Serum biomarkers can predict a change in liver fibrosis 1 year after lifestyle intervention for biopsy‐proven NASH

Background & Aims The dynamic response of serum fibrosis biomarkers to histological changes within the liver following lifestyle intervention (LI) is unknown. We explored relationships between changes in serum biomarkers and liver fibrosis in NASH patients undergoing LI. Methods Paired liver bio...

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Veröffentlicht in:Liver international 2017-12, Vol.37 (12), p.1887-1896
Hauptverfasser: Vilar‐Gomez, Eduardo, Calzadilla‐Bertot, Luis, Friedman, Scott L., Gra‐Oramas, Bienvenido, Gonzalez‐Fabian, Licet, Lazo‐del Vallin, Sacha, Diago, Moises, Adams, Leon A.
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container_end_page 1896
container_issue 12
container_start_page 1887
container_title Liver international
container_volume 37
creator Vilar‐Gomez, Eduardo
Calzadilla‐Bertot, Luis
Friedman, Scott L.
Gra‐Oramas, Bienvenido
Gonzalez‐Fabian, Licet
Lazo‐del Vallin, Sacha
Diago, Moises
Adams, Leon A.
description Background & Aims The dynamic response of serum fibrosis biomarkers to histological changes within the liver following lifestyle intervention (LI) is unknown. We explored relationships between changes in serum biomarkers and liver fibrosis in NASH patients undergoing LI. Methods Paired liver biopsies were performed in 261 NASH patients to assess fibrosis change after 1 year of LI. We explored the utility of serum fibrosis markers to predict changes in hepatic fibrosis and developed and internally validated a model for predicting fibrosis improvement in patients with baseline fibrosis. Results Regression, stabilization and worsening of fibrosis occurred in 51 (20%), 165 (63%) and 45 (17%) patients respectively. By multivariable analysis, change in HbA1c (OR, 0.39, P
doi_str_mv 10.1111/liv.13480
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We explored relationships between changes in serum biomarkers and liver fibrosis in NASH patients undergoing LI. Methods Paired liver biopsies were performed in 261 NASH patients to assess fibrosis change after 1 year of LI. We explored the utility of serum fibrosis markers to predict changes in hepatic fibrosis and developed and internally validated a model for predicting fibrosis improvement in patients with baseline fibrosis. Results Regression, stabilization and worsening of fibrosis occurred in 51 (20%), 165 (63%) and 45 (17%) patients respectively. By multivariable analysis, change in HbA1c (OR, 0.39, P<.01), platelets (OR, 1.22, P<.01) and NFS (OR, 0.27, P<.01), as well as ALT normalization (OR, 9.7, P<.01) were independently associated with fibrosis improvement, whereas change in platelets (OR, 0.96, P<.01), and NFS (OR, 1.8, P<.01) as well as ALT normalization (OR, 0.21, P<.01) were linked to fibrosis progression. A model, including change in HbA1c, platelet and ALT normalization, was significantly more accurate (AUC of 0.96, 95% CI, l0.94‐0.99) than NFS, FIB‐4 and APRI for predicting fibrosis improvement. Using a threshold of ≥0.497, positive and negative predictive values were 94% (95% CI, 84‐98) and 91% (95% CI, 81‐96) respectively. Conclusions Change in NFS, platelets and ALT normalization are associated with change in liver fibrosis after 1 year of LI. A model including change in HbA1c, platelet and ALT normalization discriminated patients with fibrosis improvement significantly better than other biomarkers.]]></description><identifier>ISSN: 1478-3223</identifier><identifier>EISSN: 1478-3231</identifier><identifier>DOI: 10.1111/liv.13480</identifier><identifier>PMID: 28544769</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Biomarkers - blood ; Cohort Studies ; Disease Progression ; Female ; Fibrosis ; fibrosis regression ; Humans ; lifestyle interventions ; Liver - pathology ; Liver Cirrhosis - blood ; Liver Cirrhosis - etiology ; Male ; Middle Aged ; Non-alcoholic Fatty Liver Disease - blood ; Non-alcoholic Fatty Liver Disease - complications ; Non-alcoholic Fatty Liver Disease - pathology ; Non-alcoholic Fatty Liver Disease - therapy ; nonalcoholic steatohepatitis ; noninvasive biomarkers ; Risk Reduction Behavior</subject><ispartof>Liver international, 2017-12, Vol.37 (12), p.1887-1896</ispartof><rights>2017 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3910-faa68bbf26f81bb326405ad4fcfc2404a85ab109c95643205a7a67dba3a1226a3</citedby><cites>FETCH-LOGICAL-c3910-faa68bbf26f81bb326405ad4fcfc2404a85ab109c95643205a7a67dba3a1226a3</cites><orcidid>0000-0003-1435-4013</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fliv.13480$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fliv.13480$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28544769$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vilar‐Gomez, Eduardo</creatorcontrib><creatorcontrib>Calzadilla‐Bertot, Luis</creatorcontrib><creatorcontrib>Friedman, Scott L.