Identification of Risk Factors for Dupilumab-associated Ocular Surface Disease in Patients with Atopic Dermatitis
Achten, Roselie E; Van Luijk, Chantal; Van der Rijst, Lisa; Bakker, Daphne; Spekhorst, Lotte; Zuithoff, Nicolaas; Schuttelaar, Marie; Romeijn, Geertruida; Voorberg, Angelique; Kamsteeg, Marijke; Haeck, Inge; De Graaf, Marlies; Thijs, Judith; De Boer, Joke; De Bruin-Weller, Marjolein
(2022) Acta Dermato-Venereologica, volume 102, pp. 1 - 7
(Article)
Abstract
This study identified risk factors for the development of dupilumab-associated ocular surface disease in patients with moderate-to-severe atopic dermatitis in a large prospective daily practice cohort. Data from the Dutch BioDay Registry were used to assess the risk of developing dupilumab-associated ocular surface disease, by performing univariate and multivariate logistic
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regression analyses. A total of 469 patients were included, of which 152/469 (32.4%) developed dupilumab-associated ocular surface disease. Multivariate analysis showed a statistically significant association of the development of dupilumab-associated ocular surface disease with a history of any eye disease (history of self-reported episodic acute allergic conjunctivitis excluded) combined with the use of ophthalmic medication at the start of dupilumab (odds ratio 5.16, 95% confidence interval 2.30-11.56, p < 0.001). In conclusion, a history of any eye disease (history of self-reported episodic acute allergic conjunctivitis excluded) combined with the use of ophthalmic medication at baseline was associated with the development of dupilumab-associated ocular surface disease in patients with atopic dermatitis.
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Keywords: DAOSD, conjunctivitis, dupilumab, dupilumab-associated ocular surface disease, Dermatology
ISSN: 0001-5555
Publisher: Medical Journals Sweden AB
Note: Funding Information: The authors thank Andrew Walker for critically reading the manuscript. Patients included in this manuscript participated in the BioDay registry sponsored by Sanofi Genzyme. Conflicts of interest: REA has nothing to disclose. CMvL is a speaker for Sanofi Genzyme. LPvdR has nothing to disclose. DSB is a speaker for Sanofi Genzyme and LEO Pharma. LSS has nothing to disclose. NPAZ has nothing to disclose. MLAS is an advisory board member and/or speaker for AbbVie, Eli Lilly, Leo Pharma, Pfizer, Regeneron, and Sanofi-Genzyme. GLER has nothing to disclose. Angelique N. Voorberg has nothing to disclose. MK is an advisory board member of LEO Pharma. IMH is an advisory board member, and/or speaker for AbbVie, Eli Lilly, Leo Pharma and Sanofi-Genzyme. MdG is a principal investigator and advisory board member and/or speaker for Sanofi Genzyme and Regene-ron Pharmaceuticals and LEO Pharma, and is an advisory board member for Eli Lilly. JLT is a speaker for Sanofi Genzyme and LEO Pharma. JHdB received research funding from Abbvie; this is outside the submitted work. MSdB-W is a consultant, advisory board member, and/or speaker for AbbVie, Almirall, Arena, Eli Lilly, Galderma, Janssen, Leo Pharma, Pfizer, Regeneron, and Sanofi-Genzyme. Publisher Copyright: © 2022, Medical Journals/Acta D-V. All rights reserved.
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