Comparison of liraglutide plus basal insulin and basal-bolus insulin therapy (BBIT) for glycemic control, body weight stability, and treatment satisfaction in patients treated using BBIT for type 2 diabetes without severe insulin deficiency: A randomized prospective pilot study

被引:11
作者
Yamamoto, Saki [1 ]
Hayashi, Toshiyuki [1 ]
Ohara, Makoto [1 ]
Goto, Satoshi [1 ]
Sato, Jun [1 ]
Nagaike, Hiroe [1 ]
Fukase, Ayako [1 ]
Sato, Nobuko [1 ]
Hiromura, Munenori [1 ]
Tomoyasu, Masako [1 ]
Nakanishi, Noriko [1 ]
Lee, Soushou [1 ]
Osamura, Anna [1 ]
Yamamoto, Takeshi [1 ]
Fukui, Tomoyasu [1 ]
Hirano, Tsutomu [1 ]
机构
[1] Showa Univ, Dept Med, Div Diabet Metab & Endocrinol, Sch Med, Tokyo, Japan
关键词
Liraglutide; Basal-bolus insulin therapy; Type; 2; diabetes; Body weight; Treatment satisfaction; JAPANESE PATIENTS; GLP-1; ANALOG; C-PEPTIDE; MELLITUS; SULFONYLUREA; EFFICACY; PEOPLE; SAFETY;
D O I
10.1016/j.diabres.2018.03.032
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: We examined whether 0.9 mg/day liraglutide plus basal insulin (Lira-basal) is superior to basal-bolus insulin therapy (BBIT) for type 2 diabetes (T2DM) without severe insulin deficiency as determined by glucagon stimulation. Methods: Fifty patients receiving BBIT were enrolled in this 24-week, prospective, randomized, open-labeled study. After excluding subjects with fasting C-peptide immunoreactivity (CPR) <1.0 ng/mL and CPR increase <1.0 ng/mL at 6 min post glucagon injection, 25 were randomly allocated to receive Lira-basal (n = 12) or continued BBIT (n = 13). Primary end-point was change in HbAlc. Secondary endpoints were changes in body weight (BW), 7-point self-monitored blood glucose (SMBG), and Diabetes Treatment Satisfaction Questionnaire status (DTSQs) scores. Result: The Lira-basal group demonstrated reduced HbAlc, whereas the BBIT group showed no change. BW was reduced in the Lira-basal group but increased in the BBIT group. The Lira-basal group also exhibited significantly reduced pre-breakfast and pre-lunch SMBG. DTSQs scores improved in the Lira-basal group but not the BBIT group. Plasma lipids, liver function, and kidney function were not significantly changed in either group. Conclusions: Lira-basal therapy is superior to BBIT for T2DM without severe insulin deficiency. (C) 2018 The Authors Published by Elsevier B.V.
引用
收藏
页码:339 / 346
页数:8
相关论文
共 32 条
[1]   A meta-analysis comparing clinical effects of short- or long-acting GLP-1 receptor agonists versus insulin treatment from head-to-head studies in type 2 diabetic patients [J].
Abd El Aziz, Mirna S. ;
Kahle, Melanie ;
Meier, Juris J. ;
Nauck, Michael A. .
DIABETES OBESITY & METABOLISM, 2017, 19 (02) :216-227
[2]  
[Anonymous], 1995, Diabetes, V44, P1249
[3]   The association between symptomatic, severe hypoglycaemia and mortality in type 2 diabetes: retrospective epidemiological analysis of the ACCORD study [J].
Bonds, Denise E. ;
Miller, Michael E. ;
Bergenstal, Richard M. ;
Buse, John B. ;
Byington, Robert P. ;
Cutler, Jeff A. ;
Dudl, R. James ;
Ismail-Beigi, Faramarz ;
Kimel, Angela R. ;
Hoogwerf, Byron ;
Horowitz, Karen R. ;
Savage, Peter J. ;
Seaquist, Elizabeth R. ;
Simmons, Debra L. ;
Sivitz, William I. ;
Speril-Hillen, Joann M. ;
Sweeney, Mary Ellen .
BMJ-BRITISH MEDICAL JOURNAL, 2010, 340 :137
[4]   MEASURES OF PSYCHOLOGICAL WELL-BEING AND TREATMENT SATISFACTION DEVELOPED FROM THE RESPONSES OF PEOPLE WITH TABLET-TREATED DIABETES [J].
BRADLEY, C ;
LEWIS, KS .
DIABETIC MEDICINE, 1990, 7 (05) :445-451
[5]   The Diabetes Treatment Satisfaction Questionnaire change version (DTSQc) evaluated in insulin glargine trials shows greater responsiveness to improvements than the original DTSQ [J].
Bradley, Clare ;
Plowright, Rosalind ;
Stewart, John ;
Valentine, John ;
Witthaus, Elke .
HEALTH AND QUALITY OF LIFE OUTCOMES, 2007, 5 (1)
[6]   One-year treatment with exenatide vs. Insulin Glargine: Effects on postprandial glycemia, lipid profiles, and oxidative stress [J].
Bunck, Mathijs C. ;
Corner, Anja ;
Eliasson, Bjorn ;
Heine, Robert J. ;
Shaginian, Rimma M. ;
Wu, Yan ;
Yan, Ping ;
Smith, Ulf ;
Yki-Jarvinen, Hannele ;
Diamant, Michaela ;
Taskinen, Marja-Riitta .
ATHEROSCLEROSIS, 2010, 212 (01) :223-229
[7]   Liraglutide reverses pronounced insulin-associated weight gain, improves glycaemic control and decreases insulin dose in patients with type 2 diabetes: a 26 week, randomised clinical trial (ELEGANT) [J].
de Wit, Helena M. ;
Vervoort, Gerald M. M. ;
Jansen, Henry J. ;
de Grauw, Wim J. C. ;
de Galan, Bastiaan E. ;
Tack, Cees J. .
DIABETOLOGIA, 2014, 57 (09) :1812-1819
[8]   Prevalence and associated metabolic factors of nonalcoholic fatty liver disease in the general population from 2009 to 2010 in Japan: a multicenter large retrospective study [J].
Eguchi, Yuichiro ;
Hyogo, Hideyuki ;
Ono, Masafumi ;
Mizuta, Toshihiko ;
Ono, Naofumi ;
Fujimoto, Kazuma ;
Chayama, Kazuaki ;
Saibara, Toshiji .
JOURNAL OF GASTROENTEROLOGY, 2012, 47 (05) :586-595
[9]   C-PEPTIDE RESPONSE TO GLUCAGON - TEST FOR RESIDUAL BETA-CELL FUNCTION IN DIABETES-MELLITUS [J].
FABER, OK ;
BINDER, C .
DIABETES, 1977, 26 (07) :605-610
[10]   The Once-Daily Human Glucagon-Like Peptide-1 (GLP-1) Analog Liraglutide Improves Postprandial Glucose Levels in Type 2 Diabetes Patients [J].
Flint, Anne ;
Kapitza, Christoph ;
Hindsberger, Charlotte ;
Zdravkovic, Milan .
ADVANCES IN THERAPY, 2011, 28 (03) :213-226