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POSTER PRESENTATION Open Access P83 - Asthma inflammatory subtype specific treatment; a randomised clinical study Doaa Youssef * , Rabab Elbhedy, Hosam Salah From 3rd Pediatric Allergy and Asthma Meeting (PAAM) Athens, Greece. 17-19 October 2013 Introduction Macrolides antibiotics, such as clarithromycine express immunomodulatory and tissue reparative effects that are distinct from their anti-infective properties, and have in vitro efficacy against neutrophils. Aim of study To determine the efficacy of add-on therapies that target eosinophilic and noneosinophilic airway inflammation and their effects on asthma control test, pulmonary function and asthma symptoms. Methods single blind randomized clinical trial; asthmatic children with persistent symptoms undergoing treatment with fluticasone 100 mg bid and b 2 agonist as required were studied. Group A (23 males / 17 females, aged 11.5±1.8 years) received fluticasone 200mg bid, and group B (21 males / 19 females, aged 11.5±1.8 years) clarithromycine 15 mg/kg bid, in addition to fluticasone 100 mg bid for 8 weeks. (FEV1%, C-CAT, SABA use, sputum induced % of eosinophils and neutrophils) were compared before and after treatment in each group. Results In group A there is significant reduction of eosinophils percentage after treatment, and non significant increase in neutrophils percentage. There was significant improvement in FEV1% predicted. While in group B there was non significant decrease in eosinophils, and significant decrease in neutrophils. In group A there was significant negative correlation between changes in FEV1% and change in eosinophils and week positive correlation between changes in FEV1% and changes in neutrophils. In group B there was significant positive correlation between basal eosinophils and change in FEV1% and significant negative correlation between basal neutrophils and change in FEV1%. Conclusion Steroids were effective in targeting eosinophilic inflamma- tion and clarithromycine target neutrophilic inflammation. High eosinophils and neutrophils percentage in sputum are best predictors of response to steroids or clarithromy- cine treatment respectively. Published: 28 February 2014 doi:10.1186/2045-7022-4-S1-P138 Cite this article as: Youssef et al.: P83 - Asthma inflammatory subtype specific treatment; a randomised clinical study. Clinical and Translational Allergy 2014 4(Suppl 1):P138. Submit your next manuscript to BioMed Central and take full advantage of: Convenient online submission Thorough peer review No space constraints or color figure charges Immediate publication on acceptance Inclusion in PubMed, CAS, Scopus and Google Scholar Research which is freely available for redistribution Submit your manuscript at www.biomedcentral.com/submit Zagazig University, Zagazig, Egypt Youssef et al. Clinical and Translational Allergy 2014, 4(Suppl 1):P138 http://www.ctajournal.com/content/4/S1/P138 © 2014 Youssef et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

P83 - Asthma inflammatory subtype specific treatment; a randomised clinical study

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POSTER PRESENTATION Open Access

P83 - Asthma inflammatory subtype specifictreatment; a randomised clinical studyDoaa Youssef*, Rabab Elbhedy, Hosam Salah

From 3rd Pediatric Allergy and Asthma Meeting (PAAM)Athens, Greece. 17-19 October 2013

IntroductionMacrolides antibiotics, such as clarithromycine expressimmunomodulatory and tissue reparative effects that aredistinct from their anti-infective properties, and have invitro efficacy against neutrophils.

Aim of studyTo determine the efficacy of add-on therapies that targeteosinophilic and noneosinophilic airway inflammationand their effects on asthma control test, pulmonaryfunction and asthma symptoms.

Methodssingle blind randomized clinical trial; asthmatic childrenwith persistent symptoms undergoing treatment withfluticasone 100 mg bid and b2 agonist as requiredwere studied. Group A (23 males / 17 females, aged11.5±1.8 years) received fluticasone 200mg bid, andgroup B (21 males / 19 females, aged 11.5±1.8 years)clarithromycine 15 mg/kg bid, in addition to fluticasone100 mg bid for 8 weeks. (FEV1%, C-CAT, SABA use,sputum induced % of eosinophils and neutrophils) werecompared before and after treatment in each group.

ResultsIn group A there is significant reduction of eosinophilspercentage after treatment, and non significant increasein neutrophils percentage. There was significantimprovement in FEV1% predicted. While in group Bthere was non significant decrease in eosinophils, andsignificant decrease in neutrophils. In group A there wassignificant negative correlation between changes inFEV1% and change in eosinophils and week positivecorrelation between changes in FEV1% and changes inneutrophils. In group B there was significant positive

correlation between basal eosinophils and change inFEV1% and significant negative correlation betweenbasal neutrophils and change in FEV1%.

ConclusionSteroids were effective in targeting eosinophilic inflamma-tion and clarithromycine target neutrophilic inflammation.High eosinophils and neutrophils percentage in sputumare best predictors of response to steroids or clarithromy-cine treatment respectively.

Published: 28 February 2014

doi:10.1186/2045-7022-4-S1-P138Cite this article as: Youssef et al.: P83 - Asthma inflammatory subtypespecific treatment; a randomised clinical study. Clinical and TranslationalAllergy 2014 4(Suppl 1):P138.

Submit your next manuscript to BioMed Centraland take full advantage of:

• Convenient online submission

• Thorough peer review

• No space constraints or color figure charges

• Immediate publication on acceptance

• Inclusion in PubMed, CAS, Scopus and Google Scholar

• Research which is freely available for redistribution

Submit your manuscript at www.biomedcentral.com/submit

Zagazig University, Zagazig, Egypt

Youssef et al. Clinical and Translational Allergy 2014, 4(Suppl 1):P138http://www.ctajournal.com/content/4/S1/P138

© 2014 Youssef et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative CommonsAttribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproductionin any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.