Epidemiology of progressive cerebellar ataxia in South Yorkshire, UK.

IF 2.6 Q3 CLINICAL NEUROLOGY
BMJ Neurology Open Pub Date : 2026-10-01 eCollection Date: 2026-01-01 DOI:10.1136/bmjno-2026-001799
Emma Foster, Priya Darshni Shanmugarajah, Suzanna Duty, Ewelina Hogg, Marios Hadjivassiliou
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引用次数: 0

Abstract

Background: Cerebellar ataxias are a heterogeneous group of rare neurological disorders characterised by progressive gait instability, limb incoordination, speech and oculomotor impairment. UK prevalence estimates remain rather limited, with the most widely cited population-based study performed in South East Wales over two decades ago. The objective is to estimate the current prevalence of progressive cerebellar ataxia within South Yorkshire using a comprehensive NHS (National Health Service) tertiary ataxia service database and to compare findings with previously published UK data.

Methods: A retrospective epidemiological analysis was undertaken using the Sheffield Ataxia Centre NHS clinical database. All alive patients aged over 18 years living in South Yorkshire with confirmed progressive cerebellar ataxia under active or historical follow-up were included, excluding static and structural ataxias where appropriate. Population sizes within South Yorkshire were derived from the 2024 Office for National Statistics (ONS) mid-year population estimates for everyone aged over 18 years and over 65 years.

Results: A total of 1204 individuals with progressive cerebellar ataxia were identified as resident in South Yorkshire, corresponding to a frequency prevalence of approximately 106 per 100 000 population (1:942). Prevalence varied by local authority, ranging from 1:647 in Sheffield to 1:1677 in Doncaster.

Conclusions: The prevalence of progressive cerebellar ataxia in South Yorkshire is substantially higher than previously reported UK figures, likely reflecting improvements in diagnostic capability, service centralisation and recognition of immune-mediated and new novel genetic ataxias. These figures have important implications for service planning and resource allocation within the NHS.

英国南约克郡进行性小脑共济失调的流行病学。
背景:小脑共济失调是一种异质性的罕见神经系统疾病,其特征是进行性步态不稳定、肢体不协调、语言和动眼肌损伤。英国的患病率估计仍然相当有限,最广泛引用的基于人口的研究是二十多年前在东南威尔士进行的。目的是利用全面的NHS(国民健康服务)三级共济失调服务数据库估计南约克郡目前进行性小脑性共济失调的患病率,并将研究结果与先前发表的英国数据进行比较。方法:使用谢菲尔德共济失调中心NHS临床数据库进行回顾性流行病学分析。所有居住在南约克郡的年龄在18岁以上的确诊进行性小脑共济失调的患者在积极或历史随访中被纳入,排除了静态和结构性共济失调。南约克郡的人口规模来自2024年国家统计局(ONS)对18岁以上和65岁以上人口的年中人口估计。结果:南约克郡共有1204名进行性小脑共济失调患者,患病率约为每10万人106人(1:942)。发病率因地方政府而异,从谢菲尔德的1:647到唐卡斯特的1:1677不等。结论:南约克郡进行性小脑共济失调的患病率大大高于先前报道的英国数据,可能反映了诊断能力,服务集中化和免疫介导和新型遗传共济失调的识别的改善。这些数字对NHS内的服务规划和资源分配具有重要意义。
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
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
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