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肌痛性脑脊髓炎/慢性疲劳综合征病例对照研究中误诊的影响

Impact of Misdiagnosis in Case-Control Studies of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

作者信息

Malato João, Graça Luís, Sepúlveda Nuno

机构信息

Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.

CEAUL-Centro de Estatística e Aplicações da Universidade de Lisboa, 1749-016 Lisboa, Portugal.

出版信息

Diagnostics (Basel). 2023 Feb 1;13(3):531. doi: 10.3390/diagnostics13030531.

Abstract

Misdiagnosis of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) can occur when different case definitions are used by clinicians (relative misdiagnosis) or when failing the genuine diagnosis of another disease (misdiagnosis in a strict sense). This problem translates to a recurrent difficulty in reproducing research findings. To tackle this problem, we simulated data from case-control studies under misdiagnosis in a strict sense. We then estimated the power to detect a genuine association between a potential causal factor and ME/CFS. A minimum power of 80% was obtained for studies with more than 500 individuals per study group. When the simulation study was extended to the situation where the potential causal factor could not be determined perfectly (e.g., seropositive/seronegative in serological association studies), the minimum power of 80% could only be achieved in studies with more than 1000 individuals per group. In conclusion, current ME/CFS studies have suboptimal power under the assumption of misdiagnosis. This power can be improved by increasing the overall sample size using multi-centric studies, reporting the excluded illnesses and their exclusion criteria, or focusing on a homogeneous cohort of ME/CFS patients with a specific pathological mechanism where the chance of misdiagnosis is reduced.

摘要

当临床医生使用不同的病例定义时(相对误诊),或者当未能正确诊断出另一种疾病时(严格意义上的误诊),可能会发生肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)的误诊。这个问题导致在重复研究结果时反复出现困难。为了解决这个问题,我们在严格误诊的情况下模拟了病例对照研究的数据。然后,我们估计了检测潜在因果因素与ME/CFS之间真实关联的检验效能。每个研究组有超过500名个体的研究获得了至少80%的检验效能。当模拟研究扩展到潜在因果因素无法完美确定的情况时(例如,血清学关联研究中的血清阳性/血清阴性),每组超过1000名个体的研究才能达到至少80%的检验效能。总之,在误诊假设下,当前的ME/CFS研究检验效能欠佳。可以通过采用多中心研究增加总体样本量、报告排除的疾病及其排除标准,或者关注具有特定病理机制且误诊可能性降低的ME/CFS患者同质队列来提高检验效能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e57/9914258/96707e40f9df/diagnostics-13-00531-g001.jpg

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