{"title":"Evaluating <sup>18</sup>F-Florzolotau tau PET for Alzheimer's disease diagnosis with <sup>18</sup>F-Flortaucipir as reference.","authors":"Qi Zhang, Jiaying Lu, Luyao Wang, Fangyang Jiao, Min Wang, Kuangyu Shi, Chuantao Zuo, Jiehui Jiang","doi":"10.1007/s00415-025-13342-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Tau protein aggregation is a hallmark of Alzheimer's disease (AD) pathology. Semi-quantitative analysis using regions of interest (ROIs)-based standardized uptake value ratios (SUVRs) serves as a major Tau positron emission tomography (PET) biomarker for AD diagnosis and staging. This study aims to evaluate the diagnostic performance of the second-generation tau tracer <sup>18</sup>F-Florzolotau, including the impact of semi-quantitative reference region and ROIs methodology and partial volume error (PVE) correction. Data from the FDA-approved tracer <sup>18</sup>F-Flortaucipir provide benchmark context, aiming to evaluate the performance.</p><p><strong>Methods: </strong>A total of 842 participants from two cohorts underwent tau PET imaging with either <sup>18</sup>F-Flortaucipir (n = 741) or <sup>18</sup>F-Florzolotau (n = 101). The <sup>18</sup>F-Flortaucipir cohort contains 384 normal controls, 292 patients with mild cognitive impairment, and 65 AD dementia. The <sup>18</sup>F-Florzolotau cohort contains 27 normal controls, 26 patients with mild cognitive impairment and 48 AD dementia. SUVRs were calculated across four ROIs using six semi-quantitative methods varying by reference region and PVE-correction application. Diagnostic performance was assessed using the area under the curve (AUC) from receiver operating characteristic analysis. Partial correlations between SUVRs and clinical severity were evaluated.</p><p><strong>Results: </strong><sup>18</sup>F-Florzolotau demonstrated high diagnostic accuracy (AUC: 0.96-0.98) for AD dementia and strong clinical correlations (|r|= 0.61-0.74). Performance varied with semi-quantitative methodology. The optimal approach used inferior cerebellar gray matter as the reference region, achieving the highest AUC and strong clinical correlations for <sup>18</sup>F-Florzolotau. Results for <sup>18</sup>F-Flortaucipir (AUC: 0.78-0.87; |r|= 0.29-0.45) provided consistent methodological insights supporting the choice of inferior cerebellar gray methodology.</p><p><strong>Conclusions: </strong><sup>18</sup>F-Florzolotau shows excellent diagnostic performance for AD dementia. The semi-quantitative methodology impacts results, with inferior cerebellar gray as the recommended reference region for optimizing <sup>18</sup>F-Florzolotau SUVR analysis in AD dementia. These findings support the clinical utility of <sup>18</sup>F-Florzolotau tau PET in AD.</p>","PeriodicalId":16558,"journal":{"name":"Journal of Neurology","volume":"272 9","pages":"597"},"PeriodicalIF":4.6000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00415-025-13342-3","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Tau protein aggregation is a hallmark of Alzheimer's disease (AD) pathology. Semi-quantitative analysis using regions of interest (ROIs)-based standardized uptake value ratios (SUVRs) serves as a major Tau positron emission tomography (PET) biomarker for AD diagnosis and staging. This study aims to evaluate the diagnostic performance of the second-generation tau tracer 18F-Florzolotau, including the impact of semi-quantitative reference region and ROIs methodology and partial volume error (PVE) correction. Data from the FDA-approved tracer 18F-Flortaucipir provide benchmark context, aiming to evaluate the performance.
Methods: A total of 842 participants from two cohorts underwent tau PET imaging with either 18F-Flortaucipir (n = 741) or 18F-Florzolotau (n = 101). The 18F-Flortaucipir cohort contains 384 normal controls, 292 patients with mild cognitive impairment, and 65 AD dementia. The 18F-Florzolotau cohort contains 27 normal controls, 26 patients with mild cognitive impairment and 48 AD dementia. SUVRs were calculated across four ROIs using six semi-quantitative methods varying by reference region and PVE-correction application. Diagnostic performance was assessed using the area under the curve (AUC) from receiver operating characteristic analysis. Partial correlations between SUVRs and clinical severity were evaluated.
Results: 18F-Florzolotau demonstrated high diagnostic accuracy (AUC: 0.96-0.98) for AD dementia and strong clinical correlations (|r|= 0.61-0.74). Performance varied with semi-quantitative methodology. The optimal approach used inferior cerebellar gray matter as the reference region, achieving the highest AUC and strong clinical correlations for 18F-Florzolotau. Results for 18F-Flortaucipir (AUC: 0.78-0.87; |r|= 0.29-0.45) provided consistent methodological insights supporting the choice of inferior cerebellar gray methodology.
Conclusions: 18F-Florzolotau shows excellent diagnostic performance for AD dementia. The semi-quantitative methodology impacts results, with inferior cerebellar gray as the recommended reference region for optimizing 18F-Florzolotau SUVR analysis in AD dementia. These findings support the clinical utility of 18F-Florzolotau tau PET in AD.
期刊介绍:
The Journal of Neurology is an international peer-reviewed journal which provides a source for publishing original communications and reviews on clinical neurology covering the whole field.
In addition, Letters to the Editors serve as a forum for clinical cases and the exchange of ideas which highlight important new findings. A section on Neurological progress serves to summarise the major findings in certain fields of neurology. Commentaries on new developments in clinical neuroscience, which may be commissioned or submitted, are published as editorials.
Every neurologist interested in the current diagnosis and treatment of neurological disorders needs access to the information contained in this valuable journal.