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Risk factors for hepatic decompensation in patients with primary biliary cirrhosis
To examine the clinical features and analyze prognostic factors in a prospective study of primary biliary cirrhosis (PBC) patients. From 1995 to 2010, PBC patients without hepatic decompensation seen at the Peking Union Medical College Hospital were enrolled. Clinical signs and manifestations (pruri...
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Published in: | World journal of gastroenterology : WJG 2013-02, Vol.19 (7), p.1111-1118 |
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description | To examine the clinical features and analyze prognostic factors in a prospective study of primary biliary cirrhosis (PBC) patients.
From 1995 to 2010, PBC patients without hepatic decompensation seen at the Peking Union Medical College Hospital were enrolled. Clinical signs and manifestations (pruritus, persistent fatigue, jaundice and pain in the right hypochondrium), laboratory parameters (auto-antibodies for autoimmune hepatic disease, biliary and hepatic enzymes, immunoglobulin, bilirubin, and albumin) and imaging findings were recorded at entry and at specific time points during follow-up. Cox regression and Kaplan-Meier analyses, respectively, assessed the risk factors for hepatic decompensation and survival.
Two hundred and sixty-two PBC patients were enrolled with a median follow-up of 75.2 mo (range, 21-201 mo). The 240 patients were aged 51.5 ± 10.2 years at diagnosis and 91.6% were female. Two hundred and forty-five (93.5%) were seropositive for anti-mitochondrial antibodies. At presentation, 170 patients (64.9%) were symptomatic, while 96 patients (36.6%) had extra-hepatic autoimmune disease. During the follow-up period, 62 (23.7%) patients developed hepatic decompensation of whom four underwent liver transplantation and 17 died. The cumulative survival rate and median survival time were 83.9% and 181.7 mo, respectively. Cox regression analysis revealed that an incomplete ursodeoxycholic acid (UDCA) response or inconsistent treatment [P < 0.001; hazard risk (HR) 95%CI = 2.423-7.541], anti-centromere antibodies (ACA) positivity (P < 0.001; HR 95%CI = 2.516-7.137), alanine aminotransferase ratio (AAR) elevations (P < 0.001; HR 95%CI = 1.357-2.678), and histological advanced liver disease (P = 0.006; HR 95%CI = 1.481-10.847) were predictors of hepatic decompensation. The clinical features and survival of PBC in China are consistent with those described in Western countries.
Incomplete UDCA response or inconsistent treatment, ACA positivity, AAR elevations, and advanced histological stage are predictors of decompensation. |
doi_str_mv | 10.3748/wjg.v19.i7.1111 |
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From 1995 to 2010, PBC patients without hepatic decompensation seen at the Peking Union Medical College Hospital were enrolled. Clinical signs and manifestations (pruritus, persistent fatigue, jaundice and pain in the right hypochondrium), laboratory parameters (auto-antibodies for autoimmune hepatic disease, biliary and hepatic enzymes, immunoglobulin, bilirubin, and albumin) and imaging findings were recorded at entry and at specific time points during follow-up. Cox regression and Kaplan-Meier analyses, respectively, assessed the risk factors for hepatic decompensation and survival.
Two hundred and sixty-two PBC patients were enrolled with a median follow-up of 75.2 mo (range, 21-201 mo). The 240 patients were aged 51.5 ± 10.2 years at diagnosis and 91.6% were female. Two hundred and forty-five (93.5%) were seropositive for anti-mitochondrial antibodies. At presentation, 170 patients (64.9%) were symptomatic, while 96 patients (36.6%) had extra-hepatic autoimmune disease. During the follow-up period, 62 (23.7%) patients developed hepatic decompensation of whom four underwent liver transplantation and 17 died. The cumulative survival rate and median survival time were 83.9% and 181.7 mo, respectively. Cox regression analysis revealed that an incomplete ursodeoxycholic acid (UDCA) response or inconsistent treatment [P < 0.001; hazard risk (HR) 95%CI = 2.423-7.541], anti-centromere antibodies (ACA) positivity (P < 0.001; HR 95%CI = 2.516-7.137), alanine aminotransferase ratio (AAR) elevations (P < 0.001; HR 95%CI = 1.357-2.678), and histological advanced liver disease (P = 0.006; HR 95%CI = 1.481-10.847) were predictors of hepatic decompensation. The clinical features and survival of PBC in China are consistent with those described in Western countries.
