautou, Pierre‐Emmanuel
Valla, Dominique
description In patients with chronic hepatitis C (CHC), cirrhosis is associated with age, gender, diabetes, alcohol abuse, and coinfection with human immunodeficiency virus (HIV) or hepatitis B virus (HBV). The effect of these factors on the outcome of cirrhosis is unknown. This study in CHC patients with cirrhosis aimed to assess the influence of these factors on decompensation, liver transplantation, and death. Consecutive patients with CHC and cirrhosis hospitalized between January 1, 2006 and December 31, 2008 were followed up until death, transplantation, or study closure in March 2013. Gender, age, Model for End‐Stage Liver Disease (MELD) score, diabetes, alcohol abuse, HIV, or HBV coinfection were collected at inclusion. The complications of cirrhosis, death, and liver transplantation were recorded at inclusion and during follow‐up. The association between baseline factors and liver‐related outcomes at inclusion and during follow‐up were tested using logistic regression and Cox's model, respectively. A total of 348 patients with CHC and cirrhosis (68% men; median age: 59 years; median MELD: 10) were included. At baseline, 40% of the patients had diabetes, 29% alcohol abuse, and 6% HIV or HBV coinfection. Baseline MELD ≥10 (P 
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The effect of these factors on the outcome of cirrhosis is unknown. This study in CHC patients with cirrhosis aimed to assess the influence of these factors on decompensation, liver transplantation, and death. Consecutive patients with CHC and cirrhosis hospitalized between January 1, 2006 and December 31, 2008 were followed up until death, transplantation, or study closure in March 2013. Gender, age, Model for End‐Stage Liver Disease (MELD) score, diabetes, alcohol abuse, HIV, or HBV coinfection were collected at inclusion. The complications of cirrhosis, death, and liver transplantation were recorded at inclusion and during follow‐up. The association between baseline factors and liver‐related outcomes at inclusion and during follow‐up were tested using logistic regression and Cox's model, respectively. A total of 348 patients with CHC and cirrhosis (68% men; median age: 59 years; median MELD: 10) were included. At baseline, 40% of the patients had diabetes, 29% alcohol abuse, and 6% HIV or HBV coinfection. Baseline MELD ≥10 (P &lt; 0.001), diabetes (P = 0.027), and HBV coinfection (P = 0.001) were independently associated with transplantation‐free survival. Baseline diabetes was independently associated with ascites (P = 0.05), bacterial infections (P = 0.001), and encephalopathy (P &lt; 0.001) at inclusion. Baseline diabetes was independently associated with development of ascites (P = 0.057), renal dysfunction (P = 0.004), bacterial infections (P = 0.007), and hepatocellular carcinoma (P = 0.016) during the follow‐up. Conclusion: In patients with CHC and cirrhosis, diabetes is an independent prognostic factor. Improving diabetes control may improve the outcome of cirrhosis. 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The effect of these factors on the outcome of cirrhosis is unknown. This study in CHC patients with cirrhosis aimed to assess the influence of these factors on decompensation, liver transplantation, and death. Consecutive patients with CHC and cirrhosis hospitalized between January 1, 2006 and December 31, 2008 were followed up until death, transplantation, or study closure in March 2013. Gender, age, Model for End‐Stage Liver Disease (MELD) score, diabetes, alcohol abuse, HIV, or HBV coinfection were collected at inclusion. The complications of cirrhosis, death, and liver transplantation were recorded at inclusion and during follow‐up. The association between baseline factors and liver‐related outcomes at inclusion and during follow‐up were tested using logistic regression and Cox's model, respectively. A total of 348 patients with CHC and cirrhosis (68% men; median age: 59 years; median MELD: 10) were included. At baseline, 40% of the patients had diabetes, 29% alcohol abuse, and 6% HIV or HBV coinfection. Baseline MELD ≥10 (P &lt; 0.001), diabetes (P = 0.027), and HBV coinfection (P = 0.001) were independently associated with transplantation‐free survival. Baseline diabetes was independently associated with ascites (P = 0.05), bacterial infections (P = 0.001), and encephalopathy (P &lt; 0.001) at inclusion. Baseline diabetes was independently associated with development of ascites (P = 0.057), renal dysfunction (P = 0.004), bacterial infections (P = 0.007), and hepatocellular carcinoma (P = 0.016) during the follow‐up. Conclusion: In patients with CHC and cirrhosis, diabetes is an independent prognostic factor. Improving diabetes control may improve the outcome of cirrhosis. 