Zhao Xiaotong, Li Yongxiangi, Chen Mingwei, Chen Yan, Dai Yao, Wang Youming, Xie Huijuan
aDepartment of Endocrinology bDivision of General Surgery cDivision of Endoscopy, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Eur J Cancer Prev. 2015 Jan;24(1):27-36. doi: 10.1097/CEJ.0000000000000078.
This research was carried out to evaluate the chemopreventive effects of different doses of metformin treatment for 6 months on rectal aberrant crypt foci (ACF) in patients with impaired glucose tolerance (IGT). A total of 120 Chinese patients with IGT were enrolled and assigned randomly to a low-dose metformin group (n=30, metformin at 250 mg/day), a middle-dose metformin group (n=30, metformin at 500 mg/day), a high-dose metformin group (n=30, metformin at 1500 mg/day), and a control (untreated with metformin) group (n=30). Each participant was followed for 6 months by protocol, and the number of ACF per patient in the above four groups was examined by magnifying colonoscopy before, and after 3 and 6 months of, treatment. The mean ACF numbers in both the middle-dose and the high-dose metformin groups were significantly decreased at 3 as well as 6 months of treatment, whereas they did not change in the low-dose metformin and the untreated groups. In the high-dose metformin group, BMI, waist circumference, fasting plasma glucose, homeostatic model assessment of insulin resistance index, and 2-h plasma glucose were significantly decreased. However, no such change was observed in the middle-dose metformin group. Changes in the ACF number correlated positively with changes in the homeostatic model assessment of insulin resistance (r=0.273, P=0.013), BMI (r=0.241, P=0.042), and 2-h plasma glucose (r=0.252, P=0.037), respectively, in the high-dose metformin group, but no such correlation was observed in the middle-dose metformin group. Metformin suppressed ACF formation in IGT patients in a dose-dependent manner, possibly through direct and indirect (attenuating insulin resistance) mechanisms.
本研究旨在评估不同剂量二甲双胍治疗6个月对糖耐量受损(IGT)患者直肠异常隐窝灶(ACF)的化学预防作用。共纳入120例中国IGT患者,随机分为低剂量二甲双胍组(n = 30,二甲双胍250 mg/天)、中剂量二甲双胍组(n = 30,二甲双胍500 mg/天)、高剂量二甲双胍组(n = 30,二甲双胍1500 mg/天)和对照组(未用二甲双胍治疗,n = 30)。按照方案对每位参与者随访6个月,并在治疗前、治疗3个月和6个月后通过放大结肠镜检查上述四组中每位患者的ACF数量。中剂量和高剂量二甲双胍组在治疗3个月和6个月时的平均ACF数量均显著减少,而低剂量二甲双胍组和未治疗组则无变化。高剂量二甲双胍组的体重指数、腰围、空腹血糖、胰岛素抵抗指数的稳态模型评估值和2小时血糖均显著降低。然而,中剂量二甲双胍组未观察到此类变化。在高剂量二甲双胍组中,ACF数量的变化分别与胰岛素抵抗的稳态模型评估值变化(r = 0.273,P = 0.013)、体重指数变化(r = 0.241,P = 0.042)和2小时血糖变化(r = 0.252,P = 0.037)呈正相关,但中剂量二甲双胍组未观察到此类相关性。二甲双胍以剂量依赖方式抑制IGT患者的ACF形成,可能是通过直接和间接(减轻胰岛素抵抗)机制实现的。