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High and typical 18F-FDG bowel uptake in patients treated with metformin
Authors:Eric Gontier  Emmanuelle Fourme  Myriam Wartski  Cyrille Blondet  Gerald Bonardel  Elise Le Stanc  Marina Mantzarides  Herve Foehrenbach  Alain-Paul Pecking  Jean-Louis Alberini
Affiliation:(1) Department of Nuclear Medicine, Military Hospital Val-de-Grace, 74, Bd de Port Royal, 75230 Paris, cedex 05, France;(2) Department of Medical Statistics, Cancer Research Center René Huguenin, Saint-Cloud, France;(3) Department of Nuclear Medicine, Cancer Research Center René Huguenin, Saint-Cloud, France;(4) Department of Nuclear Medicine, University Hospital of Strasbourg, Strasbourg, France;(5) Department of Nuclear Medicine, Foch Hospital, Suresnes, France
Abstract:Purpose This prospective and bi-centric study was conducted in order to determine the impact of antidiabetic treatments (AD) on 18F-FDG bowel uptake in type 2 diabetic patients. Methods Fifty-five patients with previously diagnosed and treated type 2 diabetes mellitus (group 1) were divided in two subgroups: AD treatment including metformin (n=32; group 1a) and AD treatment excluding metformin (n=23; group 1b). The 95 patients without diabetes mellitus made up controls (group 2). 18F-FDG uptake in small intestine and colon was visually graded and semi-quantitatively measured using the maximum standardized uptake value. Results 18F-FDG bowel uptake was significantly increased in AD patients (group 1) as compared to controls (group 2) (p<0.001). Bowel uptake was significantly higher in AD patients including metformin (group 1a) as compared to AD patients excluding metformin (group 1b) (p<0.01), whose bowel uptake was not significantly different from controls (group 2). A metformin treatment was predictive of an increased bowel uptake in the small intestine (odds ratio OR=16.9, p<0.0001) and in the colon (OR=95.3, p<0.0001), independently of the other factors considered in the multivariate analysis. Bowel uptake pattern in the patients treated with metformin was typically intense, diffuse and continuous along the bowel, strongly predominant in the colon, in both the digestive wall and lumen. Conclusion This study emphasizes that metformin significantly increases 18F-FDG uptake in colon and, to a lesser extent, in small intestine. It raises the question of stopping metformin treatment before an 18F-FDG PET/CT scan is performed for intra-abdominal neoplasic lesion assessment.
Keywords:18F-FDG PET/CT  Antidiabetic  Metformin  Bowel uptake
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