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Open AccessJournal ArticleDOI

Dipeptidyl peptidase IV inhibitors, a risk factor for bullous pemphigoid: Retrospective multicenter case-control study from France and Switzerland

TLDR
DPP4is, especially vildagliptin, are associated with an increased risk for development of BP, and their use needs to be carefully evaluated, particularly in high‐risk patients, such as males and those age 80 years or older.
Abstract
Background Case reports have suggested an association between dipeptidyl peptidase-4 inhibitors (DPP4is) and development of bullous pemphigoid (BP). Objective To evaluate the association between DPP4i treatment and development of BP. Methods We conducted a retrospective 1:2 case-control study, comparing case patients with diabetes and BP with age- and sex-matched control patients with diabetes issued from Swiss (Bern) and French (Marseille) dermatologic departments from January 1, 2014, to July 31, 2016. Results We collected 61 case patients with diabetes and BP and 122 controls. DPP4is were associated with an increased risk for development of BP (adjusted odds ratio, 2.64; 95% confidence interval, 1.19-5.85; P  = .02), with vildagliptin showing the highest adjusted odds ratio (3.57 [95% confidence interval, 1.07-11.84; P  = .04]). Stratified analysis showed a stronger association in males and patients age 80 years or older. DPP4i withdrawal and the initiation of first-line treatments led to clinical remission in 95% of cases. Limitations This was a retrospective study in tertiary referral hospitals. We focused the analysis on DPP4i intake, without analyzing the potential isolated effect of metformin. Conclusions DPP4is, especially vildagliptin, are associated with an increased risk for development of BP. Their use needs to be carefully evaluated, particularly in high-risk patients, such as males and those age 80 years or older.

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Journal ArticleDOI

The Growing Incidence of Bullous Pemphigoid: Overview and Potential Explanations.

TL;DR: A review of the current understanding of the epidemiological features of BP sheds light on the putative explanations for its growing incidence and summarizes the current awareness of the increased risk to develop BP.
Journal ArticleDOI

Dipeptidyl peptidase 4 inhibitors and their potential immune modulatory functions

TL;DR: This review focuses on the regulatory effects of DPP4is on immune functions and their possible underlying mechanisms as well as potential new drug class applied in these diseases.
Journal ArticleDOI

Association of Bullous Pemphigoid With Dipeptidyl-Peptidase 4 Inhibitors in Patients With Diabetes: Estimating the Risk of the New Agents and Characterizing the Patients.

TL;DR: A retrospective case-control study of the intake of different DPP-4 inhibitor agents and metformin and occurrence of BP among patients with diabetes in a tertiary care referral center for autoimmune bullous diseases in northern Israel found that vildagliptin and, to a lesser extent, linagli leptin are associated with an increased risk of BP.
Journal ArticleDOI

The Role of Eosinophils in Bullous Pemphigoid: A Developing Model of Eosinophil Pathogenicity in Mucocutaneous Disease.

TL;DR: The role of eosinophils in BP is reviewed and a framework for understanding eOSinophil pathogenic mechanisms in mucocutaneous disease is provided.
References
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Journal ArticleDOI

A Comparison of Oral and Topical Corticosteroids in Patients with Bullous Pemphigoid

TL;DR: Topical corticosteroid therapy is effective for both moderate and severe bullous pemphigoid and is superior to oral corticosterone therapy for extensive disease.
Journal ArticleDOI

Autoantibody Profile Differentiates between Inflammatory and Noninflammatory Bullous Pemphigoid

TL;DR: It is shown that the autoAb profile differentiates between inflammatory and noninflammatory BP, and that non inflammatory BP may be associated with dipeptidyl peptidase-IV inhibitors.
Journal ArticleDOI

Drugs Associated With Bullous Pemphigoid: A Case-Control Study

TL;DR: The results suggest that some drug therapies may be a risk factor for bullous pemphigoid, and the cause of this association should be further investigated.
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