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Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study

BACKGROUND: Sublingual immunotherapy (SLIT) has been proved to be an effective and safe treatment for allergic asthma (AS) in children. Nonetheless, several issues regarding SLIT remain to be resolved, including the information about optimal administration timing. METHODS: A total of 163 AS children...

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Autores principales: Liao, Feng, Chen, Shi, Wang, Ling, Quan, Ying-yu, Chen, Li-li, Lin, Guo-hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218255/
https://www.ncbi.nlm.nih.gov/pubmed/35757136
http://dx.doi.org/10.3389/fped.2022.892572
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author Liao, Feng
Chen, Shi
Wang, Ling
Quan, Ying-yu
Chen, Li-li
Lin, Guo-hua
author_facet Liao, Feng
Chen, Shi
Wang, Ling
Quan, Ying-yu
Chen, Li-li
Lin, Guo-hua
author_sort Liao, Feng
collection PubMed
description BACKGROUND: Sublingual immunotherapy (SLIT) has been proved to be an effective and safe treatment for allergic asthma (AS) in children. Nonetheless, several issues regarding SLIT remain to be resolved, including the information about optimal administration timing. METHODS: A total of 163 AS children aged 4-13 years were enrolled and randomized into the morning dosing (MD) group and the evening dosing (ED) group. Participants received SLIT with Dermatophagoides farinae drops between 7:00 a. m. and 9:00 a.m. (for the MD group) or between 8:00 p. m. and 10:00 p.m. (for the ED group). The total asthma symptom score (TASS), total asthma medicine score (TAMS), Asthma Control Questionnaire (ACQ), forced expiratory volume in one second (FEV(1)), FEV(1)/forced volume vital capacity (FVC), fractional exhaled nitric oxide (FeNO) and adverse events (AEs) were assessed at baseline, 0.5 and 1 year during the 1-year SLIT. RESULTS: After 1 year, 62 patients in the MD group and 63 patients in the ED group completed the entire study. The clinical efficacy, pulmonary function and FeNO in both groups improved significantly at 0.5 and 1 year (p < 0.001). Compared to the MD group, the ED group showed significant lower ACQ score at 0.5 year (p < 0.001) and lower FeNO at 1 year (p < 0.05). No significant difference between two groups was observed in AE rate (p > 0.05). All AEs occurred in the first month, with no systemic AEs reported. CONCLUSION: 1-year house dust mite (HDM) SLIT is effective and well-tolerated in AS children regardless of administration time. SLIT dosing in the evening might enhance the asthma control level and reduce FeNO level compared with SLIT dosing in the morning.
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spelling pubmed-92182552022-06-24 Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study Liao, Feng Chen, Shi Wang, Ling Quan, Ying-yu Chen, Li-li Lin, Guo-hua Front Pediatr Pediatrics BACKGROUND: Sublingual immunotherapy (SLIT) has been proved to be an effective and safe treatment for allergic asthma (AS) in children. Nonetheless, several issues regarding SLIT remain to be resolved, including the information about optimal administration timing. METHODS: A total of 163 AS children aged 4-13 years were enrolled and randomized into the morning dosing (MD) group and the evening dosing (ED) group. Participants received SLIT with Dermatophagoides farinae drops between 7:00 a. m. and 9:00 a.m. (for the MD group) or between 8:00 p. m. and 10:00 p.m. (for the ED group). The total asthma symptom score (TASS), total asthma medicine score (TAMS), Asthma Control Questionnaire (ACQ), forced expiratory volume in one second (FEV(1)), FEV(1)/forced volume vital capacity (FVC), fractional exhaled nitric oxide (FeNO) and adverse events (AEs) were assessed at baseline, 0.5 and 1 year during the 1-year SLIT. RESULTS: After 1 year, 62 patients in the MD group and 63 patients in the ED group completed the entire study. The clinical efficacy, pulmonary function and FeNO in both groups improved significantly at 0.5 and 1 year (p < 0.001). Compared to the MD group, the ED group showed significant lower ACQ score at 0.5 year (p < 0.001) and lower FeNO at 1 year (p < 0.05). No significant difference between two groups was observed in AE rate (p > 0.05). All AEs occurred in the first month, with no systemic AEs reported. CONCLUSION: 1-year house dust mite (HDM) SLIT is effective and well-tolerated in AS children regardless of administration time. SLIT dosing in the evening might enhance the asthma control level and reduce FeNO level compared with SLIT dosing in the morning. Frontiers Media S.A. 2022-06-09 /pmc/articles/PMC9218255/ /pubmed/35757136 http://dx.doi.org/10.3389/fped.2022.892572 Text en Copyright © 2022 Liao, Chen, Wang, Quan, Chen and Lin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Liao, Feng
Chen, Shi
Wang, Ling
Quan, Ying-yu
Chen, Li-li
Lin, Guo-hua
Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study
title Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study
title_full Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study
title_fullStr Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study
title_full_unstemmed Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study
title_short Morning Versus Evening Dosing of Sublingual Immunotherapy in Allergic Asthma: A Prospective Study
title_sort morning versus evening dosing of sublingual immunotherapy in allergic asthma: a prospective study
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218255/
https://www.ncbi.nlm.nih.gov/pubmed/35757136
http://dx.doi.org/10.3389/fped.2022.892572
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