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1998-2019 年英格兰运动神经元病发病率分析:三个关联数据集的应用。

Analysis of incidence of motor neuron disease in England 1998-2019: use of three linked datasets.

机构信息

Nuffield Department of Primary Care Health Sciences, Oxford University, Oxford, England.

Institute for Translational Neuroscience, University of Sheffield, Sheffield, England.

出版信息

Amyotroph Lateral Scler Frontotemporal Degener. 2022 Aug;23(5-6):363-371. doi: 10.1080/21678421.2021.2016837. Epub 2022 Feb 1.

DOI:10.1080/21678421.2021.2016837
PMID:35103515
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9344929/
Abstract

This study uses three linked datasets to provide an estimate of incidence of motor neuron disease (MND) in England from 1998 to 2019. Comparison is made to previous British studies. It examines age at diagnosis and ethnicity of those affected. The literature was searched for studies of MND incidence in Great Britain from 1995 to date. The QResearch and linked Hospital Episode Statistics and Death register databases were searched from 1998 to 2019 for cases of MND, and incidence calculated from 16.8 million adults and 112 million adult years of data. We found 6437 adults with a diagnosis of MND giving an incidence of MND of 5.69/100,000 person years (95% CI 5.51-5.88); 6.57 (6.41-6.99) in men and 4.72 (4.49-4.97) in women when age-standardized to the 2011 UK population. The median age of diagnosis was 72 years. Peak incidence occurred in the 80-84 year age group in men and 75-79 in women. Age-standardized incidence was as high in Bangladeshi, Black Caribbean, Indian, other Asian and Pakistani people as in White people. Black African and Chinese people had a lower incidence. The use of three linked national datasets captured 33% more people than a primary care dataset alone. Patients were older than in previous studies and rates were high in all ethnic groups studied except Black African and Chinese people. We present the highest incidence of MND reported globally in the past 50 years. Methodological differences may in part explain differences with previous reports. The use of national datasets may have captured additional MND patients with serious comorbidities who have not seen a neurologist before death. A limitation of this approach is that unlike population registers, which minimize false positive diagnosis by neurologist review of each patient, we cannot review diagnosis for individuals as data are anonymized.

摘要

这项研究使用三个关联数据集,提供了 1998 年至 2019 年期间英格兰运动神经元疾病(MND)发病率的估计。与之前的英国研究进行了比较。它检查了诊断时的年龄和受影响人群的种族。从 1995 年至今,对英国 MND 发病率的研究进行了文献检索。从 1998 年到 2019 年,在 QResearch 及其关联的医院事件统计和死亡登记数据库中搜索 MND 病例,并从 1680 万成年人和 1.12 亿成年人的数据中计算发病率。我们发现 6437 名成年人被诊断为 MND,发病率为 5.69/100000 人年(95%CI 5.51-5.88);男性为 6.57(6.41-6.99),女性为 4.72(4.49-4.97),年龄标准化至 2011 年英国人口。诊断的中位年龄为 72 岁。发病率峰值出现在男性 80-84 岁和女性 75-79 岁年龄组。孟加拉国人、加勒比黑人、印度人、其他亚洲人和巴基斯坦人的年龄标准化发病率与白人一样高。黑人和中国人的发病率较低。与仅使用初级保健数据集相比,使用三个关联的国家数据集捕获了 33%的更多人。患者比以前的研究更年长,除了黑人和中国人外,所有研究的种族群体发病率都很高。我们提出了过去 50 年来全球报道的最高 MND 发病率。方法学差异可能在一定程度上解释了与以前报告的差异。使用国家数据集可能会捕获更多患有严重合并症的 MND 患者,这些患者在死亡前从未看过神经科医生。这种方法的一个限制是,与人口登记不同,人口登记通过神经科医生对每个患者的诊断进行审查来最小化假阳性诊断,我们不能对个人的诊断进行审查,因为数据是匿名的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/abbfe1c14e28/IAFD_A_2016837_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/20936c56c0a5/IAFD_A_2016837_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/6bb021ff958b/IAFD_A_2016837_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/5feb6842edf4/IAFD_A_2016837_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/abbfe1c14e28/IAFD_A_2016837_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/20936c56c0a5/IAFD_A_2016837_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/6bb021ff958b/IAFD_A_2016837_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/5feb6842edf4/IAFD_A_2016837_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9efd/9344929/abbfe1c14e28/IAFD_A_2016837_F0004_C.jpg

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