</creatorcontrib><creatorcontrib>Gra‐Oramas, Bienvenido</creatorcontrib><creatorcontrib>Gonzalez‐Fabian, Licet</creatorcontrib><creatorcontrib>Lazo‐del Vallin, Sacha</creatorcontrib><creatorcontrib>Diago, Moises</creatorcontrib><creatorcontrib>Adams, Leon A.</creatorcontrib><title>Serum biomarkers can predict a change in liver fibrosis 1 year after lifestyle intervention for biopsy‐proven NASH</title><title>Liver international</title><addtitle>Liver Int</addtitle><description><![CDATA[Background & Aims The dynamic response of serum fibrosis biomarkers to histological changes within the liver following lifestyle intervention (LI) is unknown. We explored relationships between changes in serum biomarkers and liver fibrosis in NASH patients undergoing LI. Methods Paired liver biopsies were performed in 261 NASH patients to assess fibrosis change after 1 year of LI. We explored the utility of serum fibrosis markers to predict changes in hepatic fibrosis and developed and internally validated a model for predicting fibrosis improvement in patients with baseline fibrosis. Results Regression, stabilization and worsening of fibrosis occurred in 51 (20%), 165 (63%) and 45 (17%) patients respectively. By multivariable analysis, change in HbA1c (OR, 0.39, P<.01), platelets (OR, 1.22, P<.01) and NFS (OR, 0.27, P<.01), as well as ALT normalization (OR, 9.7, P<.01) were independently associated with fibrosis improvement, whereas change in platelets (OR, 0.96, P<.01), and NFS (OR, 1.8, P<.01) as well as ALT normalization (OR, 0.21, P<.01) were linked to fibrosis progression. A model, including change in HbA1c, platelet and ALT normalization, was significantly more accurate (AUC of 0.96, 95% CI, l0.94‐0.99) than NFS, FIB‐4 and APRI for predicting fibrosis improvement. Using a threshold of ≥0.497, positive and negative predictive values were 94% (95% CI, 84‐98) and 91% (95% CI, 81‐96) respectively. Conclusions Change in NFS, platelets and ALT normalization are associated with change in liver fibrosis after 1 year of LI. A model including change in HbA1c, platelet and ALT normalization discriminated patients with fibrosis improvement significantly better than other biomarkers.]]></description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Cohort Studies</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Fibrosis</subject><subject>fibrosis regression</subject><subject>Humans</subject><subject>lifestyle interventions</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - blood</subject><subject>Liver Cirrhosis - etiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Non-alcoholic Fatty Liver Disease - blood</subject><subject>Non-alcoholic Fatty Liver Disease - complications</subject><subject>Non-alcoholic Fatty Liver Disease - pathology</subject><subject>Non-alcoholic Fatty Liver Disease - therapy</subject><subject>nonalcoholic steatohepatitis</subject><subject>noninvasive biomarkers</subject><subject>Risk Reduction Behavior</subject><issn>1478-3223</issn><issn>1478-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE9OAjEUhxujUUQXXsB0qQug_6bMLAlRISG6QN1OXkur1WEGWwYzO4_gETyLR_EkFkF3dtO-1y-_134InVDSpXH1CrfqUi5SsoNaVPTTDmec7v6dGT9AhyE8EUKzLKH76ICliRB9mbVQPTW-nmPlqjn4Z-MD1lDihTczp5cYsH6E8sFgV-I4xHhsnfJVcAHTz4_GgMdgl7FdOGvCsinWZKxXply6qsS28uvoRWi-3t4Xvop9fD2Yjo7QnoUimOPt3kZ3lxe3w1FncnM1Hg4mHc0zSjoWQKZKWSZtSpXiTAqSwExYbTUTRECagKIk01kiBWfxrg-yP1PAgTImgbfR2SY3zn6p4wvzuQvaFAWUpqpDTjPCqWSSkIieb1Ad_xe8sfnCu-ikySnJ15bzKCD_sRzZ021sreZm9kf-ao1AbwO8usI0_yflk_H9JvIblmGJqA</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Vilar‐Gomez, Eduardo</creator><creator>Calzadilla‐Bertot, Luis</creator><creator>Friedman, Scott L.</creator><creator>Gra‐Oramas, Bienvenido</creator><creator>Gonzalez‐Fabian, Licet</creator><creator>Lazo‐del Vallin, Sacha</creator><creator>Diago, Moises</creator><creator>Adams, Leon A.