Early Screening for the Parkinson Variant of Multiple System Atrophy: A 6‐Item Score

Author:

Fanciulli Alessandra1ORCID,Stankovic Iva23ORCID,Avraham Omer45,Jecmenica Lukic Milica23,Ezra Adi4,Leys Fabian1,Goebel Georg6,Krismer Florian1ORCID,Petrovic Igor23,Svetel Marina23,Seppi Klaus17,Kostic Vladimir23,Giladi Nir458,Poewe Werner1,Wenning Gregor K.1,Gurevich Tanya458

Affiliation:

1. Department of Neurology Medical University of Innsbruck Innsbruck Austria

2. Neurology Clinic, University Clinical Center of Serbia Belgrade Serbia

3. Faculty of Medicine University of Belgrade Belgrade Serbia

4. Movement Disorders Unit Neurological Institute, Tel‐Aviv Medical Center Tel‐Aviv Israel

5. School of Medicine, Sagol School of Neuroscience Tel‐Aviv University Tel‐Aviv Israel

6. Institute of Medical Statistics and Informatics Medical University of Innsbruck Innsbruck Austria

7. Department of Neurology Provincial Hospital of Kufstein Kufstein Austria

8. Sagol School of Neuroscience Tel‐Aviv University Tel‐Aviv Israel

Abstract

AbstractBackgroundA 4‐item score based on ≥2 features out of orthostatic hypotension, overactive bladder, urinary retention and postural instability was previously shown to early distinguish the Parkinson‐variant of multiple system atrophy (MSA‐P) from Parkinson's disease (PD) with 78% sensitivity and 86% specificity.ObjectivesTo replicate and improve the 4‐item MSA‐P score.MethodsWe retrospectively studied 161 patients with early parkinsonism [ie, ≤2 years disease duration or no postural instability, aged 64 (57; 68) years, 44% females] and a diagnosis of clinically established MSA‐P (n = 38) or PD (n = 123) after ≥24 months follow‐up.ResultsThe 4‐item MSA‐P score had a 92% sensitivity and 78% specificity for a final MSA‐P diagnosis. By including dopaminergic responsiveness and postural deformities into a 6‐item score (range: 0–6), reaching ≥3 points at early disease identified MSA‐P patients with 89% sensitivity and 98% specificity.ConclusionsThe 6‐item MSA‐P score is a cost‐effective tool to pinpoint individuals with early‐stage MSA‐P.

Funder

Austrian Science Fund

Publisher

Wiley

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