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The obese-asthma phenotype in children: An exacerbating situation? - 05/04/18

Doi : 10.1016/j.jaci.2017.10.052 
Cristina Longo, MSc a, Gillian Bartlett, PhD a, Tibor Schuster, PhD a, Francine M. Ducharme, MSc, MD b, c, d, Brenda MacGibbon, PhD e, Tracie A. Barnett, PhD b, f,
a Department of Family Medicine, McGill University, Montreal, Quebec, Canada 
b CHU Sainte-Justine Research Centre, Montreal, Quebec, Canada 
c Department of Pediatrics, University of Montreal, Montreal, Quebec, Canada 
d Department of Social and Preventive Medicine, University of Montreal, Montreal, Quebec, Canada 
e Department of Mathematics, Université du Québec à Montréal, Montreal, Quebec, Canada 
f Department of Epidemiology and Biostatistics, INRS-Institut Armand-Frappier, Laval, Quebec, Canada 

Corresponding author: Tracie A. Barnett, PhD, INRS-Institut Armand Frappier, Centre de recherche du CHU Sainte-Justine, 5757 Avenue Decelles, Suite 100a, Montréal, Québec H3S 2C3, Canada.INRS-Institut Armand FrappierCentre de recherche du CHU Sainte-Justine5757 Avenue DecellesSuite 100aMontréalQuébecH3S 2C3Canada

Abstract

Background

Current evidence regarding the relationship between childhood obesity, decreased response to inhaled corticosteroids (ICSs), and poor asthma control is conflicting.

Objectives

We assessed whether obesity (1) is associated with time to first exacerbation among children with asthma initiating step 3 maintenance therapies and (2) modifies the effectiveness of step 3 therapies.

Methods

A retrospective cohort study was conducted from clinical data linked to health and drug administrative databases. The cohort consisted of children aged 2 to 18 years with specialist-confirmed asthma who initiated medium/high-dose ICS monotherapy or low/medium-dose ICS with leukotriene receptor antagonist/long-acting β-agonist (combination therapy) at the Montreal Children's Hospital Asthma Center from 2000 to 2007. Children were classified as exposed to step 3 therapies when they were dispensed a corresponding drug claim during follow-up, whereas those without claims were classified as nonadherers. Marginal structural Cox models were used to estimate the effect of obesity (body mass index > 97th percentile) and treatment on time to exacerbation, which was defined as any emergency department visit, hospitalization, or use of oral corticosteroids for asthma.

Results

Of the 4621 cohort patients, 231 initiated ICS monotherapy, and 97 initiated combination therapy. The hazard ratio (HR) for obesity was 1.67 (95% CI, 1.41-1.98). Compared with nonobese nonadherers, the HR for obese nonadherers was 1.54 (95% CI, 0.97-2.45); the HR for ICS monotherapy in obese and nonobese children was 0.85 (95% CI, 0.47-1.52) and 0.58 (95% CI, 0.37-0.91), respectively; and the HR for combination therapy in obese and nonobese children was 0.50 (95% CI, 0.13-1.89) and 0.46 (95% CI, 0.23-0.92), respectively.

Conclusion

Obesity might be a determinant of shorter exacerbation-free time in children with asthma; however, we could not rule out a differential response to step 3 therapies by obesity status, potentially because of a lack of precision.

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Graphical abstract




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Key words : Asthma, obesity, inhaled corticosteroid monotherapy, inhaled corticosteroid combination therapy, marginal structural Cox model

Abbreviations used : BMI, HFA-BDPeq, HR, ICD-9/ICD-10, ICS, IPCW, IPTW, LABA, LTRA, MSM, WHO


Esquema


 Supported by Fonds de la Recherche du Québec en Santé (FRQ-S). The FRQ-S had no role in the study design, data collection, analysis, interpretation, or writing of the manuscript.
 Disclosure of potential conflict of interest: F. M. Ducharme received unrestricted donations from Boehringer Ingelheim, Merck Canada, GlaxoSmithKline, and Novartis and a research grant from Merck and serves on an advisory board of Boehringer Ingelheim. The rest of the authors declare that they have no relevant conflicts of interest.


Crown Copyright © 2018  Publicado por Elsevier Masson SAS. Todos los derechos reservados.
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Vol 141 - N° 4

P. 1239 - avril 2018 Regresar al número
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