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Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study

PURPOSE: Despite ample evidence underpinning the efficacy of β(2)-agonists in asthma and chronic obstructive pulmonary disease (COPD), the occurrence of β(1)- and β(2)-adrenoceptors in the heart suggests that β(2)-agonists may have deleterious cardiac effects. We investigated the association between...

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Autores principales: Amegadzie, Joseph Emil, Gamble, John-Michael, Farrell, Jamie, Gao, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130098/
https://www.ncbi.nlm.nih.gov/pubmed/35645559
http://dx.doi.org/10.2147/COPD.S358927
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author Amegadzie, Joseph Emil
Gamble, John-Michael
Farrell, Jamie
Gao, Zhiwei
author_facet Amegadzie, Joseph Emil
Gamble, John-Michael
Farrell, Jamie
Gao, Zhiwei
author_sort Amegadzie, Joseph Emil
collection PubMed
description PURPOSE: Despite ample evidence underpinning the efficacy of β(2)-agonists in asthma and chronic obstructive pulmonary disease (COPD), the occurrence of β(1)- and β(2)-adrenoceptors in the heart suggests that β(2)-agonists may have deleterious cardiac effects. We investigated the association between new users of long-or short-acting β(2)-agonists (LABA or SABA) or ICS (inhaled corticosteroids)/LABA and major adverse cardiovascular events (MACE). METHODS: A nested case–control analysis was conducted using the UK Clinical Practice Research Datalink of patients with asthma, COPD or asthma–COPD overlap with initial treatment of LABA, SABA, ICS/LABA, ICS, long-or short-acting muscarinic antagonist (LAMA or SAMA) between 01 January 1998 and 31 July 2018. The primary outcome was MACE, defined as the first occurrence of stroke, heart failure, myocardial infarction, arrhythmia, or cardiovascular death. Each case was matched with up to 10 controls on age, sex, date of cohort-entry, and duration of follow-up. The risk of MACE associated with β(2)-agonists was estimated using conditional logistic regression after controlling for potential confounders. RESULTS: The cohort included 180,567 new users of β(2)-agonists, ICS, SAMA, or LAMA. Among asthmatics, β(2)-agonists were not associated with the risk of MACE (SABA vs ICS: HR 1.29 [0.96–1.73]; ICS/LABA vs ICS, HR 0.75 [0.33–1.73]). In contrast, among COPD patients, LABA (HR, 2.38 [1.04–5.47]), SABA (HR, 2.02 [1.13–3.59]) and ICS/LABA (HR, 2.08 [1.04–4.16]) users had an increased risk of MACE compared with SAMA users. Among patients with asthma–COPD overlap, SABA (HR, 2.57 [1.26–5.24]) was associated with an increased risk of MACE compared with ICS. CONCLUSION: In conclusion, initiation of LABA, SABA, or ICS/LABA in COPD or SABA in asthma–COPD overlap is associated with increased risk of MACE. No associations were observed among patients with asthma.
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spelling pubmed-91300982022-05-26 Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study Amegadzie, Joseph Emil Gamble, John-Michael Farrell, Jamie Gao, Zhiwei Int J Chron Obstruct Pulmon Dis Original Research PURPOSE: Despite ample evidence underpinning the efficacy of β(2)-agonists in asthma and chronic obstructive pulmonary disease (COPD), the occurrence of β(1)- and β(2)-adrenoceptors in the heart suggests that β(2)-agonists may have deleterious cardiac effects. We investigated the association between new users of long-or short-acting β(2)-agonists (LABA or SABA) or ICS (inhaled corticosteroids)/LABA and major adverse cardiovascular events (MACE). METHODS: A nested case–control analysis was conducted using the UK Clinical Practice Research Datalink of patients with asthma, COPD or asthma–COPD overlap with initial treatment of LABA, SABA, ICS/LABA, ICS, long-or short-acting muscarinic antagonist (LAMA or SAMA) between 01 January 1998 and 31 July 2018. The primary outcome was MACE, defined as the first occurrence of stroke, heart failure, myocardial infarction, arrhythmia, or cardiovascular death. Each case was matched with up to 10 controls on age, sex, date of cohort-entry, and duration of follow-up. The risk of MACE associated with β(2)-agonists was estimated using conditional logistic regression after controlling for potential confounders. RESULTS: The cohort included 180,567 new users of β(2)-agonists, ICS, SAMA, or LAMA. Among asthmatics, β(2)-agonists were not associated with the risk of MACE (SABA vs ICS: HR 1.29 [0.96–1.73]; ICS/LABA vs ICS, HR 0.75 [0.33–1.73]). In contrast, among COPD patients, LABA (HR, 2.38 [1.04–5.47]), SABA (HR, 2.02 [1.13–3.59]) and ICS/LABA (HR, 2.08 [1.04–4.16]) users had an increased risk of MACE compared with SAMA users. Among patients with asthma–COPD overlap, SABA (HR, 2.57 [1.26–5.24]) was associated with an increased risk of MACE compared with ICS. CONCLUSION: In conclusion, initiation of LABA, SABA, or ICS/LABA in COPD or SABA in asthma–COPD overlap is associated with increased risk of MACE. No associations were observed among patients with asthma. Dove 2022-05-20 /pmc/articles/PMC9130098/ /pubmed/35645559 http://dx.doi.org/10.2147/COPD.S358927 Text en © 2022 Amegadzie et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Amegadzie, Joseph Emil
Gamble, John-Michael
Farrell, Jamie
Gao, Zhiwei
Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study
title Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study
title_full Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study
title_fullStr Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study
title_full_unstemmed Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study
title_short Association between Inhaled β(2)-agonists Initiation and Risk of Major Adverse Cardiovascular Events: A Population-based Nested Case-Control Study
title_sort association between inhaled β(2)-agonists initiation and risk of major adverse cardiovascular events: a population-based nested case-control study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130098/
https://www.ncbi.nlm.nih.gov/pubmed/35645559
http://dx.doi.org/10.2147/COPD.S358927
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