Incomplete UDCA response or inconsistent treatment, ACA positivity, AAR elevations, and advanced histological stage are predictors of decompensation.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v19.i7.1111</identifier><identifier>PMID: 23467321</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Co., Limited</publisher><subject>Adult ; Biomarkers - blood ; Brief ; Chi-Square Distribution ; China ; Cholagogues and Choleretics - therapeutic use ; Disease Progression ; Female ; Humans ; Kaplan-Meier Estimate ; Liver Cirrhosis, Biliary - blood ; Liver Cirrhosis, Biliary - complications ; Liver Cirrhosis, Biliary - diagnosis ; Liver Cirrhosis, Biliary - immunology ; Liver Cirrhosis, Biliary - mortality ; Liver Cirrhosis, Biliary - therapy ; Liver Failure - blood ; Liver Failure - diagnosis ; Liver Failure - etiology ; Liver Failure - immunology ; Liver Failure - mortality ; Liver Failure - therapy ; Liver Transplantation - adverse effects ; Liver Transplantation - mortality ; Male ; Middle Aged ; Proportional Hazards Models ; Prospective Studies ; Risk Factors ; Time Factors ; Treatment Outcome ; Ursodeoxycholic Acid - therapeutic use</subject><ispartof>World journal of gastroenterology : WJG, 2013-02, Vol.19 (7), p.1111-1118</ispartof><rights>2013 Baishideng Publishing Group Co., Limited. All rights reserved. 2013</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-1997af4d77da4a179e116bf7eb6d10667e5fe56ad744a9c13f3cba1f42c71ce33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582000/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582000/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23467321$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Tian-Yan</creatorcontrib><creatorcontrib>Zhang, Li-Na</creatorcontrib><creatorcontrib>Chen, Hua</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Shen, Min</creatorcontrib><creatorcontrib>Zhang, Xuan</creatorcontrib><creatorcontrib>Zhang, Feng-Chun</creatorcontrib><title>Risk factors for hepatic decompensation in patients with primary biliary cirrhosis</title><title>World journal of gastroenterology : WJG</title><addtitle>World J Gastroenterol</addtitle><description>To examine the clinical features and analyze prognostic factors in a prospective study of primary biliary cirrhosis (PBC) patients.
From 1995 to 2010, PBC patients without hepatic decompensation seen at the Peking Union Medical College Hospital were enrolled. Clinical signs and manifestations (pruritus, persistent fatigue, jaundice and pain in the right hypochondrium), laboratory parameters (auto-antibodies for autoimmune hepatic disease, biliary and hepatic enzymes, immunoglobulin, bilirubin, and albumin) and imaging findings were recorded at entry and at specific time points during follow-up. Cox regression and Kaplan-Meier analyses, respectively, assessed the risk factors for hepatic decompensation and survival.
Two hundred and sixty-two PBC patients were enrolled with a median follow-up of 75.2 mo (range, 21-201 mo). The 240 patients were aged 51.5 ± 10.2 years at diagnosis and 91.6% were female. Two hundred and forty-five (93.5%) were seropositive for anti-mitochondrial antibodies. At presentation, 170 patients (64.9%) were symptomatic, while 96 patients (36.6%) had extra-hepatic autoimmune disease. During the follow-up period, 62 (23.7%) patients developed hepatic decompensation of whom four underwent liver transplantation and 17 died. The cumulative survival rate and median survival time were 83.9% and 181.7 mo, respectively. Cox regression analysis revealed that an incomplete ursodeoxycholic acid (UDCA) response or inconsistent treatment [P < 0.001; hazard risk (HR) 95%CI = 2.423-7.541], anti-centromere antibodies (ACA) positivity (P < 0.001; HR 95%CI = 2.516-7.137), alanine aminotransferase ratio (AAR) elevations (P < 0.001; HR 95%CI = 1.357-2.678), and histological advanced liver disease (P = 0.006; HR 95%CI = 1.481-10.847) were predictors of hepatic decompensation. The clinical features and survival of PBC in China are consistent with those described in Western countries.
