| Literature DB >> 30543900 |
Marthe Plaquevent1, Florence Tétart2, Laurence Fardet3, Saskia Ingen-Housz-Oro3, Laurence Valeyrie-Allanore3, Philippe Bernard4, Vivien Hebert2, Aude Roussel5, Martine Avenel-Audran6, Guillaume Chaby7, Michel D'Incan8, Marie-Christine Ferrier-Le-Bouedec8, Sophie Duvert-Lehembre9, Catherine Picard-Dahan10, Geraldine Jeudy11, Evelyne Collet11, Bruno Labeille12, Cécile Morice13, Marie-Aleth Richard14, Isabelle Bourgault-Villada15, Noémie Litrowski16, Corina Bara17, Emmanuel Mahe18, Catherine Prost-Squarcioni19, Marina Alexandre19, Gaelle Quereux20, Claire Bernier20, Angèle Soria21, Domitille Thomas-Beaulieu22, Christine Pauwels22, Olivier Dereure23, Jacques Benichou24, Pascal Joly2.
Abstract
Dipeptidyl peptidase-4 inhibitors have been suspected to induce bullous pemphigoid (BP). The objective of this study was to compare the observed frequency of gliptin intake in a large sample of 1,787 BP patients diagnosed between 2012 and 2015 in France, with the expected frequency after indirect age standardization on 225,412 individuals extracted from the database of the National Healthcare Insurance Agency. The secondary objective was to assess the clinical characteristics and the course of gliptin-associated BP, depending on whether gliptin was continued or stopped. The observed frequencies of intake of the whole gliptin class and that of vildagliptin in the BP population were higher than those in the general population after age standardization (whole gliptin class: 6.0%; 95% confidence interval = 4.9-7.1% vs. 3.6%, observed-to-expected drug intake ratio = 1.7; 95% confidence interval = 1.4-2.0; P < 0.0001; vildagliptin = 3.3%; 95% confidence interval = 2.5-4.1% vs. 0.7%, ratio = 4.4; 95% confidence interval = 3.5-5.7; P < 0.0001). The association of any gliptin+metformin was also higher than in the general population, ratio = 1.8 (95% confidence interval = 1.3-2.4; P < 0.0001). Gliptin-associated BP had no specific clinical characteristics. Gliptin was stopped in 48 (45.3%) cases. Median duration to achieve disease control, rate, and delay of relapse were not different whether gliptin was stopped or continued. This study strongly supports the association between gliptin intake, particularly vildagliptin, and the onset of BP.Entities:
Year: 2018 PMID: 30543900 DOI: 10.1016/j.jid.2018.10.045
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551