Gontier Eric, Fourme Emmanuelle, Wartski Myriam, Blondet Cyrille, Bonardel Gerald, Le Stanc Elise, Mantzarides Marina, Foehrenbach Herve, Pecking Alain-Paul, Alberini Jean-Louis
Department of Nuclear Medicine, Military Hospital Val-de-Grâce, 74, Bd de Port Royal, 75230, Paris, cedex 05, France.
Eur J Nucl Med Mol Imaging. 2008 Jan;35(1):95-9. doi: 10.1007/s00259-007-0563-6. Epub 2007 Sep 5.
This prospective and bi-centric study was conducted in order to determine the impact of antidiabetic treatments (AD) on (18)F-FDG bowel uptake in type 2 diabetic patients.
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). (18)F-FDG uptake in small intestine and colon was visually graded and semi-quantitatively measured using the maximum standardized uptake value.
(18)F-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.
This study emphasizes that metformin significantly increases (18)F-FDG uptake in colon and, to a lesser extent, in small intestine. It raises the question of stopping metformin treatment before an (18)F-FDG PET/CT scan is performed for intra-abdominal neoplasic lesion assessment.
本前瞻性双中心研究旨在确定抗糖尿病治疗(AD)对2型糖尿病患者肠道(18)F-FDG摄取的影响。
55例先前已诊断并接受治疗的2型糖尿病患者(第1组)分为两个亚组:包括二甲双胍的AD治疗组(n = 32;第1a组)和不包括二甲双胍的AD治疗组(n = 23;第1b组)。95例非糖尿病患者作为对照组(第2组)。对小肠和结肠的(18)F-FDG摄取进行视觉分级,并使用最大标准化摄取值进行半定量测量。
与对照组(第2组)相比,AD患者(第1组)的肠道(18)F-FDG摄取显著增加(p<0.001)。与不包括二甲双胍的AD患者(第1b组)相比,包括二甲双胍的AD患者(第1a组)的肠道摄取显著更高(p<0.01),其肠道摄取与对照组(第2组)无显著差异。二甲双胍治疗可预测小肠(优势比OR = 16.9,p<0.0001)和结肠(OR = 95.3,p<0.0001)的肠道摄取增加,独立于多变量分析中考虑的其他因素。接受二甲双胍治疗的患者的肠道摄取模式通常强烈、弥漫且沿肠道连续,在结肠中强烈占优势,在消化壁和管腔中均如此。
本研究强调二甲双胍显著增加结肠以及在较小程度上小肠的(18)F-FDG摄取。这就提出了在进行(18)F-FDG PET/CT扫描以评估腹内肿瘤病变之前停止二甲双胍治疗的问题。