Marked Improvement in Glycemic Control with Exenatide on Addition to Metformin, Sulfonylurea and Insulin Glargine in Type 2 Diabetes Mellitus, a Real World Experience

IF 1.3 4区 计算机科学 Q3 COMPUTER SCIENCE, INFORMATION SYSTEMS
Salina Esmail, S. Banzal, U. Kabadi
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Abstract

Background: The major effect of Exenatide is attributed to lowering of post-prandial glycemia, whereas insulin glargine mainly improves fasting glycemia [FPG]. Objective: Therefore, we assessed effect of Exenatide administration at 6 months and for at 1 year on glycemic control, lipids, body weight [BW], daily insulin dose and hypoglycemic events. Methods: Records of 164 subjects, 126 men and 38 women administered Exenatide between January 2011 and December 2013 are included in this report. Exenatide was initiated at 5 mcg subcutaneously twice daily [BID] in obese subjects, BMI > 30 kg/m2, with C-peptide > 1 ng/d, and HbA1c 7.5% - 9.5%, while receiving daily metformin 2000 mg, Sulfonylurea Glimepiride 8 mg and insulin Glargine [GLAR]. Exclusion criteria were creatinine > 1.5 mg/dL and liver enzymes > 2.5 times upper limit of normal. Indices of glycemic control include fasting plasma glucose levels and HbA1c. Lipids include serum concentrations of total, LDL and HDL cholesterol. Other endpoints are body weight, daily insulin dose and number of hypoglycemic events per patient during 4 weeks prior to initiation of Exenatide, at 6 months and 1 year of therapy. Results: In 37 subjects, Exenatide was discontinued within 1 - 3 weeks; 29 due to onset of nausea and vomiting. Seven of these also complained of abdominal pain and in these, serum amylase and lipase were elevated indicating presence of acute pancreatitis. One subject discontinued because of chest pain. Fasting plasma Glucose remained unchanged following Exenatide administration. However, HbA1c declined significantly denoting improvement in overall glycemic control without significant changes in body weight, daily insulin dose and hypoglycemic events. Lipid panel improved as well. Conclusion: Exenatide may be an appropriate adjuvant option in obese subjects with Type 2 diabetes mellitus with lack of desirable glycemic control while receiving therapy with Metformin, Glimepiride, and insulin Glargine. Moreover, improvement in glycemic control is likely to be secondary to lowering of post prandial hyperglycemia induced by Exenatide.
艾塞那肽加二甲双胍、磺脲和甘精胰岛素对2型糖尿病血糖控制的显著改善,一个真实的世界经验
背景:艾塞那肽的主要作用是降低餐后血糖,而甘精胰岛素主要改善空腹血糖[FPG]。目的:因此,我们评估了6个月和1年给药艾塞那肽对血糖控制、血脂、体重、每日胰岛素剂量和低血糖事件的影响。方法:收集2011年1月至2013年12月使用艾塞那肽的164例患者,其中男性126例,女性38例。体重指数> 30 kg/m2, c肽> 1 ng/d,糖化血红蛋白7.5% - 9.5%,同时每日给予二甲双胍2000 mg,磺酰脲格列美脲8 mg和甘精胰岛素[GLAR],埃塞那肽5 mcg皮下注射[BID]。排除标准为肌酐> 1.5 mg/dL,肝酶> 2.5倍正常值上限。血糖控制指标包括空腹血糖水平和糖化血红蛋白。血脂包括血清总胆固醇、低密度脂蛋白和高密度脂蛋白的浓度。其他终点是体重、每日胰岛素剂量和每名患者在艾塞那肽开始治疗前4周、治疗6个月和1年期间的低血糖事件数。结果:37例受试者在1 - 3周内停用艾塞那肽;由于恶心和呕吐。其中7人还抱怨腹痛,在这些人中,血清淀粉酶和脂肪酶升高表明存在急性胰腺炎。一名受试者因胸痛停药。服用艾塞那肽后,空腹血糖保持不变。然而,HbA1c显著下降,表明总体血糖控制得到改善,而体重、每日胰岛素剂量和低血糖事件没有显著变化。脂质组也有所改善。结论:对于接受二甲双胍、格列美脲和甘精胰岛素治疗且血糖控制不佳的肥胖2型糖尿病患者,艾塞那肽可能是一种合适的辅助选择。此外,血糖控制的改善可能继发于艾塞那肽引起的餐后高血糖的降低。
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来源期刊
Journal of Database Management
Journal of Database Management 工程技术-计算机:软件工程
CiteScore
4.20
自引率
23.10%
发文量
24
期刊介绍: The Journal of Database Management (JDM) publishes original research on all aspects of database management, design science, systems analysis and design, and software engineering. The primary mission of JDM is to be instrumental in the improvement and development of theory and practice related to information technology, information systems, and management of knowledge resources. The journal is targeted at both academic researchers and practicing IT professionals.
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