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Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study

BACKGROUND & AIMS: Liver transplantation (LT) for primary sclerosing cholangitis (PSC) is complicated by recurrence of PSC (rPSC) in up to 25% of recipients. Recurrence has been shown to be detrimental for both graft and patient survival. For both PSC and rPSC, a medical cure is not available. T...

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Autores principales: Visseren, Thijmen, Erler, Nicole S., Heimbach, Julie K., Eaton, John E., Selzner, Nazia, Gulamhusein, Aliya, van der Heide, Frans, Porte, Robert J., van Hoek, Bart, Alwayn, Ian P.J., Metselaar, Herold J., IJzermans, Jan N.M., Darwish Murad, Sarwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678780/
https://www.ncbi.nlm.nih.gov/pubmed/36426376
http://dx.doi.org/10.1016/j.jhepr.2022.100599
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author Visseren, Thijmen
Erler, Nicole S.
Heimbach, Julie K.
Eaton, John E.
Selzner, Nazia
Gulamhusein, Aliya
van der Heide, Frans
Porte, Robert J.
van Hoek, Bart
Alwayn, Ian P.J.
Metselaar, Herold J.
IJzermans, Jan N.M.
Darwish Murad, Sarwa
author_facet Visseren, Thijmen
Erler, Nicole S.
Heimbach, Julie K.
Eaton, John E.
Selzner, Nazia
Gulamhusein, Aliya
van der Heide, Frans
Porte, Robert J.
van Hoek, Bart
Alwayn, Ian P.J.
Metselaar, Herold J.
IJzermans, Jan N.M.
Darwish Murad, Sarwa
author_sort Visseren, Thijmen
collection PubMed
description BACKGROUND & AIMS: Liver transplantation (LT) for primary sclerosing cholangitis (PSC) is complicated by recurrence of PSC (rPSC) in up to 25% of recipients. Recurrence has been shown to be detrimental for both graft and patient survival. For both PSC and rPSC, a medical cure is not available. To predict and ideally to prevent rPSC, it is imperative to find risk factors for rPSC that can be potentially modified. Therefore, we aimed to identify such factors for rPSC in a large international multicentre study including 6 centres in PSC-prevalent countries. METHODS: In this international multicentre, retrospective cohort study, 531 patients who underwent transplantation for PSC were included. In 25% of cases (n = 131), rPSC was diagnosed after a median follow-up of 6.72 (3.29–10.11) years post-LT. RESULTS: In the multivariable competing risk model with time-dependent covariates, we found that factors representing an increased inflammatory state increase the risk for rPSC. Recurrent cholangitis before LT as indication for LT (hazard ratio [HR] 3.6, 95% CI 2.5–5.2), increased activity of inflammatory bowel disease after LT (HR 1.7, 95% CI 1.08–2.75), and multiple acute cellular rejections (HR: non-linear) were significantly and independently associated with an increased risk of rPSC. In contrast to the findings of previous studies, pretransplant colectomy was not found to be independently protective against the development of rPSC. CONCLUSIONS: An increased inflammatory state before and after LT may play a causal and modifiable role in the development of rPSC. Pretransplant colectomy did not reduce the risk of rPSC per se. Recurrent cholangitis as indication for LT was associated with an increased risk of rPSC. IMPACT AND IMPLICATIONS: Recurrence of PSC (rPSC) negatively affects survival after liver transplant (LT). Modifiable risk factors could guide clinical management and prevention of rPSC. We demonstrate that an increased inflammatory state both before and after LT increases the incidence of rPSC. As these are modifiable factors, they could serve as targets for future studies and therapies. We also added further evidence to the ongoing debate regarding preventive colectomy for rPSC by reporting that in our multicenter study, we could not find an independent association between colectomy and risk of rPSC.
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spelling pubmed-96787802022-11-23 Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study Visseren, Thijmen Erler, Nicole S. Heimbach, Julie K. Eaton, John E. Selzner, Nazia Gulamhusein, Aliya van der Heide, Frans Porte, Robert J. van Hoek, Bart Alwayn, Ian P.J. Metselaar, Herold J. IJzermans, Jan N.M. Darwish Murad, Sarwa JHEP Rep Research Article BACKGROUND & AIMS: Liver transplantation (LT) for primary sclerosing cholangitis (PSC) is complicated by recurrence of PSC (rPSC) in up to 25% of recipients. Recurrence has been shown to be detrimental for both graft and patient survival. For both PSC and rPSC, a medical cure is not available. To predict and ideally to prevent rPSC, it is imperative to find risk factors for rPSC that can be potentially modified. Therefore, we aimed to identify such factors for rPSC in a large international multicentre study including 6 centres in PSC-prevalent countries. METHODS: In this international multicentre, retrospective cohort study, 531 patients who underwent transplantation for PSC were included. In 25% of cases (n = 131), rPSC was diagnosed after a median follow-up of 6.72 (3.29–10.11) years post-LT. RESULTS: In the multivariable competing risk model with time-dependent covariates, we found that factors representing an increased inflammatory state increase the risk for rPSC. Recurrent cholangitis before LT as indication for LT (hazard ratio [HR] 3.6, 95% CI 2.5–5.2), increased activity of inflammatory bowel disease after LT (HR 1.7, 95% CI 1.08–2.75), and multiple acute cellular rejections (HR: non-linear) were significantly and independently associated with an increased risk of rPSC. In contrast to the findings of previous studies, pretransplant colectomy was not found to be independently protective against the development of rPSC. CONCLUSIONS: An increased inflammatory state before and after LT may play a causal and modifiable role in the development of rPSC. Pretransplant colectomy did not reduce the risk of rPSC per se. Recurrent cholangitis as indication for LT was associated with an increased risk of rPSC. IMPACT AND IMPLICATIONS: Recurrence of PSC (rPSC) negatively affects survival after liver transplant (LT). Modifiable risk factors could guide clinical management and prevention of rPSC. We demonstrate that an increased inflammatory state both before and after LT increases the incidence of rPSC. As these are modifiable factors, they could serve as targets for future studies and therapies. We also added further evidence to the ongoing debate regarding preventive colectomy for rPSC by reporting that in our multicenter study, we could not find an independent association between colectomy and risk of rPSC. Elsevier 2022-10-01 /pmc/articles/PMC9678780/ /pubmed/36426376 http://dx.doi.org/10.1016/j.jhepr.2022.100599 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Visseren, Thijmen
Erler, Nicole S.
Heimbach, Julie K.
Eaton, John E.
Selzner, Nazia
Gulamhusein, Aliya
van der Heide, Frans
Porte, Robert J.
van Hoek, Bart
Alwayn, Ian P.J.
Metselaar, Herold J.
IJzermans, Jan N.M.
Darwish Murad, Sarwa
Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study
title Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study
title_full Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study
title_fullStr Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study
title_full_unstemmed Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study
title_short Inflammatory conditions play a role in recurrence of PSC after liver transplantation: An international multicentre study
title_sort inflammatory conditions play a role in recurrence of psc after liver transplantation: an international multicentre study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678780/
https://www.ncbi.nlm.nih.gov/pubmed/36426376
http://dx.doi.org/10.1016/j.jhepr.2022.100599
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