Early Subtypes and Progressions of Progressive Supranuclear Palsy: A Data-Driven Brain Bank Study.

Daisuke Ono, Hiroaki Sekiya, Nikhil B Ghayal, Alexia R Maier, Shanu F Roemer, Ryan J Uitti, Irene Litvan, Keith A Josephs, Zbigniew K Wszolek, Dennis W Dickson
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Abstract

Background: Progressive supranuclear palsy (PSP) is typically characterized by vertical supranuclear gaze palsy and early falls, referred to as Richardson's syndrome (PSP-RS). Other presentations include postural instability (PSP-PI), parkinsonism (PSP-P), speech/language impairment (PSP-SL), frontal presentation (PSP-F), ocular motor dysfunction (PSP-OM), and corticobasal syndrome (PSP-CBS). Differences across the early presentations and in their subsequent progression have yet to be elucidated.

Objective: This study aimed to characterize early PSP subtypes and their subsequent progressions using a large postmortem dataset.

Methods: An automated pipeline incorporating fine-tuned ChatGPT models was developed. The pipeline collected 195 clinical features with onset information from autopsy-confirmed PSP cases without significant neurodegenerative co-pathologies.

Results: A structured clinicopathologic dataset from 588 patients was analyzed. After distilling results with unsupervised clustering, a decision tree model was developed. With five clinical manifestations: frontal presentation, PI, OM, SL, and parkinsonism, this mutually exclusive algorithm identified seven subtypes: PSP-PF (postural and frontal dysfunction), PSP-RS, PSP-PI, PSP-P, PSP-SL, PSP-F, and PSP-OM. PSP-PF, defined by PI and frontal presentation, showed rapid progression, the shortest median disease duration (six years), and high tau burden in cortical and subcortical regions. In PSP-F, frontal presentation preceded other symptoms by four years, and the disease duration was the second longest (nine years) after PSP-P (10 years). PSP-CBS was not identified as an independent subtype.

Conclusions: This data-driven study identified a novel, aggressive PSP phenotype characterized by early postural and frontal dysfunction. Early subtyping utilizing the decision tree would help clinicians estimate progression and facilitate early patient recruitment for clinical trials.

进行性核上性麻痹的早期亚型和进展:一个数据驱动的脑库研究。
背景:进行性核上性麻痹(PSP)的典型特征是垂直核上凝视性麻痹和早期跌倒,被称为理查森综合征(PSP- rs)。其他表现包括体位不稳(PSP-PI)、帕金森病(PSP-P)、言语/语言障碍(PSP-SL)、额部表现(PSP-F)、眼运动功能障碍(PSP-OM)和皮质基底综合征(PSP-CBS)。早期表现和随后进展的差异尚未得到阐明。目的:本研究旨在利用大型死后数据集描述早期PSP亚型及其随后的进展。方法:建立一个包含微调ChatGPT模型的自动化流水线。该研究收集了195例尸检证实的PSP病例的临床特征和发病信息,这些病例没有明显的神经退行性共病。结果:对588例患者的结构化临床病理数据集进行了分析。在对结果进行无监督聚类后,建立了决策树模型。具有5种临床表现:额部表现、PI、OM、SL和帕金森症,该算法确定了7种亚型:PSP-PF(体位和额部功能障碍)、PSP-RS、PSP-PI、PSP-P、PSP-SL、PSP-F和PSP-OM。由PI和额位表现定义的PSP-PF表现为进展迅速,中位病程最短(6年),皮层和皮层下区域的tau负担高。在PSP-F中,额部表现比其他症状早4年,病程第二长(9年),仅次于PSP-P(10年)。PSP-CBS未被确定为独立亚型。结论:这项数据驱动的研究确定了一种新的、侵袭性的PSP表型,其特征是早期姿势和额叶功能障碍。早期亚型利用决策树将有助于临床医生估计进展和促进早期患者招募临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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