4.5 Article

Clinical features of dipeptidyl peptidase-4 inhibitor-associated bullous pemphigoid in Japan: A nationwide retrospective observational study

Journal

JOURNAL OF DERMATOLOGY
Volume 49, Issue 7, Pages 697-702

Publisher

WILEY
DOI: 10.1111/1346-8138.16394

Keywords

bullous pemphigoid; dipeptidyl peptidase-4 inhibitor; non-inflammatory; spontaneous remission; vildagliptin

Categories

Funding

  1. Kawasaki Medical School
  2. Japan Agency for Medical Research and Development [20ek0410068h0001]
  3. Ministry of Health, Labor, and Welfare (MHLW) Health and Labor Sciences Research Grant for Research on Rare Intractable Dermatological Disorders as part of the MHLW Research Project on Overcoming Intractable Diseases

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This retrospective study investigated the incidence, clinical presentation, and clinical course of DPP-4i-associated bullous pemphigoid (BP) using data from a nationwide registry for BP in Japan. The results showed that DPP-4i-BP was more common in males and non-inflammatory BP was more frequently observed in DPP-4i-BP cases. Some patients achieved spontaneous remission after discontinuing DPP-4i.
Many cases of bullous pemphigoid (BP) have been reported in patients taking dipeptidyl peptidase-4 inhibitors (DPP-4i), which are the most widely used antidiabetic drug for type 2 diabetes mellitus. However, no large-scale survey has been conducted in Japan. This retrospective study investigated the incidence, clinical presentation, and clinical course of DPP-4i-associated BP (DPP-4i-BP) using epidemiological data from a nationwide registry for BP. In 2016, 713 new BP patients at 94 dermatological institutes were registered, 243 (34.1%) with DPP-4i-BP and 461 (64.7%) with non-DPP-4i-BP. The male-to-female ratio was 1.9 and 0.84, respectively. Patients with DPP-4i-BP were predominantly male. Non-inflammatory BP was more common in DPP-4i-BP (33.3%) than in non-DPP-4i-BP (14.6%), while inflammatory BP was common in both. No specific subtype or difference in disease severity was evident in DPP-4i-BP. The most common gliptins administered to DPP-4i-BP patients were vildagliptin (37.2%) and linagliptin (23.8%). DPP-4i intake was discontinued in 79.9% of cases after diagnosis. Some DPP-4i-BP patients (17.6%) achieved spontaneous remission after discontinuing DPP-4i without requiring the use of systemic corticosteroids and/or adjuvant therapy. Mean duration to achieve disease control was 2.87 months. The odds ratio for non-inflammatory BP requiring systemic corticosteroids and/or adjuvant therapy was low (0.52), suggesting that remission was achieved easily with supportive care in that phenotype. Non-inflammatory and mild cases of DPP-4i-BP may resolve spontaneously with supportive care, including the discontinuation of DPP-4i and no oral corticosteroid therapy.

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