Diagnostic Accuracy of Noninvasive Markers of Steatosis, NASH, and Liver Fibrosis in HIV-Monoinfected Individuals at Risk of Nonalcoholic Fatty Liver Disease (NAFLD): Results From the ECHAM Study
BACKGROUND:HIV-monoinfected individuals are at high risk of nonalcoholic fatty liver disease. Noninvasive tests of steatosis, nonalcoholic steatohepatitis (NASH), and fibrosis have been poorly assessed in this population. Using liver biopsy (LB) as a reference, we assessed the accuracy of noninvasiv...
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Veröffentlicht in: | Journal of acquired immune deficiency syndromes (1999) 2019-04, Vol.80 (4), p.e86-e94 |
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creator | Lemoine, Maud Assoumou, Lambert De Wit, Stephane Girard, Pierre-Marie Valantin, Marc Antoine Katlama, Christine Necsoi, Coca Campa, Pauline Huefner, Anja D Schulze zur Wiesch, Julian Rougier, Hayette Bastard, Jean-Philippe Stocker, Hartmut Mauss, Stefan Serfaty, Lawrence Ratziu, Vlad Menu, Yves Schlue, Jerome Behrens, Georg Bedossa, Pierre Capeau, Jacqueline Ingiliz, Patrick Costagliola, Dominique |
description | BACKGROUND:HIV-monoinfected individuals are at high risk of nonalcoholic fatty liver disease. Noninvasive tests of steatosis, nonalcoholic steatohepatitis (NASH), and fibrosis have been poorly assessed in this population. Using liver biopsy (LB) as a reference, we assessed the accuracy of noninvasive methods for their respective diagnosismagnetic resonance imaging proton-density-fat-fraction (MRI-PDFF), FibroScan/controlled attenuation parameter (CAP), and biochemical tests.
METHODS:We enrolled antiretroviral therapy–controlled participants with persistently elevated transaminases and/or metabolic syndrome, and/or lipodystrophy. All had hepatic MRI-PDFF, FibroScan/CAP, FibroTest/NashTest/SteatoTest, APRI, FIB-4, and nonalcoholic fatty liver disease–fibrosis score. A LB was indicated if suspected significant fibrosis (FibroScan ≥7.1 kPa and/or FibroTest ≥0.49). Performance was considered as good if area under a receiver operating characteristic curves (AUROCs) was >0.80.
RESULTS:Among the 140 patients with suspected significant fibrosis out of the 402 eligible patients, 49 had had a LBmedian age of 54 years (53–65), body mass index26 kg/m (24–30), steatosis in 37 (76%), NASH in 23 (47%), and fibrosis in 31 (63%) patients [F27 (14%); F36 (12%); and F42 (4%)]. Regarding steatosis, MRI-PDFF had excellent and CAP good performances with AUROCs at 0.98 (95% confidence interval0.96 to 1.00) and 0.88 (0.76 to 0.99), respectively, whereas the AUROCs of SteatoTest was 0.68 (0.51 to 0.85). Regarding fibrosis (≥F2), APRI and FIB-4 had good performance with AUROCs at 0.86 (0.74 to 0.98) and 0.81 (0.67 to 0.95). By contrast, FibroScan and FibroTest had poor AUROCs [0.61 (0.43 to 0.79) and 0.61 (0.44 to 0.78)], with very low specificity. Regarding NASH, alanine aminotransferase ≥36 IU/L had good performance with AUROCs of 0.83 (0.71 to 0.94), whereas the NashTest had an AUROC of 0.60 (0.44 to 0.76).
CONCLUSIONS:In HIV-monoinfected patients, MRI-PDFF and FibroScan/CAP are highly accurate for the diagnosis of steatosis. The alanine aminotransferase level and APRI should be considered for the detection of NASH and fibrosis. |
doi_str_mv | 10.1097/QAI.0000000000001936 |
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METHODS:We enrolled antiretroviral therapy–controlled participants with persistently elevated transaminases and/or metabolic syndrome, and/or lipodystrophy. All had hepatic MRI-PDFF, FibroScan/CAP, FibroTest/NashTest/SteatoTest, APRI, FIB-4, and nonalcoholic fatty liver disease–fibrosis score. A LB was indicated if suspected significant fibrosis (FibroScan ≥7.1 kPa and/or FibroTest ≥0.49). Performance was considered as good if area under a receiver operating characteristic curves (AUROCs) was >0.80.
