Gartenmann Anne C, Fossali Emilio, von Vigier Rodo O, Simonetti Giacomo D, Schmidtko Jan, Edefonti Alberto, Bianchetti Mario G
Division of Nephrology, University Children's Hospital, Inselspital, Bern, Switzerland.
Kidney Int. 2003 Oct;64(4):1450-4. doi: 10.1046/j.1523-1755.2003.00238.x.
The dihydropyridine calcium channel blocker amlodipine and the angiotensin II antagonist irbesartan effectively reduce blood pressure in hypertensive children.
Eligible for the open-label, randomized study were nephropathic children between 6.0 and 18 years of age with plasma creatinine <177 micromol/L, overt proteinuria, untreated arterial hypertension (systolic, 5 to 30 mm Hg; and diastolic, 1 to 15 mm Hg;>95th centile) and stable immunosuppressive treatment. The initial dose of amlodipine was 5 mg (body weight, 20 to 40 kg) and 10 mg (body weight,>40 kg), respectively, that of irbesartan, which was 75 mg (body weight, 20 to 40 kg) and 150 mg (body weight,>40 kg), respectively. The dosage was doubled if necessary.
A total of 26 children aged 6.1 to 17 years were allocated to receive either amlodipine (N = 13) or irbesartan (N = 13) for 16 weeks. Severe edema and headache occurred in two patients on amlodipine who withdrew from the study. No adverse experiences were noted in patients given irbesartan. Amlodipine [by 12 (10 to 14)/7 (5 to 10) mm Hg; median and interquartile range, respectively] and irbesartan [by 13 (9 to 16)/9 (7 to 11) mm Hg, respectively] reduced blood pressure (P < 0.01) in a similar fashion. Heart rate, plasma sodium, and creatinine did not change. Irbesartan slightly increased plasma potassium [by 0.1 (0.0 to 0.2) mmol/L; P < 0.05]. Plasma albumin and the urinary albumin/creatinine ratio were similar before and with amlodipine. On the contrary, irbesartan increased plasma albumin [by 4 (3 to 5) g/L; P < 0.03] and decreased the urinary albumin/creatinine ratio [by 242 (68 to 312) mg/mmol; P < 0.03].
The study demonstrates that in children the effect of angiotensin II antagonists on proteinuria is better than that of dihydropyridine calcium channel blockers.
二氢吡啶类钙通道阻滞剂氨氯地平和血管紧张素II拮抗剂厄贝沙坦可有效降低高血压儿童的血压。
本开放标签随机研究的入选对象为6.0至18岁的肾病患儿,其血浆肌酐<177微摩尔/升,有明显蛋白尿,未经治疗的动脉高血压(收缩压比同年龄、同性别儿童血压的第95百分位数高5至30毫米汞柱;舒张压高1至15毫米汞柱),且免疫抑制治疗稳定。氨氯地平的初始剂量分别为5毫克(体重20至40千克)和10毫克(体重>40千克),厄贝沙坦的初始剂量分别为75毫克(体重20至40千克)和150毫克(体重>40千克)。必要时剂量加倍。
共有26名6.1至17岁的儿童被分配接受氨氯地平(N = 13)或厄贝沙坦(N = 13)治疗16周。两名服用氨氯地平的患者出现严重水肿和头痛,退出了研究。服用厄贝沙坦的患者未出现不良事件。氨氯地平[收缩压降低12(10至14)/舒张压降低7(5至10)毫米汞柱;分别为中位数和四分位间距]和厄贝沙坦[收缩压降低13(9至