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水通道蛋白2基因突变导致的肾性尿崩症患者对1-去氨基-8-D-精氨酸加压素的正常纤溶反应。

Normal fibrinolytic responses to 1-desamino-8-D-arginine vasopressin in patients with nephrogenic diabetes insipidus caused by mutations in the aquaporin 2 gene.

作者信息

van Lieburg A F, Knoers V V, Mallmann R, Proesmans W, van den Heuvel L P, Monnens L A

机构信息

Department of Pediatrics, University Hospital Nijmegen, The Netherlands.

出版信息

Nephron. 1996;72(4):544-6. doi: 10.1159/000188936.

Abstract

Three patients with autosomal-recessive nephrogenic diabetes insipidus (NDI), homozygous for mutations in the aquaporin 2 gene (AQP2), were tested for their fibrinolytic and hemodynamic responses to intravenous administration of 1-desamino-8-D-arginine vasopressin (DDAVP). They all showed an increase of tissue-type plasminogen activator antigen, facial flushing, an increase of heart rate and a decrease of diastolic blood pressure. These results confirm the hypothesis that NDI patients with an AQP2 defect can be discriminated from NDI patients with a vasopressin type 2 receptor defect by their normal extrarenal responses to DDAVP.

摘要

对三名常染色体隐性遗传性肾性尿崩症(NDI)患者进行了测试,这些患者水通道蛋白2基因(AQP2)发生纯合突变,通过静脉注射1-去氨基-8-D-精氨酸加压素(DDAVP)来检测其纤溶和血流动力学反应。他们均表现出组织型纤溶酶原激活物抗原增加、面部潮红、心率加快和舒张压降低。这些结果证实了以下假设:具有AQP2缺陷的NDI患者可通过其对DDAVP的正常肾外反应与具有2型血管加压素受体缺陷的NDI患者区分开来。

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