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Details

Autor(en) / Beteiligte
Titel
Dipeptidyl‐peptidase IV inhibitors (DPP4i)‐associated bullous pemphigoid: Estimating the clinical profile and exploring intraclass differences
Ist Teil von
  • Dermatologic therapy, 2020-07, Vol.33 (4), p.e13790-n/a
Ort / Verlag
Hoboken, USA: John Wiley & Sons, Inc
Erscheinungsjahr
2020
Quelle
MEDLINE
Beschreibungen/Notizen
  • Data regarding the clinical characteristics of patients with dipeptidyl‐peptidase IV inhibitors (DPP4i)‐associated BP is inconclusive. We aimed to characterize the clinical features of patients with DPP4i‐associated BP, and to assess whether there are phenotypic differences associated with different agents belonging to the DPP4i class. A retrospective prevalence study was performed, including all consecutive patients diagnosed with BP throughout the years 2000 to 2019. The study included 397 patients with BP, of whom 58 (14.6%) were DPP4i‐associated. Compared to other patients with BP, patients with DPP4i‐associated BP had a more prominent male preponderance (60.3% vs 41.0%; P = .006), presented more frequently with extensive disease (60.3% vs 46.3%; P = .049), had greater truncal (96.6% vs 85.5%; P = .019) and cephalic (51.7% vs 33.6%; P = .008) involvement, and had less frequent peripheral eosinophilia (25.9% vs 51.9%; P < .001). Compared to patients with vildagliptin‐associated BP, those with linagliptin‐associated BP were managed by higher dosage of systemic corticosteroids in order to achieve disease control (prednisone > 1 mg/kg: 68.2% vs 40.0%; P = .046). In conclusion, DPP4i‐associated BP seems to have a unique clinical profile characterized by male predominance, extensive disease, truncal and cephalic involvement, and less peripheral eosinophilia. Linagliptin may be associated with a harder course necessitating more aggressive therapy.

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