Gideon M. Hirschfield

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Canada

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Articles (19)

Quantitative <scp>MRCP</scp> and metrics of bile duct disease over time in patients with primary sclerosing cholangitis: A prospective study

Summary Background Imaging markers of biliary disease in primary sclerosing cholangitis (PSC) have potential for use in clinical and trial disease monitoring. Herein, we evaluate how quantitative magnetic resonance cholangiopancreatography (MRCP) metrics change over time, as per the natural history of disease. Methods Individuals with PSC were prospectively scanned using non‐contrast MRCP. Quantitative metrics were calculated using MRCP+ post‐processing software to assess duct diameters and dilated and strictured regions. Additionally, a hepatopancreatobiliary radiologist (blinded to clinical details, biochemistry and quantitative biliary metrics) reported each scan, including ductal disease assessment according to the modified Amsterdam Cholangiographic Score (MAS). Results At baseline, 14 quantitative MRCP+ metrics were found to be significantly different in patients with PSC ( N = 55) compared to those with primary biliary cholangitis ( N = 55), autoimmune hepatitis ( N = 57) and healthy controls ( N = 18). In PSC specifically, baseline metrics quantifying the number of strictures and the number and length of bile ducts correlated with the MAS, transient elastography and serum ALP values ( p < 0.01 for all correlations). Over a median 371‐day follow‐up (range: 364–462), 29 patients with PSC underwent repeat MRCP, of whom 15 exhibited quantitative changes in MRCP+ metrics. Compared to baseline, quantitative MRCP+ identified an increasing number of strictures over time ( p < 0.05). Comparatively, no significant differences in biochemistry, elastography or the MAS were observed between timepoints. Quantitative MRCP+ metrics remained stable in non‐PSC liver disease. Conclusion Quantitative MRCP+ identifies changes in ductal disease over time in PSC, despite stability in biochemistry, liver stiffness and radiologist‐derived cholangiographic assessment (trial registration: ISRCTN39463479).

Year:

2024

Collaborators (19)

james ferguson

University of Birmingham

UNITED KINGDOM

Mark Pedersen

Assistant Professor

University of Texas Southwestern Medical Center

UNITED STATES

Jessica Katharine Dyson

Honorary Clinical Senior Lecturer

Newcastle University

UNITED KINGDOM

Charles McWherter

President and Chief Scientific Officer

-

UNITED STATES

Palak J. Trivedi

-

UNITED KINGDOM

Stephen D. Ryder

-

UNITED KINGDOM

Ellina Lytvyak

Assistant Professor

University of Alberta

CANADA

Emily Russell

University of Oxford

UNITED KINGDOM

PIETRO ANDREONE

Professor of Medicine and Surgery

Università degli Studi di Roma Tor Vergata Facoltà di Medicina e Chirurgia

ITALY

Anna Rowe

University of Birmingham

UNITED KINGDOM

Hanns-Ulrich Marschall

University of Gothenburg

SWEDEN

Stephen A. Harrison

University of Oxford

UNITED KINGDOM

David Sheridan

Associate Professor (Senior Lecturer)

Plymouth University Peninsula Schools of Medicine and Dentistry

UNITED KINGDOM

Cynthia Levy

Professor of Medicine

University of Miami

UNITED STATES

Deirdre Kelly

Professor

-

UNITED KINGDOM

Julian Hercun

Université de Montréal

CANADA

Kristel Leung

Assistant Professor

Queen's University

CANADA

Julie McDonald

Lecturer

Imperial College London

UNITED KINGDOM

John Vierling

Professor of Medicine and Surgery (tenured); Chief of Hepatology

Baylor College of Medicine

UNITED STATES
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