Evidence map›Paper›PMID 41781912›Full record

ArticleBMC medical imaging2026

Periductal iron-corrected T1 is a predictor of adverse outcomes in large-duct primary sclerosing cholangitis.

Emmanuel A Selvaraj, Ahmed Ba-Ssalamah, Sarah Poetter-Lang, Bruno Paun, Gerard R Ridgway, Cayden Beyer, Anneli Andersson, Sir Michael Brady, Michele Pansini, Emma L Culver and 2 more

Abstract read
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Article in BMC medical imaging, 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

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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

12 authors.

Emmanuel A SelvarajOxford Centre for Clinical Magnetic Resonance Research (OCMR), Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Ahmed Ba-SsalamahDepartment of Biomedical Imaging and Image- guided Therapy, Medical University of Vienna, General Hospital of Vienna (AKH), Vienna, Austria.
Sarah Poetter-LangDepartment of Biomedical Imaging and Image- guided Therapy, Medical University of Vienna, General Hospital of Vienna (AKH), Vienna, Austria.
Bruno PaunPerspectum Ltd., Oxford, UK.
Gerard R RidgwayOxford Brain Diagnostics Ltd., Oxford, UK.
Cayden BeyerPerspectum Ltd., Oxford, UK.
Anneli AnderssonPerspectum Ltd., Oxford, UK. anneli.andersson@perspectum.com.
Sir Michael BradyPerspectum Ltd., Oxford, UK.
Michele PansiniPerspectum Ltd., Oxford, UK.
Emma L CulverTranslational Gastroenterology and Liver Unit, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Adam BaileyTranslational Gastroenterology and Liver Unit, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Michael Pavlides DPhilOxford Centre for Clinical Magnetic Resonance Research (OCMR), Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConcentric periductal fibrosis, commonly referred to as “onion skin” fibrosis, is a histological hallmark of primary sclerosing cholangitis (PSC) and associated with the development of biliary-type cirrhosis and end-stage liver disease. Our aim was to investigate whether non-contrast enhanced quantitative MRI can provide a noninvasive biomarker of periductal fibro-inflammation in large-duct PSC.

methodsThis prospective cohort study included adults with diagnosis of large-duct PSC, at baseline and 1-year follow-up, and healthy volunteers (HV) at baseline. MRCP + and LiverMultiScan (both Perspectum, UK) were used to align 3D biliary tree models with axial iron-corrected T1 (cT1) maps to quantify cT1 around the bile ducts (periductal-cT1; Pd-cT1). Regions of interest (ROIs) were defined as rings of tissue at increasing distance from the bile duct (1.5–3.5 mm (1), 3.5–5.5 mm (2), 5.5–7.5 mm (3) or 7.5–9.5 mm (4), whole liver (5)). Pd-cT1 was compared between high-risk or low-risk groups using existing markers of risk in PSC and Cox proportional hazard model was used for prediction of outcomes by elevated (> 800ms) Pd-cT1.

resultsFrom 80 recruited participants with PSC, n = 72 had available Pd-cT1 at baseline (median age 44 years; 65% male) and n = 20 HV were included (median age 35 years; 65% male). In PSC, Pd-cT1 in ROIs 1 and 2 was higher than ROIs 3–4 and whole liver cT1 (p < 0.0001) at baseline and follow-up, while there were no differences between ROIs in HV. Participants with high risk stratified by liver stiffness (LS) > 9.6 kPa, enhanced liver fibrosis (ELF) test > 9.8 and Amsterdam-Oxford Model (AOM) > 2 had significantly higher Pd-cT1 than those with low risk classification. In a median follow-up of 49 months (range: 14–66), elevated baseline Pd-cT1 could predict adverse events (cholangitis, hepatic decompensation, liver transplantation and all-cause mortality) in patients with large-duct PSC.

conclusionsPd-cT1, a novel quantitative MRI method combining biliary and parenchymal technologies, detected periductal liver abnormalities in PSC and was associated with increased risk of clinical outcomes. This work proposes a non-invasive, objective biomarker of fibro-inflammation in the periductal parenchyma in PSC which, once validated, may have utility as a monitoring biomarker in clinical trials for large-duct PSC.

Indexed as

Cholangitis, SclerosingMagnetic Resonance ImagingAdultFemaleHumansIronMaleMiddle AgedProspective StudiesIronBile ductCholestasiscT1Liver fibrosisMagnetic resonance imagingMRCPPeribiliary inflammationPSC

Identifiers

PMID41781912
PMCPMC13067436

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LicenceCC BY
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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.