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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 haemo...

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Autores principales: Harding, Barbara N, Whitney, Bridget M, Nance, Robin M, Crane, Heidi M, Burkholder, Greer, Moore, Richard D, Mathews, W Christopher, Eron, Joseph J, Hunt, Peter W, Volberding, Paul, Rodriguez, Benigno, Mayer, Kenneth, Saag, Michael S, Kitahata, Mari M, Heckbert, Susan R, Delaney, Joseph A C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103836/
https://www.ncbi.nlm.nih.gov/pubmed/32198297
http://dx.doi.org/10.1136/bmjopen-2019-031487
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author Harding, Barbara N
Whitney, Bridget M
Nance, Robin M
Crane, Heidi M
Burkholder, Greer
Moore, Richard D
Mathews, W Christopher
Eron, Joseph J
Hunt, Peter W
Volberding, Paul
Rodriguez, Benigno
Mayer, Kenneth
Saag, Michael S
Kitahata, Mari M
Heckbert, Susan R
Delaney, Joseph A C
author_facet Harding, Barbara N
Whitney, Bridget M
Nance, Robin M
Crane, Heidi M
Burkholder, Greer
Moore, Richard D
Mathews, W Christopher
Eron, Joseph J
Hunt, Peter W
Volberding, Paul
Rodriguez, Benigno
Mayer, Kenneth
Saag, Michael S
Kitahata, Mari M
Heckbert, Susan R
Delaney, Joseph A C
author_sort Harding, Barbara N
collection PubMed
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 pubmed-71038362020-03-31 Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study Harding, Barbara N Whitney, Bridget M Nance, Robin M Crane, Heidi M Burkholder, Greer Moore, Richard D Mathews, W Christopher Eron, Joseph J Hunt, Peter W Volberding, Paul Rodriguez, Benigno Mayer, Kenneth Saag, Michael S Kitahata, Mari M Heckbert, Susan R Delaney, Joseph A C BMJ Open HIV/AIDS 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. BMJ Publishing Group 2020-03-19 /pmc/articles/PMC7103836/ /pubmed/32198297 http://dx.doi.org/10.1136/bmjopen-2019-031487 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle HIV/AIDS
Harding, Barbara N
Whitney, Bridget M
Nance, Robin M
Crane, Heidi M
Burkholder, Greer
Moore, Richard D
Mathews, W Christopher
Eron, Joseph J
Hunt, Peter W
Volberding, Paul
Rodriguez, Benigno
Mayer, Kenneth
Saag, Michael S
Kitahata, Mari M
Heckbert, Susan R
Delaney, Joseph A C
Antiretroviral drug class and anaemia risk in the current treatment era among people living with HIV in the USA: a clinical cohort study
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
topic HIV/AIDS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103836/
https://www.ncbi.nlm.nih.gov/pubmed/32198297
http://dx.doi.org/10.1136/bmjopen-2019-031487
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