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
相关论文
共 81 条
[51]   Efficacy and Safety Profile of Exenatide Once Weekly Compared With Insulin Once Daily in Japanese Patients With Type 2 Diabetes Treated With Oral Antidiabetes Drug(s): Results From a 26-Week, Randomized, Open-Label, Parallel-Group, Multicenter, Noninferiority Study [J].
Inagaki, Nobuya ;
Atsumi, Yoshihito ;
Oura, Tomonori ;
Saito, Hitoshi ;
Imaoka, Takeshi .
CLINICAL THERAPEUTICS, 2012, 34 (09) :1892-1908
[52]   Glucagon-like peptide- I receptor agonists: a systematic review of comparative effectiveness research [J].
Levin, Philip A. ;
Nguyen, Hiep ;
Wittbrodt, Eric T. ;
Kim, Seoyoung C. .
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY, 2017, 10 :123-139
[53]   Efficacy and Acceptability of Glycemic Control of Glucagon-Like Peptide-1 Receptor Agonists among Type 2 Diabetes: A Systematic Review and Network Meta-Analysis [J].
Li, Zhixia ;
Zhang, Yuan ;
Quan, Xiaochi ;
Yang, Zhirong ;
Zeng, Xiantao ;
Ji, Linong ;
Sun, Feng ;
Zhan, Siyan .
PLOS ONE, 2016, 11 (05)
[54]   Effect of Insulin Glargine Up-titration vs Insulin Degludec/Liraglutide on Glycated Hemoglobin Levels in Patients With Uncontrolled Type 2 Diabetes The DUAL V Randomized Clinical Trial [J].
Lingvay, Ildiko ;
Perez Manghi, Federico ;
Garcia-Hernandez, Pedro ;
Norwood, Paul ;
Lehmann, Lucine ;
Tarp-Johansen, Mads Jeppe ;
Buse, John B. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 315 (09) :898-907
[55]   Trends in Medicaid Reimbursements for Insulin From 1991 Through 2014 [J].
Luo, Jing ;
Avorn, Jerry ;
Kesselheim, Aaron S. .
JAMA INTERNAL MEDICINE, 2015, 175 (10) :1681-1686
[56]   Free and fixed-ratio combinations of basal insulin and GLP-1 receptor agonists versus basal insulin intensification in type 2 diabetes: A systematic review and meta-analysis of randomized controlled trials [J].
Maiorino, Maria Ida ;
Chiodini, Paolo ;
Bellastella, Giuseppe ;
Scappaticcio, Lorenzo ;
Longo, Miriam ;
Esposito, Katherine ;
Giugliano, Dario .
DIABETES OBESITY & METABOLISM, 2018, 20 (09) :2309-2313
[57]   Efficacy and Safety of Degludec versus Glargine in Type 2 Diabetes [J].
Marso, Steven P. ;
McGuire, Darren K. ;
Zinman, Bernard ;
Poulter, Neil R. ;
Emerson, Scott S. ;
Pieber, Thomas R. ;
Pratley, Richard E. ;
Haahr, Poul-Martin ;
Lange, Martin ;
Brown-Frandsen, Kirstine ;
Moses, Alan ;
Skibsted, Simon ;
Kvist, Kajsa ;
Buse, John B. ;
Buse, John B. ;
Hansen, Liliana ;
Marso, Steven P. ;
Rabol, Rasmus ;
Zinman, Bernard ;
Bethel, Angelyn ;
de Lemos, James A. ;
Senn, Stephen ;
Schwamm, Lee ;
Timmis, Adam ;
Alshekhlee, Amer ;
Bach, Richard G. ;
Bertram, Therese M. ;
Chaitman, Bernard R. ;
Cruz-Flores, Salvador ;
Eckstein, Jane F. ;
Feen, Eliahu S. ;
Fisher, Simon J. ;
Gosselin, Gilbert ;
Lim, Michael J. ;
Rosenzweig, James L. ;
Sherwin, Robert S. ;
Tobin, Garry S. ;
Vetrovec, George ;
Ziemer, David C. ;
Daugaard, Gedske ;
Ozlem, Er ;
Pollak, Michael ;
Sengelov, Lisa ;
Ahn, Yu-Bae ;
Amod, Aslam ;
Benroubi, Mariana ;
Boonyavarakul, Apussanee ;
Canecki-Varzic, Silvija ;
Consoli, Agostino ;
Eliaschewitz, Freddy G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (08) :723-732
[58]   Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes [J].
Marso, Steven P. ;
Daniels, Gilbert H. ;
Brown-Frandsen, Kirstine ;
Kristensen, Peter ;
Mann, Johannes F. E. ;
Nauck, Michael A. ;
Nissen, Steven E. ;
Pocock, Stuart ;
Poulter, Neil R. ;
Ravn, Lasse S. ;
Steinberg, William M. ;
Stockner, Mette ;
Zinman, Bernard ;
Bergenstal, Richard M. ;
Buse, John B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (04) :311-322
[59]   A comparison of adding liraglutide versus a single daily dose of insulin aspart to insulin degludec in subjects with type 2 diabetes (BEGIN: VICTOZA ADD-ON) [J].
Mathieu, C. ;
Rodbard, H. W. ;
Cariou, B. ;
Handelsman, Y. ;
Philis-Tsimikas, A. ;
Francisco, A. M. Ocampo ;
Rana, A. ;
Zinman, B. .
DIABETES OBESITY & METABOLISM, 2014, 16 (07) :636-644
[60]   Is there a justification for classifying GLP-1 receptor agonists as basal and prandial? [J].
Minambres, Inka ;
Perez, Antonio .
DIABETOLOGY & METABOLIC SYNDROME, 2017, 9