Your browser doesn't support javascript.
loading
Coupling of the spatial distributions between sMRI and PET reveals the progression of Alzheimer's disease.
Zhao, Kun; Lin, Jiaji; Dyrba, Martin; Wang, Dong; Che, Tongtong; Wu, Haoyang; Wang, Jingyu; Liu, Yong; Li, Shuyu.
Afiliación
  • Zhao K; Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing, China.
  • Lin J; Department of Neurology, Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
  • Dyrba M; German Center for Neurodegenerative Diseases (DZNE), Rostock, Germany.
  • Wang D; School of Information Science and Engineering, Shandong Normal University, Jinan, China.
  • Che T; Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing, China.
  • Wu H; School of Basic Medicine, Air Force Medical University, Xi'an, China.
  • Wang J; School of Basic Medicine, Air Force Medical University, Xi'an, China.
  • Liu Y; School of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.
  • Li S; State Key Laboratory of Cognition Neuroscience and Learning, Beijing Normal University, Beijing, China.
Netw Neurosci ; 7(1): 86-101, 2023.
Article en En | MEDLINE | ID: mdl-37334010
ABSTRACT
Amyloid-beta (Aß) deposition and altered brain structure are the most relevant neuroimaging biomarkers for Alzheimer's disease (AD). However, their spatial inconsistency was always confusing and misleading. Furthermore, the relationship between this spatial inconsistency and AD progression is unclear. The current study introduced a regional radiomics similarity network (R2SN) to map structural MRI and Aß positron emission tomography (PET) images to study their cross-modal interregional coupling. A total of 790 participants (248 normal controls, 390 mild cognitive impaired patients, and 152 AD patients) with their structural MRI and PET images were studied. The results showed that global and regional R2SN coupling significantly decreased according to the severity of cognitive decline, from mild cognitive impairment to AD dementia. The global coupling patterns are discriminative between different APOE ε4, Aß, and Tau subgroups. R2SN coupling was probed for relationships with neuropsychiatric measures and peripheral biomarkers. Kaplan-Meier analysis showed that lower global coupling scores could reveal worse clinical progression of dementia. The R2SN coupling scores derived from the coupling between Aß and atrophy over individual brain regions could reflect the specific pathway of AD progression, which would be a reliable biomarker for AD.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Netw Neurosci Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Netw Neurosci Año: 2023 Tipo del documento: Article País de afiliación: China