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培哚普利与坎地沙坦治疗2型糖尿病高血压患者的随机、双盲、对照、平行组比较

A randomized, double-blind, controlled, parallel-group comparison of perindopril and candesartan in hypertensive patients with type 2 diabetes mellitus.

作者信息

Derosa Giuseppe, Cicero Arrigo F G, Ciccarelli Leonardina, Fogari Roberto

机构信息

Department of Internal Medicine and Therapeutics, University of Pavia, IRCCS Policlinico S. Matteo, Pavia, Italy.

出版信息

Clin Ther. 2003 Jul;25(7):2006-21. doi: 10.1016/s0149-2918(03)80201-1.

Abstract

BACKGROUND

When choosing an antihypertensive drug for patients with hypertension and diabetes mellitus (DM), the metabolic side effects, possibility of improving some metabolic parameters, and need for adequate blood pressure control must all be considered.

OBJECTIVE

The goal of this study was to compare the impacts of perindopril and candesartan on blood pressure, glucose metabolism, serum lipid profile, and metabolic parameters in patients with mild hypertension and type 2 DM during therapy and after a 1-month washout period.

METHODS

Type 2 DM patients with mild hypertension and good glucose control who were not taking hypercholesterolemic drugs were enrolled. Perindopril 4 mg QD or candesartan 16 mg QD was administered for 12 months in this randomized, double-blind, controlled, parallel-group clinical trial. Fasting plasma glucose (FPG), fasting plasma insulin (FPI), glycosylated hemoglobin, homeostasis model assessment (HOMA) index, systolic blood pressure (SBP), diastolic blood pressure (DBP), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol, triglycerides, lipoprotein(a) (Lp[a]), plasminogen activator inhibitor 1 (PAI-1), homocysteine, body mass index (BMI), and albumin excretion rate (AER) were assessed.

RESULTS

Ninety-six patients (49 women and 47 men; mean [SD] ages, 53 [10] years [perindopril] and 55 [9] years [candesartan]) were enrolled. Mean (SD) body weight, height, and BMI were 78.2 (9.4) kg, 1.69 (0.05) m, and 27.2 (2.0) kg/m(2) in the perindopril group and 77.5 (8.6) kg, 1.70 (0.06) m, and 26.8 (2.5) kg/m(2) in the candesartan group. A significant change occurred from baseline to month 12 during treatment with perindopril in SBP and DBP (both P < 0.01), FPG (P < 0.05), FPI (P < 0.05), TC (P < 0.05), LDL-C (P < 0.05), Lp(a) (P < 0.05), PAM (P < 0.05), and AER (P < 0.05). Significant changes from baseline to month 12 occurred with candesartan in SBP and DBP (both P < 0.01) and AER (P < 0.05). The HOMA index was significantly lower at month 12 in the perindopril group than in the candesartan group (P < 0.05). When we interrupted perindopril and candesartan therapy for a 1-month washout period, changes in SBP and DBP values were significant compared with month 12 in both groups (all P < 0.05). Changes in TC and LDL-C from month 12 to the end of washout were significant only in the perindopril group (both P < 0.05).

CONCLUSIONS

Perindopril and candesartan both effectively lowered blood pressure in this group of patients with mild hypertension and type 2 DM. Perindopril showed an improvement on some metabolic parameters compared with candesartan. However, the inclusion/exclusion criteria could limit the ability to extrapolate the results to a general population.

摘要

背景

为高血压合并糖尿病(DM)患者选择抗高血压药物时,必须综合考虑药物的代谢副作用、改善某些代谢参数的可能性以及充分控制血压的必要性。

目的

本研究旨在比较培哚普利和坎地沙坦对轻度高血压合并2型DM患者治疗期间及1个月洗脱期后的血压、糖代谢、血脂谱和代谢参数的影响。

方法

纳入未服用降胆固醇药物、轻度高血压且血糖控制良好的2型DM患者。在这项随机、双盲、对照、平行组临床试验中,给予培哚普利4mg每日一次或坎地沙坦16mg每日一次,治疗12个月。评估空腹血糖(FPG)、空腹血浆胰岛素(FPI)、糖化血红蛋白、稳态模型评估(HOMA)指数、收缩压(SBP)、舒张压(DBP)、总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇、甘油三酯、脂蛋白(a)[Lp(a)]、纤溶酶原激活物抑制剂1(PAI-1)、同型半胱氨酸、体重指数(BMI)和白蛋白排泄率(AER)。

结果

共纳入96例患者(49例女性和47例男性;培哚普利组平均[标准差]年龄为53[10]岁,坎地沙坦组为55[9]岁)。培哚普利组的平均(标准差)体重、身高和BMI分别为78.2(9.4)kg、1.69(0.05)m和27.2(2.0)kg/m²,坎地沙坦组分别为77.5(8.6)kg、1.70(0.06)m和26.8(2.5)kg/m²。培哚普利治疗期间,从基线到第12个月,SBP和DBP(均P<0.01)、FPG(P<0.05)、FPI(P<0.05)、TC(P<0.05)、LDL-C(P<0.05)、Lp(a)(P<0.05)、PAI-1(P<0.05)和AER(P<0.05)均发生显著变化。坎地沙坦治疗期间,从基线到第12个月,SBP和DBP(均P<0.01)以及AER(P<0.05)发生显著变化。培哚普利组第12个月时的HOMA指数显著低于坎地沙坦组(P<0.05)。当我们中断培哚普利和坎地沙坦治疗1个月洗脱期时,两组的SBP和DBP值变化与第12个月相比均有显著性(均P<0.05)。仅培哚普利组从第12个月到洗脱期末TC和LDL-C有显著变化(均P<0.05)。

结论

培哚普利和坎地沙坦均可有效降低本组轻度高血压合并2型DM患者的血压。与坎地沙坦相比,培哚普利在某些代谢参数方面有所改善。然而,纳入/排除标准可能会限制将结果外推至一般人群的能力。

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