Incomplete UDCA response or inconsistent treatment, ACA positivity, AAR elevations, and advanced histological stage are predictors of decompensation.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Brief</subject><subject>Chi-Square Distribution</subject><subject>China</subject><subject>Cholagogues and Choleretics - therapeutic use</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Liver Cirrhosis, Biliary - blood</subject><subject>Liver Cirrhosis, Biliary - complications</subject><subject>Liver Cirrhosis, Biliary - diagnosis</subject><subject>Liver Cirrhosis, Biliary - immunology</subject><subject>Liver Cirrhosis, Biliary - mortality</subject><subject>Liver Cirrhosis, Biliary - therapy</subject><subject>Liver Failure - blood</subject><subject>Liver Failure - diagnosis</subject><subject>Liver Failure - etiology</subject><subject>Liver Failure - immunology</subject><subject>Liver Failure - mortality</subject><subject>Liver Failure - therapy</subject><subject>Liver Transplantation - adverse effects</subject><subject>Liver Transplantation - mortality</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Ursodeoxycholic Acid - therapeutic use</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpVUU1LAzEQDaLYWj17kxy9bM0k2U33IkjxCwpC0XPIZpM2dbupybbFf29Ka9G5DDPz5s1jHkLXQIZM8NHddjEbbqAcOjGEFCeoTymUGR1xcor6QIjISkZFD13EuCCEMpbTc9SjjBeCUeij6dTFT2yV7nyI2PqA52alOqdxbbRfrkwbU-Vb7Fq865u2i3jrujleBbdU4RtXrnG7rF0Icx9dvERnVjXRXB3yAH08Pb6PX7LJ2_Pr-GGSaVayLoOyFMryWohacQWiNABFZYWpihpIUQiTW5MXqhacq1IDs0xXCiynWoA2jA3Q_Z53ta6WptZJWlCNPOiSXjn5f9K6uZz5jWT5iBJCEsHtgSD4r7WJnVy6qE3TqNb4dZTAIC_SpzhN0Ls9VAcfYzD2eAaI3DkhkxMyOSGdkDsn0sbNX3VH_O_r2Q-jcYiX</recordid><startdate>20130221</startdate><enddate>20130221</enddate><creator>Shi, Tian-Yan</creator><creator>Zhang, Li-Na</creator><creator>Chen, Hua</creator><creator>Wang, Li</creator><creator>Shen, Min</creator><creator>Zhang, Xuan</creator><creator>Zhang, Feng-Chun</creator><general>Baishideng Publishing Group Co., Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130221</creationdate><title>Risk factors for hepatic decompensation in patients with primary biliary cirrhosis</title><author>Shi, Tian-Yan ; Zhang, Li-Na ; Chen, Hua ; Wang, Li ; Shen, Min ; Zhang, Xuan ; Zhang, Feng-Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-1997af4d77da4a179e116bf7eb6d10667e5fe56ad744a9c13f3cba1f42c71ce33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>Brief</topic><topic>Chi-Square Distribution</topic><topic>China</topic><topic>Cholagogues and Choleretics - therapeutic use</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Liver Cirrhosis, Biliary - blood</topic><topic>Liver Cirrhosis, Biliary - complications</topic><topic>Liver Cirrhosis, Biliary - diagnosis</topic><topic>Liver Cirrhosis, Biliary - immunology</topic><topic>Liver Cirrhosis, Biliary - mortality</topic><topic>Liver Cirrhosis, Biliary - therapy</topic><topic>Liver Failure - blood</topic><topic>Liver Failure - diagnosis</topic><topic>Liver Failure - etiology</topic><topic>Liver Failure - immunology</topic><topic>Liver Failure - mortality</topic><topic>Liver Failure - therapy</topic><topic>Liver Transplantation - adverse effects</topic><topic>Liver Transplantation - mortality</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Ursodeoxycholic Acid - therapeutic use</topic><toplevel>online_resources</toplevel><creatorcontrib>Shi, Tian-Yan</creatorcontrib><creatorcontrib>Zhang, Li-Na</creatorcontrib><creatorcontrib>Chen, Hua</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Shen, Min</creatorcontrib><creatorcontrib>Zhang, Xuan</creatorcontrib><creatorcontrib>Zhang, Feng-Chun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Tian-Yan</au><au>Zhang, Li-Na</au><au>Chen, Hua</au><au>Wang, Li</au><au>Shen, Min</au><au>Zhang, Xuan</au><au>Zhang, Feng-Chun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk factors for hepatic decompensation in patients with primary biliary cirrhosis</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World J Gastroenterol</addtitle><date>2013-02-21</date><risdate>2013</risdate><volume>19</volume><issue>7</issue><spage>1111</spage><epage>1118</epage><pages>1111-1118</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>To examine the clinical features and analyze prognostic factors in a prospective study of primary biliary cirrhosis (PBC) patients.
