Proesmans Willem, Van Dyck Maria
Renal Unit, Department of Pediatrics, University Hospital Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium.
Pediatr Nephrol. 2004 Mar;19(3):271-5. doi: 10.1007/s00467-003-1366-z. Epub 2004 Jan 24.
Ten pediatric patients with Alport syndrome received enalapril for 5 years. There were nine boys. Eight patients have the X-linked form of the disease and two the autosomal recessive form. The median age at the start of treatment was 10.25 years. Only one patient was hypertensive. The starting dose of enalapril was 0.05 mg/kg; the target dose was 0.5 mg/kg per day. The median dose given effectively was 0.24, 0.37, 0.45, 0.43, and 0.49 mg/kg per day at years of study 1, 2, 3, 4, and 5, respectively. The median urinary protein/creatinine ratio was 1.58 g/g (range 0.49-4.60) before treatment. This decreased to 0.98, 1.09, 1.35, 1.11, and 1.38 g/g after 1, 2, 3, 4, and 5 years, respectively. The median creatinine clearance at baseline was 100 ml/min per 1.73 m2 (range 82-133) and after 5 years 92 ml/min per 1.73 m2 (range 22-115). Three patients did not reach the target dose of enalapril because of orthostatic hypotension. One of them was the only patient to develop chronic renal failure within 5 years. The present study indicates that enalapril reduces urinary protein excretion and preserves glomerular filtration in Alport patients as a group. However, there was individual variation, as in most studies of patients with proteinuric nephropathies given inhibitors of the angiotensin-converting enzyme.
十名患有Alport综合征的儿科患者接受依那普利治疗达5年。其中有9名男孩。8名患者为X连锁型疾病,2名患者为常染色体隐性遗传型。治疗开始时的中位年龄为10.25岁。只有一名患者患有高血压。依那普利的起始剂量为0.05mg/kg;目标剂量为每日0.5mg/kg。在研究的第1、2、3、4和5年,有效给予的中位剂量分别为每日0.24、0.37、0.45、0.43和0.49mg/kg。治疗前尿蛋白/肌酐比值的中位数为1.58g/g(范围0.49 - 4.60)。在1、2、3、4和5年后分别降至0.98、1.09、1.35、1.11和1.38g/g。基线时肌酐清除率的中位数为每1.73m²每分钟100ml(范围82 - 133);5年后为每1.73m²每分钟92ml(范围22 - 115)。三名患者因体位性低血压未达到依那普利的目标剂量。其中一人是唯一在5年内发展为慢性肾衰竭的患者。本研究表明,作为一个群体,依那普利可减少Alport患者的尿蛋白排泄并保留肾小球滤过功能。然而,正如大多数对给予血管紧张素转换酶抑制剂的蛋白尿性肾病患者的研究所显示的那样,存在个体差异。