Suppr超能文献

法罗群岛的肌张力障碍患病率很高:一项基于人群的研究。

High Prevalence of Dystonia in the Faroe Islands: A Population-Based Study.

机构信息

Department of Neurology, Yale School of Medicine, Yale University, New Haven, Connecticut, USA,

Department of Chronic Disease Epidemiology, Yale School of Public Health, Yale University, New Haven, Connecticut, USA,

出版信息

Neuroepidemiology. 2019;53(3-4):220-224. doi: 10.1159/000502455. Epub 2019 Aug 20.

Abstract

BACKGROUND

There are fewer than 5 population-based studies of dystonia worldwide. Only one utilized a movement disorders neurologist. Given the potential for founder effects, and the highly genetic nature of dystonia, the Faroe Islands provide a particularly interesting setting to study the prevalence of dystonia.

OBJECTIVE

To estimate the prevalence of dystonia.

METHODS

We used a 2-phase, population-based design, screening 1,334 randomly selected Faroese individuals aged ≥40 years from which a subsample of 227 participated in an in-person clinical evaluation. Dystonia was assessed by 2 movement disorder neurologists using videotaped examinations.

RESULTS

Two of 227 (0.88%, 95% CI -0.33 to 2.09%) were diagnosed with cervical or segmental dystonia. An unusual form of thumb flexion dystonia was noted in 75 more, yielding a combined prevalence of 33.92% (95% CI 27.73-40.11%).

CONCLUSIONS

The prevalence of cervical or segmental dystonia was as high as in one prior population-based study using similar methods. Furthermore, an unusual form of thumb flexion dystonia was uncovered, which yielded an extraordinarily high prevalence of dystonia in this population. Although our methods likely contributed to more complete capture of subtle dystonia, founder effects are highly likely to have been an additional major contributor to these findings.

摘要

背景

全球仅有不到 5 项基于人群的研究探讨了肌张力障碍。仅有一项研究使用了运动障碍神经科医生。鉴于可能存在创始效应,以及肌张力障碍高度遗传性,法罗群岛为研究肌张力障碍的患病率提供了一个特别有趣的环境。

目的

估计肌张力障碍的患病率。

方法

我们采用了 2 阶段、基于人群的设计,对随机选择的 1334 名年龄≥40 岁的法罗群岛个体进行筛查,其中 227 名个体参与了现场临床评估。两名运动障碍神经科医生使用录像检查评估了肌张力障碍。

结果

227 名个体中有 2 名(0.88%,95%CI -0.33 至 2.09%)被诊断为颈段或节段性肌张力障碍。另外 75 名个体还存在一种不常见的拇指屈肌痉挛,总体患病率为 33.92%(95%CI 27.73-40.11%)。

结论

颈段或节段性肌张力障碍的患病率与采用类似方法的一项先前基于人群的研究相当。此外,还发现了一种不常见的拇指屈肌痉挛,使该人群的肌张力障碍患病率非常高。虽然我们的方法可能有助于更全面地发现微妙的肌张力障碍,但创始效应极有可能是这些发现的另一个主要促成因素。

相似文献

引用本文的文献

本文引用的文献

5
Update on the Genetics of Dystonia.扭转痉挛遗传学研究进展。
Curr Neurol Neurosci Rep. 2017 Mar;17(3):26. doi: 10.1007/s11910-017-0735-0.
7
Familial aggregation of Parkinson's disease in the Faroe Islands.法罗群岛帕金森病的家族聚集性。
Mov Disord. 2015 Apr;30(4):538-44. doi: 10.1002/mds.26132. Epub 2015 Jan 20.
9
Parkinson's disease, genetic variability and the Faroe Islands.帕金森病、基因变异性与法罗群岛
Parkinsonism Relat Disord. 2015 Jan;21(1):75-8. doi: 10.1016/j.parkreldis.2014.10.027. Epub 2014 Nov 4.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验