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Inhaled corticosteroids, blood eosinophils, and FEV1 decline in patients with COPD in a large UK primary health care setting.

Whittaker, HR; Müllerova, H; Jarvis, D; Barnes, NC; Jones, PW; Compton, CH; Kiddle, SJ; Quint, JK (2019) Inhaled corticosteroids, blood eosinophils, and FEV1 decline in patients with COPD in a large UK primary health care setting. Int J Chron Obstruct Pulmon Dis, 14. pp. 1063-1073. ISSN 1178-2005 https://doi.org/10.2147/COPD.S200919
SGUL Authors: Jones, Paul Wyatt

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Abstract

Background: Inhaled corticosteroid (ICS)-containing medications slow rate of decline of FEV1. Blood eosinophil (EOS) levels are associated with the degree of exacerbation reduction with ICS. Purpose: We investigated whether FEV1 decline differs between patients with and without ICS, stratified by blood EOS level. Patients and methods: The UK Clinical Practice Research Datalink (primary care records) and Hospital Episode Statistics (hospital records) were used to identify COPD patients aged 35 years or older, who were current or ex-smokers with ≥2 FEV1 measurements ≥6 months apart. Prevalent ICS use and the nearest EOS count to start of follow-up were identified. Patients were classified at baseline as higher stratum EOS (≥150 cell/µL) on ICS; higher stratum EOS not on ICS; lower stratum EOS (<150 cells/µL) on ICS; and lower stratum EOS not on ICS. In addition, an incident ICS cohort was used to investigate the rate of FEV1 change by EOS and incident ICS use. Mixed-effects linear regression was used to compare rates of FEV1 change in mL/year. Results: A total of 26,675 COPD patients met our inclusion criteria (median age 69, 46% female). The median duration of follow up was 4.2 years. The rate of FEV1 change in prevalent ICS users was slower than non-ICS users (-12.6 mL/year vs -21.1 mL/year; P =0.001). The rate of FEV1 change was not significantly different when stratified by EOS level. The rate of FEV1 change in incident ICS users increased (+4.2 mL/year) vs -21.2 mL/year loss in non-ICS users; P<0.001. In patients with high EOS, incident ICS patients showed an increase in FEV1 (+12 mL/year) compared to non-ICS users whose FEV1 decreased (-20.8 mL/year); P<0.001. No statistical difference was seen in low EOS patients. Incident ICS use is associated with an improvement in FEV1 change, however, over time this association is lost. Conclusion: Regardless of blood EOS level, prevalent ICS use is associated with slower rates of FEV1 decline in COPD.

Item Type: Article
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Keywords: COPD, eosinophil, inhaled corticosteroids, lung function, Administration, Inhalation, Adrenal Cortex Hormones, Aged, Aged, 80 and over, Disease Progression, Electronic Health Records, England, Eosinophils, Female, Forced Expiratory Volume, Humans, Leukocyte Count, Lung, Male, Middle Aged, Predictive Value of Tests, Pulmonary Disease, Chronic Obstructive, Risk Factors, Time Factors, Treatment Outcome, Lung, Eosinophils, Humans, Pulmonary Disease, Chronic Obstructive, Disease Progression, Adrenal Cortex Hormones, Forced Expiratory Volume, Leukocyte Count, Treatment Outcome, Administration, Inhalation, Risk Factors, Predictive Value of Tests, Time Factors, Aged, Aged, 80 and over, Middle Aged, England, Female, Male, Electronic Health Records, COPD, lung function, eosinophil, inhaled corticosteroids, COPD, eosinophil, inhaled corticosteroids, lung function, Administration, Inhalation, Adrenal Cortex Hormones, Aged, Aged, 80 and over, Disease Progression, Electronic Health Records, England, Eosinophils, Female, Forced Expiratory Volume, Humans, Leukocyte Count, Lung, Male, Middle Aged, Predictive Value of Tests, Pulmonary Disease, Chronic Obstructive, Risk Factors, Time Factors, Treatment Outcome, 1102 Cardiorespiratory Medicine and Haematology, Respiratory System
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Int J Chron Obstruct Pulmon Dis
ISSN: 1178-2005
Language: eng
Dates:
DateEvent
23 May 2019Published
1 April 2019Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 3.0
Projects:
Project IDFunderFunder ID
MR/P021573/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
PubMed ID: 31213788
Web of Science ID: WOS:000469120100001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113698
Publisher's version: https://doi.org/10.2147/COPD.S200919

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