Trachtman Howard, Greenbaum Laurence A, McCarthy Ellen T, Sharma Mukut, Gauthier Bernard G, Frank Rachel, Warady Bradley, Savin Virginia J
Department of Pediatrics, Division of Nephrology, Schneider Children's Hospital of North Shore-Long Island Jewish Health System, Long Island Campus for Albert Einstein College of Medicine, New Hyde Park, NY 11040, USA.
Am J Kidney Dis. 2004 Oct;44(4):604-10.
A circulating factor that increases in vitro glomerular permeability to albumin (P alb ) has been isolated from patients with recurrence of focal segmental glomerulosclerosis in their renal allografts. The prevalence and prognostic significance of permeability activity has not been examined in children with idiopathic nephrotic syndrome (INS).
P alb activity level was determined in sera from 26 children with new-onset INS before the initiation of therapy by using an in vitro assay. Permeability factor was considered present if P alb was greater than 0.5. The following clinical and laboratory data for patients were tabulated: demographic information, serum albumin and cholesterol concentrations, calculated glomerular filtration rate, age at disease onset, response to corticosteroid treatment, and long-term outcome.
Patients ranged in age from 2 to 18 years, and 19 patients (73%) were male. Mean P alb was 0.45 +/- 0.04 (SEM). P alb in patients with a steroid-responsive course (n = 17) did not differ from that of patients with steroid-resistant disease (n = 9). Percentages with P alb greater than 0.5 did not differ between patients with steroid-responsive and steroid-resistant disease (47% and 33%, respectively). P alb was determined after 41 +/- 5 months in 6 patients with steroid-responsive INS. These patients had normal serum creatinine concentrations, and 4 of 6 patients were in prolonged remission. P alb at the onset of INS before therapy was 0.51 +/- 0.09 (P alb > 0.5 in 2 patients) and was not changed at follow-up (P alb = 0.40 +/- 0.12; P alb > 0.5 in 2 patients).
Permeability activity, defined as P alb greater than 0.5, is present in pretreatment serum samples from nearly half the children with INS. The presence of permeability activity does not predict clinical response to steroid treatment, renal histopathologic characteristics, or clinical outcome at up to 5 years of follow-up.
从肾移植后局灶节段性肾小球硬化复发患者中分离出一种可增加体外肾小球对白蛋白通透性(Palb)的循环因子。尚未在特发性肾病综合征(INS)患儿中检测通透性活性的患病率及其预后意义。
采用体外测定法,对26例初发INS患儿治疗开始前的血清进行Palb活性水平测定。若Palb大于0.5,则认为存在通透性因子。将患者的以下临床和实验室数据制成表格:人口统计学信息、血清白蛋白和胆固醇浓度、计算的肾小球滤过率、发病年龄、对皮质类固醇治疗的反应以及长期预后。
患者年龄在2至18岁之间,19例(73%)为男性。平均Palb为0.45±0.04(标准误)。激素反应型病程患者(n = 17)的Palb与激素抵抗型疾病患者(n = 9)的Palb无差异。激素反应型和激素抵抗型疾病患者中Palb大于0.5的百分比无差异(分别为47%和33%)。对6例激素反应型INS患者在41±5个月后测定Palb。这些患者血清肌酐浓度正常,6例患者中有4例处于长期缓解状态。INS治疗开始前的Palb为0.51±0.09(2例患者Palb>0.5),随访时未改变(Palb = 0.40±0.12;2例患者Palb>0.5)。
定义为Palb大于0.5的通透性活性存在于近半数INS患儿的治疗前血清样本中。通透性活性的存在不能预测对类固醇治疗的临床反应、肾脏组织病理学特征或长达5年随访的临床结局。