Systematic review of risk factors for fibrosis progression in non-alcoholic steatohepatitis
Background/Aims Non-alcoholic steatohepatitis (NASH) is a growing public health problem. Evaluation of risk factors for fibrosis in NASH will help to target resources to reduce development of cirrhosis. This study had two aims; the first to compile longitudinal histological data to characterize the...
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description | Background/Aims Non-alcoholic steatohepatitis (NASH) is a growing public health problem. Evaluation of risk factors for fibrosis in NASH will help to target resources to reduce development of cirrhosis. This study had two aims; the first to compile longitudinal histological data to characterize the natural history of fibrosis progression in NASH, and second, to identify predictive factors for progression to advanced fibrosis (stage 3 or greater) in NASH. Methods Subjects had to have a histological diagnosis compatible with NASH on their initial biopsy, received no intervention of proven histological benefit, and undergone two liver biopsies with at least an interval of one year between them. Results Ten studies were selected comprising 221 patients. 37.6% had progressive fibrosis over a mean follow-up interval of 5.3 years (SD, 4.2 years, median, 3.7 years, range 1.0–21.3 years). Proportional hazards regression analysis demonstrated that age (HR = 0.98, p = 0.009) and inflammation on initial biopsy (any inflammation, HR = 2.5, p = 0.001; grade 1, HR = 2.5, p = 0.001; grade 2, HR = 2.4, p = 0.003) are independent predictors of progression to advanced fibrosis. Other traditional parameters (e.g. obesity, diabetes, hypertension) were not statistically significant predictors. Conclusions Presence of inflammation on the initial biopsy and age are independent predictors of progression to advanced fibrosis in patients with NASH. |
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Evaluation of risk factors for fibrosis in NASH will help to target resources to reduce development of cirrhosis. This study had two aims; the first to compile longitudinal histological data to characterize the natural history of fibrosis progression in NASH, and second, to identify predictive factors for progression to advanced fibrosis (stage 3 or greater) in NASH. Methods Subjects had to have a histological diagnosis compatible with NASH on their initial biopsy, received no intervention of proven histological benefit, and undergone two liver biopsies with at least an interval of one year between them. Results Ten studies were selected comprising 221 patients. 37.6% had progressive fibrosis over a mean follow-up interval of 5.3 years (SD, 4.2 years, median, 3.7 years, range 1.0–21.3 years). Proportional hazards regression analysis demonstrated that age (HR = 0.98, p = 0.009) and inflammation on initial biopsy (any inflammation, HR = 2.5, p = 0.001; grade 1, HR = 2.5, p = 0.001; grade 2, HR = 2.4, p = 0.003) are independent predictors of progression to advanced fibrosis. Other traditional parameters (e.g. obesity, diabetes, hypertension) were not statistically significant predictors. Conclusions Presence of inflammation on the initial biopsy and age are independent predictors of progression to advanced fibrosis in patients with NASH.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2009.03.019</identifier><identifier>PMID: 19501928</identifier><identifier>CODEN: JOHEEC</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Adult ; Age Factors ; Aged ; Biological and medical sciences ; Cirrhosis ; Fatty liver ; Fatty Liver - complications ; Fatty Liver - pathology ; Female ; Fibrosis ; Gastroenterology and Hepatology ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Inflammation ; Kaplan-Meier Estimate ; Liver Cirrhosis - etiology ; Liver Cirrhosis - pathology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Other diseases. Semiology ; Prognosis ; Proportional Hazards Models ; Risk Factors ; Steatohepatitis ; Time Factors</subject><ispartof>Journal of hepatology, 2009-08, Vol.51 (2), p.371-379</ispartof><rights>European Association for the Study of the Liver</rights><rights>2009 European Association for the Study of the Liver</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-a5744eb1ed4186a8515a73cefa6743912b8a77e83a2080d0ff4701ea0cd2f5b73</citedby><cites>FETCH-LOGICAL-c531t-a5744eb1ed4186a8515a73cefa6743912b8a77e83a2080d0ff4701ea0cd2f5b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168827809002608$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21742250$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19501928$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Argo, Curtis K</creatorcontrib><creatorcontrib>Northup, Patrick G</creatorcontrib><creatorcontrib>Al-Osaimi, Abdullah M.S</creatorcontrib><creatorcontrib>Caldwell, Stephen H</creatorcontrib><title>Systematic review of risk factors for fibrosis progression in non-alcoholic steatohepatitis</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Background/Aims Non-alcoholic steatohepatitis (NASH) is a growing public health problem. Evaluation of risk factors for fibrosis in NASH will help to target resources to reduce development of cirrhosis. This study had two aims; the first to compile longitudinal histological data to characterize the natural history of fibrosis progression in NASH, and second, to identify predictive factors for progression to advanced fibrosis (stage 3 or greater) in NASH. Methods Subjects had to have a histological diagnosis compatible with NASH on their initial biopsy, received no intervention of proven histological benefit, and undergone two liver biopsies with at least an interval of one year between them. Results Ten studies were selected comprising 221 patients. 