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Cutaneous microbiome effects of fluticasone propionate cream and adjunctive bleach baths in childhood atopic dermatitis - 17/08/16

Doi : 10.1016/j.jaad.2016.04.066 
Mercedes E. Gonzalez, MD a, Julie V. Schaffer, MD a, Seth J. Orlow, MD, PhD a, Zhan Gao, MD d, Huilin Li, PhD b, Alexander V. Alekseyenko, PhD c, Martin J. Blaser, MD d,
a Ronald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York 
b Department of Population Health, Division of Biostatistics, New York University School of Medicine, New York, New York 
c Center for Health Informatics and Bioinformatics, Department of Medicine, Division of Translational Medicine, New York University School of Medicine, New York, New York 
d Department of Medicine, New York University Langone Medical Center, New York, New York 

Correspondence to: Martin J. Blaser, MD, New York University Langone Medical Center, 550 First Ave, Bellevue CD 689, New York, NY 10016.New York University Langone Medical Center550 First Ave, Bellevue CD 689New YorkNY10016

Abstract

Background

Patients with atopic dermatitis (AD) are prone to skin infections, with microbes such as Staphylococcus aureus suspected of contributing to pathogenesis. Bleach baths might improve AD by reducing skin microbial burden.

Objective

We sought to characterize the microbiota of lesional and nonlesional skin in young children with AD and control subjects and compare changes after treatment with a topical corticosteroid (TCS) alone or TCS + dilute bleach bath.

Methods

In a randomized, placebo-controlled, single-blinded clinical trial in 21 children with AD and 14 healthy children, lesional and nonlesional AD skin was examined at baseline and after 4-week treatment with TCS alone or TCS plus bleach bath. Microbial DNA was extracted for quantitative polymerase chain reaction of predominant genera and 16S rRNA sequencing.

Results

At baseline, densities of total bacteria and Staphylococcus, including Staphylococcus aureus, were significantly higher at the worst AD lesional site than nonlesional (P = .001) or control (P < .001) skin; bacterial communities on lesional and nonlesional AD skin significantly differed from each other (P = .04) and from control (P < .001). After TCS + bleach bath or TCS alone, bacterial compositions on lesional skin normalized (P < .0001), resembling nonlesional skin, with microbial diversity restored to control skin levels.

Limitations

The 4-week time period and/or the twice-weekly baths may not have been sufficient for additional impact on the cutaneous microbiome. More detailed sequencing may allow better characterization of the distinguishing taxa with bleach bath treatment.

Conclusions

Treatment with a TCS cream suffices to normalize the cutaneous microbiota on lesional AD; after treatment, bacterial communities on lesional skin resemble nonlesional skin but remain distinct from control.

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Key words : atopic dermatitis, bleach baths, cutaneous microbiome, quantitative polymerase chain reaction, 16S sequencing, Staphylococcus aureus, topical corticosteroids

Abbreviations used : AD, EASI, NYU, NYULMC, PCR, qPCR, rRNA, TCS


Plan


 Dr Gonzalez was a recipient of a Pediatric Dermatology Fellowship Award from the Dermatology Foundation and Dr Schaffer received a Medical Dermatology Career Development Award from the Dermatology Foundation. Dr Gonzalez was supported in part by a gift from the Bohnert Foundation. This work used computing resources at the High Performance Computing Facility of the Center for Health Informatics and Bioinformatics at the New York University Langone Medical Center. Supported in part by UH2 AR057506 and New York University Clinical and Translational Science Awards grant UL1 TR000038 from the National Institutes of Health, and by the Diane Belfer Program in Human Microbial Ecology, and C&D Research Fund.
 Conflicts of interest: None declared.
 Supplementary items are available at www.jaad.org/.
 Reprints not available from the authors.


© 2016  American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 75 - N° 3

P. 481 - septembre 2016 Retour au numéro
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