Luckett, PH;
              
      
            
                McCullough, A;
              
      
            
                Gordon, BA;
              
      
            
                Strain, J;
              
      
            
                Flores, S;
              
      
            
                Dincer, A;
              
      
            
                McCarthy, J;
              
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
          
      
            
            
            ... Dominantly Inherited Alzheimer Network (DIAN), .; + view all
            
          
      
        
        
        
    
  
(2021)
  Modeling autosomal dominant Alzheimer's disease with machine learning.
Alzheimer's & Dementia
, 17
       (6)
    
     pp. 1005-1016.
    
         10.1002/alz.12259.
  
  
       
    
  
| Preview | Text Modeling autosomal dominant AlzDem - final accepted ms.pdf - Accepted Version Download (1MB) | Preview | 
Abstract
INTRODUCTION: Machine learning models were used to discover novel disease trajectories for autosomal dominant Alzheimer's disease. METHODS: Longitudinal structural magnetic resonance imaging, amyloid positron emission tomography (PET), and fluorodeoxyglucose PET were acquired in 131 mutation carriers and 74 non-carriers from the Dominantly Inherited Alzheimer Network; the groups were matched for age, education, sex, and apolipoprotein ε4 (APOE ε4). A deep neural network was trained to predict disease progression for each modality. Relief algorithms identified the strongest predictors of mutation status. RESULTS: The Relief algorithm identified the caudate, cingulate, and precuneus as the strongest predictors among all modalities. The model yielded accurate results for predicting future Pittsburgh compound B (R2 = 0.95), fluorodeoxyglucose (R2 = 0.93), and atrophy (R2 = 0.95) in mutation carriers compared to non-carriers. DISCUSSION: Results suggest a sigmoidal trajectory for amyloid, a biphasic response for metabolism, and a gradual decrease in volume, with disease progression primarily in subcortical, middle frontal, and posterior parietal regions.
| Type: | Article | 
|---|---|
| Title: | Modeling autosomal dominant Alzheimer's disease with machine learning | 
| Location: | United States | 
| Open access status: | An open access version is available from UCL Discovery | 
| DOI: | 10.1002/alz.12259 | 
| Publisher version: | https://doi.org/10.1002/alz.12259 | 
| Language: | English | 
| Additional information: | This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions. | 
| Keywords: | Pittsburgh compound B (PiB), autosomal dominant Alzheimer's disease (ADAD), fluorodeoxyglucose (FDG), machine learning, magnetic resonance imaging (MRI) | 
| UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases | 
| URI: | https://discovery.ucl.ac.uk/id/eprint/10120804 | 
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