首页> 外文期刊>Diabetes, obesity & metabolism >Comparison between a basal-bolus and a premixed insulin regimen in individuals with type 2 diabetes-results of the GINGER study.
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Comparison between a basal-bolus and a premixed insulin regimen in individuals with type 2 diabetes-results of the GINGER study.

机译:GINGER研究的2型糖尿病患者基础推注和预混胰岛素方案之间的比较。

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AIM: To compare the efficacy and safety of an intensified insulin regimen, using insulin glargine (glargine) once daily and pre-meal insulin glulisine (glulisine) (basal-bolus), with a conventional therapy, using premixed insulin (premix) twice daily. METHODS: This 52-week, open-label, randomized, multinational, multicentre trial included 310 subjects with type 2 diabetes (T2D) on premix, with or without metformin, who were randomized to a basal-bolus regimen with glargine and glulisine (n = 153; mean +/- s.d. age 60.2 +/- 7.5 years; HbA1c 8.6 +/- 0.8%; weight 87.0 +/- 15.1 kg; T2D duration 12.8 +/- 5.8 years) or twice-daily premix (n = 157; age 60.9 +/- 7.8 years; HbA1c 8.5 +/- 0.9%; weight 84.3 +/- 15.0 kg; T2D duration 12.5 +/- 6.8 years). The primary endpoint was change in HbA1c from baseline to endpoint. RESULTS: Mean decrease in baseline-to-endpoint HbA1c for basal-bolus vs. premix was -1.31 vs. -0.80% (difference: -0.476%; 95% Cl: -0.714, -0.238; p = 0.0001, ancova). More subjects reached HbA1c < or = 7.0% in the basal-bolus group than in the premix group [68 (46.6%) vs. 43 (27.9%); p = 0.0004], while they also experienced significantly lower mean +/- s.d. daytime (-2.7 +/- 2.3 vs. -2.3 +/- 2.5 mmol/l; p = 0.0033) and postprandial (-3.1 +/- 2.6 vs. -2.5 +/- 2.8 mmol/l; p < 0.0001) blood glucose. Endpoint daily insulin doses were 98.0 +/- 48.7 vs. 91.3 +/- 44.3 IU (p = 0.2104); mean weight gain was +3.6 +/- 4.0 vs. +2.2 +/- 4.5 kg (p = 0.0073). Mean number of overall hypoglycaemic events with basal-bolus and premix was 13.99 and 18.54 events/patient year, respectively (difference: -3.90; 95% CI: -10.40, 2.60; p = 0.2385). CONCLUSIONS: An intensified basal-bolus regimen using glargine/glulisine results in a significantly superior glycaemic control vs. premix therapy in a population with long-standing insulin-treated T2D, with no increase in the rates of hypoglycaemia.
机译:目的:为了比较强化胰岛素治疗的有效性和安全性,采用传统方法,每天两次使用预混胰岛素(预混合物),每天一次使用甘精胰岛素(甘精胰岛素)和餐前胰岛素谷胱甘肽(谷氨酰胺)(基础推注) 。方法:这项为期52周,开放标签,随机,跨国,多中心的试验,包括310名患有预混剂的2型糖尿病(T2D)受试者,有或没有二甲双胍,他们随机分配了含甘精氨酸和甘氨酸的基础推注方案(n = 153;平均+/- sd年龄60.2 +/- 7.5岁; HbA1c 8.6 +/- 0.8%;体重87.0 +/- 15.1公斤; T2D持续时间12.8 +/- 5.8年)或每天两次预混(n = 157 ;年龄60.9 +/- 7.8岁; HbA1c 8.5 +/- 0.9%;体重84.3 +/- 15.0公斤; T2D持续时间12.5 +/- 6.8岁。主要终点是HbA1c从基线到终点的变化。结果:基础推注与预混物相比,基线至终点HbA1c的平均降低为-1.31对-0.80%(差异:-0.476%; 95%Cl:-0.714,-0.238; p = 0.0001,ancova)。基础推注组中的HbA1c <或= 7.0%的受试者多于预混组[68(46.6%)vs. 43(27.9%); p = 0.0004],而他们的平均+/- s.d也显着降低。白天(-2.7 +/- 2.3与-2.3 +/- 2.5 mmol / l; p = 0.0033)和餐后(-3.1 +/- 2.6与-2.5 +/- 2.8 mmol / l; p <0.0001)葡萄糖。端点每日胰岛素剂量为98.0 +/- 48.7 IU与91.3 +/- 44.3 IU(p = 0.2104);平均体重增加+3.6 +/- 4.0公斤,而+2.2 +/- 4.5公斤(p = 0.0073)。含基础推注和预混剂的总体降血糖事件的平均数分别为每患者年13.99和18.54事件(差异:-3.90; 95%CI:-10.40,2.60; p = 0.2385)。结论:在长期使用胰岛素治疗的T2D人群中,使用甘精胰岛素/谷氨酰胺加强基础推注方案可显着优于预混疗法,且血糖升高率没有增加。

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