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Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors

Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH....

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Published in:Digestive diseases and sciences 2011-01, Vol.56 (1), p.227-235
Main Authors: Eapen, C. E, Nightingale, Peter, Hubscher, Stefan G, Lane, Peter J, Plant, Timothy, Velissaris, Dimitris, Elias, Elwyn
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container_title Digestive diseases and sciences
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creator Eapen, C. E
Nightingale, Peter
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description Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH.
doi_str_mv 10.1007/s10620-010-1278-2
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E ; Nightingale, Peter ; Hubscher, Stefan G ; Lane, Peter J ; Plant, Timothy ; Velissaris, Dimitris ; Elias, Elwyn</creator><creatorcontrib>Eapen, C. E ; Nightingale, Peter ; Hubscher, Stefan G ; Lane, Peter J ; Plant, Timothy ; Velissaris, Dimitris ; Elias, Elwyn</creatorcontrib><description>Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1007/s10620-010-1278-2</identifier><identifier>PMID: 20499175</identifier><identifier>CODEN: DDSCDJ</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Analysis ; Antibodies, Anticardiolipin - blood ; Anticardiolipin antibodies ; Biochemistry ; Biological and medical sciences ; Biopsy ; Celiac Disease - diagnosis ; Celiac Disease - epidemiology ; Celiac Disease - mortality ; Cohort Studies ; Colitis, Ulcerative - diagnosis ; Colitis, Ulcerative - epidemiology ; Colitis, Ulcerative - mortality ; Comorbidity ; Feeding. Feeding behavior ; Female ; Follow-Up Studies ; Fundamental and applied biological sciences. Psychology ; Gastroenterology ; Gastroenterology. Liver. Pancreas. Abdomen ; Hepatology ; Humans ; Hypertension, Portal - diagnosis ; Hypertension, Portal - epidemiology ; Hypertension, Portal - mortality ; Immunoglobulin A ; Kaplan-Meier Estimate ; Liver ; Liver - pathology ; Liver cirrhosis ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Lupus Coagulation Inhibitor - blood ; Male ; Medical research ; Medical sciences ; Medicine ; Medicine &amp; Public Health ; Medicine, Experimental ; Middle Aged ; Oncology ; Original Article ; Other diseases. Semiology ; Portal hypertension ; Prognosis ; Regression Analysis ; Retrospective Studies ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Survival Rate ; Transplant Surgery ; Ulcerative colitis ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Young Adult</subject><ispartof>Digestive diseases and sciences, 2011-01, Vol.56 (1), p.227-235</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2011 Springer</rights><rights>Springer Science+Business Media, LLC 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c590t-27d76ac04d7d9394bc56e25371a0ce6941936dcb7c61d35b97a0a3ddf7b88b6c3</citedby><cites>FETCH-LOGICAL-c590t-27d76ac04d7d9394bc56e25371a0ce6941936dcb7c61d35b97a0a3ddf7b88b6c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23838137$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20499175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eapen, C. E</creatorcontrib><creatorcontrib>Nightingale, Peter</creatorcontrib><creatorcontrib>Hubscher, Stefan G</creatorcontrib><creatorcontrib>Lane, Peter J</creatorcontrib><creatorcontrib>Plant, Timothy</creatorcontrib><creatorcontrib>Velissaris, Dimitris</creatorcontrib><creatorcontrib>Elias, Elwyn</creatorcontrib><title>Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><addtitle>Dig Dis Sci</addtitle><description>Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analysis</subject><subject>Antibodies, Anticardiolipin - blood</subject><subject>Anticardiolipin antibodies</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Celiac Disease - diagnosis</subject><subject>Celiac Disease - epidemiology</subject><subject>Celiac Disease - mortality</subject><subject>Cohort Studies</subject><subject>Colitis, Ulcerative - diagnosis</subject><subject>Colitis, Ulcerative - epidemiology</subject><subject>Colitis, Ulcerative - mortality</subject><subject>Comorbidity</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Hypertension, Portal - diagnosis</subject><subject>Hypertension, Portal - epidemiology</subject><subject>Hypertension, Portal - mortality</subject><subject>Immunoglobulin A</subject><subject>Kaplan-Meier Estimate</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Liver cirrhosis</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Lupus Coagulation Inhibitor - blood</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Medicine, Experimental</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Other diseases. Semiology</subject><subject>Portal hypertension</subject><subject>Prognosis</subject><subject>Regression Analysis</subject><subject>Retrospective Studies</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. 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E</au><au>Nightingale, Peter</au><au>Hubscher, Stefan G</au><au>Lane, Peter J</au><au>Plant, Timothy</au><au>Velissaris, Dimitris</au><au>Elias, Elwyn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors</atitle><jtitle>Digestive diseases and sciences</jtitle><stitle>Dig Dis Sci</stitle><addtitle>Dig Dis Sci</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>56</volume><issue>1</issue><spage>227</spage><epage>235</epage><pages>227-235</pages><issn>0163-2116</issn><eissn>1573-2568</eissn><coden>DDSCDJ</coden><abstract>Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>20499175</pmid><doi>10.1007/s10620-010-1278-2</doi><tpages>9</tpages></addata></record>
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ispartof Digestive diseases and sciences, 2011-01, Vol.56 (1), p.227-235
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Analysis
Antibodies, Anticardiolipin - blood
Anticardiolipin antibodies
Biochemistry
Biological and medical sciences
Biopsy
Celiac Disease - diagnosis
Celiac Disease - epidemiology
Celiac Disease - mortality
Cohort Studies
Colitis, Ulcerative - diagnosis
Colitis, Ulcerative - epidemiology
Colitis, Ulcerative - mortality
Comorbidity
Feeding. Feeding behavior
Female
Follow-Up Studies
Fundamental and applied biological sciences. Psychology
Gastroenterology
Gastroenterology. Liver. Pancreas. Abdomen
Hepatology
Humans
Hypertension, Portal - diagnosis
Hypertension, Portal - epidemiology
Hypertension, Portal - mortality
Immunoglobulin A
Kaplan-Meier Estimate
Liver
Liver - pathology
Liver cirrhosis
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Lupus Coagulation Inhibitor - blood
Male
Medical research
Medical sciences
Medicine
Medicine & Public Health
Medicine, Experimental
Middle Aged
Oncology
Original Article
Other diseases. Semiology
Portal hypertension
Prognosis
Regression Analysis
Retrospective Studies
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Survival Rate
Transplant Surgery
Ulcerative colitis
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Young Adult
title Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors
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