1. Olmesartan-associated enteropathy: results of a national survey.
- Author
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Marthey, L., Cadiot, G., Seksik, P., Pouderoux, P., Lacroute, J., Skinazi, F., Mesnard, B., Chayvialle, J. A., Savoye, G., Druez, A., Parlier, D., Abitbol, V., Gompel, M., Eoche, M., Poncin, E., Bobichon, R., Colardelle, P., Wils, P., Salloum, H., and Peschard, S.
- Subjects
INTESTINAL diseases ,GASTROENTEROLOGY ,HISTOLOGICAL techniques ,DIARRHEA ,THERAPEUTICS ,TRANSGLUTAMINASE regulation - Abstract
Background Recently, a new enteropathy has been described: olmesartan-associated enteropathy. However, the association has been questioned: a phase 3 trial and a cohort study found no association between gastrointestinal events and olmesartan. Aim To collect French cases of sartan-associated enteropathy to describe further this entity, confirm or refute causality, and determine if the association exists with other sartans. Methods French gastroenterologists were invited to report cases of sartan-associated enteropathy and collect clinical, biological and histological data. Patients with diarrhoea and histological duodenal abnormalities were included. Results Thirty-six patients with olmesartan-associated enteropathy were reported, including 32 with villous atrophy and four without. There was only one patient with irbesartan-associated enteropathy. None of the patients died. Patients with villous atrophy had diarrhoea, vomiting, renal failure, hypokalaemia, body weight loss and hypoalbuminaemia. Thirty-one patients were hospitalised; four required intensive care. Anti-transglutaminase and anti-enterocyte antibodies were negative; anti-nuclear antibodies were positive (9/11). Endoscopic duodenal biopsies showed villous atrophy (32/32) and polyclonal intra-epithelial CD3+CD8+ lymphocytosis (11/11). Exactly, 14/15 patients responded to steroids and/or immunosuppressants, prescribed because of suspected autoimmune enteropathy. Ten olmesartan interruptions were followed by reintroductions before steroids or immunosuppressants. Interruptions were followed by remissions (9/10), but reintroductions were followed by relapses (9/9). Twenty-nine patients were in remission since olmesartan interruption, including 26 without immunosuppressants. Patients with normal villi had similar clinical characteristics, but mild histological abnormalities (intra-epithelial lymphocytosis and lamina propria lymphocytic infiltration). Conclusions Olmesartan causes a severe and immune-mediated enteropathy, with or without villous atrophy. Enteropathy associated with other sartans seems to be very rare. [ABSTRACT FROM AUTHOR]
- Published
- 2014
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