Evidence map›Paper›PMID 40091087›Full record

ArticleEJNMMI research2025

Multinomial logistic regression algorithm for the classification of patients with parkinsonisms.

Eva Štokelj, Tomaž Rus, Jan Jamšek, Maja Trošt, Urban Simončič

Abstract read
In one paragraph

Article in EJNMMI research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Eva ŠtokeljFaculty of Mathematics and Physics, University of Ljubljana, Jadranska ulica 19, 1000, Ljubljana, Slovenia.
Tomaž RusDepartment of Neurology, University Medical Centre Ljubljana, Zaloška cesta 2, 1000, Ljubljana, Slovenia.
Jan JamšekDepartment of Nuclear Medicine, University Medical Centre Ljubljana, Zaloška cesta 7, 1000, Ljubljana, Slovenia.
Maja TroštDepartment of Neurology, University Medical Centre Ljubljana, Zaloška cesta 2, 1000, Ljubljana, Slovenia.
Urban SimončičFaculty of Mathematics and Physics, University of Ljubljana, Jadranska ulica 19, 1000, Ljubljana, Slovenia. urban.simoncic@fmf.uni-lj.si.

Funding

Javna Agencija za Raziskovalno Dejavnost RS J7-2600Javna Agencija za Raziskovalno Dejavnost RS J7-3150Javna Agencija za Raziskovalno Dejavnost RS P1-0389
6 · The paper itself

Abstract

backgroundAccurate differential diagnosis of neurodegenerative parkinsonisms is challenging due to overlapping early symptoms and high rates of misdiagnosis. To improve the diagnostic accuracy, we developed an integrated classification algorithm using multinomial logistic regression and Scaled Subprofile Model/Principal Component Analysis (SSM/PCA) applied to

resultsThe Area Under the Curve (AUC) values were the highest for progressive supranuclear palsy (PSP) (AUC = 0.95), followed by Parkinson's disease (PD) (AUC = 0.93) and multiple system atrophy (MSA) (AUC = 0.90). When classifying the patients based on their calculated probability for each group, the desired tradeoff between sensitivity and specificity had to be selected. With a 99% probability threshold for classification into a disease group, 82% of PD patients, 29% of MSA patients, and 77% of PSP patients were correctly identified. Only 5% of PD, 6% of MSA and 6% of PSP patients were misclassified, whereas the remaining patients (13% of PD, 65% of MSA and 18% of PSP) are undetermined by our classification algorithm.

conclusionsCompared to existing algorithms, this approach offers comparable accuracy and reliability in diagnosing PD, MSA, and PSP with no need of healthy control images. It can also distinguish between multiple types of parkinsonisms simultaneously and offers the flexibility to easily accommodate new groups.

Indexed as

FDG-PETMetabolic brain patternMultinomial logistic regressionParkinsonismsSSM/PCA

Identifiers

PMID40091087
PMCPMC11911283

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.