T1 mapping in Alzheimer’s disease: a quantitative MRI study with amyloid-PET correlation

Abstract Objectives Quantitative T1 mapping (qT1) is a magnetic resonance imaging (MRI) biomarker of brain microstructural changes; however, its application in Alzheimer disease (AD) remains limited. We compared cortico-limbic qT1 values between patients with AD and healthy controls (HCs) and examined their relationship with amyloid burden measured by amyloid-positron emission tomography (PET). Materials and methods We retrospectively identified subjects with mild cognitive impairment due to AD and HCs who underwent 3-T MRI, including a compressed-sensing MP2RAGE sequence, generating three-dimensional T1-weighted images and qT1 maps. Amyloid-PET was available for 16 patients. Hippocampal qT1 and volume were compared between groups, adjusting for age and sex; analyses were repeated after stratifying patients by Mini-Mental State Examination (MMSE). Voxel-wise group comparison was performed using SPM 12. The qT1-standardized uptake value ratio (SUVr) association was assessed with a linear mixed-effects model applied to voxel-level data, accounting for partial volume effects. Results Thirty-three AD subjects, aged 69.3 ± 8.2 years (mean ± standard deviation), 18 females, and 22 HCs aged 70.5 ± 13.3 years, 15 females, were evaluated. Regional hippocampal qT1 was higher in AD (1,398 ± 53.0 ms versus 1,349 ± 53.4 ms; p = 0.002), without difference across cognitive subgroups stratified by MMSE. AD subjects exhibited increased qT1 in mesial temporal gray matter and temporo-parieto-occipital cortices (1,448 ± 55.7 ms versus 1,344 ± 51.6 ms; p < 0.001). Voxel-level modelling revealed a positive association between qT1 and amyloid-PET SUVr ( p < 0.001; d = 0.223). Conclusion qT1 mapping can be sensitive to changes related to brain amyloidosis, supporting its role as a promising, noninvasive imaging biomarker in AD. Key Points Question Can qT1 mapping detect AD-related microstructural changes in the cortico-limbic gray matter? Findings Participants with AD showed increased cortico-limbic qT1 values. A subtle yet consistent positive association was observed between cortical qT1 values and amyloid-PET SUVr. Relevance statement qT1 mapping captures microstructural tissue alterations related to amyloid pathology in Alzheimer’s disease, supporting its role as a potential non-invasive imaging biomarker in this condition.

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Journal
European Radiology Experimental
Published
2026-09-21
DOI
https://doi.org/10.1186/s41747-026-00792-1
Primary Topic
Dementia and Cognitive Impairment Research
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article
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article

T1 mapping in Alzheimer’s disease: a quantitative MRI study with amyloid-PET correlation

Emanuele Pravatà, Tom Hilbert, Stefano Raffa, Luca Roccatagliata et al.
European Radiology Experimental
Dementia and Cognitive Impairment Research
article

T1 mapping in Alzheimer’s disease: a quantitative MRI study with amyloid-PET correlation

Emanuele Pravatà, Tom Hilbert, Stefano Raffa, Luca Roccatagliata, Enrico Peira, Luigi Lorenzini, Gianmario Sambuceti, Andrea Diociasi, Massimo Caulo, Gian Franco Piredda, Domenico Zacà, Lorenzo Gualco, Maria Pia Sormani, Mauro Costagli, Noemi Montobbio, Matteo Pardini, Tobias Kober, A. Chincarini, Dario Arnaldi, Lucia Argenti, Mattia Losa, Luca Sofia, Silvia Morbelli, Beatrice Orso, Martina Pulze, Federico Massa, Marco Bozzali
article en

Abstract

Abstract Objectives Quantitative T1 mapping (qT1) is a magnetic resonance imaging (MRI) biomarker of brain microstructural changes; however, its application in Alzheimer disease (AD) remains limited. We compared cortico-limbic qT1 values between patients with AD and healthy controls (HCs) and examined their relationship with amyloid burden measured by amyloid-positron emission tomography (PET). Materials and methods We retrospectively identified subjects with mild cognitive impairment due to AD and HCs who underwent 3-T MRI, including a compressed-sensing MP2RAGE sequence, generating three-dimensional T1-weighted images and qT1 maps. Amyloid-PET was available for 16 patients. Hippocampal qT1 and volume were compared between groups, adjusting for age and sex; analyses were repeated after stratifying patients by Mini-Mental State Examination (MMSE). Voxel-wise group comparison was performed using SPM 12. The qT1-standardized uptake value ratio (SUVr) association was assessed with a linear mixed-effects model applied to voxel-level data, accounting for partial volume effects. Results Thirty-three AD subjects, aged 69.3 ± 8.2 years (mean ± standard deviation), 18 females, and 22 HCs aged 70.5 ± 13.3 years, 15 females, were evaluated. Regional hippocampal qT1 was higher in AD (1,398 ± 53.0 ms versus 1,349 ± 53.4 ms; p = 0.002), without difference across cognitive subgroups stratified by MMSE. AD subjects exhibited increased qT1 in mesial temporal gray matter and temporo-parieto-occipital cortices (1,448 ± 55.7 ms versus 1,344 ± 51.6 ms; p < 0.001). Voxel-level modelling revealed a positive association between qT1 and amyloid-PET SUVr ( p < 0.001; d = 0.223). Conclusion qT1 mapping can be sensitive to changes related to brain amyloidosis, supporting its role as a promising, noninvasive imaging biomarker in AD. Key Points Question Can qT1 mapping detect AD-related microstructural changes in the cortico-limbic gray matter? Findings Participants with AD showed increased cortico-limbic qT1 values. A subtle yet consistent positive association was observed between cortical qT1 values and amyloid-PET SUVr. Relevance statement qT1 mapping captures microstructural tissue alterations related to amyloid pathology in Alzheimer’s disease, supporting its role as a potential non-invasive imaging biomarker in this condition.

European Radiology ExperimentalVol. 10(1)
Siemens (Germany) (DE), University of Chieti-Pescara (IT), Azienda Ospedaliera Citta' della Salute e della Scienza di Torino (IT), Ospedale Policlinico San Martino (IT), Piedmont Reference Center for Epidemiology and Cancer Prevention (IT), Siemens Healthcare (United States) (US), Siemens Healthineers (Germany) (DE), Azienda Ospedaliera Nazionale SS. Antonio e Biagio e Cesare Arrigo (IT), École Polytechnique Fédérale de Lausanne (CH), National Cancer Research Institute (GB), University of Turin (IT), University of Genoa (IT), Vrije Universiteit Amsterdam (NL), University of Lausanne (CH)
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Openalex Percentile: Top 10%
Dementia and Cognitive Impairment Research
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