Evidence map›Paper›PMID 40127396›Full record

ArticlePloS one2025

Weighted-VAE: A deep learning approach for multimodal data generation applied to experimental T. cruzi infection.

Blanca Vazquez, Nidiyare Hevia-Montiel, Jorge Perez-Gonzalez, Paulina Haro

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Multimodal graph learning for chagas disease classification.Medical & biological engineering & computing · 2026
    Article
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  3. Article
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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

4 authors.

Blanca VazquezUnidad Académica del Instituto de Investigaciones en Matemáticas Aplicadas y en Sistemas del Estado de Yucatán, Universidad Nacional Autónoma de México, Mérida, Yucatán, Mexico.ORCID 0000-0001-7708-8424
Nidiyare Hevia-MontielUnidad Académica del Instituto de Investigaciones en Matemáticas Aplicadas y en Sistemas del Estado de Yucatán, Universidad Nacional Autónoma de México, Mérida, Yucatán, Mexico.ORCID 0000-0003-4238-7496
Jorge Perez-GonzalezUnidad Académica del Instituto de Investigaciones en Matemáticas Aplicadas y en Sistemas del Estado de Yucatán, Universidad Nacional Autónoma de México, Mérida, Yucatán, Mexico.
Paulina HaroInstituto de Investigaciones en Ciencias Veterinarias, Universidad Autónoma de Baja California, Mexicali, Baja California, Mexico.ORCID 0000-0003-0101-8512

Funding

UNAM-PAPIIT Program IT101422 AND IA100924‘UNAM Posdoctoral Program (POSDOC)’
6 · The paper itself

Abstract

Chagas disease (CD), caused by the protozoan parasite Trypanosoma cruzi (T. cruzi), represents a major public health concern in most of the American continent and causes 12,000 deaths every year. CD clinically manifests in two phases (acute and chronic), and the diagnosis can result in complications due to the difference between phases and the long period between them. Still, strategies are lacking for the automatic diagnosis of healthy and T. cruzi-infected individuals with missing and limited data. In this work, we propose a Weighted Variational Auto-Encoder (W-VAE) for imputing and augmenting multimodal data to classify healthy individuals and individuals in the acute or chronic phases of T. cruzi infection from a murine model. W-VAE is a deep generative architecture trained with a new proposed loss function to which we added a weighting factor and a masking mechanism to improve the quality of the data generated. We imputed and augmented data using four modalities: electrocardiography signals, echocardiography images, Doppler spectrum, and ELISA antibody titers. We evaluated the generated data through different multi-classification tasks to identify healthy individuals and individuals in the acute or chronic phase of infection. In each multi-classification task, we assessed several classifiers, missing rates, and feature-selection methods. The best obtained accuracy was 92 ± 4% in training and 95% in the final test using a Gaussian Process Classifier with a missing rate of 50%. The accuracy achieved was 95% for individuals in healthy and acute phase and 100% for individuals in the chronic phase. Our approach can be useful in generating data to study the phases of T. cruzi infection.

Indexed as

Chagas DiseaseDeep LearningTrypanosoma cruziAnimalsDisease Models, AnimalEchocardiographyElectrocardiographyHumansMice

Identifiers

PMID40127396
PMCPMC11932709

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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.