From 1995 to 2010, PBC patients without hepatic decompensation seen at the Peking Union Medical College Hospital were enrolled. Clinical signs and manifestations (pruritus, persistent fatigue, jaundice and pain in the right hypochondrium), laboratory parameters (auto-antibodies for autoimmune hepatic disease, biliary and hepatic enzymes, immunoglobulin, bilirubin, and albumin) and imaging findings were recorded at entry and at specific time points during follow-up. Cox regression and Kaplan-Meier analyses, respectively, assessed the risk factors for hepatic decompensation and survival.
Two hundred and sixty-two PBC patients were enrolled with a median follow-up of 75.2 mo (range, 21-201 mo). The 240 patients were aged 51.5 ± 10.2 years at diagnosis and 91.6% were female. Two hundred and forty-five (93.5%) were seropositive for anti-mitochondrial antibodies. At presentation, 170 patients (64.9%) were symptomatic, while 96 patients (36.6%) had extra-hepatic autoimmune disease. During the follow-up period, 62 (23.7%) patients developed hepatic decompensation of whom four underwent liver transplantation and 17 died. The cumulative survival rate and median survival time were 83.9% and 181.7 mo, respectively. Cox regression analysis revealed that an incomplete ursodeoxycholic acid (UDCA) response or inconsistent treatment [P < 0.001; hazard risk (HR) 95%CI = 2.423-7.541], anti-centromere antibodies (ACA) positivity (P < 0.001; HR 95%CI = 2.516-7.137), alanine aminotransferase ratio (AAR) elevations (P < 0.001; HR 95%CI = 1.357-2.678), and histological advanced liver disease (P = 0.006; HR 95%CI = 1.481-10.847) were predictors of hepatic decompensation. The clinical features and survival of PBC in China are consistent with those described in Western countries.
Incomplete UDCA response or inconsistent treatment, ACA positivity, AAR elevations, and advanced histological stage are predictors of decompensation.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Co., Limited</pub><pmid>23467321</pmid><doi>10.3748/wjg.v19.i7.1111</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biomarkers - blood Brief Chi-Square Distribution China Cholagogues and Choleretics - therapeutic use Disease Progression Female Humans Kaplan-Meier Estimate Liver Cirrhosis, Biliary - blood Liver Cirrhosis, Biliary - complications Liver Cirrhosis, Biliary - diagnosis Liver Cirrhosis, Biliary - immunology Liver Cirrhosis, Biliary - mortality Liver Cirrhosis, Biliary - therapy Liver Failure - blood Liver Failure - diagnosis Liver Failure - etiology Liver Failure - immunology Liver Failure - mortality Liver Failure - therapy Liver Transplantation - adverse effects Liver Transplantation - mortality Male Middle Aged Proportional Hazards Models Prospective Studies Risk Factors Time Factors Treatment Outcome Ursodeoxycholic Acid - therapeutic use |
title | Risk factors for hepatic decompensation in patients with primary biliary cirrhosis |
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