Intestinal Bacteremia After Liver Transplantation Is a Risk Factor for Recurrence of Primary Sclerosing Cholangitis

Author:

Mammadov Ruslan A.12,Selten Jasmijn W.1,Roest Henk P.1,Verhoeven Cornelia J.13,Maroni Luca45,Bril Sandra I.1,Tolenaars Dagmar4,Gadjradj Pravesh S.1,van de Graaf Stan F.J.4,Oude Elferink Ronald P.J.4,Kwekkeboom Jaap2,Metselaar Herold J.2,Peppelenbosch Maikel P.2,Beuers Ulrich4,IJzermans Jan N.M.1,van der Laan Luc J.W.1

Affiliation:

1. Department of Surgery, Erasmus MC Transplant Institute, University Medical Center Rotterdam, The Netherlands.

2. Department of Gastroenterology and Hepatology, Erasmus University Medical Center Rotterdam, The Netherlands.

3. Department of Otorhinolaryngology, University Medical Center Groningen, The Netherlands.

4. Amsterdam UMC, University of Amsterdam, Department of Gastroenterology and Hepatology, Tytgat Institute for Liver and Intestinal Research, Amsterdam, The Netherlands.

5. Department of Gastroenterology, Marche Polytechnic University, Ancona, Italy.

Abstract

Background. Primary sclerosing cholangitis (PSC) is a chronic progressive pathological process, related to inflammatory bowel disease and subsequent bacterial translocation. Liver transplantation (LT) is the only curative therapy, but outcomes are compromised by recurrence of PSC (rPSC). The aim of the study was to investigate a potential link between intestinal bacteremia, fucosyltransferase-2 (FUT2), and rPSC after LT. Methods. LT recipients with PSC (n = 81) or without PSC (n = 271) were analyzed for clinical outcomes and positive bacterial blood cultures. A link between bacteremia and the genetic variant of the FUT2 gene was investigated. Results. The incidence of inflammatory bowel disease was significantly higher in PSC recipients but not associated with rPSC. Bacteremia occurred in 31% of PSC recipients. The incidence of rPSC was 37% and was significantly more common in patients with intestinal bacteremia versus no bacteremia (82% versus 30%; P = 0.003). The nonsecretor polymorphism of the FUT2 gene was identified as a genetic risk factor for both intestinal bacteremia and rPSC. Combined FUT2 genotype and intestinal bacteremia in recipients resulted in the highest risk for rPSC (hazard ratio, 15.3; P < 0.001). Conclusions. Thus, in this article, we showed that bacterial translocation is associated with rPSC after LT and related to the FUT2 nonsecretor status.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation

Reference50 articles.

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