Graft Fibrosis Over 10 to 15 Years in Pediatric Liver Transplant Recipients: Multicenter Study of Paired, Longitudinal Surveillance Biopsies.


Journal

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
ISSN: 1527-6473
Titre abrégé: Liver Transpl
Pays: United States
ID NLM: 100909185

Informations de publication

Date de publication:
06 2022
Historique:
revised: 19 12 2021
received: 15 09 2021
accepted: 22 12 2021
pubmed: 15 1 2022
medline: 20 5 2022
entrez: 14 1 2022
Statut: ppublish

Résumé

Previous single-center, cross-sectional studies have reported a steep increase in the prevalence and severity of fibrosis through 10 to 15 years after pediatric liver transplantation. We report a multicenter study of paired surveillance biopsies in a contemporary cohort. Children who underwent liver transplant when younger than 6 years old and had paired surveillance liver biopsies were enrolled (n = 78, 35% girls, median 1.2 years old at transplant). A central pathologist graded inflammation, assessed rejection activity index, and staged fibrosis in the portal, sinusoidal, and perivenular compartments, allowing for calculation of the Liver Allograft Fibrosis Score (LAFSc). Analysis of variance tested associations between fibrosis progression and clinical parameters. The first biopsy, at a median 8.2 years (interquartile range, 5.9-11.6 years) after transplantation, showed absent to mild fibrosis (LAFSc 0-2) in 29%, moderate (LAFSc 3-5) in 56%, and severe (LAFSc 6-7) in 14% of patients. The second biopsy, at a median 4.7 years (IQR, 4.3-5.1 years) later, showed fibrosis progression (LAFSc increased by ≥3) in 10 (13%) and regression (LAFSc decreased by ≥3) in 4 (5%) patients. After adjusting for baseline LAFSc, younger age at transplant was the only risk factor for fibrosis progression. Although fibrosis prevalence and severity 6 to 12 years after transplant was similar to previous reports, fibrosis trajectory during the next 4 to 5 years was stable. Our data may be reassuring for children with consistently normal liver tests. A comprehensive understanding of factors determining allograft health during the very long term is essential to optimizing allograft and patient health.

Identifiants

pubmed: 35029022
doi: 10.1002/lt.26409
pii: 01445473-202206000-00021
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1051-1062

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK114180
Pays : United States

Informations de copyright

© 2022 by the American Association for the Study of Liver Diseases.

Références

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Auteurs

Emily R Perito (ER)

Department of Pediatrics, Department of Epidemiology and Biostatistics University of California, San Francisco San Francisco CA Institute of Liver Studies King's College London London UK Department of Pediatrics, Mount Sinai Kravis Children's Hospital and Recanati/Miller Transplantation Institute Mount Sinai Health System New York NY Department of Surgery, Center for Liver Diseases and Transplantation Columbia University Irving Medical Center New York NY Department of Pediatrics, Siragusa Transplantation Center Ann & Robert H. Lurie Children's Hospital of Chicago Chicago IL Department of Pediatrics University of Pittsburgh Medical CenterChildren's Hospital of Pittsburgh Pittsburgh PA Department of Pathology University of Pittsburgh Pittsburgh PA 8785 Department of Surgery University of California San Francisco San Francisco CA.

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