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AuthorAl Chalabi, Radi
AuthorSherbash, Mohamed
AuthorAl-Marri, Fahad
AuthorIqneibi, Mariam
AuthorJoy, Febu Elizabeth
AuthorJochebeth, Anh
AuthorAl-Khawaga, Sara
AuthorBuddenkotte, Joerg
AuthorSteinhoff, Martin
Available date2024-12-24T10:20:42Z
Publication Date2024-04-23
Publication NameJournal of the European Academy of Dermatology and Venereology
Identifierhttp://dx.doi.org/10.1111/jdv.20037
CitationAl Chalabi, R., Sherbash, M., Al-Marri, F., Iqneibi, M., Joy, F. E., Jochebeth, A., ... & Steinhoff, M. (2024). Severe atopic dermatitis in an Asian-Arabic population treated with dupilumab: A retrospective observational study. Journal of the European Academy of Dermatology and Venereology: JEADV.
ISSN0926-9959
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85191192738&origin=inward
URIhttp://hdl.handle.net/10576/61993
AbstractAtopic dermatitis (AD) is a common, inflammatory skin disease characterized by a TH2-deviated immune response in the acute phase and a TH2/TH1/TH17/TH22-skewed immune response in the chronic phase1 associated with pruritus. Dupilumab, a therapeutic targeting IL-4, IL-13 signalling pathways2, 3 and the first biologic approved for the treatment of moderate-to-severe AD4 demonstrated substantial efficacy, minor side effects and good tolerability.2 Long term real-world studies investigating the efficacy, safety and tolerability of dupilumab in AD patients have been conducted mainly in Caucasians, Hispanic and southeast Asian populations but not Asian-Arabic descent population. To fill this gap, we investigated dupilumab in AD patients among Asian-Arabic population of Qatari descent.
SponsorSupported by Internal Research Grand Competition (IRGC-04-SI-17-151) of the MRC fund, Hamad Medical Corporation, Qatar (to M.S. and J.B.).
Languageen
PublisherJohn Wiley and Sons
Subjectdupilumab
Atopic dermatitis
TitleSevere atopic dermatitis in an Asian-Arabic population treated with dupilumab: A retrospective observational study
TypeOther
Issue Number11
Volume Number38
ESSN1468-3083
dc.accessType Full Text


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