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Grab-AD: Generalizability and reproducibility of altered brain activity and diagnostic classification in Alzheimer's Disease.
Jin, Dan; Wang, Pan; Zalesky, Andrew; Liu, Bing; Song, Chengyuan; Wang, Dawei; Xu, Kaibin; Yang, Hongwei; Zhang, Zengqiang; Yao, Hongxiang; Zhou, Bo; Han, Tong; Zuo, Nianming; Han, Ying; Lu, Jie; Wang, Qing; Yu, Chunshui; Zhang, Xinqing; Zhang, Xi; Jiang, Tianzi; Zhou, Yuying; Liu, Yong.
Afiliación
  • Jin D; Brainnetome Center & National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing, China.
  • Wang P; School of Artificial Intelligence, University of Chinese Academy of Sciences, Beijing, China.
  • Zalesky A; Department of Neurology, Tianjin Huanhu Hospital, Tianjin University, Tianjin, China.
  • Liu B; Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne and Melbourne Health, Melbourne, Victoria, Australia.
  • Song C; Department of Biomedical Engineering, University of Melbourne, Melbourne, Victoria, Australia.
  • Wang D; Brainnetome Center & National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing, China.
  • Xu K; School of Artificial Intelligence, University of Chinese Academy of Sciences, Beijing, China.
  • Yang H; Center for Excellence in Brain Science and Intelligence Technology, Institute of Automation, Chinese Academy of Sciences, Beijing, China.
  • Zhang Z; Department of Neurology, Qilu Hospital of Shandong University, Ji'nan, China.
  • Yao H; Department of Radiology, Qilu Hospital of Shandong University, Ji'nan, China.
  • Zhou B; Brainnetome Center & National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing, China.
  • Han T; Department of Radiology, Xuanwu Hospital of Capital Medical University, Beijing, China.
  • Zuo N; Branch of Chinese PLA General Hospital, Sanya, China.
  • Han Y; Department of Radiology, the Second Medical Centre, National Clinical Research Centre for Geriatric Diseases, Chinese PLA General Hospital, Beijing, China.
  • Lu J; Department of Neurology, the Second Medical Centre, National Clinical Research Centre for Geriatric Diseases, Chinese PLA General Hospital, Beijing, China.
  • Wang Q; Department of Radiology, Tianjin Huanhu Hospital, Tianjin, China.
  • Yu C; Brainnetome Center & National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing, China.
  • Zhang X; School of Artificial Intelligence, University of Chinese Academy of Sciences, Beijing, China.
  • Zhang X; Department of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China.
  • Jiang T; Beijing Institute of Geriatrics, Beijing, China.
  • Zhou Y; National Clinical Research Center for Geriatric Disorders, Beijing, China.
  • Liu Y; Center of Alzheimer's Disease, Beijing Institute for Brain Disorders, Beijing, China.
Hum Brain Mapp ; 41(12): 3379-3391, 2020 08 15.
Article en En | MEDLINE | ID: mdl-32364666
ABSTRACT
Alzheimer's disease (AD) is associated with disruptions in brain activity and networks. However, there is substantial inconsistency among studies that have investigated functional brain alterations in AD; such contradictions have hindered efforts to elucidate the core disease mechanisms. In this study, we aim to comprehensively characterize AD-associated functional brain alterations using one of the world's largest resting-state functional MRI (fMRI) biobank for the disorder. The biobank includes fMRI data from six neuroimaging centers, with a total of 252 AD patients, 221 mild cognitive impairment (MCI) patients and 215 healthy comparison individuals. Meta-analytic techniques were used to unveil reliable differences in brain function among the three groups. Relative to the healthy comparison group, AD was associated with significantly reduced functional connectivity and local activity in the default-mode network, basal ganglia and cingulate gyrus, along with increased connectivity or local activity in the prefrontal lobe and hippocampus (p < .05, Bonferroni corrected). Moreover, these functional alterations were significantly correlated with the degree of cognitive impairment (AD and MCI groups) and amyloid-ß burden. Machine learning models were trained to recognize key fMRI features to predict individual diagnostic status and clinical score. Leave-one-site-out cross-validation established that diagnostic status (mean area under the receiver operating characteristic curve 0.85) and clinical score (mean correlation coefficient between predicted and actual Mini-Mental State Examination scores 0.56, p < .0001) could be predicted with high accuracy. Collectively, our findings highlight the potential for a reproducible and generalizable functional brain imaging biomarker to aid the early diagnosis of AD and track its progression.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ganglios Basales / Corteza Cerebral / Péptidos beta-Amiloides / Enfermedad de Alzheimer / Disfunción Cognitiva / Conectoma / Aprendizaje Automático / Red en Modo Predeterminado Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Hum Brain Mapp Asunto de la revista: CEREBRO Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ganglios Basales / Corteza Cerebral / Péptidos beta-Amiloides / Enfermedad de Alzheimer / Disfunción Cognitiva / Conectoma / Aprendizaje Automático / Red en Modo Predeterminado Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Hum Brain Mapp Asunto de la revista: CEREBRO Año: 2020 Tipo del documento: Article País de afiliación: China