</creator><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><orcidid>https://orcid.org/0000-0003-1435-4013</orcidid></search><sort><creationdate>201712</creationdate><title>Serum biomarkers can predict a change in liver fibrosis 1 year after lifestyle intervention for biopsy‐proven NASH</title><author>Vilar‐Gomez, Eduardo ; Calzadilla‐Bertot, Luis ; Friedman, Scott L. ; Gra‐Oramas, Bienvenido ; Gonzalez‐Fabian, Licet ; Lazo‐del Vallin, Sacha ; Diago, Moises ; Adams, Leon A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3910-faa68bbf26f81bb326405ad4fcfc2404a85ab109c95643205a7a67dba3a1226a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>Cohort Studies</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Fibrosis</topic><topic>fibrosis regression</topic><topic>Humans</topic><topic>lifestyle interventions</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - blood</topic><topic>Liver Cirrhosis - etiology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Non-alcoholic Fatty Liver Disease - blood</topic><topic>Non-alcoholic Fatty Liver Disease - complications</topic><topic>Non-alcoholic Fatty Liver Disease - pathology</topic><topic>Non-alcoholic Fatty Liver Disease - therapy</topic><topic>nonalcoholic steatohepatitis</topic><topic>noninvasive biomarkers</topic><topic>Risk Reduction Behavior</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vilar‐Gomez, Eduardo</creatorcontrib><creatorcontrib>Calzadilla‐Bertot, Luis</creatorcontrib><creatorcontrib>Friedman, Scott L.</creatorcontrib><creatorcontrib>Gra‐Oramas, Bienvenido</creatorcontrib><creatorcontrib>Gonzalez‐Fabian, Licet</creatorcontrib><creatorcontrib>Lazo‐del Vallin, Sacha</creatorcontrib><creatorcontrib>Diago, Moises</creatorcontrib><creatorcontrib>Adams, Leon A.</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><jtitle>Liver international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vilar‐Gomez, Eduardo</au><au>Calzadilla‐Bertot, Luis</au><au>Friedman, Scott L.</au><au>Gra‐Oramas, Bienvenido</au><au>Gonzalez‐Fabian, Licet</au><au>Lazo‐del Vallin, Sacha</au><au>Diago, Moises</au><au>Adams, Leon A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum biomarkers can predict a change in liver fibrosis 1 year after lifestyle intervention for biopsy‐proven NASH</atitle><jtitle>Liver international</jtitle><addtitle>Liver Int</addtitle><date>2017-12</date><risdate>2017</risdate><volume>37</volume><issue>12</issue><spage>1887</spage><epage>1896</epage><pages>1887-1896</pages><issn>1478-3223</issn><eissn>1478-3231</eissn><abstract><![CDATA[Background & Aims The dynamic response of serum fibrosis biomarkers to histological changes within the liver following lifestyle intervention (LI) is unknown. We explored relationships between changes in serum biomarkers and liver fibrosis in NASH patients undergoing LI. Methods Paired liver biopsies were performed in 261 NASH patients to assess fibrosis change after 1 year of LI. We explored the utility of serum fibrosis markers to predict changes in hepatic fibrosis and developed and internally validated a model for predicting fibrosis improvement in patients with baseline fibrosis. Results Regression, stabilization and worsening of fibrosis occurred in 51 (20%), 165 (63%) and 45 (17%) patients respectively. By multivariable analysis, change in HbA1c (OR, 0.39, P<.01), platelets (OR, 1.22, P<.01) and NFS (OR, 0.27, P<.01), as well as ALT normalization (OR, 9.7, P<.01) were independently associated with fibrosis improvement, whereas change in platelets (OR, 0.96, P<.01), and NFS (OR, 1.8, P<.01) as well as ALT normalization (OR, 0.21, P<.01) were linked to fibrosis progression. A model, including change in HbA1c, platelet and ALT normalization, was significantly more accurate (AUC of 0.96, 95% CI, l0.94‐0.99) than NFS, FIB‐4 and APRI for predicting fibrosis improvement. Using a threshold of ≥0.497, positive and negative predictive values were 94% (95% CI, 84‐98) and 91% (95% CI, 81‐96) respectively. Conclusions Change in NFS, platelets and ALT normalization are associated with change in liver fibrosis after 1 year of LI. A model including change in HbA1c, platelet and ALT normalization discriminated patients with fibrosis improvement significantly better than other biomarkers.]]></abstract><cop>United States</cop><pmid>28544769</pmid><doi>10.1111/liv.13480</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-1435-4013</orcidid></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Biomarkers - blood
Cohort Studies
Disease Progression
Female
Fibrosis
fibrosis regression
Humans
lifestyle interventions
Liver - pathology
Liver Cirrhosis - blood
Liver Cirrhosis - etiology
Male
Middle Aged
Non-alcoholic Fatty Liver Disease - blood
Non-alcoholic Fatty Liver Disease - complications
Non-alcoholic Fatty Liver Disease - pathology
Non-alcoholic Fatty Liver Disease - therapy
nonalcoholic steatohepatitis
noninvasive biomarkers
Risk Reduction Behavior
title Serum biomarkers can predict a change in liver fibrosis 1 year after lifestyle intervention for biopsy‐proven NASH
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