RESULTS:Among the 140 patients with suspected significant fibrosis out of the 402 eligible patients, 49 had had a LBmedian age of 54 years (53–65), body mass index26 kg/m (24–30), steatosis in 37 (76%), NASH in 23 (47%), and fibrosis in 31 (63%) patients [F27 (14%); F36 (12%); and F42 (4%)]. Regarding steatosis, MRI-PDFF had excellent and CAP good performances with AUROCs at 0.98 (95% confidence interval0.96 to 1.00) and 0.88 (0.76 to 0.99), respectively, whereas the AUROCs of SteatoTest was 0.68 (0.51 to 0.85). Regarding fibrosis (≥F2), APRI and FIB-4 had good performance with AUROCs at 0.86 (0.74 to 0.98) and 0.81 (0.67 to 0.95). By contrast, FibroScan and FibroTest had poor AUROCs [0.61 (0.43 to 0.79) and 0.61 (0.44 to 0.78)], with very low specificity. Regarding NASH, alanine aminotransferase ≥36 IU/L had good performance with AUROCs of 0.83 (0.71 to 0.94), whereas the NashTest had an AUROC of 0.60 (0.44 to 0.76).
CONCLUSIONS:In HIV-monoinfected patients, MRI-PDFF and FibroScan/CAP are highly accurate for the diagnosis of steatosis. The alanine aminotransferase level and APRI should be considered for the detection of NASH and fibrosis.</description><identifier>ISSN: 1525-4135</identifier><identifier>EISSN: 1944-7884</identifier><identifier>DOI: 10.1097/QAI.0000000000001936</identifier><identifier>PMID: 30570529</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Adipokines - blood ; Aged ; AIDS/HIV ; Alanine ; Alanine transaminase ; Anti-Retroviral Agents - therapeutic use ; Antiretroviral agents ; Antiretroviral therapy ; Attenuation ; Belgium ; Biochemical tests ; Biopsy ; Body mass ; Body mass index ; Body size ; Confidence intervals ; Diagnosis ; Diagnostic systems ; Elasticity Imaging Techniques ; Fatty liver ; Female ; Fibrosis ; France ; Germany ; Health risks ; HIV ; HIV Infections - drug therapy ; HIV Infections - pathology ; Human immunodeficiency virus ; Humans ; Lipodystrophy ; Liver ; Liver Cirrhosis - diagnosis ; Liver Cirrhosis - diagnostic imaging ; Liver diseases ; Magnetic Resonance Imaging ; Male ; Metabolic disorders ; Metabolic syndrome ; Middle Aged ; NMR ; Non-alcoholic Fatty Liver Disease - diagnosis ; Non-alcoholic Fatty Liver Disease - diagnostic imaging ; Nuclear magnetic resonance ; Prospective Studies ; Steatosis ; Transaminases ; Ultrasonography</subject><ispartof>Journal of acquired immune deficiency syndromes (1999), 2019-04, Vol.80 (4), p.e86-e94</ispartof><rights>Copyright © 2019 Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright Lippincott Williams & Wilkins Ovid Technologies Apr 1, 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4306-5eea237c15cfd9a5c85afd5af2baafb5ba70912819975bb7dfffed7082721e043</citedby><cites>FETCH-LOGICAL-c4306-5eea237c15cfd9a5c85afd5af2baafb5ba70912819975bb7dfffed7082721e043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30570529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lemoine, Maud</creatorcontrib><creatorcontrib>Assoumou, Lambert</creatorcontrib><creatorcontrib>De Wit, Stephane</creatorcontrib><creatorcontrib>Girard, Pierre-Marie</creatorcontrib><creatorcontrib>Valantin, Marc