17种神经肌肉疾病的患病率和发病率:最新文献综述。

IF 3.4 4区 医学 Q2 CLINICAL NEUROLOGY
Johanna Cw Deenen, André Lm Verbeek, Jan Jgm Verschuuren, Baziel Gm van Engelen, Nicol C Voermans
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引用次数: 0

摘要

背景:流行病学频率测量可作为患者、临床医生、研究人员和决策者的参考点。之前,我们发表了一篇关于神经肌肉临床中常见的30种神经肌肉疾病的患病率和发病率的文献综述。当时还没有荟萃分析。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,我们的目标是更新我们之前的综述。方法:在Pubmed检索17种获得性和遗传性神经肌肉疾病的“发病率”和“患病率”,以确定1990年至2023年的同行评议文献。如果发现多个患病率和发病率,则通过提供平均值、平均值所依据的估计值的数量和这些估计值的范围来总结这些估计值。此外,我们检索了meta分析,以比较基于单个研究总结得出的平均患病率与基于meta分析得出的综合患病率。结果:17种疾病的平均患病率估计范围从兰波特-伊顿肌无力综合征、糖原症V型和线状肌病的0.3/10万人到沙克-玛丽-图斯病i型的20/10万人。我们发现8种疾病的年发病率范围从进行性(脊髓)肌肉萎缩和面肩肱肌萎缩的0.3/10万人到沙克-玛丽-图斯病1型和肌强直性营养不良1型的1/10万人。将当前研究的平均患病率估计值与8项荟萃分析的汇总患病率估计值进行对比,结果显示出合理的一致性。结论:神经肌肉疾病的流行病学频率,特别是发病率的数据很少。基于最近发表的关于个体队列的研究得出的平均患病率估计值与较少进行的荟萃分析的结果吻合得很好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence and incidence rates of 17 neuromuscular disorders: An updated review of the literature.

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.

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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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