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Licensed Unlicensed Requires Authentication Published by De Gruyter May 29, 2015

Swallowed glucocorticoid therapy for eosinophilic esophagitis in children does not suppress adrenal function

  • Katherine Q. Philla EMAIL logo , Steve B. Min , Jody N. Hefner , Robin S. Howard , Brian J. Reinhardt , Luz G. Nazareno and Karen S. Vogt

Abstract

Objective: The purpose of this study was to examine the effect of chronic swallowed glucocorticoids on adrenal function during the treatment of eosinophilic esophagitis (EoE) in children.

Methods: Serum cortisol levels were obtained in children with EoE pre- and post-treatment with swallowed glucocorticoids. Exclusion criteria included those on any additional steroid therapy. Once diagnosed with EoE by esophageal biopsy, subjects were treated based on current standard of care with either swallowed fluticasone or budesonide. At the time of follow-up, esophagogastroduodenoscopy and blood sampling was repeated. Both pre- and post-treatment serum cortisol samples were collected fasting, between 07:00 and 10:00, and determined using a competitive binding method assay. The distribution of differences in cortisol levels between the pre- and post-treatment samples satisfied the assumption for normality and were subsequently analyzed using the paired t-test.

Results: Pre- and post-treatment serum cortisol levels were examined in 14 children who met clinical and histological diagnostic criteria for EoE. Mean age was 10.1 years (range 2–17 years) with 71% male and 29% female subjects. Swallowed glucocorticoid treatment included fluticasone in 79% and budesonide in 21% of subjects. Mean dosage of fluticasone was 704 μg daily (range 220–880 μg daily) and budesonide 0.8 mg daily (range 0.5–1 mg daily), along with a mean treatment length of 17 weeks (range 8–43 weeks). No significant difference in serum cortisol was found following treatment with swallowed fluticasone or budesonide (mean change 1.9 μg/dL, p=0.75, SD of the change=21.2).

Conclusions: Swallowed glucocorticoid therapy does not appear to significantly affect the adrenal axis in children, and therefore, may represent a safe therapy for EoE.


Corresponding author: Katherine Q. Philla, MD, Department of Pediatric Endocrinology, Walter Reed National Military Medical Center, 8901 Wisconsin Avenue, Bethesda, MD 20889, USA, Phone: +1-301-295-4959, Fax: +1-301-295-6173, E-mail:
aConceptualized and designed the study, revised and submitted Institutional Review Board protocol addendum, contributed to the data analysis, drafted the initial manuscript, edited the manuscript, and approved the final manuscript as submitted.bAssisted with the design of the study, submitted Institutional Review Board protocol, recruited subjects, consented subjects, reviewed and revised the manuscript, and approved the final manuscript as submitted.cAssisted with review and multiple revisions of the manuscript along with approval of the final manuscript as submitted.dDesigned the data collection instruments, assisted with organization and analysis of the data, and approved the final manuscript as submitted.ePerformed assay testing and approved the final manuscript as submitted.fAssisted with subject recruitment, consent, data preparation and analysis, and approved the final manuscript as submitted.gAssisted with Institutional Review Board protocol addendum submission, reviewed and revised the manuscript, and approved the final manuscript as submitted.

Acknowledgments

The authors wish to thank the patients and their families for participating in this study.

Conflict of interest statement: The authors have no conflicts of interest to disclose. The authors have no financial relationships relevant to this article to disclose. No external funding was secured for this study.

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Received: 2014-6-16
Accepted: 2015-4-9
Published Online: 2015-5-29
Published in Print: 2015-9-1

©2015 by De Gruyter

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