Antoine</creatorcontrib><creatorcontrib>Katlama, Christine</creatorcontrib><creatorcontrib>Necsoi, Coca</creatorcontrib><creatorcontrib>Campa, Pauline</creatorcontrib><creatorcontrib>Huefner, Anja D</creatorcontrib><creatorcontrib>Schulze zur Wiesch, Julian</creatorcontrib><creatorcontrib>Rougier, Hayette</creatorcontrib><creatorcontrib>Bastard, Jean-Philippe</creatorcontrib><creatorcontrib>Stocker, Hartmut</creatorcontrib><creatorcontrib>Mauss, Stefan</creatorcontrib><creatorcontrib>Serfaty, Lawrence</creatorcontrib><creatorcontrib>Ratziu, Vlad</creatorcontrib><creatorcontrib>Menu, Yves</creatorcontrib><creatorcontrib>Schlue, Jerome</creatorcontrib><creatorcontrib>Behrens, Georg</creatorcontrib><creatorcontrib>Bedossa, Pierre</creatorcontrib><creatorcontrib>Capeau, Jacqueline</creatorcontrib><creatorcontrib>Ingiliz, Patrick</creatorcontrib><creatorcontrib>Costagliola, Dominique</creatorcontrib><creatorcontrib>ANRS-ECHAM Group</creatorcontrib><creatorcontrib>on behalf of the ANRS-ECHAM Group</creatorcontrib><title>Diagnostic Accuracy of Noninvasive Markers of Steatosis, NASH, and Liver Fibrosis in HIV-Monoinfected Individuals at Risk of Nonalcoholic Fatty Liver Disease (NAFLD): Results From the ECHAM Study</title><title>Journal of acquired immune deficiency syndromes (1999)</title><addtitle>J Acquir Immune Defic Syndr</addtitle><description>BACKGROUND:HIV-monoinfected individuals are at high risk of nonalcoholic fatty liver disease. Noninvasive tests of steatosis, nonalcoholic steatohepatitis (NASH), and fibrosis have been poorly assessed in this population. Using liver biopsy (LB) as a reference, we assessed the accuracy of noninvasive methods for their respective diagnosismagnetic resonance imaging proton-density-fat-fraction (MRI-PDFF), FibroScan/controlled attenuation parameter (CAP), and biochemical tests.
METHODS:We enrolled antiretroviral therapy–controlled participants with persistently elevated transaminases and/or metabolic syndrome, and/or lipodystrophy. All had hepatic MRI-PDFF, FibroScan/CAP, FibroTest/NashTest/SteatoTest, APRI, FIB-4, and nonalcoholic fatty liver disease–fibrosis score. A LB was indicated if suspected significant fibrosis (FibroScan ≥7.1 kPa and/or FibroTest ≥0.49). Performance was considered as good if area under a receiver operating characteristic curves (AUROCs) was >0.80.
RESULTS:Among the 140 patients with suspected significant fibrosis out of the 402 eligible patients, 49 had had a LBmedian age of 54 years (53–65), body mass index26 kg/m (24–30), steatosis in 37 (76%), NASH in 23 (47%), and fibrosis in 31 (63%) patients [F27 (14%); F36 (12%); and F42 (4%)]. Regarding steatosis, MRI-PDFF had excellent and CAP good performances with AUROCs at 0.98 (95% confidence interval0.96 to 1.00) and 0.88 (0.76 to 0.99), respectively, whereas the AUROCs of SteatoTest was 0.68 (0.51 to 0.85). Regarding fibrosis (≥F2), APRI and FIB-4 had good performance with AUROCs at 0.86 (0.74 to 0.98) and 0.81 (0.67 to 0.95). By contrast, FibroScan and FibroTest had poor AUROCs [0.61 (0.43 to 0.79) and 0.61 (0.44 to 0.78)], with very low specificity. Regarding NASH, alanine aminotransferase ≥36 IU/L had good performance with AUROCs of 0.83 (0.71 to 0.94), whereas the NashTest had an AUROC of 0.60 (0.44 to 0.76).
