Evidence map›Paper›PMID 41162156›Full record

Observational studyJournal of clinical pathology2026

AI portal tract detection and characterisation for a regional analysis of steatosis and inflammation in MASLD, MASH and AIH.

Dylan Windell, Alastair Magness, Cayden Beyer, Helena Thomaides Brears, Sarah Larkin, Kezia Hobson, Paul Aljabar, Kenneth Fleming, Eve Fryer, Timothy James Kendall and 5 more

Abstract readObservational Study
In one paragraph

Observational study in Journal of clinical pathology, 2026. 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
  2. Review
  3. 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

15 authors.

Dylan WindellPerspectum Ltd, Oxford, UK dylan.windell@perspectum.com.ORCID http://orcid.org/0000-0002-8188-6573
Alastair MagnessPerspectum Ltd, Oxford, UK.
Cayden BeyerPerspectum Ltd, Oxford, UK.
Helena Thomaides BrearsPerspectum Ltd, Oxford, UK.
Sarah LarkinPerspectum Ltd, Oxford, UK.
Kezia HobsonPerspectum Ltd, Oxford, UK.
Paul AljabarPerspectum Ltd, Oxford, UK.
Kenneth FlemingPerspectum Ltd, Oxford, UK.
Eve FryerCellular Pathology, Oxford University Hospitals NHS Trust, Oxford, UK.
Timothy James KendallCentre for Inflammation Research, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-4174-2786
Reema KainthPerspectum Ltd, Oxford, UK.
Phil WakefieldPerspectum Ltd, Oxford, UK.
Caitlin Rose LangfordPerspectum Ltd, Oxford, UK.ORCID http://orcid.org/0000-0003-0730-7091
Pierre BedossaLiverPat, Paris, France.
Robert GoldinImperial College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsAnnotation of liver biopsies for disease staging is increasingly aided by digital pathology; however, existing systems do not quantify inflammation and steatosis within an anatomical framework. We hypothesise that an artificial intelligence (AI) system that quantifies portal tracts (PT) and the anatomical distribution of steatotic vesicles and inflammatory cells will align with manual pathologist scoring and stratify liver diseases.

methodsIn this observational, cross-sectional study, digitised images of haematoxylin and eosin-stained specimens were pooled from four independent cohorts of metabolic dysfunction-associated steatotic liver disease (MASLD) or steatohepatitis (MASH) or autoimmune hepatitis (AIH) (n=390: 89 MASLD, 238 MASH, 63 AIH). PT, steatosis, and inflammation were quantified using a proprietary AI system and scored by expert pathologists.

resultsThe percentage of steatosis was higher in MASH (7.5%) than in MASLD (3.2%). Lobular regions had larger steatotic vesicles (260 vs 190 μm

conclusionA new AI system for anatomical quantification of liver biopsy features measured variation in fat and inflammation across the lobule. It showed that inflammation burden was higher in AIH than MASLD/MASH, despite equivalent portal grades, providing objective support for histological scoring.

Indexed as

Artificial IntelligenceFatty LiverHepatitis, AutoimmuneImage Interpretation, Computer-AssistedLiverAdultBiopsyCross-Sectional StudiesFemaleHumansInflammationMaleMiddle AgedArtificial IntelligenceDIGITAL PATHOLOGYHistologyINFLAMMATIONLiver Diseases

Identifiers

PMID41162156
PMCPMC13018851

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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.