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Postprandial blood glucose response to a standard test meal in insulin-requiring patients with diabetes treated with insulin lispro mix 50 or human insulin mix 50

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单位: [1]Peking Univ, Hosp 1, Dept Endocrinol, Beijing 100871, Peoples R China [2]Sino Japan Friendship Hosp, Dept Endocrinol, Beijing, Peoples R China [3]Sun Yat Sen Univ, Affiliated Hosp 2, Dept Endocrinol, Guangzhou 510275, Guangdong, Peoples R China [4]Eli Lilly Asia Inc, Shanghai Rap Off 21F, Shanghai 200021, Peoples R China
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Aim: To compare the 2-h postprandial blood glucose (PPBG) excursion following a standard test meal in insulin-requiring patients with diabetes treated twice daily with human insulin mix 50 vs. insulin lispro mix 50 (LM50). Methods: This was a multicentre, randomised, open-label, crossover comparison of two insulin treatments for two 12-week treatment periods in 120 Chinese patients. One- and 2-h PPBG and excursion values were obtained following a standardised test meal. Fasting blood glucose (FBG), haemoglobin A1c (HbA1c), insulin dose, rate of hypoglycaemia and safety data were obtained. A crossover analysis using SAS Proc MIXED was employed. Results: Mean 2-h PPBG excursion decreased from 6.32 +/- 3.07 mmol/l at baseline to 3.47 +/- 2.97 mmol/l at end-point in the LM50 group, and from 6.31 +/- 2.88 at baseline to 5.02 +/- 3.32 mmol/l at end-point in the human insulin mix 50 group (p < 0.001). Two-hour PPBG (p = 0.004) and 1-h PPBG excursion (p < 0.001) were significantly lower with LM50 as compared with human insulin mix 50. Both treatment groups were equivalent for HbA1c control, 1-h PPBG and insulin dose requirements. Mean FBG was higher with LM50 than with human insulin mix 50 (p = 0.023). The overall incidence of treatment-emergent adverse events and hypoglycaemia rate per 30 days were similar between treatment groups. Conclusions: Insulin lispro mix 50 provided better postprandial glycaemic control compared with human insulin mix 50 while providing the convenience of injecting immediately before meals. Both treatments were generally well tolerated by all randomly assigned patients.

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出版当年[2007]版:
大类 | 4 区 医学
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 医学:内科
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出版当年[2006]版:
Q3 MEDICINE, GENERAL & INTERNAL
最新[2023]版:
Q2 MEDICINE, GENERAL & INTERNAL

影响因子: 最新[2023版] 最新五年平均[2021-2025] 出版当年[2006版] 出版当年五年平均[2002-2006] 出版前一年[2005版] 出版后一年[2007版]

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第一作者单位: [1]Peking Univ, Hosp 1, Dept Endocrinol, Beijing 100871, Peoples R China
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通讯机构: [4]Eli Lilly Asia Inc, Shanghai Rap Off 21F, Shanghai 200021, Peoples R China [*1]Eli Lilly Asia Inc, Shanghai Rap Off 21F, 1 Corp Ave 222,Hu Bin Rd, Shanghai 200021, Peoples R China
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