TY - JOUR
T1 - Association of Metformin Initiation and Risk of Asthma Exacerbation A Claims-based Cohort Study
AU - Wu, Tianshi David
AU - Keet, Corinne A.
AU - Fawzy, Ashraf
AU - Segal, Jodi B.
AU - Brigham, Emily P.
AU - McCormack, Meredith C.
N1 - Funding Information:
Supported by the National Institutes of Health (NIH), National Institute of Environmental Health Sciences, under grants F32ES028578 (T.D.W.), R01ES026170 (C.A.K.), R01ES023447 (C.A.K.), F32ES028576 (A.F.), and P50ES018176 (M.C.M.); by the National Institute of Allergy and Infectious Diseases under grant U01AI125290 (C.A.K.); by the National Center for Advancing Translational Sciences under grant K23ES029105 (E.P.B.); and by the U.S. Environmental Protection Agency (EPA) under grant RD83615201 (M.C.M.). This research has not been reviewed by the NIH or the EPA and does not represent the official views or policies of these organizations.
Publisher Copyright:
Copyright © 2019 by the American Thoracic Society
PY - 2019
Y1 - 2019
N2 - Rationale: Diabetes and metabolic syndrome have been associated with worsened asthma control. Metformin improves insulin resistance and metabolic function. Experimental studies suggest that metformin may improve pathologic features of asthma, but evidence of clinical benefit is limited. Objectives: To determine if treatment with metformin in a cohort of individuals with asthma and diabetes is associated with lower risk of asthma exacerbation. Methods: A 6-year retrospective cohort of individuals over age 18 with asthma and diabetes was assembled from a national administrative claims database. New users of metformin were matched to nonusers by propensity score on the basis of demographic, comorbidity, and medication-use characteristics. An exacerbation was defined as an asthma-related hospitalization, emergency department visit, or filling of a systemic corticosteroid prescription within 14 days of an asthma-related ambulatory visit. Cox proportional hazards estimated the change in hazard of asthma exacerbation associated with metformin initiation. Results: In a cohort of 23,920 individuals with asthma and diabetes, metformin initiation was associated with lower hazard of asthma exacerbation (hazard ratio [HR], 0.92; 95% confidence interval [CI], 0.86–0.98), driven by lower hazards of asthma-related emergency department visits (HR, 0.81; 95% CI, 0.74–0.88) and hospitalization (HR, 0.67; 95% CI, 0.50–0.91), without differences in corticosteroid use (HR, 0.96; 95% CI, 0.86–1.03). Conclusions: In an administrative cohort of individuals with asthma and diabetes, metformin initiation was associated with a lower hazard of asthma-related emergency department visits and hospitalizations. These findings suggest a possible benefit of metformin in more severe asthma exacerbations. Investigation within cohorts with more detailed participant characterization is necessary.
AB - Rationale: Diabetes and metabolic syndrome have been associated with worsened asthma control. Metformin improves insulin resistance and metabolic function. Experimental studies suggest that metformin may improve pathologic features of asthma, but evidence of clinical benefit is limited. Objectives: To determine if treatment with metformin in a cohort of individuals with asthma and diabetes is associated with lower risk of asthma exacerbation. Methods: A 6-year retrospective cohort of individuals over age 18 with asthma and diabetes was assembled from a national administrative claims database. New users of metformin were matched to nonusers by propensity score on the basis of demographic, comorbidity, and medication-use characteristics. An exacerbation was defined as an asthma-related hospitalization, emergency department visit, or filling of a systemic corticosteroid prescription within 14 days of an asthma-related ambulatory visit. Cox proportional hazards estimated the change in hazard of asthma exacerbation associated with metformin initiation. Results: In a cohort of 23,920 individuals with asthma and diabetes, metformin initiation was associated with lower hazard of asthma exacerbation (hazard ratio [HR], 0.92; 95% confidence interval [CI], 0.86–0.98), driven by lower hazards of asthma-related emergency department visits (HR, 0.81; 95% CI, 0.74–0.88) and hospitalization (HR, 0.67; 95% CI, 0.50–0.91), without differences in corticosteroid use (HR, 0.96; 95% CI, 0.86–1.03). Conclusions: In an administrative cohort of individuals with asthma and diabetes, metformin initiation was associated with a lower hazard of asthma-related emergency department visits and hospitalizations. These findings suggest a possible benefit of metformin in more severe asthma exacerbations. Investigation within cohorts with more detailed participant characterization is necessary.
KW - Administrative data
KW - Metabolic dysfunction
KW - Metformin
KW - Pharmacoepidemiology
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U2 - 10.1513/AnnalsATS.201812-897OC
DO - 10.1513/AnnalsATS.201812-897OC
M3 - Article
C2 - 31415212
AN - SCOPUS:85075797016
SN - 2325-6621
VL - 16
SP - 1527
EP - 1533
JO - Annals of the American Thoracic Society
JF - Annals of the American Thoracic Society
IS - 12
ER -