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作 者:李顺斌[1] 邱蔚[1] 王文华[1] 施万春[1] 郑淑莺[1] 沈建国[2]
机构地区:[1]湖州市中心医院内分泌科,313000 [2]浙江大学附属第一医院内分泌科
出 处:《浙江医学》2014年第13期1141-1143,共3页Zhejiang Medical Journal
基 金:湖州市自然科学基金项目(2010YZ14)
摘 要:目的观察二肽基肽酶IV抑制剂沙格列汀对多种口服降糖药物治疗3个月以上血糖控制不良的2型糖尿病患者的疗效和安全性。方法入选研究对象90例,比较沙格列汀治疗前后空腹血糖、空腹胰岛素、服糖后1、2、3h血糖和胰岛素、糖化血红蛋白(HbA_1c)、TG、TC、LDL-C、HDL-C、胰高血糖素、BMI、胰高血糖素/胰岛素比值及稳态模型评估-胰岛素抵抗指数(HOMA-IR)。结果治疗后患者空腹血糖由(9.5±2.6)mmol/L降至(6.8±1.8)mmol/L、服糖后2h血糖由(14.8±3.2)mmol/L降至(8.9±2.3)mmol/L、HbA_1c由(8.4±2.2)%降至(7.0±1.3)%、服糖后2h胰高血糖素由(169.6±50.6)ng/L降至(101.4±40.8)ng/L,与治疗前比较均有统计学差异(均P<0.01),且无低血糖及体重增加等不良反应。结论沙格列汀能有效降低多种口服降糖药控制不良的2型糖尿病患者的血糖水平,具有良好的安全性。Objective To evaluate the efficacy and safety of dipeptidy1 peptidase- 4 inhibitor saxagliptin in patients with type 2 diabetes who were poorly control ed by multiple oral antidiabetic drugs. Methods Ninety type 2 diabetic patients who were poorly control ed by previous administration of oral antidiabetic drugs for at least 3 months were treated with saxagliptin. The changes of fasting plasma glucose (FPG), fasting plasma insulin (FINS), postprandial glucose and insulin (1, 2, 3h), HbA1c, TG, TC, LDL- C, HDL- C, glucagon, BMI, glucagon/insulin and HOMA- IR were measured before and after treatment. Results FPG, 2h postprandial glucose(2h PPG), HbA1c, 2h postprandial glucagon decreased significantly after saxagliptin treatment [(9.5±2.6) mmol/L vs (6.8±1.8)mmol/L, (14.8±3.2)mmol/Lvs (8.9±2.3)mmol/L, (8.4±2.2)%vs (7.0±1.3)%, (169.6±50.6)ng/L vs(101.4± 40.8)ng/L,respectively, al P〈0.01].There was no hypoglycemia, weight gain or other adverse reactions. Conclusion Saxagliptin can effectively reduce the blood sugar leve1s in type 2 diabetics poorly control ed by multiple oral antidiabetic drugs with an excellent safety profile.
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