The effects of exenatide twice daily compared to insulin lispro added to basal insulin in Latin American patients with type 2 diabetes: A retrospective analysis of the 4B trial

被引:2
|
作者
Beatriz Gorban de Lapertosa, Silvia [1 ]
Frechtel, Gustavo [2 ]
Hardy, Elise [3 ]
Sauque-Reyna, Leobardo [4 ]
机构
[1] Natl Univ Northeast, Sch Med, Corrientes, Argentina
[2] Univ Buenos Aires, Hosp Clin, Cordoba 2351,C1120AAR CABA, RA-1419 Buenos Aires, DF, Argentina
[3] AstraZeneca, Gaithersburg, MD USA
[4] Soc Civil, Inst Diabet Obesidad & Nutr, Cuernavaca, Morelos, Mexico
关键词
Exenatide; Insulin lispro; Type; 2; diabetes; Latin America; RECEPTOR AGONISTS; SAFETY DATA; EFFICACY; CLASSIFICATION; LIRAGLUTIDE; STATEMENT; UPDATE;
D O I
10.1016/j.diabres.2016.10.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: Socioeconomic changes in Latin American countries have led to an increased prevalence of type 2 diabetes (T2D). We examined the effects of exenatide twice daily (BID) or insulin lispro, each added to insulin glargine, in Latin American patients with T2D. Methods: This was a subgroup analysis of patients from Argentina and Mexico in the 4B study (N = 114). Patients with glycated hemoglobin (HbA1c) of 7.0-10.0% (53-86 mmol/mol) after 12 weeks of intensive basal insulin optimization were randomized to exenatide BID or thrice-daily insulin lispro added to insulin glargine and metformin. Results: After 30 weeks, addition of exenatide BID or insulin lispro resulted in significant (P < 0.0001) reductions in HbA1c (exenatide BID: -0.9% [-10 mmol/mol]; insulin lispro: -1.2% [-13 mmol/mol]). Weight was stable in the exenatide BID group (-0.1 kg) and increased significantly (+3.4 kg; P < 0.0001) with insulin lispro. Major and minor hypoglycemia occurred less frequently (40 vs. 253 events) with exenatide BID compared with insulin lispro. Gastrointestinal adverse events of nausea, diarrhea, and vomiting occurred more frequently with exenatide BID than with insulin lispro. Conclusions: Both exenatide BID and prandial insulin lispro, each added to basal insulin glargine, were effective at reducing HbA1c in Latin American patients. Treatment with exenatide BID resulted in stable weight but more gastrointestinal adverse events. Treatment with insulin lispro resulted in weight gain and an increased risk of hypoglycemia. These findings support the addition of exenatide BID to insulin glargine as an option for Latin American patients unable to achieve glycemic control on basal insulin alone. (C) 2016 The Authors. Published by Elsevier Ireland Ltd.
引用
收藏
页码:38 / 45
页数:8
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