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Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART)

BACKGROUND: De novo steatosis is the main criteria for non-alcoholic fatty liver disease (NAFLD), which is becoming a clinically relevant comorbidity in HIV-infected patients. This may be due to the HIV virus itself, as well as long-term toxicities deriving from antiretroviral therapy. Therefore, HI...

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Autores principales: Bischoff, Jenny, Gu, Wenyi, Schwarze-Zander, Carolynne, Boesecke, Christoph, Wasmuth, Jan-Christian, van Bremen, Kathrin, Dold, Leona, Rockstroh, Jürgen K, Trebicka, Jonel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427211/
https://www.ncbi.nlm.nih.gov/pubmed/34522873
http://dx.doi.org/10.1016/j.eclinm.2021.101116
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author Bischoff, Jenny
Gu, Wenyi
Schwarze-Zander, Carolynne
Boesecke, Christoph
Wasmuth, Jan-Christian
van Bremen, Kathrin
Dold, Leona
Rockstroh, Jürgen K
Trebicka, Jonel
author_facet Bischoff, Jenny
Gu, Wenyi
Schwarze-Zander, Carolynne
Boesecke, Christoph
Wasmuth, Jan-Christian
van Bremen, Kathrin
Dold, Leona
Rockstroh, Jürgen K
Trebicka, Jonel
author_sort Bischoff, Jenny
collection PubMed
description BACKGROUND: De novo steatosis is the main criteria for non-alcoholic fatty liver disease (NAFLD), which is becoming a clinically relevant comorbidity in HIV-infected patients. This may be due to the HIV virus itself, as well as long-term toxicities deriving from antiretroviral therapy. Therefore, HIV infected patients require prevention and monitoring regarding NAFLD. METHODS: This study investigated the differential role of body mass index (BMI) and combination antiretroviral treatment (cART) drugs on NAFLD progression. This single center prospective longitudinal observational study enrolled HIV monoinfected individuals between August 2013 to December 2018 with yearly visits. Each visit included liver stiffness and steatosis [defined as controlled attenuation parameter (CAP)>237 dB/m] assessment by annually transient elastography using an M- or XL-probe of FibroScan, and calculation of the novel FibroScan-AST (FAST) score. Risk factors for denovo/progressed steatosis and tripling of FAST-score increase were investigated using Cox regression model with time-dependent covariates. FINDINGS: 319 monoinfected HIV positive patients with at least two visits were included into the study, of which 301 patients had at least two valid CAP measurements. 51·5%(155) patients did not have steatosis at first assessment, of which 45%(69) developed steatosis during follow-up. A BMI>23 kg/m(2) (OR: 4·238, 95% CI: 2·078–8·938; p < 0·0001), tenofovir-alafenamid (TAF) (OR: 5·073, 95% CI: 2·362–10·899); p < 0·0001) and integrase strand transfer inhibitors (INSTI) (OR: 2·354, 95% CI: 1·370–4·048; p = 0·002), as well as type 2 diabetes mellitus (OR: 7·605, 95% CI: 2·315–24·981; p < 0·0001) were independent predictors of de novo steatosis in multivariable analysis. Tenofovir disoproxilfumarate (TDF) was associated with a lower risk for weight gain and steatosis progression/onset using CAP value (HR: 0·28, 95% CI: 0·12–0·64; p = 0·003) and FAST scores (HR: 0·31, 95% CI: 0·101–0·945; p = 0·04). INTERPRETATION: Steatosis can develop despite non-obese BMI in patients with HIV monoinfection under cART, especially in male patients with BMI over 23 kg/m(2). While TAF and INSTI increase the risk of progression of steatosis, TDF was found to be independently associated with a lower risk of a clinically significant weight gain and thereby, might slow down development and progression of steatosis. FUNDING: There was no additional funding received for this project. All funders mentioned in the ‘declaration of interests’ section had no influence on study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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spelling pubmed-84272112021-09-13 Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART) Bischoff, Jenny Gu, Wenyi Schwarze-Zander, Carolynne Boesecke, Christoph Wasmuth, Jan-Christian van Bremen, Kathrin Dold, Leona Rockstroh, Jürgen K Trebicka, Jonel EClinicalMedicine Research Paper BACKGROUND: De novo steatosis is the main criteria for non-alcoholic fatty liver disease (NAFLD), which is becoming a clinically relevant comorbidity in HIV-infected patients. This may be due to the HIV virus itself, as well as long-term toxicities deriving from antiretroviral therapy. Therefore, HIV infected patients require prevention and monitoring regarding NAFLD. METHODS: This study investigated the differential role of body mass index (BMI) and combination antiretroviral treatment (cART) drugs on NAFLD progression. This single center prospective longitudinal observational study enrolled HIV monoinfected individuals between August 2013 to December 2018 with yearly visits. Each visit included liver stiffness and steatosis [defined as controlled attenuation parameter (CAP)>237 dB/m] assessment by annually transient elastography using an M- or XL-probe of FibroScan, and calculation of the novel FibroScan-AST (FAST) score. Risk factors for denovo/progressed steatosis and tripling of FAST-score increase were investigated using Cox regression model with time-dependent covariates. FINDINGS: 319 monoinfected HIV positive patients with at least two visits were included into the study, of which 301 patients had at least two valid CAP measurements. 51·5%(155) patients did not have steatosis at first assessment, of which 45%(69) developed steatosis during follow-up. A BMI>23 kg/m(2) (OR: 4·238, 95% CI: 2·078–8·938; p < 0·0001), tenofovir-alafenamid (TAF) (OR: 5·073, 95% CI: 2·362–10·899); p < 0·0001) and integrase strand transfer inhibitors (INSTI) (OR: 2·354, 95% CI: 1·370–4·048; p = 0·002), as well as type 2 diabetes mellitus (OR: 7·605, 95% CI: 2·315–24·981; p < 0·0001) were independent predictors of de novo steatosis in multivariable analysis. Tenofovir disoproxilfumarate (TDF) was associated with a lower risk for weight gain and steatosis progression/onset using CAP value (HR: 0·28, 95% CI: 0·12–0·64; p = 0·003) and FAST scores (HR: 0·31, 95% CI: 0·101–0·945; p = 0·04). INTERPRETATION: Steatosis can develop despite non-obese BMI in patients with HIV monoinfection under cART, especially in male patients with BMI over 23 kg/m(2). While TAF and INSTI increase the risk of progression of steatosis, TDF was found to be independently associated with a lower risk of a clinically significant weight gain and thereby, might slow down development and progression of steatosis. FUNDING: There was no additional funding received for this project. All funders mentioned in the ‘declaration of interests’ section had no influence on study design, data collection and analysis, decision to publish, or preparation of the manuscript. Elsevier 2021-09-05 /pmc/articles/PMC8427211/ /pubmed/34522873 http://dx.doi.org/10.1016/j.eclinm.2021.101116 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Bischoff, Jenny
Gu, Wenyi
Schwarze-Zander, Carolynne
Boesecke, Christoph
Wasmuth, Jan-Christian
van Bremen, Kathrin
Dold, Leona
Rockstroh, Jürgen K
Trebicka, Jonel
Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART)
title Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART)
title_full Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART)
title_fullStr Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART)
title_full_unstemmed Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART)
title_short Stratifying the risk of NAFLD in patients with HIV under combination antiretroviral therapy (cART)
title_sort stratifying the risk of nafld in patients with hiv under combination antiretroviral therapy (cart)
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427211/
https://www.ncbi.nlm.nih.gov/pubmed/34522873
http://dx.doi.org/10.1016/j.eclinm.2021.101116
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