Basal‐prandial versus premixed insulin in patients with type 2 diabetes requiring insulin intensification after basal insulin optimization: A 24‐week randomized non‐inferiority trial1. (29th June 2015)
- Record Type:
- Journal Article
- Title:
- Basal‐prandial versus premixed insulin in patients with type 2 diabetes requiring insulin intensification after basal insulin optimization: A 24‐week randomized non‐inferiority trial1. (29th June 2015)
- Main Title:
- Basal‐prandial versus premixed insulin in patients with type 2 diabetes requiring insulin intensification after basal insulin optimization: A 24‐week randomized non‐inferiority trial1
- Authors:
- Jin, Sang‐Man
Kim, Jae Hyeon
Min, Kyung Wan
Lee, Ji Hyun
Ahn, Kue Jeong
Park, Jeong Hyun
Jang, Hak Chul
Park, Seok Won
Lee, Kwan Woo
Won, Kyu Chang
Kim, Young‐Il
Chung, Choon Hee
Park, Tae Sun
Lee, Jee‐Hyun
Lee, Moon‐Kyu - Abstract:
- Abstract: Background: The aim of the present 24‐week multicentre randomized non‐inferiority trial was to compare the efficacy and safety of two insulin intensification strategies in uncontrolled type 2 diabetes despite optimized basal insulin therapy. Methods: Patients with fasting plasma glucose (FPG) <130 mg/dL and HbA1c 7.0%–10.0% while on insulin glargine were randomized to a basal‐prandial group (stepwise addition of insulin glulisine) or a premixed insulin group (insulin aspart/insulin aspart protamine 30/70 starting with 6 IU twice daily). The primary endpoint was the change in HbA1c after 24 weeks (non‐inferiority margin 0.4%). Results: At Week 24, the adjusted mean change from baseline HbA1c was –0.94 ± 0.09% and –1.04 ± 0.09% in basal‐prandial and premixed insulin groups, respectively, with a mean difference of –0.09% (95% confidence interval [CI] –0.35, 0.16). A lower rate of hypoglycemia with a similar reduction in HbA1c was observed during stabilization of the total daily insulin dose in the premixed insulin group (Weeks 0–12). After stabilization of the total daily insulin dose, the rate of hypoglycemia and the total daily insulin dose were similar in the two groups. Conclusions: The efficacy and safety of the two intensifying regimens were similar after stabilization of the total daily insulin dose when oral agents were maintained. Starting with a lower total daily insulin dose with a gradual change in the treatment regimen was helpful in reducing the rate ofAbstract: Background: The aim of the present 24‐week multicentre randomized non‐inferiority trial was to compare the efficacy and safety of two insulin intensification strategies in uncontrolled type 2 diabetes despite optimized basal insulin therapy. Methods: Patients with fasting plasma glucose (FPG) <130 mg/dL and HbA1c 7.0%–10.0% while on insulin glargine were randomized to a basal‐prandial group (stepwise addition of insulin glulisine) or a premixed insulin group (insulin aspart/insulin aspart protamine 30/70 starting with 6 IU twice daily). The primary endpoint was the change in HbA1c after 24 weeks (non‐inferiority margin 0.4%). Results: At Week 24, the adjusted mean change from baseline HbA1c was –0.94 ± 0.09% and –1.04 ± 0.09% in basal‐prandial and premixed insulin groups, respectively, with a mean difference of –0.09% (95% confidence interval [CI] –0.35, 0.16). A lower rate of hypoglycemia with a similar reduction in HbA1c was observed during stabilization of the total daily insulin dose in the premixed insulin group (Weeks 0–12). After stabilization of the total daily insulin dose, the rate of hypoglycemia and the total daily insulin dose were similar in the two groups. Conclusions: The efficacy and safety of the two intensifying regimens were similar after stabilization of the total daily insulin dose when oral agents were maintained. Starting with a lower total daily insulin dose with a gradual change in the treatment regimen was helpful in reducing the rate of hypoglycemia during initial stabilization of the total daily insulin dose. … (more)
- Is Part Of:
- Journal of diabetes. Volume 8:Number 3(2016:May)
- Journal:
- Journal of diabetes
- Issue:
- Volume 8:Number 3(2016:May)
- Issue Display:
- Volume 8, Issue 3 (2016)
- Year:
- 2016
- Volume:
- 8
- Issue:
- 3
- Issue Sort Value:
- 2016-0008-0003-0000
- Page Start:
- 405
- Page End:
- 413
- Publication Date:
- 2015-06-29
- Subjects:
- basal‐prandial -- glargine -- glulisine -- premixed insulin
基础‐餐时 -- 甘精胰岛素 -- 赖谷胰岛素 -- 预混胰岛素
Diabetes -- Periodicals
618.3646005 - Journal URLs:
- http://www3.interscience.wiley.com/journal/118902543/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1753-0407.12312 ↗
- Languages:
- English
- ISSNs:
- 1753-0393
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4969.405000
British Library DSC - BLDSS-3PM
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- 1234.xml