37.6% had progressive fibrosis over a mean follow-up interval of 5.3 years (SD, 4.2 years, median, 3.7 years, range 1.0–21.3 years). Proportional hazards regression analysis demonstrated that age (HR = 0.98, p = 0.009) and inflammation on initial biopsy (any inflammation, HR = 2.5, p = 0.001; grade 1, HR = 2.5, p = 0.001; grade 2, HR = 2.4, p = 0.003) are independent predictors of progression to advanced fibrosis. Other traditional parameters (e.g. obesity, diabetes, hypertension) were not statistically significant predictors. Conclusions Presence of inflammation on the initial biopsy and age are independent predictors of progression to advanced fibrosis in patients with NASH.</description><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Cirrhosis</subject><subject>Fatty liver</subject><subject>Fatty Liver - complications</subject><subject>Fatty Liver - pathology</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Gastroenterology and Hepatology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Kaplan-Meier Estimate</subject><subject>Liver Cirrhosis - etiology</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Risk Factors</subject><subject>Steatohepatitis</subject><subject>Time Factors</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhi1ERZfCH-CAcoFb0rHzYUdCSFXFl1SJQ-HEwXKcMXWatRdPlmr_PY52BRKHnnx55p3XzzD2ikPFgXeXUzXd4a4SAH0FdQW8f8I2vAMooWv4U7bJkCqVkOqcPSeaAKCGvnnGznnfZlqoDftxe6AFt2bxtkj42-NDEV2RPN0XztglJipcTIXzQ4rkqdil-DMhkY-h8KEIMZRmtvEuzjkgJ5kl5k45bvH0gp05MxO-PL0X7PvHD9-uP5c3Xz99ub66KW1b86U0rWwaHDiODVedUS1vjawtOtPJpu65GJSRElVtBCgYwblGAkcDdhSuHWR9wd4ec3O5X3ukRW89WZxnEzDuSa8xjYIVFEfQ5s9QQqd3yW9NOmgOelWqJ70q1atSDbXOkvLQ61P6ftji-G_k5DADb06AIWtml0ywnv5ygstGiBYy9-7IYXaRTSdN1mOwOPqEdtFj9I_3eP_fuJ198HnjPR6QprhPIVvWXJPQoG_X46-3hx5AdKDqPySUqt8</recordid><startdate>20090801</startdate><enddate>20090801</enddate><creator>Argo, Curtis K</creator><creator>Northup, Patrick G</creator><creator>Al-Osaimi, Abdullah M.S</creator><creator>Caldwell, Stephen H</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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></search><sort><creationdate>20090801</creationdate><title>Systematic review of risk factors for fibrosis progression in non-alcoholic steatohepatitis</title><author>Argo, Curtis K ; Northup, Patrick G ; Al-Osaimi, Abdullah M.S ; Caldwell, Stephen H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-a5744eb1ed4186a8515a73cefa6743912b8a77e83a2080d0ff4701ea0cd2f5b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Cirrhosis</topic><topic>Fatty liver</topic><topic>Fatty Liver - complications</topic><topic>Fatty Liver - pathology</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Gastroenterology and Hepatology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Kaplan-Meier Estimate</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Risk Factors</topic><topic>Steatohepatitis</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Argo, Curtis K</creatorcontrib><creatorcontrib>Northup, Patrick G</creatorcontrib><creatorcontrib>Al-Osaimi, Abdullah M.S</creatorcontrib><creatorcontrib>Caldwell, Stephen H</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Argo, Curtis K</au><au>Northup, Patrick G</au><au>Al-Osaimi, Abdullah M.S</au><au>Caldwell, Stephen H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systematic review of risk factors for fibrosis progression in non-alcoholic steatohepatitis</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2009-08-01</date><risdate>2009</risdate><volume>51</volume><issue>2</issue><spage>371</spage><epage>379</epage><pages>371-379</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><coden>JOHEEC</coden><abstract>Background/Aims Non-alcoholic steatohepatitis (NASH) is a growing public health problem. Evaluation of risk factors for fibrosis in NASH will help to target resources to reduce development of cirrhosis. This study had two aims; the first to compile longitudinal histological data to characterize the natural history of fibrosis progression in NASH, and second, to identify predictive factors for progression to advanced fibrosis (stage 3 or greater) in NASH. Methods Subjects had to have a histological diagnosis compatible with NASH on their initial biopsy, received no intervention of proven histological benefit, and undergone two liver biopsies with at least an interval of one year between them. Results Ten studies were selected comprising 221 patients. 37.6% had progressive fibrosis over a mean follow-up interval of 5.3 years (SD, 4.2 years, median, 3.7 years, range 1.0–21.3 years). Proportional hazards regression analysis demonstrated that age (HR = 0.98, p = 0.009) and inflammation on initial biopsy (any inflammation, HR = 2.5, p = 0.001; grade 1, HR = 2.5, p = 0.001; grade 2, HR = 2.4, p = 0.003) are independent predictors of progression to advanced fibrosis. Other traditional parameters (e.g. obesity, diabetes, hypertension) were not statistically significant predictors. Conclusions Presence of inflammation on the initial biopsy and age are independent predictors of progression to advanced fibrosis in patients with NASH.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>19501928</pmid><doi>10.1016/j.jhep.2009.03.019</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Age Factors Aged Biological and medical sciences Cirrhosis Fatty liver Fatty Liver - complications Fatty Liver - pathology Female Fibrosis Gastroenterology and Hepatology Gastroenterology. Liver. Pancreas. Abdomen Humans Inflammation Kaplan-Meier Estimate Liver Cirrhosis - etiology Liver Cirrhosis - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Other diseases. Semiology Prognosis Proportional Hazards Models Risk Factors Steatohepatitis Time Factors |
title | Systematic review of risk factors for fibrosis progression in non-alcoholic steatohepatitis |
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