Initial injectable therapy in type 2 diabetes: Key considerations when choosing between glucagon-like peptide 1 receptor agonists and insulin

被引:19
作者
Alexopoulos, Anastasia-Stefania [1 ]
Buse, John B. [2 ]
机构
[1] Duke Univ, Med Ctr, Durham, NC 27708 USA
[2] Univ N Carolina, Chapel Hill, NC 27515 USA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2019年 / 98卷
基金
美国国家卫生研究院;
关键词
FIXED-RATIO COMBINATION; ACHIEVE GLYCEMIC CONTROL; ONCE-WEEKLY SEMAGLUTIDE; OPEN-LABEL; BASAL INSULIN; PARALLEL-GROUP; WEEKLY EXENATIDE; WEIGHT-GAIN; CARDIOVASCULAR OUTCOMES; CLINICAL-TRIAL;
D O I
10.1016/j.metabol.2019.06.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Managing type 2 diabetes is complex and necessitates careful consideration of patient factors such as engagement in self-care, comorbidities and costs. Since type 2 diabetes is a progressive disease, many patients will require injectable agents, usually insulin. Recent ADA-EASD guidelines recommend glucagon-like peptide 1 receptor agonists (GLP-1 RAs) as first injectable therapy in most cases. The basis for this recommendation is the similar glycemic efficacy of GLP-1 RAs and insulin, but with GLP-1 RAs promoting weight loss instead of weight gain, at lower hypoglycemia risk, and with cardiovascular benefits in patients with pre-existing cardiovascular disease. GLP-1 RAs also reduce burden of glucose self-monitoring. However, tolerability and costs are important considerations, and notably, rates of drug discontinuation are often higher for GLP-1 RAs than basal insulin. To minimize risk of gastrointestinal symptoms patients should be started on lowest doses of GLP-1 RAs and up-titrated slowly. Overall healthcare costs may be lower with GLP-1 RAs compared to insulin. Though patient-level costs may still be prohibitive, GLP-1 RAs can replace 50-80 units of insulin daily and reduce costs associated with glucose self-monitoring. Decisions regarding initiating injectable therapy should be individualized. This review provides a framework to guide decision-making in the real-world setting. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:104 / 111
页数:8
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