日本小儿肌张力障碍流行病学研究:基于问卷的调查。

IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Brain & Development Pub Date : 2024-06-27 DOI:10.1016/j.braindev.2024.06.002
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引用次数: 0

摘要

研究目的本研究旨在调查日本小儿肌张力障碍的临床特征,解决因症状变化和病因多样性而产生的诊断难题:从 2020 年到 2022 年,日本儿童神经病学学会向 1218 名经委员会认证的儿童神经病学家(BCCN)发放了调查问卷。在初级调查中,参与者被要求报告在其治疗下的小儿肌张力障碍患者人数。随后进行的后续二次调查则要求提供有关这些患者临床特征的更多信息:主要调查从 BCCN 获得了 550 份回复(回复率:45%),涉及 736 名肌张力障碍患者。主要病因包括遗传性病例(DYT10最为常见,其次是DYT5和ATP1A3相关神经系统疾病)、获得性病例(围产期异常最为常见)和特发性病例。二次调查提供了来自 82 个 BCCN 的 308 个病例的临床资料。婴儿期发病的肌张力障碍表现为持续性和全身性,症状多样,主要与 ATP1A3 相关神经系统疾病和其他类似获得性肌张力障碍的遗传疾病有关。相反,儿童/青少年期肌张力障碍表现为阵发性、波动性病程,主要累及四肢。最常见的病因是 DYT5 和 DYT10,从而导致治疗性诊断:结论:在日本,28%的 BCCN 治疗过小儿肌张力障碍。大多数病例是遗传性的,DYT5 和 DYT10 的发病率很高。婴幼儿期肌张力障碍的病因和症状多种多样,因此需要进行包括基因检测在内的各种检查。尽管本研究存在问卷调查的局限性,但这些发现极大地促进了我们对日本儿童发病型肌张力障碍的了解。
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Epidemiological study on pediatric-onset dystonia in Japan: A questionnaire-based survey

Objective

This study aimed to investigate the clinical characteristics of pediatric-onset dystonia in Japan, addressing the diagnostic challenges arising from symptom variations and etiological diversity.

Methods

From 2020 to 2022, questionnaires were distributed to 1218 board certified child neurologists (BCCNs) by Japanese Society of Child Neurology. In the primary survey, participants were asked to report the number of patients with pediatric-onset dystonia under their care. Subsequently, the follow-up secondary survey sought additional information on the clinical characteristics of these patients.

Results

The primary survey obtained 550 responses (response rate: 45 %) from BCCNs for their 736 patients with dystonia. The predominant etiologies included inherited cases (with DYT10  <PxMD-PRRT2> being the most prevalent, followed by DYT5 <DYT/PARK-GCH1> and ATP1A3-related neurologic disorders), acquired cases (with perinatal abnormalities being the most common), and idiopathic cases. The secondary survey provided clinical insights into 308 cases from 82 BCCNs. Infancy-onset dystonia presented as persistent and generalized with diverse symptoms, primarily linked to ATP1A3-related neurologic disorders and other genetic disorders resembling acquired dystonia. Conversely, childhood/adolescent-onset dystonia showed paroxysmal, fluctuating courses, predominantly affecting limbs. The most common etiologies were DYT5 <DYT/PARK-GCH1> and DYT10 <PxMD-PRRT2>, leading to therapeutic diagnoses.

Conclusion

Pediatric-onset dystonia in Japan was treated by 28 % of BCCNs. The majority of cases were inherited, with high prevalence rates of DYT5 <DYT/PARK-GCH1> and DYT10 <PxMD-PRRT2>. Infancy-onset dystonia exhibits diverse etiologies and symptoms, emphasizing the utility of various examinations, including genetic testing. These findings significantly contribute to our understanding of pediatric-onset dystonia in Japan, although this study has the limitation of questionnaire survey.

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来源期刊
Brain & Development
Brain & Development 医学-临床神经学
CiteScore
3.60
自引率
0.00%
发文量
153
审稿时长
50 days
期刊介绍: Brain and Development (ISSN 0387-7604) is the Official Journal of the Japanese Society of Child Neurology, and is aimed to promote clinical child neurology and developmental neuroscience. The journal is devoted to publishing Review Articles, Full Length Original Papers, Case Reports and Letters to the Editor in the field of Child Neurology and related sciences. Proceedings of meetings, and professional announcements will be published at the Editor''s discretion. Letters concerning articles published in Brain and Development and other relevant issues are also welcome.
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