Evidence map›Paper›PMID 40416329›Full record

ArticleNature machine intelligence2025

A personalized time-resolved 3D mesh generative model for unveiling normal heart dynamics.

Mengyun Qiao, Kathryn A McGurk, Shuo Wang, Paul M Matthews, Declan P O'Regan, Wenjia Bai

Abstract read
In one paragraph

Article in Nature machine intelligence, 2025. 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. Review
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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

6 authors.

Mengyun QiaoDepartment of Brain Sciences, Imperial College London, London, UK.ORCID 0000-0002-5157-1079
Kathryn A McGurkMRC Laboratory of Medical Sciences, Imperial College London, London, UK.
Shuo WangData Science Institute, Imperial College London, London, UK.
Paul M MatthewsDepartment of Brain Sciences, Imperial College London, London, UK.ORCID 0000-0002-1619-8328
Declan P O'ReganMRC Laboratory of Medical Sciences, Imperial College London, London, UK.
Wenjia BaiDepartment of Brain Sciences, Imperial College London, London, UK.ORCID 0000-0003-2943-7698

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the structure and motion of the heart is crucial for diagnosing and managing cardiovascular diseases, the leading cause of global death. There is wide variation in cardiac shape and motion patterns, influenced by demographic, anthropometric and disease factors. Unravelling normal patterns of shape and motion, and understanding how each individual deviates from the norm, would facilitate accurate diagnosis and personalized treatment strategies. Here, to this end, we developed a conditional generative model, MeshHeart, to learn the distribution of shape and motion patterns for the left and right ventricles of the heart. To model the high-dimensional spatio-temporal mesh data, MeshHeart uses a geometric encoder to represent cardiac meshes in a latent space and a temporal transformer to model the motion dynamics of latent representations. Based on MeshHeart, we investigate the latent space of 3D + t cardiac mesh sequences and propose a distance metric, latent delta, which quantifies the deviation of a real heart from its personalized normative pattern. Here, 3D + t refers to three-dimensional data evolving over time. In experiments using a large cardiac magnetic resonance image dataset of 38,309 participants from the UK Biobank, MeshHeart demonstrates high performance in cardiac mesh sequence reconstruction and generation. Latent space features are discriminative for cardiac disease classification, whereas latent delta exhibits strong correlations with clinical phenotypes in phenome-wide association studies.

Indexed as

Cardiovascular diseasesMagnetic resonance imaging

Identifiers

PMID40416329
PMCPMC12101970

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