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对多巴胺能缺乏无影像学证据(SWEDD)的患者进行多巴反应性肌张力障碍筛查。

Screening for dopa-responsive dystonia in patients with Scans Without Evidence of Dopaminergic Deficiency (SWEDD).

作者信息

De Rosa Anna, Carducci Claudia, Carducci Carla, Peluso Silvio, Lieto Maria, Mazzella Andrea, Saccà Francesco, Brescia Morra Vincenzo, Pappatà Sabina, Leuzzi Vincenzo, De Michele Giuseppe

机构信息

Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Via Pansini 5, 80131, Naples, Italy,

出版信息

J Neurol. 2014 Nov;261(11):2204-8. doi: 10.1007/s00415-014-7477-6. Epub 2014 Sep 3.

Abstract

The clinical diagnosis of Parkinson's Disease (PD) is not supported by Single Photon Emission Computed Tomography (SPECT) using dopamine transporter radioligand in 4-15 % of patients. It has been hypothesized that this phenomenon, named "Scans Without Evidence of Dopaminergic Deficiency" (SWEDD), may be an adult-onset dystonia. We investigated the hypothesis that these patients might be affected by Dopa-Responsive Dystonia (DRD). We enrolled eleven unrelated patients (8 F and 3 M) with clinical parkinsonism and normal [(123)I]FP-CIT SPECT. The GTP-cyclohydrolase1 (GCH1) gene was sequenced in all patients; urine biopterin and neopterin analysis was carried out in nine and oral phenylalanine (Phe) loading in seven. Neurological examination showed bradykinesia and resting/postural tremor in all patients, and rigidity in ten, suggesting a clinical diagnosis of PD. We detected mild dystonic signs in eight cases. In particular, five of them presented cranial dyskinesias. No mutation of the GCH1 gene was found. The results of the urine biopterin and neopterin analysis and the oral Phe loading did not reveal biochemical abnormalities suggestive of reduced GCH1 activity. We confirm that some clinical features, namely the presence of focal or segmental dystonia, suggest an adult-onset dystonia in SWEDD cases. However, we exclude DRD caused by GCH1 gene mutations in the present series.

摘要

在4%-15%的患者中,使用多巴胺转运体放射性配体的单光子发射计算机断层扫描(SPECT)不支持帕金森病(PD)的临床诊断。据推测,这种被称为“无多巴胺能缺乏证据的扫描”(SWEDD)的现象可能是成人起病的肌张力障碍。我们研究了这些患者可能受多巴反应性肌张力障碍(DRD)影响的假说。我们纳入了11例无亲缘关系的临床帕金森综合征患者且[(123)I]FP-CIT SPECT检查正常(8例女性和3例男性)。对所有患者的GTP环化水解酶1(GCH1)基因进行测序;9例患者进行了尿生物蝶呤和新蝶呤分析,7例患者进行了口服苯丙氨酸(Phe)负荷试验。神经学检查显示所有患者均有运动迟缓及静息/姿势性震颤,10例有肌强直,提示临床诊断为PD。我们在8例患者中检测到轻度肌张力障碍体征。特别是其中5例出现头颅运动障碍。未发现GCH1基因突变。尿生物蝶呤和新蝶呤分析以及口服Phe负荷试验结果未显示提示GCH1活性降低生化异常。我们证实,一些临床特征,即局灶性或节段性肌张力障碍的存在,提示SWEDD病例为成人起病的肌张力障碍。然而,在本系列研究中,我们排除了由GCH1基因突变引起的DRD。

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