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17种神经肌肉疾病的患病率和发病率:文献综述更新

Prevalence and incidence rates of 17 neuromuscular disorders: An updated review of the literature.

作者信息

Deenen Johanna Cw, Verbeek André Lm, Verschuuren Jan Jgm, van Engelen Baziel Gm, Voermans Nicol C

机构信息

Department of Neurology, Radboud university medical center, PO Box 9101, 6500 HB Nijmegen, the Netherlands.

Department for Health Evidence, Radboud university medical center, PO Box 9101, 6500 HB Nijmegen, the Netherlands.

出版信息

J Neuromuscul Dis. 2025 Mar 4:22143602241313118. doi: 10.1177/22143602241313118.

Abstract

BACKGROUND

Epidemiological frequency measures serve as reference point for patients, clinicians, researchers, and policymakers. Previously, we published a comprehensive review of the literature with prevalence and incidence rates for thirty neuromuscular disorders frequently encountered in the neuromuscular clinic. No meta-analyses were available at the time.

OBJECTIVE

We included various new studies and meta-analyses that have been published since 2014, we aim to update our previous review.

METHODS

Pubmed was searched for 'incidence' and 'prevalence' in combination with seventeen acquired and inherited neuromuscular disorders to identify peer-reviewed literature from 1990 to 2023. If multiple prevalence and incidence rates were found, these were summarized by providing the mean, the number of the estimates on which the mean was based and the range of these estimates. Additionally, we searched for meta-analyses to compare the found mean prevalence rates based on the summary of individual studies with the pooled prevalence rates based on the meta-analyses.

RESULTS

The mean prevalence estimates for 17 disorders ranged from 0.3/100,000 population for Lambert-Eaton myasthenic syndrome, glycogenosis type V and nemaline myopathy to 20/100,000 for Charcot-Marie-Tooth disease type I. We found annual incidence rates for eight disorders, ranging from 0.3/100,000 population for progressive (spinal) muscular atrophy and facioscapulohumeral muscular atrophy to 1/100,000 for Charcot-Marie-Tooth disease type 1 and myotonic dystrophy type 1. Plotting the mean prevalence estimates from the current study against the pooled prevalence estimates from eight meta-analyses showed reasonable agreement.

CONCLUSIONS

Epidemiological frequencies about neuromuscular diseases- and in particular data on incidence are scarce. The mean prevalence estimates based on recently published studies on individual cohorts correspond well with the findings from the sparingly performed meta-analyses.

摘要

背景

流行病学频率测量为患者、临床医生、研究人员和政策制定者提供了参考依据。此前,我们发表了一篇全面的文献综述,介绍了神经肌肉诊所中常见的30种神经肌肉疾病的患病率和发病率。当时尚无荟萃分析。

目的

我们纳入了自2014年以来发表的各种新研究和荟萃分析,旨在更新我们之前的综述。

方法

在PubMed上搜索“发病率”和“患病率”,并结合17种获得性和遗传性神经肌肉疾病,以识别1990年至2023年的同行评审文献。如果发现多个患病率和发病率,通过提供平均值、该平均值所基于的估计数以及这些估计数的范围来进行总结。此外,我们搜索了荟萃分析,以比较基于个体研究总结得出的平均患病率与基于荟萃分析得出的合并患病率。

结果

17种疾病的平均患病率估计值范围从兰伯特-伊顿肌无力综合征、Ⅴ型糖原贮积病和杆状体肌病的每10万人口0.3例到Ⅰ型遗传性运动感觉神经病的每10万人口20例。我们发现了8种疾病的年发病率,范围从进行性(脊髓性)肌萎缩和面肩肱型肌营养不良的每10万人口0.3例到Ⅰ型遗传性运动感觉神经病和Ⅰ型强直性肌营养不良的每10万人口1例。将本研究的平均患病率估计值与八项荟萃分析的合并患病率估计值进行对比,结果显示吻合度良好。

结论

关于神经肌肉疾病的流行病学频率,尤其是发病率数据稀缺。基于近期发表的个体队列研究得出的平均患病率估计值与少量进行的荟萃分析结果吻合度良好。

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