Evidence map›Paper›PMID 41717278›Full record

ArticleFrontiers in neuroimaging2026

Deep learning to predict future cognitive decline: a multimodal approach using brain MRI and clinical data.

Tamoghna Chattopadhyay, Pavithra Senthilkumar, Rahul H Ankarath, Christopher Patterson, Emma J Gleave, Sophia I Thomopoulos, Heng Huang, Li Shen, Lei You, Degui Zhi and 1 more

Abstract read
In one paragraph

Article in Frontiers in neuroimaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Tamoghna ChattopadhyayImaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, United States.
Pavithra SenthilkumarImaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, United States.
Rahul H AnkarathImaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, United States.
Christopher PattersonImaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, United States.
Emma J GleaveImaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, United States.
Sophia I ThomopoulosImaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, United States.
Heng HuangDepartment of Computer Science, University of Maryland, College Park, MD, United States.
Li ShenDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Lei YouMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX, United States.
Degui ZhiMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX, United States.
Paul M ThompsonImaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Predicting the trajectory of clinical decline in aging individuals is a pressing challenge, especially for people with mild cognitive impairment, Alzheimer's disease, Parkinson's disease, or vascular dementia. Accurate predictions can guide treatment decisions, identify risk factors, and optimize clinical trials. In this study, we compared two deep learning approaches for forecasting changes, over a 2-year interval, in the Clinical Dementia Rating scale 'sum of boxes' score (sobCDR), as a continuous outcome (regression). This is a key metric in dementia research and clinical trials, and scores range from 0 (no impairment) to 18 (severe impairment). To predict decline, we trained a hybrid convolutional neural network (CNN) that integrates 3D T1-weighted brain MRI scans with tabular clinical and demographic features (including age, sex, body mass index (BMI), and baseline sobCDR). We benchmarked its performance against AutoGluon, an automated multimodal machine learning framework that selects an appropriate neural network architecture (an 'autoML' approach). We evaluated the models using data from 2,319 unique participants drawn from three independent cohorts-ADNI, OASIS-3, and NACC. For each participant, we used one T1-weighted brain MRI scan along with corresponding clinical and demographic information. Our results demonstrate the importance of combining image and tabular data in predictive modeling for this clinical application. Deep learning algorithms can fuse information from image-based brain signatures and tabular clinical data, with potential for personalized prognostics in aging and dementia. Rather than concluding that multimodal fusion uniformly improves performance, our results show that deep learning applied to volumetric MRI data may struggle to add predictive value, particularly when clinical covariates explain substantial variance and provide a strong baseline. In other conditions and tasks, it may help to have a hybrid system that can learn from both data types, and their relative value may be different. Conversely, AutoML-based multimodal fusion provides a robust baseline when tabular data already provide strong predictive value for the task. These insights clarify how different multimodal strategies could be selected in clinical prognostic applications.

Indexed as

Alzheimer’s disease prognosticsartificial intelligence in hospitalsAutoGluonclinical decision support systemsclinical declineclinical dementia ratingdeep learningmultimodal analysis

Identifiers

PMID41717278
PMCPMC12913073

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.