UCL Discovery Stage
UCL home » Library Services » Electronic resources » UCL Discovery Stage

Pathological Validation of the MDS Criteria for the Diagnosis of Multiple System Atrophy

Virameteekul, Sasivimol; Revesz, Tamas; Jaunmuktane, Zane; Warner, Thomas T; De Pablo-Fernández, Eduardo; (2023) Pathological Validation of the MDS Criteria for the Diagnosis of Multiple System Atrophy. Movement Disorders 10.1002/mds.29304. (In press).

[thumbnail of De Pablo Fernandez_Pathological Validation of The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy_R2_Clear.pdf] Text
De Pablo Fernandez_Pathological Validation of The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy_R2_Clear.pdf
Access restricted to UCL open access staff

Download (209kB)
[thumbnail of De Pablo Fernandez_Supplementary material_R2.pdf] Text
De Pablo Fernandez_Supplementary material_R2.pdf
Access restricted to UCL open access staff

Download (157kB)
[thumbnail of De Pablo Fernandez_Tables_R2.pdf] Text
De Pablo Fernandez_Tables_R2.pdf
Access restricted to UCL open access staff

Download (68kB)

Abstract

BACKGROUND: The recent International Parkinson and Movement Disorder Society diagnostic criteria for multiple system atrophy (MDS-MSA) have been developed to improve diagnostic accuracy although their diagnostic properties have not been evaluated. OBJECTIVES: The aims were to validate the MDS-MSA diagnostic criteria against neuropathological diagnosis and compare their diagnostic performance to previous criteria and diagnosis in clinical practice. METHODS: Consecutive patients with sporadic, progressive, adult-onset parkinsonism, or cerebellar ataxia from the Queen Square Brain Bank between 2009 and 2019 were selected and divided based on neuropathological diagnosis into MSA and non-MSA. Medical records were systematically reviewed, and clinical diagnosis was documented by retrospectively applying the MDS-MSA criteria, second consensus criteria, and diagnosis according to treating clinicians at early (within 3 years of symptom onset) and final stages. Diagnostic parameters (sensitivity, specificity, positive/negative predictive value, and accuracy) were calculated using neuropathological diagnosis as gold standard and compared between different criteria. RESULTS: Three hundred eighteen patients (103 MSA and 215 non-MSA) were included, comprising 248 patients with parkinsonism and 70 with cerebellar ataxia. Clinically probable MDS-MSA showed excellent sensitivity (95.1%), specificity (94.0%), and accuracy (94.3%), although their sensitivity at early stages was modest (62.1%). Clinically probable MDS-MSA outperformed diagnosis by clinicians and by second consensus criteria. Clinically established MDS-MSA showed perfect specificity (100%) even at early stages although to the detriment of low sensitivity. MDS-MSA diagnostic accuracy did not differ according to clinical presentation (ataxia vs. parkinsonism). CONCLUSIONS: MDS-MSA criteria demonstrated excellent diagnostic performance against neuropathological diagnosis and are useful diagnostic tools for clinical practice and research. © 2023 International Parkinson and Movement Disorder Society.

Type: Article
Title: Pathological Validation of the MDS Criteria for the Diagnosis of Multiple System Atrophy
Location: United States
DOI: 10.1002/mds.29304
Publisher version: https://doi.org/10.1002/mds.29304
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: diagnosis, diagnostic accuracy, diagnostic criteria, multiple system atrophy, pathological validation
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences
URI: https://discovery-pp.ucl.ac.uk/id/eprint/10163115
Downloads since deposit
228Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item