Gliptin-Induced Bullous Pemphigoid: Canadian Case Series of 10 Patients
Miriam Armanious, Mohannad Abu‐Hilal
Abstract
BACKGROUND: Bullous pemphigoid (BP) is a chronic immune-mediated vesiculobullous disorder. Recently, several reports have described dipeptidyl peptidase-4 inhibitors, also known as gliptins, as causative agents for drug-induced BP. OBJECTIVE: To report and describe clinical and histologic characteristics of 10 cases of gliptin-induced BP. RESULTS: We identified 10 patients with gliptin-induced BP. Nine were secondary to linagliptin, and 1 case was attributed to sitagliptin. All patients showed significant improvement after withdrawal of gliptin medications and proper medical treatment. There has been no evidence of relapse after 4 months of follow-up. CONCLUSION: This report supports the proposed association between gliptins and BP. Physicians should be aware of this potential adverse effect, as gliptin-induced BP can be reversible once identified and the responsible medication is stopped. Early withdrawal of the offending drug and proper treatment can lead to rapid improvement and reduced morbidity.