Abstract
Background: Although the association of bullous pemphigoid (BP) and psoriasis is well-established, the clinical and immunological features of patients with coexisting BP and psoriasis are yet to be investigated. Objective: We aimed to estimate the prevalence of psoriasis amongst patients with BP and to elucidate the clinical and immunological characteristics of BP patients with comorbid psoriasis. Methods: A retrospective cohort study including all consecutive patients diagnosed with BP throughout the years 2009–2019 in a tertiary referral centre. Results: The study encompassed 273 patients with BP, of whom 11 (4.0%; 95% CI, 2.3–7.1%) had comorbid psoriasis. The onset of psoriasis preceded that of BP in 81.8% of patients by a median (range) latency of 26.5 (5.0–34.0) years. Compared to BP patients without psoriasis, those with BP and comorbid psoriasis were significantly younger at the onset of BP [71.8 (9.3) vs. 79.4 (9.8) years; P = 0.023], had a milder erosive phenotype [erosion/blister BPDAI mean (SD)score; 5 (4.1) vs. 22.3 (15.2); P = 0.025], lower levels of anti-BP180 NC16A serum autoantibodies [236.6 (266.3) vs. 556.2 (1323.6) U/mL; P = 0.008] and a higher prevalence of isolated linear C3 deposits (36.4% vs. 14.1%; P = 0.043) and a lower prevalence of linear immunoglobulin G deposits (36.4% vs. 68.7%; P = 0.025) along the dermal–epidermal junction by direct immunofluorescence microscopy. Conclusions: Patients with BP and comorbid psoriasis present at a younger age with milder erosive phenotype and lower levels of pathogenic autoantibodies.
Original language | English |
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Pages (from-to) | 981-987 |
Number of pages | 7 |
Journal | Journal of the European Academy of Dermatology and Venereology |
Volume | 35 |
Issue number | 4 |
DOIs | |
State | Published - Apr 2021 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2020 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology
Funding
sources Clinical Research Unit Pemphigoid Diseases (KFO 303) and Cluster of Excellence Precision Medicine in Chronic Inflammation (EXC 2167), both from the Deutsche Forschungsgemeinschaft.The patients presented in this manuscript have given written informed consent to publication of their case details. Open access funding enabled and organized by Projekt DEAL.