Volume 39, Issue 2 pp. 371-381
AUTOIMMUNE AND CHOLESTATIC LIVER DISEASE

Circulating markers of gut barrier function associated with disease severity in primary sclerosing cholangitis

Amandeep K. Dhillon

Amandeep K. Dhillon

Norwegian PSC Center, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway

Institute of Clinical Medicine, University of Oslo, Oslo, Norway

Research Institute of Internal Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway

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Martin Kummen

Martin Kummen

Norwegian PSC Center, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway

Institute of Clinical Medicine, University of Oslo, Oslo, Norway

Research Institute of Internal Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway

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Marius Trøseid

Marius Trøseid

Institute of Clinical Medicine, University of Oslo, Oslo, Norway

Research Institute of Internal Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway

Section of Clinical Immunology and Infectious Diseases, Oslo University Hospital, Oslo, Norway

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Sissel Åkra

Sissel Åkra

Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital, Ullevål, Norway

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Evaggelia Liaskou

Evaggelia Liaskou

Centre for Liver Research, NIHR Birmingham Liver Biomedical Research Centre, Institute of Immunology & Immunotherapy, University of Birmingham, Birmingham, UK

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Bjørn Moum

Bjørn Moum

Institute of Clinical Medicine, University of Oslo, Oslo, Norway

Department of Gastroenterology, Division of Medicine, Oslo University Hospital Ullevål, Oslo, Norway

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Mette Vesterhus

Mette Vesterhus

Norwegian PSC Center, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway

Department of Medicine, Haraldsplass Deaconess Hospital, Bergen, Norway

Department of Clinical Science, University of Bergen, Bergen, Norway

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Tom H. Karlsen

Tom H. Karlsen

Norwegian PSC Center, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway

Institute of Clinical Medicine, University of Oslo, Oslo, Norway

Research Institute of Internal Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway

Section of Gastroenterology, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway

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Ingebjørg Seljeflot

Ingebjørg Seljeflot

Institute of Clinical Medicine, University of Oslo, Oslo, Norway

Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital, Ullevål, Norway

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Johannes R. Hov

Corresponding Author

Johannes R. Hov

Norwegian PSC Center, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway

Institute of Clinical Medicine, University of Oslo, Oslo, Norway

Research Institute of Internal Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway

Section of Gastroenterology, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway

Correspondence

Johannes R. Hov, Norwegian PSC Research Centre, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital Rikshospitalet, Oslo, Norway.

Email: [email protected]

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First published: 30 September 2018
Citations: 60

FUNDING INFORMATION

AKD and JRH are funded by the Research Council of Norway (no. 240787/F20). MK is funded by the Regional Health Authority of South-Eastern Norway (no. 2016067).

Abstract

Background & Aims

One important hypothesis in primary sclerosing cholangitis pathophysiology suggests that bacterial products from an inflamed leaky gut lead to biliary inflammation. We aimed to investigate whether circulating markers of bacterial translocation were associated with survival in a Norwegian primary sclerosing cholangitis cohort.

Methods

Serum levels of zonulin, intestinal fatty acid binding protein, soluble CD14, lipopolysaccharide and lipopolysaccharide-binding protein were measured in 166 primary sclerosing cholangitis patients and 100 healthy controls.

Results

Lipopolysaccharide-binding protein and soluble CD14 were elevated in primary sclerosing cholangitis compared with healthy controls (median 13 662 vs 12 339 ng/mL, P = 0.010 and 1657 vs 1196 ng/mL, P < 0.001, respectively). High soluble CD14 and lipopolysaccharide-binding protein (values >optimal cut-off using receiver operating characteristics) were associated with reduced liver transplantation–free survival (P < 0.001 and P = 0.005, respectively). The concentration of soluble CD14 was higher in patients with hepatobiliary cancer compared to other primary sclerosing cholangitis patients and healthy controls. Zonulin was lower in primary sclerosing cholangitis than controls, but when excluding primary sclerosing cholangitis patients with increased prothrombin time zonulin concentrations were similar in primary sclerosing cholangitis and healthy controls. Concomitant inflammatory bowel disease did not influence the results, while inflammatory bowel disease patients without primary sclerosing cholangitis (n = 40) had lower concentration of soluble CD14. In multivariable Cox regression, high soluble CD14 and high lipopolysaccharide-binding protein were associated with transplantation-free survival, independent from Mayo risk score (HR: 2.26 [95% CI: 1.15-4.43], P = 0.018 and HR: 2.00 [95% CI: 1.17-3.43], P = 0.011, respectively).

Conclusions

Primary sclerosing cholangitis patients show increased levels of circulating markers of bacterial translocation. High levels are associated with poor prognosis measured by transplantation-free survival, indicating that ongoing gut leakage could have clinical impact in primary sclerosing cholangitis.

CONFLICT OF INTEREST

There was no conflict of interest.

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