Evidence map›Paper›PMID 38384484›Full record

ArticleFrontiers in neuroscience2024

Differential diagnosis of frontotemporal dementia subtypes with explainable deep learning on structural MRI.

Da Ma, Jane Stocks, Howard Rosen, Kejal Kantarci, Samuel N Lockhart, James R Bateman, Suzanne Craft, Metin N Gurcan, Karteek Popuri, Mirza Faisal Beg and 2 more

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. 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

12 authors.

Da Ma *Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Jane Stocks *Department of Psychiatry and Behavioral Health, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Howard RosenWeill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
Kejal KantarciDepartment of Radiology, Mayo Clinic, Rochester, MN, United States.
Samuel N LockhartDepartment of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
James R BatemanDepartment of Neurology, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Suzanne CraftDepartment of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Metin N GurcanDepartment of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Karteek PopuriDepartment of Computer Science, Memorial University of Newfoundland, St. John's, NL, Canada.
Mirza Faisal BegSchool of Engineering Science, Simon Fraser University, Burnaby, BC, Canada.
Lei WangDepartment of Psychiatry and Behavioral Health, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
ALLFTD consortium

Funding

Research Education Core FP30AG072977 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ROBERT J VASSAR · 2021 to 2026
$26.3M
Wake Forest University School of Medicine Alzheimer's Disease Research CenterP30AG072947 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUZANNE CRAFT · 2021 to 2026
$24.3M
PREDOCTORAL AND POSTDOCTORAL TRAINING PROGRAM IN AGING AND DEMENTIAT32AG020506 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ROBERT J VASSAR, SANDRA WEINTRAUB · 2002 to 2026
$9.9M
PREDICT-ADFTD: Multimodal Imaging Prediction of AD/FTD and Differential DiagnosisR01AG055121 · NIA · OHIO STATE UNIVERSITY · PI ROSEN, HOWARD J, WANG, LEI · 2017 to 2020
$2.8M
PREDICT-FTD: Multimodal Imaging Prediction of FTLD Subtypes.R56AG055121 · NIA · OHIO STATE UNIVERSITY · PI ROSEN, HOWARD J, WANG, LEI · 2023 to 2023
$1.4M
NIA NIH HHS P30 AG072947NIA NIH HHS P30 AG072977NIA NIH HHS R01 AG055121NIA NIH HHS R56 AG055121NIA NIH HHS T32 AG020506
6 · The paper itself

Abstract

Background: Frontotemporal dementia (FTD) represents a collection of neurobehavioral and neurocognitive syndromes that are associated with a significant degree of clinical, pathological, and genetic heterogeneity. Such heterogeneity hinders the identification of effective biomarkers, preventing effective targeted recruitment of participants in clinical trials for developing potential interventions and treatments. In the present study, we aim to automatically differentiate patients with three clinical phenotypes of FTD, behavioral-variant FTD (bvFTD), semantic variant PPA (svPPA), and nonfluent variant PPA (nfvPPA), based on their structural MRI by training a deep neural network (DNN). Methods: Data from 277 FTD patients (173 bvFTD, 63 nfvPPA, and 41 svPPA) recruited from two multi-site neuroimaging datasets: the Frontotemporal Lobar Degeneration Neuroimaging Initiative and the ARTFL-LEFFTDS Longitudinal Frontotemporal Lobar Degeneration databases. Raw T1-weighted MRI data were preprocessed and parcellated into patch-based ROIs, with cortical thickness and volume features extracted and harmonized to control the confounding effects of sex, age, total intracranial volume, cohort, and scanner difference. A multi-type parallel feature embedding framework was trained to classify three FTD subtypes with a weighted cross-entropy loss function used to account for unbalanced sample sizes. Feature visualization was achieved through post-hoc analysis using an integrated gradient approach. Results: The proposed differential diagnosis framework achieved a mean balanced accuracy of 0.80 for bvFTD, 0.82 for nfvPPA, 0.89 for svPPA, and an overall balanced accuracy of 0.84. Feature importance maps showed more localized differential patterns among different FTD subtypes compared to groupwise statistical mapping. Conclusion: In this study, we demonstrated the efficiency and effectiveness of using explainable deep-learning-based parallel feature embedding and visualization framework on MRI-derived multi-type structural patterns to differentiate three clinically defined subphenotypes of FTD: bvFTD, nfvPPA, and svPPA, which could help with the identification of at-risk populations for early and precise diagnosis for intervention planning.

Indexed as

bvFTDdifferential diagnosis algorithmexplainable deep learningFTD (frontotemporal dementia)multi-level feature fusionmulti-type featuresnfvPPAsvPPA

Identifiers

PMID38384484
PMCPMC10879283

What OpenQuestion holds

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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.