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肾病综合征患儿的组织因子途径抑制剂

Tissue factor pathway inhibitor in paediatric patients with nephrotic syndrome.

作者信息

Farid Farida Ahmed, Mohammed Ahmed Abdullah, Afifi Hanaa Mohammed, Beltagi Rania Saleh

机构信息

Department of Paediatrics Ain Shams University, Cairo, Egypt.

出版信息

SAJCH. 2011 Dec;5(4):107-111.

Abstract

BACKGROUND

Tissue factor pathway inhibitor is an endogenous protease inhibitor that regulates the initiation of the extrinsic coagulation pathway by producing factor Xa-mediated feedback inhibition of the tissue factor/factor VIIa (TF/VIIA) catalytic complex. OBJECTIVES: To evaluate plasma TFPI levels in paediatric patients with nephrotic syndrome and its correlation with disease activity. SUBJECTS AND METHODS: Fifteen nephrotic patients in relapse (proteinuria>40mg/m2/hour, hypoalbuminemia, and edema) before initiating steroid therapy (Group I), and another15 nephrotic patients in remission after withdrawal of steroid therapy (Group II) were compared to 15 age- and sex-matched healthy children (Group III). Besides clinical evaluation and routine laboratory investigations of nephrotic syndrome, tissue factor pathway inhibitor levels in plasma were measured by ELISA. RESULTS: Plasma TFPI level was higher in nephrotic patients during relapse (Group I) and during remission (Group II) [102.53±14.23 and 82.93±3.83ng/ml respectively] compared to that in the control group (62.40 ± 7.53 ng/ml) (p< 0.0001). In children with nephrotic syndrome Plasma TFPI level was higher during relapse (Group I) compared to that in remission (Group II) (p< 0.0001). There was a negative correlation between plasma TFPI level and total protein and serum albumin, and there was a positive correlation between plasma TFPI level and urine protein /creatinine ratio with a statistically significant difference (p< 0.05). CONCLUSION: Nephrotic syndrome was associated with increased level of plasma tissue factor pathway inhibitor in comparison to control group and the increase was more apparent in patients with active disease.

摘要

背景

组织因子途径抑制物是一种内源性蛋白酶抑制剂,通过产生因子Xa介导的对组织因子/因子VIIa(TF/VIIa)催化复合物的反馈抑制来调节外源性凝血途径的启动。目的:评估肾病综合征患儿的血浆TFPI水平及其与疾病活动度的相关性。对象与方法:将15例复发期肾病患者(蛋白尿>40mg/m²/小时、低白蛋白血症和水肿)在开始使用类固醇治疗前(I组),以及另外15例在停用类固醇治疗后缓解期的肾病患者(II组)与15例年龄和性别匹配的健康儿童(III组)进行比较。除了对肾病综合征进行临床评估和常规实验室检查外,采用酶联免疫吸附测定法测定血浆组织因子途径抑制物水平。结果:与对照组(62.40±7.53ng/ml)相比,复发期(I组)和缓解期(II组)肾病患者的血浆TFPI水平更高[分别为102.53±14.23和82.93±3.83ng/ml](p<0.0001)。肾病综合征患儿复发期(I组)的血浆TFPI水平高于缓解期(II组)(p<0.0001)。血浆TFPI水平与总蛋白和血清白蛋白呈负相关,与尿蛋白/肌酐比值呈正相关,差异有统计学意义(p<0.05)。结论:与对照组相比,肾病综合征患者血浆组织因子途径抑制物水平升高,且在疾病活动期患者中升高更为明显。

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