Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study

Objective Anaemia is common among people living with HIV (PLWH) and has been associated with certain, often older, antiretroviral medications. Information on current antiretroviral therapy (ART) and anaemia is limited. The objective was to compare the associations between anaemia incidence or haemog...

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Main Authors: Richard D Moore, Kenneth Mayer, Greer Burkholder, Susan R Heckbert, Barbara N Harding, Bridget M Whitney, Robin M Nance, Heidi M Crane, W Christopher Mathews, Joseph J Eron, Peter W Hunt, Paul Volberding, Michael S Saag, Mari M Kitahata, Joseph A C Delaney
Format: Article
Language:English
Published: BMJ Publishing Group 2020-03-01
Series:BMJ Open
Online Access:https://bmjopen.bmj.com/content/10/3/e031487.full
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author Richard D Moore
Kenneth Mayer
Greer Burkholder
Susan R Heckbert
Barbara N Harding
Bridget M Whitney
Robin M Nance
Heidi M Crane
W Christopher Mathews
Joseph J Eron
Peter W Hunt
Paul Volberding
Michael S Saag
Mari M Kitahata
Joseph A C Delaney
author_facet Richard D Moore
Kenneth Mayer
Greer Burkholder
Susan R Heckbert
Barbara N Harding
Bridget M Whitney
Robin M Nance
Heidi M Crane
W Christopher Mathews
Joseph J Eron
Peter W Hunt
Paul Volberding
Michael S Saag
Mari M Kitahata
Joseph A C Delaney
author_sort Richard D Moore
collection DOAJ
description Objective Anaemia is common among people living with HIV (PLWH) and has been associated with certain, often older, antiretroviral medications. Information on current antiretroviral therapy (ART) and anaemia is limited. The objective was to compare the associations between anaemia incidence or haemoglobin change with core ART classes in the current ART era.Design Retrospective cohort study.Setting USA-based prospective clinical cohort of PLWH aged 18 and above receiving care at eight sites between January 2010 and March 2018.Participants 16 505 PLWH were included in this study.Main outcome measures Anaemia risk and haemoglobin change were estimated among PLWH for person-time on a protease inhibitor (PI) or an integrase strand transfer inhibitor (INSTI)-based regimen, relative to a non-nucleoside reverse transcriptase inhibitor (NNRTI)-based reference. We also examined PLWH on regimens containing multiple core classes. Cox proportional hazards regression analyses were conducted to measure the associations between time-updated ART classes and incident anaemia or severe anaemia. Linear mixed effects models were used to examine the relationships between ART classes and haemoglobin change.Results During a median of 4.9 years of follow-up, 1040 developed anaemia and 488 developed severe anaemia. Compared with NNRTI use, INSTI-based regimens were associated with an increased risk of anaemia (adjusted HR (aHR) 1.26, 95% CI 1.00 to 1.58) and severe anaemia (aHR 1.51, 95% CI 1.07 to 2.11) and a decrease in haemoglobin level. Time on multiple core classes was also associated with increased anaemia risk (aHR 1.39, 95% CI 1.13 to 1.70), while no associations were found for PI use.Conclusion These findings suggest INSTI use may increase the risk of anaemia. If confirmed, screening for anaemia development in users of INSTIs may be beneficial. Further research into the underlying mechanisms is warranted.
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spelling doaj-art-28b59c9b068d4cb99df435f2a86b8ae02024-12-07T06:45:09ZengBMJ Publishing GroupBMJ Open2044-60552020-03-0110310.1136/bmjopen-2019-031487Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort studyRichard D Moore0Kenneth Mayer1Greer Burkholder2Susan R Heckbert3Barbara N Harding4Bridget M Whitney5Robin M Nance6Heidi M Crane7W Christopher Mathews8Joseph J Eron9Peter W Hunt10Paul Volberding11Michael S Saag12Mari M Kitahata13Joseph A C Delaney144 Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA10 The Fenway Institute at Fenway Health, Boston, Massachusetts, USA2University of Alabama at Birmingham, Medicine, Birmingham, USAEpidemiology, University of Washington, Seattle, WA, USA1Barcelona Institute for Global Health (ISGlobal), Barcelona, Spain1 Department of Epidemiology, University of Washington, Seattle, Washington, USA1 Department of Epidemiology, University of Washington, Seattle, Washington, USA2 Medicine, University of Washington, Seattle, Washington, USA5 University of California, San Diego, La Jolla, California, USA6 University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA7 University of California San Francisco, San Francisco, California, USA8 Medicine, University of California, San Francisco, San Francisco, California, USA6 Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA2 Medicine, University of Washington, Seattle, Washington, USApostdoctoral fellowObjective Anaemia is common among people living with HIV (PLWH) and has been associated with certain, often older, antiretroviral medications. Information on current antiretroviral therapy (ART) and anaemia is limited. The objective was to compare the associations between anaemia incidence or haemoglobin change with core ART classes in the current ART era.Design Retrospective cohort study.Setting USA-based prospective clinical cohort of PLWH aged 18 and above receiving care at eight sites between January 2010 and March 2018.Participants 16 505 PLWH were included in this study.Main outcome measures Anaemia risk and haemoglobin change were estimated among PLWH for person-time on a protease inhibitor (PI) or an integrase strand transfer inhibitor (INSTI)-based regimen, relative to a non-nucleoside reverse transcriptase inhibitor (NNRTI)-based reference. We also examined PLWH on regimens containing multiple core classes. Cox proportional hazards regression analyses were conducted to measure the associations between time-updated ART classes and incident anaemia or severe anaemia. Linear mixed effects models were used to examine the relationships between ART classes and haemoglobin change.Results During a median of 4.9 years of follow-up, 1040 developed anaemia and 488 developed severe anaemia. Compared with NNRTI use, INSTI-based regimens were associated with an increased risk of anaemia (adjusted HR (aHR) 1.26, 95% CI 1.00 to 1.58) and severe anaemia (aHR 1.51, 95% CI 1.07 to 2.11) and a decrease in haemoglobin level. Time on multiple core classes was also associated with increased anaemia risk (aHR 1.39, 95% CI 1.13 to 1.70), while no associations were found for PI use.Conclusion These findings suggest INSTI use may increase the risk of anaemia. If confirmed, screening for anaemia development in users of INSTIs may be beneficial. Further research into the underlying mechanisms is warranted.https://bmjopen.bmj.com/content/10/3/e031487.full
spellingShingle Richard D Moore
Kenneth Mayer
Greer Burkholder
Susan R Heckbert
Barbara N Harding
Bridget M Whitney
Robin M Nance
Heidi M Crane
W Christopher Mathews
Joseph J Eron
Peter W Hunt
Paul Volberding
Michael S Saag
Mari M Kitahata
Joseph A C Delaney
Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study
BMJ Open
title Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study
title_full Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study
title_fullStr Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study
title_full_unstemmed Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study
title_short Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study
title_sort antiretroviral drug class and anaemia risk in the current treatment era among people living with hiv in the usa a clinical cohort study
url https://bmjopen.bmj.com/content/10/3/e031487.full
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