Evidence map›Paper›PMID 40575353›Full record

ArticleGenetics in medicine open2025

Early diagnosis of vascular Ehlers-Danlos syndrome through AI-powered facial analysis: Results from the Montalcino Aortic Consortium.

David R Murdock, Adarsh Suresh, Ernesto Calderon Martinez, Isabella Marin, Frances Marin, Alan C Braverman, Angela T Yetman, Shaine A Morris, Dianna M Milewicz

Abstract read
In one paragraph

Article in Genetics in medicine open, 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. Review
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

9 authors.

David R MurdockDivision of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX.
Adarsh SureshDivision of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX.
Ernesto Calderon MartinezDivision of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX.
Isabella MarinDivision of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX.
Frances MarinDivision of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX.
Alan C BravermanCardiovascular Division, Department of Medicine, Washington University in St Louis, St Louis, MI.
Angela T YetmanDepartment of Pediatrics, Children's Hospital and Medical Center of Omaha, Omaha, NE.
Shaine A MorrisSection of Pediatric Cardiology, Department of Pediatrics, Texas Children's Hospital and Baylor College of Medicine, Houston, TX.
Dianna M MilewiczDivision of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Vascular Ehlers-Danlos syndrome (vEDS), which is caused by Methods: We implemented an artificial intelligence (AI) facial analysis model based on the PhenoScore framework using a support vector machine trained on facial images of 30 individuals, aged 6 to 65 years, with vEDS from the Montalcino Aortic Consortium, control images from the Chicago Face Database, and publicly available images of individuals with hEDS. Cross-validation was used to train the support vector machine, and statistical measures to evaluate the model performance were calculated. Local Interpretable Model-agnostic Explanations was used to generate facial heatmaps highlighting the features driving the model's predictions. Results: The AI classifier showed excellent performance with as few as 13 vEDS training images and distinguished vEDS from both controls and individuals with hEDS with high accuracy, achieving an area under the receiver operating characteristic curve ≥ 0.97. Local Interpretable Model-agnostic Explanations highlighted facial regions already established to characterize the facial features of vEDS patients (eg, prominent eyes). Conclusion: Our results demonstrate the potential of AI-based facial analysis for diagnosing vEDS. This method democratizes the early diagnosis of vEDS by reducing dependence on genetic testing, enabling optimal management and improved outcomes, particularly in resource-limited areas.

Indexed as

AI-based screeningFacial phenotype analysisLIMEMachine learningvEDS

Identifiers

PMID40575353
PMCPMC12197971

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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.