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    • Rapid Communication2

    Author

    • Cho, Kyu Yong1
    • Försti, Anna-Kaisa1
    • Huilaja, Laura1
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    • Iwata, Hiroaki1
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    • Journal of Investigative Dermatology2

    Keyword

    • BP2
    • bullous pemphigoid2
    • dipeptidyl peptidase-4 inhibitor2
    • BPDAI1
    • Bullous Pemphigoid Disease Area Index1
    • COL171
    • type XVII collagen1

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    • Letter to the Editor
      Open Archive

      Vildagliptin Significantly Increases the Risk of Bullous Pemphigoid: A Finnish Nationwide Registry Study

      Journal of Investigative Dermatology
      Vol. 138Issue 7p1659–1661Published online: February 7, 2018
      • Outi Varpuluoma
      • Anna-Kaisa Försti
      • Jari Jokelainen
      • Miia Turpeinen
      • Markku Timonen
      • Laura Huilaja
      • and others
      Cited in Scopus: 81
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        Bullous pemphigoid (BP) is the most common autoimmune blistering skin disease (Schmidt and Zillikens, 2013). BP has become more common over the past two decades (Försti et al., 2014; Joly et al., 2012; Langan et al., 2008). However, the underlying causes of the increasing incidence of BP are poorly understood. Altogether, over 50 drugs have been reported to induce BP (Stavropoulos et al., 2014). The use of dipeptidyl peptidase-4 inhibitors (DPP-4i), a class of drug used for the treatment of diabetes, has recently been scrutinized as a risk factor for BP, both in case reports (see Supplementary Table S1 online) and in national pharmacovigilance database reports (Bene et al., 2016; García et al., 2016), but large population-based studies are lacking.
      • Letter to the Editor
        Open Archive

        HLA-DQB1*03:01 as a Biomarker for Genetic Susceptibility to Bullous Pemphigoid Induced by DPP-4 Inhibitors

        Journal of Investigative Dermatology
        Vol. 138Issue 5p1201–1204Published online: December 1, 2017
        • Hideyuki Ujiie
        • Ken Muramatsu
        • Taisei Mushiroda
        • Takeshi Ozeki
        • Hideaki Miyoshi
        • Hiroaki Iwata
        • and others
        Cited in Scopus: 75
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          Dipeptidyl peptidase-4 inhibitor (DPP-4i) has been widely used to treat type 2 diabetes. DPP-4 inactivates incretins by catalyzing the cleavage of those proteins to inactive forms (Drucker, 2007). DPP-4i works by inhibiting the action of this enzyme and improves glycemic control (Aschner and Kipnes, 2006). DPP-4i has been known as a safe drug; however, an increased risk of bullous pemphigoid (BP) during DPP-4i exposure has been reported in diabetic patients administered DPP-4i (Béné et al., 2016).
          HLA-DQB1*03:01 as a Biomarker for Genetic Susceptibility to Bullous Pemphigoid Induced by DPP-4 Inhibitors
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