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

被引:1
|
作者
Mammadov, Ruslan A. [1 ,2 ]
Selten, Jasmijn W. [1 ]
Roest, Henk P. [1 ]
Verhoeven, Cornelia J. [1 ,3 ]
Maroni, Luca [4 ,5 ]
Bril, Sandra I. [1 ]
Tolenaars, Dagmar [4 ]
Gadjradj, Pravesh S. [1 ]
van de Graaf, Stan F. J. [4 ]
Elferink, Ronald P. J. Oude [4 ]
Kwekkeboom, Jaap [2 ]
Metselaar, Herold J. [2 ]
Peppelenbosch, Maikel P. [2 ]
Beuers, Ulrich [4 ]
IJzermans, Jan N. M. [1 ]
van der Laan, Luc J. W. [1 ]
机构
[1] Univ Med Ctr Rotterdam, Erasmus MC Transplant Inst, Dept Surg, Rotterdam, Netherlands
[2] Erasmus Univ, Dept Gastroenterol & Hepatol, Med Ctr Rotterdam, Rotterdam, Netherlands
[3] Univ Med Ctr Groningen, Dept Otorhinolaryngol, Groningen, Netherlands
[4] Univ Amsterdam, Tytgat Inst Liver & Intestinal Res, Dept Gastroenterol & Hepatol, Amsterdam UMC, Amsterdam, Netherlands
[5] Marche Polytech Univ, Dept Gastroenterol, Ancona, Italy
关键词
ANASTOMOTIC BILIARY STRICTURES; GENOME-WIDE ASSOCIATION; FUCOSYL-TRANSFERASE; NON-SECRETOR STATUS; ULCERATIVE-COLITIS; GUT MICROBIOTA; DISEASE; FEATURES;
D O I
10.1097/TP.0000000000004563
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1764 / 1775
页数:12
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