Evidence map›Paper›PMID 42069469›Full record

ArticlePlacenta2026

Biologically inspired digital histology for deep phenotyping of placental composition changes across major lesion types.

Emma Clare Walker, Claudia Vanea, Karen Meir, Drorith Hochner-Celnikier, Hagit Hochner, Triin Laisk, Cecilia Lindgren, Craig A Glastonbury, Linda M Ernst, Christoffer Nellaker

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Article in Placenta, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Emma Clare WalkerNuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom; Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK. Electronic address: emma.walker@wrh.ox.ac.uk.
Claudia VaneaNuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom; Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK.
Karen MeirDepartment of Pathology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
Drorith Hochner-CelnikierFaculty of Medicine, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
Hagit HochnerBraun School of Public Health, Hebrew University of Jerusalem, Jerusalem, Israel.
Triin LaiskInstitute of Genomics, University of Tartu, Tartu, Estonia.
Cecilia LindgrenBig Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK; Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, United Kingdom; Broad Institute of Harvard and MIT, Cambridge MA, USA; Nuffield Department of Population Health, University of Oxford, United Kingdom.
Craig A GlastonburyNuffield Department of Medicine, University of Oxford, United Kingdom; Human Technopole, Viale Rita Levi-Montalcini 1, 20157, Milan, Italy.
Linda M ErnstDepartment of Pathology and Laboratory Medicine, Endeavor Health, Evanston, IL, USA; Department of Pathology, University of Chicago Pritzker School of Medicine, Chicago, IL, USA.
Christoffer NellakerNuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom; Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK. Electronic address: christoffer.nellaker@wrh.ox.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlacental histopathology provides important insights into maternal and fetal health, yet the organ's spatial heterogeneity poses significant challenges for objective and reproducible histological analysis. Systematic assessment of cellular and structural composition across placental slides remains limited by the scale and subjectivity of manual evaluation. Quantitative approaches are therefore needed to characterise placental responses to injury beyond visually apparent lesions.

methodsWe applied the Histology Analysis Pipeline.PY (HAPPY), a biologically inspired hierarchical deep learning framework for quantitative single-cell-resolution analysis of Haematoxylin and Eosin (H&E) slides, to 130 placental parenchyma slides from 62 singleton full-term live births. The dataset included healthy normal controls and four common placental lesion types: infarction, perivillous fibrin, avascular villi, and intervillous thrombosis. Cell-type and tissue-structure compositions were quantified, and slide-level deviation from a healthy reference was assessed using compositional data analysis.

resultsPlacental slides with lesions exhibited significant cellular composition differences compared with healthy controls, including increased extravillous trophoblast and leukocyte densities and decreased Hofbauer cell densities. These cellular changes were accompanied by tissue-level alterations, particularly increased fibrin deposition and changes in villous structure. Compositional deviation increased with infarction size but not with other lesion types. Notably, compositional differences were also detected in slides without an apparent lesion from placentas with lesion(s) elsewhere, indicating organ-wide responses extending beyond focal pathology.

conclusionsQuantitative deep phenotyping reveals widespread cellular and structural changes associated with placental lesions, including effects not evident on routine histological assessment. These findings demonstrate the potential of AI-based digital histology to complement conventional placental pathology in research and clinical settings.

Indexed as

Artificial intelligenceDigital pathologyHistologyPlacentaPlacenta lesionsWhole slide imaging

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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.