Viswanathan Prabhakar, Chaudhuri Ajay, Bhatia Ruchi, Al-Atrash Fida, Mohanty Priya, Dandona Paresh
The Division of Endocrinology, Diabetes, and Metabolism, State University of New York, Buffalo, and Kaleida Health, Buffalo, New York, USA.
Endocr Pract. 2007 Sep;13(5):444-50. doi: 10.4158/EP.13.5.444.
To evaluate the effect of exenatide on clinical parameters in obese patients with type 2 diabetes mellitus whose hyperglycemia is not adequately controlled despite treatment with oral hypoglycemic agents and insulin.
In this retrospective analysis, clinical progress of 52 obese patients with type 2 diabetes treated with exenatide, 5 mcg twice daily, in an outpatient setting was reviewed. Treatment initiation was between September and December 2005. Mean follow-up period was 26 weeks. Thirty-eight patients took exenatide regularly (Group A); 14 patients discontinued exenatide because of insurance, personal, or economic reasons (Group B). Measurements at baseline and at follow-up included body weight; blood pressure; and levels of hemoglobin A1c (HbA1c), high-sensitivity C-reactive protein (CRP), and plasma lipids. Insulin dosage requirements were assessed.
Mean body weight (+/- standard error of the mean) decreased by 6.46 +/- 0.8 kg (P<.001) in Group A and increased by 2.4 +/- 0.6 kg in Group B (P<001). In Group A, mean HbA1c decreased by 0.6 +/- 0.21% (P = .007), and the insulin dosage requirement decreased for rapid-acting and mixed insulins (P<.02). In Group A, means of the following parameters decreased: serum total cholesterol by 8.5 +/- 3.3% (P = .03), triglycerides by 26 +/- 7.6% (P = .01), systolic blood pressure by 9.2 +/- 3.3 mm Hg (P = .02), and high-sensitivity CRP by 34 +/- 14.3% (P = .05). These indices did not change in Group B.
Exenatide effectively treats obese patients with type 2 diabetes on insulin, leading to weight loss and reduction in levels of HbA1c, systolic blood pressure, triglycerides, and high-sensitivity CRP.
评估艾塞那肽对尽管接受口服降糖药和胰岛素治疗但血糖控制不佳的肥胖2型糖尿病患者临床参数的影响。
在这项回顾性分析中,回顾了52例在门诊接受每日两次5微克艾塞那肽治疗的肥胖2型糖尿病患者的临床进展。治疗开始于2005年9月至12月。平均随访期为26周。38例患者规律服用艾塞那肽(A组);14例患者因保险、个人或经济原因停用艾塞那肽(B组)。基线和随访时的测量指标包括体重、血压、糖化血红蛋白(HbA1c)水平、高敏C反应蛋白(CRP)水平和血脂水平。评估胰岛素剂量需求。
A组平均体重(±平均标准误差)下降了6.46±0.8千克(P<0.001),B组增加了2.4±0.6千克(P<0.001)。在A组中,平均HbA1c下降了0.6±0.21%(P = 0.007),速效胰岛素和预混胰岛素的剂量需求降低(P<0.02)。在A组中,以下参数的均值下降:血清总胆固醇下降8.5±3.3%(P = 0.03),甘油三酯下降26±7.6%(P = 0.01),收缩压下降9.2±3.3毫米汞柱(P = 0.02),高敏CRP下降34±14.3%(P = 0.05)。这些指标在B组中未发生变化。
艾塞那肽可有效治疗接受胰岛素治疗的肥胖2型糖尿病患者,导致体重减轻以及HbA1c、收缩压、甘油三酯和高敏CRP水平降低。