Similar glucose control with basal bolus regimen of insulin detemir plus insulin aspart and thrice-daily biphasic insulin aspart 30 in insulin-naive patients with type 2 diabetes: Results of a 50-week randomized clinical trial of stepwise insulin intensification

被引:15
|
作者
Malek, R. [1 ]
Ajili, F. [2 ]
Assaad-Khalil, S. H. [3 ]
Shinde, A. [4 ]
Chen, J. W. [5 ]
Van den Berg, E. [6 ]
机构
[1] Saadna Univ Hosp, Dept Internal Med, Setif, Algeria
[2] Mil Hosp Tunis, Dept Internal Med, Tunis, Tunisia
[3] Univ Alexandria, Fac Med, Alexandria, Egypt
[4] FZ LLC, Novo Nordisk Pharma Gulf, Dubai, U Arab Emirates
[5] Novo Nordisk Reg Int Operat AS, Zurich, Switzerland
[6] Zuid Afrikaanse Hosp, Pretoria, South Africa
关键词
Type; 2; diabetes; Insulin intensification; Insulin detemir; Biphasic insulin aspart; Basal-bolus insulin; Premixed insulin; THERAPY; MANAGEMENT; GLARGINE; MELLITUS; HYPERGLYCEMIA; DRUGS;
D O I
10.1016/j.diabet.2014.11.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. This study aimed to demonstrate the non-inferiority of 50-week treatment with stepwise insulin intensification of basal bolus insulin analogues [insulin detemir (IDet) and aspart (IAsp)] versus biphasic insulin aspart 30 (BIAsp30) in insulin-naive type 2 diabetes mellitus (T2DM) patients not controlled by oral glucose-lowering drugs (OGLDs). Research design and methods. In this open-label multicentre, multinational, randomized, parallel-arm treat-to-target trial, 403 insulin-naive patients with T2DM in four African countries were randomized to either an IDet + IAsp (n=200) or BIAspl-2-3 (n=203) treatment group. Stepwise insulin intensification was performed at the end of 14, 26 and 38 weeks, depending on HbA(1c) values. The primary endpoint was change in HbA(1c) after 50 weeks of treatment. Safety variables were hypoglycaemia incidence, occurrence of adverse events and weight gain. Results. Non-inferiority of the IDet + IAsp versus BIAspl-2-3 treatment regimen was demonstrated by their similar HbA(1c) levels at the end of trial (IDet + IAsp: baseline 8.6%, 50 weeks 7.4%; BIAspl-2-3: baseline 8.7%, 50 weeks 7.3%; full analysis set difference: 0.1% [95% CI: 0.1, 0.3]; per protocol: 0.2% [95% CI: 0.1, 0.4]). At week 50, 40.3 and 44.9% of patients achieved HbA(1c) <7.0% with IDet + IAsp and BIAspl-2-3, respectively. The rate of overall hypoglycaemia during the trial was also similar in both groups (IDet + IAsp: 9.4 events/patient-year; BIAspl-2-3: 9.8 events/patient-year). Conclusion. Insulin initiation and intensification using IDet + IAsp was not inferior to BIAspl-2-3 in insulin-naive patients with T2DM not controlled by OGLDs. Both regimens led to similar reductions in HbA(1c) values after 50 weeks of treatment. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:223 / 230
页数:8
相关论文
共 50 条
  • [41] Efficacy and Safety of Once-Daily Insulin Degludec/Insulin Aspart versus Insulin Glargine (U100) for 52 Weeks in Insulin-Naive Patients with Type 2 Diabetes: A Randomized Controlled Trial
    Kumar, Ajay
    Franek, Edward
    Wise, Jonathan
    Niemeyer, Marcus
    Mersebach, Henriette
    Simo, Rafael
    PLOS ONE, 2016, 11 (10):
  • [42] Efficacy of biphasic insulin aspart 70/30 in insulin-naive patients with type 2 diabetes mellitus not achieving glycemic targets on oral antidiabetic agents
    Garber, Alan J.
    Jain, Rajeev
    Wahl, Timothy
    Moses, Alan
    Cao, Anjun
    Bressler, Peter
    DIABETES, 2006, 55 : A477 - A477
  • [43] Insulin detemir is associated with more predictable glycemic control and reduced risk of hypoglycemia than NPH insulin in patients with type 1 diabetes on a basal-bolus regimen with premeal insulin aspart
    Vague, P
    Selam, JL
    Skeie, S
    De Leeuw, I
    Elte, JWF
    Haahr, H
    Kristensen, A
    Draeger, E
    DIABETES CARE, 2003, 26 (03) : 590 - 596
  • [44] Insulin degludec/insulin aspart versus biphasic insulin aspart 30 in Asian patients with type 2 diabetes inadequately controlled on basal or pre-/self-mixed insulin: A 26-week, randomised, treat-to-target trial
    Kaneko, Shizuka
    Chow, Francis
    Choi, Dong Seop
    Taneda, Shinji
    Hirao, Koichi
    Park, Yongsoo
    Andersen, Thomas Hasseriis
    Gall, Mari-Anne
    Christiansen, Jens Sandahl
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2015, 107 (01) : 139 - 147
  • [45] Once weekly basal insulin Fc demonstrated similar glycaemic control to once daily insulin degludec in insulin-naive patients with type 2 diabetes
    Bue-Valleskey, J. M.
    Kazda, C.
    Ma, C.
    Chien, J.
    Zhang, Q.
    Chigutsa, E.
    Landschulz, W.
    Swan, J.
    Haupt, A.
    Frias, J.
    DIABETOLOGIA, 2022, 65 (SUPPL 1) : S334 - S334
  • [46] 28-week, randomized, multicenter, open-label, parallel-group phase III trial to investigate the efficacy and safety of biphasic insulin aspart 70 thrice-daily injections vs twice-daily injections of biphasic insulin aspart 30 in patients with type 2 diabetes
    Kadowaki, Takashi
    Nishida, Tomoyuki
    Kaku, Kohei
    JOURNAL OF DIABETES INVESTIGATION, 2010, 1 (03) : 103 - 110
  • [47] Switching to biphasic insulin aspart 30/50/70 from biphasic human insulin 30/50 in patients with type 2 diabetes in normal clinical practice: observational study results
    Nobels, Frank
    D'Hooge, Dirk
    Crenier, Laurent
    CURRENT MEDICAL RESEARCH AND OPINION, 2012, 28 (06) : 1017 - 1026
  • [48] Comparison of Insulin Detemir and Insulin Glargine in a Basal-Bolus Regimen, With Insulin Aspart as the Mealtime Insulin, in Patients With Type 1 Diabetes: A 52-Week, Multinational, Randomized, Open-Label, Parallel-Group, Treat-to-Target Noninferiority Trial
    Heller, Simon
    Koenen, Christoph
    Bode, Bruce
    CLINICAL THERAPEUTICS, 2009, 31 (10) : 2086 - 2097
  • [49] Patients with type 2 diabetes mellitus poorly controlled on biphasic human insulin alone show improved glucose control with biphasic insulin aspart 30
    Shestakova, Marina V.
    Lebedev, Nikolay
    Bech, Ole M.
    DIABETES, 2008, 57 : A560 - A560
  • [50] A randomized, treat-to-target trial comparing insulin lispro protamine suspension and insulin detemir in insulin-naive patients with Type 2 diabetes
    Fogelfeld, L.
    Dharmalingam, M.
    Robling, K.
    Jones, C.
    Swanson, D.
    Jacober, S.
    DIABETIC MEDICINE, 2010, 27 (02) : 181 - 188