CONCLUSIONS:In HIV-monoinfected patients, MRI-PDFF and FibroScan/CAP are highly accurate for the diagnosis of steatosis. The alanine aminotransferase level and APRI should be considered for the detection of NASH and fibrosis.</description><subject>Adipokines - blood</subject><subject>Aged</subject><subject>AIDS/HIV</subject><subject>Alanine</subject><subject>Alanine transaminase</subject><subject>Anti-Retroviral Agents - therapeutic use</subject><subject>Antiretroviral agents</subject><subject>Antiretroviral therapy</subject><subject>Attenuation</subject><subject>Belgium</subject><subject>Biochemical tests</subject><subject>Biopsy</subject><subject>Body mass</subject><subject>Body mass index</subject><subject>Body size</subject><subject>Confidence intervals</subject><subject>Diagnosis</subject><subject>Diagnostic systems</subject><subject>Elasticity Imaging Techniques</subject><subject>Fatty liver</subject><subject>Female</subject><subject>Fibrosis</subject><subject>France</subject><subject>Germany</subject><subject>Health risks</subject><subject>HIV</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - pathology</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Lipodystrophy</subject><subject>Liver</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Cirrhosis - diagnostic imaging</subject><subject>Liver diseases</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Metabolic disorders</subject><subject>Metabolic syndrome</subject><subject>Middle Aged</subject><subject>NMR</subject><subject>Non-alcoholic Fatty Liver Disease - diagnosis</subject><subject>Non-alcoholic Fatty Liver Disease - diagnostic imaging</subject><subject>Nuclear magnetic resonance</subject><subject>Prospective Studies</subject><subject>Steatosis</subject><subject>Transaminases</subject><subject>Ultrasonography</subject><issn>1525-4135</issn><issn>1944-7884</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd1u0zAYhiMEYj9wBwhZ4mRIy7CdOI53FrUrrdQWsQGnkWN_oV7TeNhOp17fbgxXLQjtAEuWLfv5Hv-8SfKO4CuCBf_0tZpd4X8aEVnxIjklIs9TXpb5yzhnlKU5ydhJcub9fWSKPBevk5MMM44ZFafJ09jIn731wShUKTU4qXbItmhpe9NvpTdbQAvp1uD8fvkugAzWG3-JltXd9BLJXqN5hByamMbtd5Dp0XT2I13Y3pq-BRVAo1mvzdboQXYeyYBujV8fT5GdsivbxeMnMoTdUTY2HqQHdLGsJvPxx2t0C37ogkcTZzcorADdjKbVIt5n0Ls3yas2iuHtcTxPvk9uvo2m6fzL59momqcqz3CRMgBJM64IU60WkqmSyVbHThsp24Y1kmNBaEmE4KxpuG7bFjTHJeWUAM6z8-Ti4H1w9tcAPtQb4xV0nezBDr6mhImMFhnPIvrhGXpvBxcfGylKRZEVotwL8wOl4s95B2394MxGul1NcL0PuY4h189DjmXvj_Kh2YD-W_Qn1QiUB-DRdiEmt-6GR3D1CmQXVv93_wa_ObO6</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Lemoine, Maud</creator><creator>Assoumou, Lambert</creator><creator>De Wit, Stephane</creator><creator>Girard, Pierre-Marie</creator><creator>Valantin, Marc Antoine</creator><creator>Katlama, Christine</creator><creator>Necsoi, Coca</creator><creator>Campa, Pauline</creator><creator>Huefner, Anja D</creator><creator>Schulze zur Wiesch, Julian</creator><creator>Rougier, Hayette</creator><creator>Bastard, Jean-Philippe</creator><creator>Stocker, Hartmut</creator><creator>Mauss, Stefan</creator><creator>Serfaty, Lawrence</creator><creator>Ratziu, Vlad</creator><creator>Menu, Yves</creator><creator>Schlue, Jerome</creator><creator>Behrens, Georg</creator><creator>Bedossa, Pierre</creator><creator>Capeau, Jacqueline</creator><creator>Ingiliz, Patrick</creator><creator>Costagliola, Dominique</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><general>Lippincott Williams & Wilkins Ovid Technologies</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>7T2</scope><scope>7T5</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20190401</creationdate><title>Diagnostic Accuracy of Noninvasive Markers of Steatosis, NASH, and Liver Fibrosis in HIV-Monoinfected Individuals at Risk of Nonalcoholic Fatty Liver Disease (NAFLD): Results From the ECHAM Study</title><author>Lemoine, Maud ; Assoumou, Lambert ; De Wit, Stephane ; Girard, Pierre-Marie ; Valantin, Marc Antoine ; Katlama, Christine ; Necsoi, Coca ; Campa, Pauline ; Huefner, Anja D ; Schulze zur Wiesch, Julian ; Rougier, Hayette ; Bastard, Jean-Philippe ; Stocker, Hartmut ; Mauss, Stefan ; Serfaty, Lawrence ; Ratziu, Vlad ; Menu, Yves ; Schlue, Jerome ; Behrens, Georg ; Bedossa, Pierre ; Capeau, Jacqueline ; Ingiliz, Patrick ; Costagliola, Dominique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4306-5eea237c15cfd9a5c85afd5af2baafb5ba70912819975bb7dfffed7082721e043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adipokines - blood</topic><topic>Aged</topic><topic>AIDS/HIV</topic><topic>Alanine</topic><topic>Alanine transaminase</topic><topic>Anti-Retroviral Agents - therapeutic use</topic><topic>Antiretroviral agents</topic><topic>Antiretroviral therapy</topic><topic>Attenuation</topic><topic>Belgium</topic><topic>Biochemical tests</topic><topic>Biopsy</topic><topic>Body mass</topic><topic>Body mass index</topic><topic>Body size</topic><topic>Confidence intervals</topic><topic>Diagnosis</topic><topic>Diagnostic systems</topic><topic>Elasticity Imaging Techniques</topic><topic>Fatty liver</topic><topic>Female</topic><topic>Fibrosis</topic><topic>France</topic><topic>Germany</topic><topic>Health risks</topic><topic>HIV</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - pathology</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Lipodystrophy</topic><topic>Liver</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver Cirrhosis - diagnostic imaging</topic><topic>Liver diseases</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Metabolic disorders</topic><topic>Metabolic syndrome</topic><topic>Middle Aged</topic><topic>NMR</topic><topic>Non-alcoholic Fatty Liver Disease - diagnosis</topic><topic>Non-alcoholic Fatty Liver Disease - diagnostic imaging</topic><topic>Nuclear magnetic resonance</topic><topic>Prospective Studies</topic><topic>Steatosis</topic><topic>Transaminases</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lemoine, Maud</creatorcontrib><creatorcontrib>Assoumou, Lambert</creatorcontrib><creatorcontrib>De Wit, Stephane</creatorcontrib><creatorcontrib>Girard, Pierre-Marie</creatorcontrib><creatorcontrib>Valantin, Marc Antoine</creatorcontrib><creatorcontrib>Katlama, Christine</creatorcontrib><creatorcontrib>Necsoi, Coca</creatorcontrib><creatorcontrib>Campa, Pauline</creatorcontrib><creatorcontrib>Huefner, Anja D</creatorcontrib><creatorcontrib>Schulze zur Wiesch, Julian</creatorcontrib><creatorcontrib>Rougier, Hayette</creatorcontrib><creatorcontrib>Bastard, Jean-Philippe</creatorcontrib><creatorcontrib>Stocker, Hartmut</creatorcontrib><creatorcontrib>Mauss, Stefan</creatorcontrib><creatorcontrib>Serfaty, Lawrence</creatorcontrib><creatorcontrib>Ratziu, Vlad</creatorcontrib><creatorcontrib>Menu, Yves</creatorcontrib><creatorcontrib>Schlue, Jerome</creatorcontrib><creatorcontrib>Behrens, Georg</creatorcontrib><creatorcontrib>Bedossa, Pierre</creatorcontrib><creatorcontrib>Capeau, Jacqueline</creatorcontrib><creatorcontrib>Ingiliz, Patrick</creatorcontrib><creatorcontrib>Costagliola, Dominique</creatorcontrib><creatorcontrib>ANRS-ECHAM Group</creatorcontrib><creatorcontrib>on behalf of the ANRS-ECHAM Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lemoine, Maud</au><au>Assoumou, Lambert</au><au>De Wit, Stephane</au><au>Girard, Pierre-Marie</au><au>Valantin, Marc Antoine</au><au>Katlama, Christine</au><au>Necsoi, Coca</au><au>Campa, Pauline</au><au>Huefner, Anja D</au><au>Schulze zur Wiesch, Julian</au><au>Rougier, Hayette</au><au>Bastard, Jean-Philippe</au><au>Stocker, Hartmut</au><au>Mauss, Stefan</au><au>Serfaty, Lawrence</au><au>Ratziu, Vlad</au><au>Menu, Yves</au><au>Schlue, Jerome</au><au>Behrens, Georg</au><au>Bedossa, Pierre</au><au>Capeau, Jacqueline</au><au>Ingiliz, Patrick</au><au>Costagliola, Dominique</au><aucorp>ANRS-ECHAM Group</aucorp><aucorp>on behalf of the ANRS-ECHAM Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic Accuracy of Noninvasive Markers of Steatosis, NASH, and Liver Fibrosis in HIV-Monoinfected Individuals at Risk of Nonalcoholic Fatty Liver Disease (NAFLD): Results From the ECHAM Study</atitle><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle><addtitle>J Acquir Immune Defic Syndr</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>80</volume><issue>4</issue><spage>e86</spage><epage>e94</epage><pages>e86-e94</pages><issn>1525-4135</issn><eissn>1944-7884</eissn><abstract>BACKGROUND:HIV-monoinfected individuals are at high risk of nonalcoholic fatty liver disease. Noninvasive tests of steatosis, nonalcoholic steatohepatitis (NASH), and fibrosis have been poorly assessed in this population. Using liver biopsy (LB) as a reference, we assessed the accuracy of noninvasive methods for their respective diagnosismagnetic resonance imaging proton-density-fat-fraction (MRI-PDFF), FibroScan/controlled attenuation parameter (CAP), and biochemical tests.
