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药物控制 Alport 综合征患者的蛋白尿。

Drugs controlling proteinuria of patients with Alport syndrome.

机构信息

Department of Pediatrics, Peking University First Hospital, Beijing, 100034, China.

出版信息

World J Pediatr. 2009 Nov;5(4):308-11. doi: 10.1007/s12519-009-0059-5. Epub 2009 Nov 13.

DOI:10.1007/s12519-009-0059-5
PMID:19911149
Abstract

BACKGROUND

Proteinuria is one of the risk factors for the progression of renal diseases including Alport syndrome (AS), a hereditary glomerular renal disease. This study aimed to evaluate the efficacy of angiotensin converting enzyme inhibitors (ACEIs) and/or tripterygium, a Chinese herbal medicine widely used in Chinese patients with hematuria and proteinuria, on proteinuria in patients with AS.

METHODS

Twenty-nine children were enrolled into this retrospective study. Patients were divided into 3 therapy groups: ACEI group, tripterygium group, and ACEI plus tripterygium group.

RESULTS

In the 29 children, 23 were male and 6 female. In the ACEI group and the tripterygium group, the effective rate was 87.5% and 25.0%, respectively and in the ACEI plus tripterygium group was 42.9%.

CONCLUSIONS

ACEI is effective in controlling proteinuria of AS patients. Tripterygium should be carefully administered in controlling proteinuria of AS patients.

摘要

背景

蛋白尿是包括 Alport 综合征(AS)在内的多种肾脏疾病进展的风险因素之一,AS 是一种遗传性肾小球肾病。本研究旨在评估血管紧张素转换酶抑制剂(ACEI)和/或雷公藤(一种在中国广泛用于血尿和蛋白尿患者的中药)对 AS 患者蛋白尿的疗效。

方法

本回顾性研究纳入了 29 名儿童。患者被分为 3 个治疗组:ACEI 组、雷公藤组和 ACEI 加雷公藤组。

结果

在 29 名儿童中,男性 23 名,女性 6 名。在 ACEI 组和雷公藤组中,有效率分别为 87.5%和 25.0%,而在 ACEI 加雷公藤组中为 42.9%。

结论

ACEI 可有效控制 AS 患者的蛋白尿。雷公藤在控制 AS 患者蛋白尿方面应谨慎使用。

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本文引用的文献

1
Triptolide protects podocytes from puromycin aminonucleoside induced injury in vivo and in vitro.雷公藤甲素在体内和体外均可保护足细胞免受嘌呤霉素氨基核苷诱导的损伤。
Kidney Int. 2008 Sep;74(5):596-612. doi: 10.1038/ki.2008.203. Epub 2008 May 28.
2
[Effects of multi-glycoside of Tripterygium wilfordii Hook. f. on proteinuria and expression of slit diaphragm-associated molecules in rats with anti-thy1.1 glomerulonephritis].雷公藤多苷对抗thy1.1肾小球肾炎大鼠蛋白尿及裂孔隔膜相关分子表达的影响
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2006 Dec;26(12):1094-102.
3
Resolution of proteinuria in a patient with X-linked Alport syndrome treated with cyclosporine.
血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂对Alport综合征患儿的长期治疗
Pediatr Nephrol. 2016 Jan;31(1):67-72. doi: 10.1007/s00467-015-3184-5. Epub 2015 Aug 7.
4
HDAC inhibitors in experimental liver and kidney fibrosis.实验性肝肾纤维化中的组蛋白去乙酰化酶抑制剂
Fibrogenesis Tissue Repair. 2013 Jan 2;6(1):1. doi: 10.1186/1755-1536-6-1.
5
Glomerular pathology in Alport syndrome: a molecular perspective.Alport 综合征的肾小球病理学:分子视角。
Pediatr Nephrol. 2012 Jun;27(6):885-90. doi: 10.1007/s00467-011-1868-z. Epub 2011 Apr 1.
6
Ventricular septal defect in a child with Alport syndrome: a case report.儿童 Alport 综合征合并室间隔缺损 1 例报告
BMC Cardiovasc Disord. 2010 Oct 5;10:48. doi: 10.1186/1471-2261-10-48.
一名接受环孢素治疗的X连锁Alport综合征患者蛋白尿的消退
Scand J Urol Nephrol. 2006;40(6):522-5. doi: 10.1080/00365590600830417.
4
The effect of aldosterone blockade in patients with Alport syndrome.醛固酮阻断对阿尔波特综合征患者的影响。
Pediatr Nephrol. 2006 Dec;21(12):1824-9. doi: 10.1007/s00467-006-0270-8. Epub 2006 Oct 13.
5
Cyclosporin therapy in patients with Alport syndrome.患有奥尔波特综合征患者的环孢素治疗。
Pediatr Nephrol. 2007 Jan;22(1):57-63. doi: 10.1007/s00467-006-0227-y. Epub 2006 Sep 21.
6
Cyclosporine a slows the progressive renal disease of alport syndrome (X-linked hereditary nephritis): results from a canine model.环孢素A减缓奥尔波特综合征(X连锁遗传性肾炎)的进行性肾病:来自犬类模型的结果
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8
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Clin Nephrol. 2000 Jun;53(6):432-6.
9
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J Am Soc Nephrol. 2000 Apr;11(4):649-657. doi: 10.1681/ASN.V114649.