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一项关于阿卡波糖治疗2型糖尿病的随机双盲试验显示,在3年时间里血糖控制得到改善(英国前瞻性糖尿病研究44)。

A randomized double-blind trial of acarbose in type 2 diabetes shows improved glycemic control over 3 years (U.K. Prospective Diabetes Study 44).

作者信息

Holman R R, Cull C A, Turner R C

机构信息

Diabetes Research Laboratories, University of Oxford, Radcliffe Infirmary, U.K.

出版信息

Diabetes Care. 1999 Jun;22(6):960-4. doi: 10.2337/diacare.22.6.960.

Abstract

OBJECTIVE

To determine the degree to which alpha-glucosidase inhibitors, with their unique mode of action primarily reducing postprandial hyperglycemia, offer an additional therapeutic approach in the long-term treatment of type 2 diabetes.

RESEARCH DESIGN AND METHODS

We studied 1,946 patients (63% men) who were previously enrolled in the U.K. Prospective Diabetes Study (UKPDS). The patients were randomized to acarbose (n = 973), titrating to a maximum dose of 100 mg three times per day, or to matching placebo (n = 973). Mean +/- SD age was 59 +/- 9 years, body weight 84 +/- 17 kg, diabetes duration 7.6 +/- 2.9 years, median (interquartile range) HbA1c 7.9% (6.7-9.5), and fasting plasma glucose (FPG) 8.7 mmol/l (6.8-11.1). Fourteen percent of patients were treated with diet alone, 52% with monotherapy, and 34% with combined therapy. Patients were monitored in UKPDS clinics every 4 months for 3 years. The main outcome measures were HbA1c, FPG, body weight, compliance with study medication, incidence of side effects, and frequency of major clinical events.

RESULTS

At 3 years, a lower proportion of patients were taking acarbose compared with placebo (39 vs. 58%, P < 0.0001), the main reasons for noncompliance being flatulence (30 vs. 12%, P < 0.0001) and diarrhea (16 vs. 8%, P < 0.05). Analysis by intention to treat showed that patients allocated to acarbose, compared with placebo, had 0.2% significantly lower median HbA1c at 3 years (P < 0.001). In patients remaining on their allocated therapy, the HbA1c difference at 3 years (309 acarbose, 470 placebo) was 0.5% lower median HbA1c (8.1 vs. 8.6%, P < 0.0001). Acarbose appeared to be equally efficacious when given in addition to diet alone; in addition to monotherapy with a sulfonylurea, metformin, or insulin; or in combination with more complex treatment regimens. No significant differences were seen in FPG, body weight, incidence of hypoglycemia, or frequency of major clinical events.

CONCLUSIONS

Acarbose significantly improved glycemic control over 3 years in patients with established type 2 diabetes, irrespective of concomitant therapy for diabetes. Careful titration of acarbose is needed in view of the increased noncompliance rate seen secondary to the known side effects.

摘要

目的

确定α-葡萄糖苷酶抑制剂以其主要降低餐后高血糖的独特作用方式,在2型糖尿病长期治疗中提供额外治疗方法的程度。

研究设计与方法

我们研究了1946例患者(63%为男性),这些患者先前参加了英国前瞻性糖尿病研究(UKPDS)。患者被随机分为阿卡波糖组(n = 973),滴定至最大剂量每日3次,每次100 mg,或匹配的安慰剂组(n = 973)。平均±标准差年龄为59±9岁,体重84±17 kg,糖尿病病程7.6±2.9年,HbA1c中位数(四分位间距)为7.9%(6.7 - 9.5),空腹血糖(FPG)为8.7 mmol/l(6.8 - 11.1)。14%的患者仅接受饮食治疗,52%接受单一疗法,34%接受联合疗法。患者在UKPDS诊所每4个月监测一次,为期3年。主要结局指标为HbA1c、FPG、体重、研究药物依从性、副作用发生率及主要临床事件发生频率。

结果

3年后,与安慰剂组相比,服用阿卡波糖的患者比例更低(39%对58%,P < 0.0001),不依从的主要原因是肠胃胀气(30%对12%,P < 0.0001)和腹泻(16%对8%,P < 0.05)。意向性分析表明,与安慰剂组相比,分配到阿卡波糖组的患者在3年后HbA1c中位数显著低0.2%(P < 0.001)。在继续接受分配治疗的患者中,3年后(309例阿卡波糖组,470例安慰剂组)HbA1c差异为中位数低0.5%(8.1%对8.6%,P < 0.0001)。阿卡波糖在仅饮食治疗基础上、在磺脲类、二甲双胍或胰岛素单一疗法基础上、或在更复杂治疗方案联合使用时似乎同样有效。在FPG、体重、低血糖发生率或主要临床事件发生频率方面未观察到显著差异。

结论

阿卡波糖在3年时间里显著改善了已确诊2型糖尿病患者的血糖控制,无论糖尿病的伴随治疗如何。鉴于已知副作用导致的不依从率增加,需要谨慎滴定阿卡波糖剂量。

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