METHODS:We enrolled antiretroviral therapy–controlled participants with persistently elevated transaminases and/or metabolic syndrome, and/or lipodystrophy. All had hepatic MRI-PDFF, FibroScan/CAP, FibroTest/NashTest/SteatoTest, APRI, FIB-4, and nonalcoholic fatty liver disease–fibrosis score. A LB was indicated if suspected significant fibrosis (FibroScan ≥7.1 kPa and/or FibroTest ≥0.49). Performance was considered as good if area under a receiver operating characteristic curves (AUROCs) was >0.80.
RESULTS:Among the 140 patients with suspected significant fibrosis out of the 402 eligible patients, 49 had had a LBmedian age of 54 years (53–65), body mass index26 kg/m (24–30), steatosis in 37 (76%), NASH in 23 (47%), and fibrosis in 31 (63%) patients [F27 (14%); F36 (12%); and F42 (4%)]. Regarding steatosis, MRI-PDFF had excellent and CAP good performances with AUROCs at 0.98 (95% confidence interval0.96 to 1.00) and 0.88 (0.76 to 0.99), respectively, whereas the AUROCs of SteatoTest was 0.68 (0.51 to 0.85). Regarding fibrosis (≥F2), APRI and FIB-4 had good performance with AUROCs at 0.86 (0.74 to 0.98) and 0.81 (0.67 to 0.95). By contrast, FibroScan and FibroTest had poor AUROCs [0.61 (0.43 to 0.79) and 0.61 (0.44 to 0.78)], with very low specificity. Regarding NASH, alanine aminotransferase ≥36 IU/L had good performance with AUROCs of 0.83 (0.71 to 0.94), whereas the NashTest had an AUROC of 0.60 (0.44 to 0.76).
CONCLUSIONS:In HIV-monoinfected patients, MRI-PDFF and FibroScan/CAP are highly accurate for the diagnosis of steatosis. The alanine aminotransferase level and APRI should be considered for the detection of NASH and fibrosis.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>30570529</pmid><doi>10.1097/QAI.0000000000001936</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1525-4135 |
ispartof | Journal of acquired immune deficiency syndromes (1999), 2019-04, Vol.80 (4), p.e86-e94 |
issn | 1525-4135 1944-7884 |
language | eng |
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source | MEDLINE; Journals@Ovid LWW Legacy Archive; Free E- Journals |
subjects | Adipokines - blood Aged AIDS/HIV Alanine Alanine transaminase Anti-Retroviral Agents - therapeutic use Antiretroviral agents Antiretroviral therapy Attenuation Belgium Biochemical tests Biopsy Body mass Body mass index Body size Confidence intervals Diagnosis Diagnostic systems Elasticity Imaging Techniques Fatty liver Female Fibrosis France Germany Health risks HIV HIV Infections - drug therapy HIV Infections - pathology Human immunodeficiency virus Humans Lipodystrophy Liver Liver Cirrhosis - diagnosis Liver Cirrhosis - diagnostic imaging Liver diseases Magnetic Resonance Imaging Male Metabolic disorders Metabolic syndrome Middle Aged NMR Non-alcoholic Fatty Liver Disease - diagnosis Non-alcoholic Fatty Liver Disease - diagnostic imaging Nuclear magnetic resonance Prospective Studies Steatosis Transaminases Ultrasonography |
title | Diagnostic Accuracy of Noninvasive Markers of Steatosis, NASH, and Liver Fibrosis in HIV-Monoinfected Individuals at Risk of Nonalcoholic Fatty Liver Disease (NAFLD): Results From the ECHAM Study |
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