Evidence map›Paper›PMID 41132780›Full record

ArticleJournal of medical imaging (Bellingham, Wash.)2025

Benchmarking 3D generative autoencoders for pseudo-healthy reconstruction of brain

Ravi Hassanaly, Maëlys Solal, Olivier Colliot, Ninon Burgos, Alzheimer’s Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in Journal of medical imaging (Bellingham, Wash.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Ravi HassanalySorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié Salpêtrière, Paris, France.ORCID https://orcid.org/0009-0009-1304-5906
Maëlys SolalSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié Salpêtrière, Paris, France.ORCID https://orcid.org/0000-0001-9333-9238
Olivier ColliotSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié Salpêtrière, Paris, France.ORCID https://orcid.org/0000-0002-9836-654X
Ninon BurgosSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié Salpêtrière, Paris, France.ORCID https://orcid.org/0000-0002-4668-2006
Alzheimer’s Disease Neuroimaging Initiative

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Many deep generative models have been proposed to reconstruct pseudo-healthy images for anomaly detection. Among these models, the variational autoencoder (VAE) has emerged as both simple and efficient. Although significant progress has been made in refining the VAE within the field of computer vision, these advancements have not been extensively applied to medical imaging applications. Approach: We present a benchmark that assesses the ability of multiple VAEs to reconstruct pseudo-healthy neuroimages for anomaly detection in the context of dementia. We first propose a rigorous methodology to define the optimal architecture of the vanilla VAE and select through random searches the best hyperparameters of the VAE variants. Relying on a simulation-based evaluation framework, we thoroughly assess the ability of 20 VAE models to reconstruct pseudo-healthy images for the detection of dementia-related anomalies in 3D brain Results: This benchmark demonstrated that the majority of the VAE models tested were able to reconstruct images of good quality and generate healthy-looking images from simulated images presenting anomalies. Conclusions: Even if no model clearly outperformed all the others, the benchmark allowed identifying a few models that perform slightly better than the vanilla VAE. It further showed that many VAE-based models can generalize to the detection of anomalies of various intensities, shapes, and locations in 3D brain FDG PET.

Indexed as

Alzheimer’s diseasedeep generative modelspositron emission tomographyunsupervised anomaly detectionvariational autoencoder

Identifiers

PMID41132780
PMCPMC12543032

What OpenQuestion holds

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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.