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The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship
RATIONALE: DPP-4 may regulate immunological pathways implicated in asthma. Assessing whether DPP-4 inhibitor (DPP-4i) use might affect asthma control is clinically important because DPP-4i use in type 2 diabetes mellitus management (T2DM) is increasing. This study evaluated associations between DPP-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716303/ https://www.ncbi.nlm.nih.gov/pubmed/29238240 http://dx.doi.org/10.2147/POR.S144018 |
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author | Colice, Gene Price, David Gerhardsson de Verdier, Maria Rabon-Stith, Karma Ambrose, Christopher Cappell, Katherine Irwin, Debra E Juneau, Paul Vlahiotis, Anna |
author_facet | Colice, Gene Price, David Gerhardsson de Verdier, Maria Rabon-Stith, Karma Ambrose, Christopher Cappell, Katherine Irwin, Debra E Juneau, Paul Vlahiotis, Anna |
author_sort | Colice, Gene |
collection | PubMed |
description | RATIONALE: DPP-4 may regulate immunological pathways implicated in asthma. Assessing whether DPP-4 inhibitor (DPP-4i) use might affect asthma control is clinically important because DPP-4i use in type 2 diabetes mellitus management (T2DM) is increasing. This study evaluated associations between DPP-4i use and asthma control. METHODS: This was a retrospective, observational, matched cohort study using administrative claims in the MarketScan(®) Commercial Claims and Encounters (Commercial) and Medicare Supplemental and Coordination of Benefits (Medicare Supplemental) databases. Adult asthma patients initiating an oral DPP-4i or a non-DPP-4i between November 1, 2006 and March 31, 2014 were included. Patients were followed for asthma-related outcomes for 12 months after initiation of the antidiabetes medication. Outcomes included risk-domain asthma control (RDAC), defined as no asthma hospitalizations, no lower respiratory tract infections, and no oral corticosteroid (OCS) prescriptions; overall asthma control (RDAC criteria plus limited short-acting beta agonist use); treatment stability (RDAC criteria plus no increase of ≥50% in inhaled corticosteroid dose or addition of other asthma therapy); and severe asthma exacerbation rates (asthma-related hospitalizations, emergency room visits, or acute treatments with OCS). Comparisons were made between two matched cohorts (DPP-4i vs. non-DPP-4i initiators) using multivariable logistic regression and generalized linear modeling. Covariates included baseline demographic and clinical characteristics related to asthma and T2DM. RESULTS: The adjusted odds of achieving RDAC (odds ratio [OR]: 1.05; 95% CI: 0.964 to 1.147), overall asthma control (OR: 1.04; 95% CI: 0.956 to 1.135), and treatment stability (OR: 1.04; 95% CI: 0.949 to 1.115) did not differ between the DPP-4i and non-DPP-4i cohorts. A difference was not found between cohorts in severe asthma exacerbation rates during the 12 months following initiation of antidiabetes treatment (mean = 0.32 vs. 0.34 exacerbations per subject-year, respectively; p=0.064). CONCLUSION: Asthma control was similar between patients initiating DPP-4i and non-DPP-4i antidiabetes medications, suggesting no association between DPP-4i use and asthma control. |
format | Online Article Text |
id | pubmed-5716303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57163032017-12-13 The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship Colice, Gene Price, David Gerhardsson de Verdier, Maria Rabon-Stith, Karma Ambrose, Christopher Cappell, Katherine Irwin, Debra E Juneau, Paul Vlahiotis, Anna Pragmat Obs Res Original Research RATIONALE: DPP-4 may regulate immunological pathways implicated in asthma. Assessing whether DPP-4 inhibitor (DPP-4i) use might affect asthma control is clinically important because DPP-4i use in type 2 diabetes mellitus management (T2DM) is increasing. This study evaluated associations between DPP-4i use and asthma control. METHODS: This was a retrospective, observational, matched cohort study using administrative claims in the MarketScan(®) Commercial Claims and Encounters (Commercial) and Medicare Supplemental and Coordination of Benefits (Medicare Supplemental) databases. Adult asthma patients initiating an oral DPP-4i or a non-DPP-4i between November 1, 2006 and March 31, 2014 were included. Patients were followed for asthma-related outcomes for 12 months after initiation of the antidiabetes medication. Outcomes included risk-domain asthma control (RDAC), defined as no asthma hospitalizations, no lower respiratory tract infections, and no oral corticosteroid (OCS) prescriptions; overall asthma control (RDAC criteria plus limited short-acting beta agonist use); treatment stability (RDAC criteria plus no increase of ≥50% in inhaled corticosteroid dose or addition of other asthma therapy); and severe asthma exacerbation rates (asthma-related hospitalizations, emergency room visits, or acute treatments with OCS). Comparisons were made between two matched cohorts (DPP-4i vs. non-DPP-4i initiators) using multivariable logistic regression and generalized linear modeling. Covariates included baseline demographic and clinical characteristics related to asthma and T2DM. RESULTS: The adjusted odds of achieving RDAC (odds ratio [OR]: 1.05; 95% CI: 0.964 to 1.147), overall asthma control (OR: 1.04; 95% CI: 0.956 to 1.135), and treatment stability (OR: 1.04; 95% CI: 0.949 to 1.115) did not differ between the DPP-4i and non-DPP-4i cohorts. A difference was not found between cohorts in severe asthma exacerbation rates during the 12 months following initiation of antidiabetes treatment (mean = 0.32 vs. 0.34 exacerbations per subject-year, respectively; p=0.064). CONCLUSION: Asthma control was similar between patients initiating DPP-4i and non-DPP-4i antidiabetes medications, suggesting no association between DPP-4i use and asthma control. Dove Medical Press 2017-12-01 /pmc/articles/PMC5716303/ /pubmed/29238240 http://dx.doi.org/10.2147/POR.S144018 Text en © 2017 Colice et al. 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/). 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. |
spellingShingle | Original Research Colice, Gene Price, David Gerhardsson de Verdier, Maria Rabon-Stith, Karma Ambrose, Christopher Cappell, Katherine Irwin, Debra E Juneau, Paul Vlahiotis, Anna The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship |
title | The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship |
title_full | The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship |
title_fullStr | The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship |
title_full_unstemmed | The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship |
title_short | The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship |
title_sort | effect of dpp-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716303/ https://www.ncbi.nlm.nih.gov/pubmed/29238240 http://dx.doi.org/10.2147/POR.S144018 |
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