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Ceramide-dominant barrier repair lipids alleviate childhood atopic dermatitis: Changes in barrier function provide a sensitive indicator of disease activity,☆☆,,★★

A preliminary report of these results was presented at the Society for Investigative Dermatology meeting in Washington, DC, May 9-12, 2001. In addition, a preliminary report describing the first 6 weeks' data will appear as a Letter to the Editor in the Archives of Dermatology.
https://doi.org/10.1067/mjd.2002.124617Get rights and content

Abstract

Background: It is currently fashionable to consider atopic dermatitis (AD), like other inflammatory dermatoses, as immunologic in pathogenesis (“inside-outside” hypothesis). Accordingly, topical glucocorticoids and other immunosuppressive agents are mainstays of therapy, but the risk of toxicity from these agents is not insignificant, particularly in children. Alternatively, because stratum corneum (SC) permeability barrier function is also abnormal in AD, it has been hypothesized that the barrier abnormality could drive disease activity. Yet commonly used emollients and moisturizers do not correct the SC ceramide deficiency, the putative cause of the barrier abnormality. Objectives: We assessed the efficacy of a newly developed, ceramide-dominant, physiologic lipid-based emollient, when substituted for currently used moisturizers, in 24 children who were also receiving standard therapy for stubborn-to-recalcitrant AD. Methods: All subjects continued prior therapy (eg, topical tacrolimus or corticosteroids), only substituting the barrier repair emollient for their prior moisturizer. Follow-up evaluations, which included severity scoring of atopic dermatitis (SCORAD) values and several biophysical measures of SC function, were performed every 3 weeks for 20 to 21 weeks. Results: SCORAD values improved significantly in 22 of 24 patients by 3 weeks, with further progressive improvement in all patients between 6 and 20 or 21 weeks. Transepidermal water loss levels (TEWL), which were elevated over involved and uninvolved areas at entry, decreased in parallel with SCORAD scores and continued to decline even after SCORAD scores plateaued. Both SC integrity (cohesion) and hydration also improved slowly but significantly during therapy. Finally, the ultrastructure of the SC, treated with ceramide-dominant emollient, revealed extracellular lamellar membranes, which were largely absent in baseline SC samples. Conclusion: These studies suggest that (1) a ceramide-dominant, barrier repair emollient represents a safe, useful adjunct to the treatment of childhood AD and (2) TEWL is at least as sensitive an indicator of fluctuations in AD disease activity as are SCORAD values. These studies support the outside-inside hypothesis as a component of pathogenesis in AD and other inflammatory dermatoses that are accompanied by a barrier abnormality. (J Am Acad Dermatol 2002;47:198-208.)

Section snippets

Subjects and clinical assessments

All subjects entered the study between the end of September and the beginning of November 2000 and were followed up until February 2001 at the intervals specified below. A concomitant seasonal decline in outside temperatures and inside humidity prevailed in San Francisco during the entire study period. All subjects were recruited from the larger pool of children attending the Pediatric Dermatology Clinics at the Mt Zion Medical Center, University of California, San Francisco. The study protocol

Comparison of clinical response to changes in biophysical parameters

As seen in Fig 1, A, the combined SCORAD values for all participants declined rapidly, reaching a plateau after 6 weeks despite ongoing use of the ceramide-dominant preparation.

. Changes in clinical scores and functional parameters for group as a whole. A, Clinical severity scoring of atopic dermatitis (SCORAD) improved dramatically 3 weeks and 6 weeks after treatment with the ceramide-dominant barrier repair preparation, and then leveled off at 12 and 20 or 21 weeks. B, Transepidermal water

Discussion

When emollients or moisturizers are used in the treatment of AD and other inflammatory dermatoses, the purported aim is limited to an improvement in skin hydration, that is, mitigation of the xerosis (scaling) abnormality. No reduction in inflammatory disease activity is expected, and such activity has been documented only infrequently.27 Yet the results of this uncontrolled trial suggest, first, that substitution of a ceramide-dominant barrier repair formulation for standard, nonphysiologic

Acknowledgements

We thank Ms Sue Allen, Laura Teale, Katie O'Donnell, and Jerelyn Magnusson for excellent editorial assistance and Debra Crumrine for preparing the specimens for electron microscopy.

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  • Cited by (0)

    *Both contributed equally and should be considered co-first authors.

    ☆☆

    Funding sources: National Institutes of Health grant AR-19098, the Medical Research Service, Department of Veterans Affairs, and a grant from Osmotics Corporation, Denver, Colorado.

    Disclosure: Dr Elias is a consultant for Osmotics Corporation.

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    Reprints not available from authors.

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