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成人特发性肌张力障碍:一项全国性数据链接研究,旨在确定流行病学、社会剥夺和死亡率特征。

Adult-onset idiopathic dystonia: A national data-linkage study to determine epidemiological, social deprivation, and mortality characteristics.

机构信息

Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, UK.

Swansea University Medical School, Swansea, UK.

出版信息

Eur J Neurol. 2022 Jan;29(1):91-104. doi: 10.1111/ene.15114. Epub 2021 Oct 15.

Abstract

BACKGROUND AND PURPOSE

Accurate epidemiological information is essential for the improved understanding of dystonia syndromes, as well as better provisioning of clinical services and providing context for diagnostic decision-making. Here, we determine epidemiological, social deprivation, and mortality characteristics of adult-onset idiopathic dystonia in the Welsh population.

METHODS

A retrospective population-based cohort study using anonymized electronic health care data in Wales was conducted to identify individuals with dystonia between 1 January 1994 and 31 December 2017. We developed a case-ascertainment algorithm to determine dystonia incidence and prevalence, as well as characterization of the dystonia cohort, based on social deprivation and mortality.

RESULTS

The case-ascertainment algorithm (79% sensitivity) identified 54,966 cases; of these cases, 41,660 had adult-onset idiopathic dystonia (≥20 years). Amongst the adult-onset form, the median age at diagnosis was 41 years, with males significantly older at time of diagnosis compared to females. Prevalence rates ranged from 0.02% in 1994 to 1.2% in 2017. The average annual incidence was 87.7/100,000/year, increasing from 49.9/100,000/year (1994) to 96.21/100,000/year (2017). In 2017, people with dystonia had a similar life expectancy to the Welsh population.

CONCLUSIONS

We have developed a case-ascertainment algorithm, supported by the introduction of a neurologist-reviewed validation cohort, providing a platform for future population-based dystonia studies. We have established robust population-level prevalence and incidence values for adult-onset idiopathic forms of dystonia, with this reflecting increasing clinical recognition and identification of causal genes. Underlying causes of death mirrored those of the general population, including circulatory disorders, respiratory disorders, cancers, and dementia.

摘要

背景与目的

准确的流行病学信息对于深入了解肌张力障碍综合征至关重要,同时也有助于改善临床服务,并为诊断决策提供背景。本研究旨在确定威尔士人群成年起病特发性肌张力障碍的流行病学、社会剥夺和死亡率特征。

方法

我们采用基于人群的回顾性队列研究,使用威尔士匿名电子医疗保健数据,确定 1994 年 1 月 1 日至 2017 年 12 月 31 日期间患有肌张力障碍的个体。我们开发了一种病例确定算法,以根据社会剥夺和死亡率确定肌张力障碍的发病率和患病率,并对肌张力障碍队列进行特征描述。

结果

病例确定算法(敏感性 79%)确定了 54966 例病例;其中 41660 例为成年起病特发性肌张力障碍(≥20 岁)。在成年起病的病例中,诊断时的中位年龄为 41 岁,男性的诊断年龄明显大于女性。患病率从 1994 年的 0.02%到 2017 年的 1.2%不等。年平均发病率为 87.7/100000/年,从 1994 年的 49.9/100000/年增加到 2017 年的 96.21/100000/年。2017 年,肌张力障碍患者的预期寿命与威尔士人群相似。

结论

我们开发了一种病例确定算法,通过引入神经科医生审查的验证队列提供支持,为未来的基于人群的肌张力障碍研究提供了一个平台。我们确定了成年起病特发性肌张力障碍的可靠的人群水平患病率和发病率值,这反映了临床识别和病因基因鉴定的增加。死亡的根本原因与一般人群相似,包括循环系统疾病、呼吸系统疾病、癌症和痴呆症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c931/9377012/57eb4d7a0f85/ENE-29-91-g004.jpg

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