Treat-to-target comparison between once daily biphasic insulin aspart 30 and insulin glargine in Chinese and Japanese insulin-naive subjects with type 2 diabetes

被引:16
作者
Yang, Wenying [1 ]
Xu, Xiangjin [2 ]
Liu, Xiaomin [3 ]
Yang, Gangyi [4 ]
Seino, Yutaka [5 ]
Andersen, Henning [6 ]
Jinnouchi, Hideaki [7 ]
机构
[1] China Japan Friendship Hosp, Dept Endocrinol, Beijing 100029, Peoples R China
[2] Fuzhou Gen Hosp, Dept Endocrinol, Fuzhou, Peoples R China
[3] Harbin Med Univ, Hosp 1, Dept Endocrinol, Harbin, Peoples R China
[4] Chongqing Med Univ, Affiliated Hosp 2, Dept Endocrinol, Chongqing, Peoples R China
[5] Kansai Elect Power Hosp, Osaka, Japan
[6] Novo Nordisk AS, Dept Med & Sci Ins & Dev, Soborg, Denmark
[7] Jinnouchi Hosp, Dept Internal Med, Kumamoto, Japan
关键词
Biphasic insulin aspart 30; Insulin glargine; Insulin initiation; Insulin naive; Insulin therapy; Type 2 diabetes mellitus; GLYCEMIC CONTROL; AMERICAN ASSOCIATION; BASAL INSULIN; MELLITUS; HYPERGLYCEMIA; COMBINATION; THERAPY; GLUCOSE;
D O I
10.1185/03007995.2013.838155
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To investigate whether once daily biphasic insulin aspart 30 (BIAsp 30) is noninferior to once daily insulin glargine (IGlar) among Chinese and Japanese insulin-naive subjects with type 2 diabetes mellitus (T2DM). Research design and methods: This was a 24 week treat-to-target trial (NCT01123980) that included patients with T2DM who were poorly controlled on a combination of metformin and insulin secretagogue (or with a maximum of one more OAD) for 6 months. Patients were randomized to once daily BIAsp 30 or once daily IGlar and their secretagogue standardized to glimepiride 4 mg/day, metformin to 1500 or 2500 mg/day before randomization. Results: At Week 24, mean change from baseline in HbA1c was -0.78 +/- 0.88% (mean +/- SD) and -0.65 +/- 0.92% (-8.49 +/- 9.65 and -7.08 +/- 10.1 mmol/mol) for the BIAsp 30 (n=261) and IGlar (n=260) groups, respectively. The stimated between-group difference (BIAsp 30 vs IGlar) in HbA1c change was -0.12% (95% Cl: -0.25, 0.02) (-1.28 mmol/mol [95% Cl: -2.75, 0.19]), thus treatment with BIAsp 30 was noninferior to IGlar with respect to HbA1c (non-inferiority margin 0.4%). Although reduction in mean 9-point self-measured plasma glucose (SMPG) profile was comparable between the two groups, BIAsp 30 showed significantly lower PG levels at three time points post-dinner and a higher PG level before dinner compared to the IGlar group (all p<0.05). Comparable number of subjects reported hypoglycemic events (155 [59.4%] for BIAsp 30, 148 [56.9%] for IGlar). Conclusions: BIAsp 30 once daily showed similar HbA1c reduction and a similar safety profile to IGlar when used in insulin-naive Chinese and Japanese patients on metformin and a sulfonylurea. Moreover, it provided a better coverage of post-dinner glycemic control needs than those who received IGlar. The open-label design and insufficient insulin dose titration were the main limitations of the study.
引用
收藏
页码:1599 / 1608
页数:10
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