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001     282561
005     20251202143603.0
024 7 _ |a 10.1002/mds.70026
|2 doi
024 7 _ |a pmid:40884249
|2 pmid
024 7 _ |a pmc:PMC12661634
|2 pmc
024 7 _ |a 0885-3185
|2 ISSN
024 7 _ |a 1531-8257
|2 ISSN
037 _ _ |a DZNE-2025-01324
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Quattrone, Andrea
|0 P:(DE-2719)9002627
|b 0
|u dzne
245 _ _ |a Brain Atrophy Does Not Predict Clinical Progression in Progressive Supranuclear Palsy.
260 _ _ |a New York, NY
|c 2025
|b Wiley
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1764681380_28230
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Clinical progression rate is the typical primary endpoint measure in progressive supranuclear palsy (PSP) clinical trials.This longitudinal multicohort study investigated whether baseline clinical severity and regional brain atrophy could predict clinical progression in PSP-Richardson's syndrome (PSP-RS).PSP-RS patients (n = 309) from the placebo arms of clinical trials (NCT03068468, NCT01110720, NCT02985879, NCT01049399) and DescribePSP cohort were included. We investigated associations of baseline clinical and volumetric magnetic resonance imaging (MRI) data with 1-year longitudinal PSP rating scale (PSPRS) change. Machine learning (ML) models were tested to predict individual clinical trajectories.PSP-RS patients showed a mean PSPRS score increase of 10.3 points/yr. The frontal lobe volume showed the strongest association with subsequent clinical progression (β: -0.34, P < 0.001). However, ML models did not accurately predict individual progression rates (R2 <0.15).Baseline clinical severity and brain atrophy could not predict individual clinical progression, suggesting no need for MRI-based stratification of patients in future PSP trials. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
536 _ _ |a 353 - Clinical and Health Care Research (POF4-353)
|0 G:(DE-HGF)POF4-353
|c POF4-353
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de
650 _ 7 |a atlas‐based volumetry
|2 Other
650 _ 7 |a clinical trials
|2 Other
650 _ 7 |a outcome
|2 Other
650 _ 7 |a progression
|2 Other
650 _ 7 |a progressive supranuclear palsy
|2 Other
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Supranuclear Palsy, Progressive: pathology
|2 MeSH
650 _ 2 |a Supranuclear Palsy, Progressive: diagnostic imaging
|2 MeSH
650 _ 2 |a Disease Progression
|2 MeSH
650 _ 2 |a Atrophy: pathology
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Magnetic Resonance Imaging
|2 MeSH
650 _ 2 |a Brain: pathology
|2 MeSH
650 _ 2 |a Brain: diagnostic imaging
|2 MeSH
650 _ 2 |a Middle Aged
|2 MeSH
650 _ 2 |a Longitudinal Studies
|2 MeSH
650 _ 2 |a Severity of Illness Index
|2 MeSH
650 _ 2 |a Machine Learning
|2 MeSH
693 _ _ |0 EXP:(DE-2719)DESCRIBE-PSP-20160101
|5 EXP:(DE-2719)DESCRIBE-PSP-20160101
|e DZNE Clinical Registry Study of Neurodegenerative Diseases in Patients with Progressive Supranuclear Paresis (PSP)
|x 0
700 1 _ |a Franzmeier, Nicolai
|b 1
700 1 _ |a Huppertz, Hans-Jürgen
|b 2
700 1 _ |a Seneca, Nicholas
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700 1 _ |a Petzold, Gabor C
|0 P:(DE-2719)2810273
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700 1 _ |a Spottke, Annika
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700 1 _ |a Levin, Johannes
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700 1 _ |a Prudlo, Johannes
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700 1 _ |a Düzel, Emrah
|0 P:(DE-2719)2000005
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700 1 _ |a PASSPORT Study Group, the AL-108-231 Investigators, the Arise Investigators, the Tauros MRI Investigators, the DESCRIBE-PSP group
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700 1 _ |a Höglinger, Günter U
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700 1 _ |a Wagner, Michael
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700 1 _ |a Weidinger, Endy
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700 1 _ |a Wiltfang, Jens
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700 1 _ |a Wolfsgruber, Steffen
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700 1 _ |a Zollver, Adelgunde
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773 _ _ |a 10.1002/mds.70026
|g Vol. 40, no. 11, p. 2517 - 2530
|0 PERI:(DE-600)2041249-6
|n 11
|p 2517 - 2530
|t Movement disorders
|v 40
|y 2025
|x 0885-3185
856 4 _ |u https://pub.dzne.de/record/282561/files/DZNE-2025-01324.pdf
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Marc 21