Mapping cell-to-tissue graphs across human placenta histology whole slide images using deep learning with HAPPY.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
28 Mar 2024
Historique:
received: 22 11 2022
accepted: 15 03 2024
medline: 29 3 2024
pubmed: 29 3 2024
entrez: 29 3 2024
Statut: epublish

Résumé

Accurate placenta pathology assessment is essential for managing maternal and newborn health, but the placenta's heterogeneity and temporal variability pose challenges for histology analysis. To address this issue, we developed the 'Histology Analysis Pipeline.PY' (HAPPY), a deep learning hierarchical method for quantifying the variability of cells and micro-anatomical tissue structures across placenta histology whole slide images. HAPPY differs from patch-based features or segmentation approaches by following an interpretable biological hierarchy, representing cells and cellular communities within tissues at a single-cell resolution across whole slide images. We present a set of quantitative metrics from healthy term placentas as a baseline for future assessments of placenta health and we show how these metrics deviate in placentas with clinically significant placental infarction. HAPPY's cell and tissue predictions closely replicate those from independent clinical experts and placental biology literature.

Identifiants

pubmed: 38548713
doi: 10.1038/s41467-024-46986-2
pii: 10.1038/s41467-024-46986-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2710

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : INV-024200
Pays : United States

Informations de copyright

© 2024. The Author(s).

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Auteurs

Claudia Vanea (C)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK. claudia.vanea@wrh.ox.ac.uk.
Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK. claudia.vanea@wrh.ox.ac.uk.

Jelisaveta Džigurski (J)

Institute of Genomics, University of Tartu, Tartu, Estonia.

Valentina Rukins (V)

Institute of Genomics, University of Tartu, Tartu, Estonia.

Omri Dodi (O)

Faculty of Medicine, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

Siim Siigur (S)

Department of Pathology, Tartu University Hospital, Tartu, Estonia.

Liis Salumäe (L)

Department of Pathology, Tartu University Hospital, Tartu, Estonia.

Karen Meir (K)

Department of Pathology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

W Tony Parks (WT)

Department of Laboratory Medicine & Pathobiology, University of Toronto, Toronto, Canada.

Drorith Hochner-Celnikier (D)

Faculty of Medicine, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

Abigail Fraser (A)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.

Hagit Hochner (H)

Braun School of Public Health, Hebrew University of Jerusalem, Jerusalem, Israel.

Triin Laisk (T)

Institute of Genomics, University of Tartu, Tartu, Estonia.

Linda M Ernst (LM)

Department of Pathology and Laboratory Medicine, NorthShore University HealthSystem, Chicago, USA.
Department of Pathology, University of Chicago Pritzker School of Medicine, Chicago, USA.

Cecilia M Lindgren (CM)

Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK.
Centre for Human Genetics, Nuffield Department, University of Oxford, Oxford, UK.
Broad Institute of Harvard and MIT, Cambridge, MA, USA.
Nuffield Department of Population Health Health, University of Oxford, Oxford, UK.

Christoffer Nellåker (C)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK. christoffer.nellaker@bdi.ox.ac.uk.
Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK. christoffer.nellaker@bdi.ox.ac.uk.

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