Decreased homovanillic acid and 5-hydroxyindoleacetic acid levels in the cerebrospinal fluid of patients with Dravet syndrome with parkinsonism.

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY
Epilepsia Open Pub Date : 2025-04-04 DOI:10.1002/epi4.70034
Ryo Sugiyama, Takashi Saito, Atsuko Katsumoto, Shota Yoneno, Tomoyuki Akiyama, Hirofumi Komaki
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Abstract

Dravet syndrome (DS) is an early onset, developmental, and epileptic encephalopathy characterized by drug-resistant seizures and multiple comorbidities. It has been reported that in adulthood, it may be accompanied by parkinsonism, but the pathogenesis of this condition remains unclear. We performed dopamine transporter single-photon emission computed tomography (DAT SPECT) and measured monoamine metabolite levels in the cerebrospinal fluid (CSF) in two adult patients with DS who developed parkinsonism around the age of 30 years. DAT SPECT showed no abnormalities in either patient, whereas CSF tests revealed significant decreases in the levels of homovanillic and 5-hydroxyindoleacetic acids. One patient with severe symptoms was treated with levodopa-carbidopa, which improved parkinsonism manifestations. The other patient initiated treatment with a low dose and has been continuing the treatment without any reported side effects. In conclusion, CSF testing can detect a decrease in dopamine synthesis and may be useful in monitoring the efficacy of levodopa treatment in patients with DS and parkinsonism. PLAIN LANGUAGE SUMMARY: Dravet syndrome (DS) is an early onset, developmental, and epileptic encephalopathy. DS can lead to the development of parkinsonism in adulthood, a clinical syndrome characterized by tremor, slowed movements, and rigidity. Although parkinsonism is a significant issue for patients, its underlying pathology has not yet been elucidated. In this study, we confirmed that the levels of monoamine metabolites in the CSF were low in two patients, potentially shedding light on the pathology involved.

Dravet综合征合并帕金森病患者脑脊液中同型香草酸和5-羟基吲哚乙酸水平降低
Dravet综合征(DS)是一种以耐药癫痫发作和多种合并症为特征的早发性发育性癫痫性脑病。据报道,在成年期,它可能伴有帕金森病,但这种情况的发病机制尚不清楚。我们对两名30岁左右发展为帕金森的成年DS患者进行了多巴胺转运体单光子发射计算机断层扫描(DAT SPECT)并测量了脑脊液(CSF)中单胺代谢物的水平。数据SPECT显示两例患者均无异常,而脑脊液检查显示同型香草酸和5-羟基吲哚乙酸水平显著降低。1例重症患者用左旋多巴-卡比多巴治疗,帕金森症状得到改善。另一名患者以低剂量开始治疗,并一直在继续治疗,没有任何副作用的报道。综上所述,脑脊液检测可以检测多巴胺合成的减少,可能有助于监测左旋多巴治疗退行性痴呆和帕金森病患者的疗效。摘要:Dravet综合征(DS)是一种早发性发育性癫痫性脑病。退行性椎体滑移可导致成年期帕金森病的发展,这是一种以震颤、运动缓慢和僵硬为特征的临床综合征。虽然帕金森氏症是一个重要的问题,其潜在的病理尚未阐明。在这项研究中,我们证实了两名患者脑脊液中单胺代谢物的水平较低,这可能会揭示所涉及的病理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
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