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.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 04 2019
Historique:
pubmed: 21 12 2018
medline: 19 12 2019
entrez: 21 12 2018
Statut: ppublish

Résumé

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 diagnosis: magnetic resonance imaging proton-density-fat-fraction (MRI-PDFF), FibroScan/controlled attenuation parameter (CAP), and biochemical tests. 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. Among the 140 patients with suspected significant fibrosis out of the 402 eligible patients, 49 had had a LB: median age of 54 years (53-65), body mass index: 26 kg/m (24-30), steatosis in 37 (76%), NASH in 23 (47%), and fibrosis in 31 (63%) patients [F2: 7 (14%); F3: 6 (12%); and F4: 2 (4%)]. Regarding steatosis, MRI-PDFF had excellent and CAP good performances with AUROCs at 0.98 (95% confidence interval: 0.96 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). 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.

Sections du résumé

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 diagnosis: magnetic 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 LB: median age of 54 years (53-65), body mass index: 26 kg/m (24-30), steatosis in 37 (76%), NASH in 23 (47%), and fibrosis in 31 (63%) patients [F2: 7 (14%); F3: 6 (12%); and F4: 2 (4%)]. Regarding steatosis, MRI-PDFF had excellent and CAP good performances with AUROCs at 0.98 (95% confidence interval: 0.96 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.

Identifiants

pubmed: 30570529
doi: 10.1097/QAI.0000000000001936
doi:

Substances chimiques

Adipokines 0
Anti-Retroviral Agents 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e86-e94

Auteurs

Maud Lemoine (M)

Liver Unit, Department of Surgery and Cancer, St Mary's Hospital, Imperial College London, London, United Kingdom.

Lambert Assoumou (L)

Institut Pierre Louis d'Épidémiologie et de Santé Publique (IPLESP), INSERM, Sorbonne Université, Paris, France.

Stephane De Wit (S)

Department of Infectious Diseases and Tropical Medicine, CHU Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.

Pierre-Marie Girard (PM)

Department of Infectious disease and Tropical Medicine, Saint-Antoine Hospital, University Paris 6, Paris, France.

Marc Antoine Valantin (MA)

Department of Infectious disease and Tropical Medicine, Pitie-Salpetriere Hospital, University Paris 6, Paris, France.

Christine Katlama (C)

Department of Infectious disease and Tropical Medicine, Pitie-Salpetriere Hospital, University Paris 6, Paris, France.

Coca Necsoi (C)

Department of Infectious Diseases and Tropical Medicine, CHU Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.

Pauline Campa (P)

Department of Infectious disease and Tropical Medicine, Saint-Antoine Hospital, University Paris 6, Paris, France.

Anja D Huefner (AD)

Infectious Disease Unit, University Medical Center, Hamburg-Eppendorf, Hamburg, Germany.

Julian Schulze Zur Wiesch (J)

Infectious Disease Unit, University Medical Center, Hamburg-Eppendorf, Hamburg, Germany.

Hayette Rougier (H)

Department of Infectious disease and Tropical Medicine, Saint-Antoine Hospital, University Paris 6, Paris, France.

Jean-Philippe Bastard (JP)

Service de Biochimie, UF Bio-marqueurs Inflammatoires et Métaboliques, AP-HP, Hôpital Tenon, Paris, France.
INSERM, CRSA, UMR_S 938, Faculté de Médecine, Sorbonne Université, Paris, France.

Hartmut Stocker (H)

Department of Infectious Diseases, Vivantes Auguste-Viktoria-Klinikum, Berlin, Germany.

Stefan Mauss (S)

Center for HIV and Hepatogastroenterology, Düsseldorf, Germany.

Lawrence Serfaty (L)

Department of Hepato-Gastroenterology, Hautepierre Hospital, Hôpitaux Universitaires de Strasbourg, INSERM UMR-S938, Paris Sorbonne University, Paris, France.

Vlad Ratziu (V)

Department of Hepatology, Pitie-Salpetriere Hospital, University Paris 6, Paris, France.

Yves Menu (Y)

Department of Radiology, Saint-Antoine Hospital, University Paris 6, Paris, France.

Jerome Schlue (J)

Department of Clinical Immunology and Rheumatology, Hannover Medical School, Hannover, Germany.

Georg Behrens (G)

Institute of Pathology, Hannover Medical School, Hannover, Germany.

Pierre Bedossa (P)

Department of Histopathology, Beaujon Hospital, Clichy, France.

Jacqueline Capeau (J)

Service de Biochimie, UF Bio-marqueurs Inflammatoires et Métaboliques, AP-HP, Hôpital Tenon, Paris, France.
INSERM, CRSA, UMR_S 938, Faculté de Médecine, Sorbonne Université, Paris, France.

Patrick Ingiliz (P)

Center for Infectiology (CIB), Berlin, Germany.

Dominique Costagliola (D)

Institut Pierre Louis d'Épidémiologie et de Santé Publique (IPLESP), INSERM, Sorbonne Université, Paris, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH