Evidence map›Paper›PMID 41747709›Full record

ArticleAPMIS : acta pathologica, microbiologica, et immunologica Scandinavica2026

Quantitative Histological Insights Into Sudden Arrhythmic Death Syndrome: Findings From a Forensic Autopsy Cohort.

Pernille Heimdal Holm, Thomas Hartvig Lindkær Jensen, Joseph Westaby, Mary Sheppard, Stine Bøttcher Jacobsen, Mikkel Eriksen Dupont, Jeppe Dyrberg Andersen, Bo Gregers Winkel, Jacob Tfelt-Hansen, Jytte Banner and 1 more

Abstract read
In one paragraph

Article in APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 2026. 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

11 authors.

Pernille Heimdal HolmSection of Forensic Pathology, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-6613-6280
Thomas Hartvig Lindkær JensenDepartment of Pathology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Joseph WestabyCRY Cardiovascular Pathology Unit, Cardiovascular Clinical Academic Group, Cardiovascular and Genetic Research Institute, City St George's University of London, London, UK.
Mary SheppardCRY Cardiovascular Pathology Unit, Cardiovascular Clinical Academic Group, Cardiovascular and Genetic Research Institute, City St George's University of London, London, UK.
Stine Bøttcher JacobsenDepartment of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Mikkel Eriksen DupontDepartment of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Jeppe Dyrberg AndersenSection of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Bo Gregers WinkelDepartment of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Jacob Tfelt-HansenDepartment of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Jytte BannerSection of Forensic Pathology, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Kristine Boisen OlsenSection of Forensic Pathology, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-8675-8589

Funding

BETA.HEALTH Innovation Platform 2022-1133Danish Cardiovascular AcademyNovo Nordisk Fonden 0088546Novo Nordisk Fonden NNF23OC0082432University of Copenhagen
6 · The paper itself

Abstract

Sudden arrhythmic death syndrome (SADS) is a major cause of sudden cardiac death in young individuals, characterized by structurally normal hearts and negative toxicology. Although guidelines recommend family screening, phenotyping remains challenging. This study applied quantitative histology and deep-learning-based cell segmentation to investigate morphological features in SADS compared to controls. We conducted a retrospective autopsy study of 77 SADS cases and 41 age- and sex-matched controls (aged 1-49 years) who died from trauma or suicide. Cardiac tissue was analyzed using QuPath and deep learning-based image processing (Quan10). Random Forest classification and recursive feature elimination were used to identify discriminating features. Quantitative analysis found subtle but significant morphological differences. SADS cases had reduced residual myocardium in overall tissue (53% vs. 56%, p = 0.02) and endocardial regions (49% vs. 54%, p < 0.001). Endocardial and epicardial adipocyte density were key discriminators in the model. Genetic analysis identified pathogenic variants in six cases and three controls. AI-driven histology detected differences in hearts previously considered normal, suggesting subgroups within SADS. These findings support the use of quantitative tools in postmortem phenotyping, with potential to refine diagnosis, guide family screening, and improve understanding of arrhythmic mechanisms.

Indexed as

Arrhythmias, CardiacDeath, Sudden, CardiacMyocardiumAdolescentAdultAutopsyCase-Control StudiesChildChild, PreschoolDeep LearningFemaleForensic PathologyHumansInfantMaleMiddle Agedartificial intelligence (AI)cardiac morphologypostmortemsudden arrhythmic death syndrome (SADS)sudden cardiac death (SCD)

Identifiers

PMID41747709
PMCPMC12945455

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.