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皮质类固醇加重安徒生综合征家族中的症状。

Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred.

作者信息

Bendahhou Saïd, Fournier Emmanuel, Gallet Serge, Ménard Dominique, Larroque Marie-Madeleine, Barhanin Jacques

机构信息

Institut de Pharmacologie Moléculaire et Cellulaire, UMR 6097 CNRS, Université de Nice Sophia Antipolis, France.

出版信息

Hum Mol Genet. 2007 Apr 15;16(8):900-6. doi: 10.1093/hmg/ddm034. Epub 2007 Feb 26.

Abstract

Periodic paralysis, cardiac arrhythmia and bone features are the hallmark of Andersen's syndrome (AS), a rare disorder caused by mutations in the KCNJ2 gene that encodes for the inward rectifier K(+)-channel Kir2.1. Rest following strenuous physical activity, carbohydrate ingestion, emotional stress and exposure to cold are the precipitating triggers. Most of the mutations act in a dominant-negative fashion, either through a trafficking dysfunction or through Kir2.1-phosphatidyl inositol bisphosphate binding defect. We have identified two families that were diagnosed with periodic paralysis and cardiac abnormalities, but only discrete development features. The proband in one of the two families reported having his symptoms occurring twice within the day following corticosteroids ingestion, and alleviated after stopping the corticosteroid treatment. Electromyographic evaluations pointed out to a typical hypokalemic periodic paralysis pattern. Molecular screening of the KCNJ2 gene identified two mutations leading to C54F and T305P substitutions in the Kir2.1 protein. Functional expression in mammalian cells revealed a loss-of-function of the mutated channels and a dominant-negative effect when both mutants and wild-type channels are present in the same cell. However, channel trafficking and assembly are not affected. Substitutions at these residues may interfere with phosphatidyl inositol bisphosphate binding to Kir2.1 channels. Sensitivity of our patients to multiple corticosteroid administrations shows that care must be taken in the use of such treatments in AS patients. Taken together, our data suggest the inclusion of the KCNJ2 gene in the molecular screening of patients with periodic paralysis, even when the classical AS dysmorphic features are not present.

摘要

周期性瘫痪、心律失常和骨骼特征是安德森综合征(AS)的标志性表现,AS是一种由KCNJ2基因突变引起的罕见疾病,该基因编码内向整流钾离子通道Kir2.1。剧烈体力活动后休息、摄入碳水化合物、情绪应激和暴露于寒冷环境是诱发因素。大多数突变以显性负性方式起作用,要么通过转运功能障碍,要么通过Kir2.1-磷脂酰肌醇二磷酸结合缺陷。我们鉴定了两个被诊断为周期性瘫痪和心脏异常,但仅有离散发育特征的家系。两个家系之一的先证者报告称,在摄入皮质类固醇后一天内症状出现两次,停止皮质类固醇治疗后症状缓解。肌电图评估显示为典型的低钾性周期性瘫痪模式。对KCNJ2基因的分子筛查鉴定出两个导致Kir2.1蛋白中C54F和T305P替代的突变。在哺乳动物细胞中的功能表达显示突变通道功能丧失,且当突变体和野生型通道存在于同一细胞中时具有显性负性效应。然而,通道转运和组装不受影响。这些残基处的替代可能会干扰磷脂酰肌醇二磷酸与Kir2.1通道的结合。我们的患者对多次给予皮质类固醇敏感,这表明在AS患者中使用此类治疗时必须谨慎。综上所述,我们的数据表明,即使不存在经典的AS畸形特征,在周期性瘫痪患者的分子筛查中也应纳入KCNJ2基因。

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