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Chouinard, Pascale ; Bendersky, Noelle ; Hajage, David ; Larroque, Béatrice ; Babany, Gérard ; Kutala, Blaise ; Francoz, Claire ; Boyer, Nathalie ; Moreau, Richard ; Durand, François ; Marcellin, Patrick ; Rautou, Pierre‐Emmanuel ; Valla, Dominique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4218-6dd7ae58afe4cf5939739a4c05b84d08b36c2a92093905f0091932688dd8bb123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Bacterial infections</topic><topic>Carcinoma, Hepatocellular - epidemiology</topic><topic>Carcinoma, Hepatocellular - etiology</topic><topic>Carcinoma, Hepatocellular - virology</topic><topic>Diabetes</topic><topic>Diabetes Complications - diagnosis</topic><topic>Diabetes Complications - mortality</topic><topic>Diabetes Complications - virology</topic><topic>Female</topic><topic>France - epidemiology</topic><topic>Hepatitis</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis C</topic><topic>Hepatitis C, Chronic - complications</topic><topic>Hepatitis C, Chronic - epidemiology</topic><topic>Hepatitis C, Chronic - virology</topic><topic>Hepatology</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Liver cirrhosis</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver Cirrhosis - mortality</topic><topic>Liver Cirrhosis - virology</topic><topic>Liver Neoplasms - epidemiology</topic><topic>Liver Neoplasms - etiology</topic><topic>Liver Neoplasms - virology</topic><topic>Liver Transplantation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elkrief, Laure</creatorcontrib><creatorcontrib>Chouinard, Pascale</creatorcontrib><creatorcontrib>Bendersky, Noelle</creatorcontrib><creatorcontrib>Hajage, David</creatorcontrib><creatorcontrib>Larroque, Béatrice</creatorcontrib><creatorcontrib>Babany, Gérard</creatorcontrib><creatorcontrib>Kutala, Blaise</creatorcontrib><creatorcontrib>Francoz, Claire</creatorcontrib><creatorcontrib>Boyer, Nathalie</creatorcontrib><creatorcontrib>Moreau, Richard</creatorcontrib><creatorcontrib>Durand, François</creatorcontrib><creatorcontrib>Marcellin, Patrick</creatorcontrib><creatorcontrib>Rautou, Pierre‐Emmanuel</creatorcontrib><creatorcontrib>Valla, Dominique</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elkrief, Laure</au><au>Chouinard, Pascale</au><au>Bendersky, Noelle</au><au>Hajage, David</au><au>Larroque, Béatrice</au><au>Babany, Gérard</au><au>Kutala, Blaise</au><au>Francoz, Claire</au><au>Boyer, Nathalie</au><au>Moreau, Richard</au><au>Durand, François</au><au>Marcellin, Patrick</au><au>Rautou, Pierre‐Emmanuel</au><au>Valla, Dominique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diabetes mellitus is an independent prognostic factor for major liver‐related outcomes in patients with cirrhosis and chronic hepatitis C</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2014-09</date><risdate>2014</risdate><volume>60</volume><issue>3</issue><spage>823</spage><epage>831</epage><pages>823-831</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>In patients with chronic hepatitis C (CHC), cirrhosis is associated with age, gender, diabetes, alcohol abuse, and coinfection with human immunodeficiency virus (HIV) or hepatitis B virus (HBV). The effect of these factors on the outcome of cirrhosis is unknown. This study in CHC patients with cirrhosis aimed to assess the influence of these factors on decompensation, liver transplantation, and death. Consecutive patients with CHC and cirrhosis hospitalized between January 1, 2006 and December 31, 2008 were followed up until death, transplantation, or study closure in March 2013. Gender, age, Model for End‐Stage Liver Disease (MELD) score, diabetes, alcohol abuse, HIV, or HBV coinfection were collected at inclusion. The complications of cirrhosis, death, and liver transplantation were recorded at inclusion and during follow‐up. The association between baseline factors and liver‐related outcomes at inclusion and during follow‐up were tested using logistic regression and Cox's model, respectively. A total of 348 patients with CHC and cirrhosis (68% men; median age: 59 years; median MELD: 10) were included. At baseline, 40% of the patients had diabetes, 29% alcohol abuse, and 6% HIV or HBV coinfection. Baseline MELD ≥10 (P &lt; 0.001), diabetes (P = 0.027), and HBV coinfection (P = 0.001) were independently associated with transplantation‐free survival. Baseline diabetes was independently associated with ascites (P = 0.05), bacterial infections (P = 0.001), and encephalopathy (P &lt; 0.001) at inclusion. Baseline diabetes was independently associated with development of ascites (P = 0.057), renal dysfunction (P = 0.004), bacterial infections (P = 0.007), and hepatocellular carcinoma (P = 0.016) during the follow‐up. Conclusion: In patients with CHC and cirrhosis, diabetes is an independent prognostic factor. Improving diabetes control may improve the outcome of cirrhosis. (Hepatology 2014;60:823–831)</abstract><cop>United States</cop><pub>Wolters Kluwer Health, Inc</pub><pmid>24841704</pmid><doi>10.1002/hep.27228</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Bacterial infections
Carcinoma, Hepatocellular - epidemiology
Carcinoma, Hepatocellular - etiology
Carcinoma, Hepatocellular - virology
Diabetes
Diabetes Complications - diagnosis
Diabetes Complications - mortality
Diabetes Complications - virology
Female
France - epidemiology
Hepatitis
Hepatitis B - complications
Hepatitis C
Hepatitis C, Chronic - complications
Hepatitis C, Chronic - epidemiology
Hepatitis C, Chronic - virology
Hepatology
HIV
Human immunodeficiency virus
Humans
Liver cirrhosis
Liver Cirrhosis - diagnosis
Liver Cirrhosis - mortality
Liver Cirrhosis - virology
Liver Neoplasms - epidemiology
Liver Neoplasms - etiology
Liver Neoplasms - virology
Liver Transplantation
Male
Middle Aged
Prognosis
Retrospective Studies
Risk Factors
title Diabetes mellitus is an independent prognostic factor for major liver‐related outcomes in patients with cirrhosis and chronic hepatitis C
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