Literature DB >> 24914389

Protocol liver biopsy is the only examination that can detect mid-term graft fibrosis after pediatric liver transplantation.

Yukihiro Sanada1, Koshi Matsumoto1, Taizen Urahashi1, Yoshiyuki Ihara1, Taiichi Wakiya1, Noriki Okada1, Naoya Yamada1, Yuta Hirata1, Koichi Mizuta1.   

Abstract

AIM: To assessed the clinical significance of protocol liver biopsy (PLB) in pediatric liver transplantation (LT).
METHODS: Between July 2008 and August 2012, 89 and 55 PLBs were performed in pediatric patients at two and five years after LT, respectively. We assessed the histopathological findings using the Metavir scoring system, including activity (A) and fibrosis (F), and we identified factors associated with scores of ≥ A1 and ≥ F1. Our results clarified the timing and effectiveness of PLB.
RESULTS: The incidences of scores of ≥ A1 and ≥ F1 were 24.7% and 24.7%, respectively, at two years after LT and 42.3% and 34.5%, respectively, at five years. Independent risk factors in a multivariate analysis of a score of ≥ A1 at two years included ≥ 2 h of cold ischemic time, no acute cellular rejection and an alanine amino transaminase (ALT) level of ≥ 20 IU/L (P = 0.028, P = 0.033 and P = 0.012, respectively); however, no risk factors were identified for a score of ≥ F1. Furthermore, no independent risk factors associated with scores of ≥ A1 and ≥ F1 at five years were identified using multivariate analysis. A ROC curve analysis of ALT at two years for a score of ≥ A1 demonstrated the recommended cutoff value for diagnosing ≥ A1 histology to be 20 IU/L. The incidence of scores of ≥ A2 or ≥ F2 at two years after LT was 3.4% (three cases), and all patients had an absolute score of ≥ A2. In contrast to that observed for PLBs at five years after LT, the incidence of scores of ≥ A2 or ≥ F2 was 20.0% (11 cases), and all patients had an absolute score of ≥ F2. In all cases, the dose of immunosuppressants was increased after the PLB, and all ten patients who underwent a follow-up liver biopsy improved to scores of ≤ A1 or F1.
CONCLUSION: PLB at two years after LT is an unnecessary examination, because the serum ALT level reflects portal inflammation. In addition, immunosuppressive therapy should be modulated to maintain the ALT concentration at a level less than 20 IU/L. PLB at five years is an excellent examination for the detection of early reversible graft fibrosis because no serum markers reflect this finding.

Entities:  

Keywords:  Graft fibrosis; Immunosuppression; Liver function test; Pediatric liver transplantation; Protocol liver biopsy

Mesh:

Substances:

Year:  2014        PMID: 24914389      PMCID: PMC4047353          DOI: 10.3748/wjg.v20.i21.6638

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  36 in total

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Review 2.  Liver biopsy interpretation for causes of late liver allograft dysfunction.

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Journal:  Hepatology       Date:  2006-08       Impact factor: 17.425

Review 3.  Histological grading and staging of chronic hepatitis.

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5.  Withdrawal of steroids: a randomized prospective study of prednisone and tacrolimus versus mycophenolate mofetil and tacrolimus in liver transplant recipients with autoimmune hepatitis.

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7.  Novel histologic scoring system for long-term allograft fibrosis after liver transplantation in children.

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9.  All liver recipients benefit from the protocol 10-year liver biopsies.

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Journal:  Hepatology       Date:  2003-06       Impact factor: 17.425

10.  Long-term survival and late graft loss in pediatric liver transplant recipients--a 15-year single-center experience.

Authors:  Michael A Wallot; Michael Mathot; Magda Janssen; Tanja Hölter; Kilic Paul; Jean Paul Buts; Raymond Reding; Jean Bernard Otte; Etienne M Sokal
Journal:  Liver Transpl       Date:  2002-07       Impact factor: 5.799

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  9 in total

Review 1.  ABO-compatible liver allograft antibody-mediated rejection: an update.

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3.  Neutrophil-to-lymphocyte ratio predicts early acute cellular rejection in living donor liver transplantation.

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4.  Acute Rejection Increases Risk of Graft Failure and Death in Recent Liver Transplant Recipients.

Authors:  Josh Levitsky; David Goldberg; Abigail R Smith; Sarah A Mansfield; Brenda W Gillespie; Robert M Merion; Anna S F Lok; Gary Levy; Laura Kulik; Michael Abecassis; Abraham Shaked
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Review 6.  Role of Histopathologist in Liver Transplantation.

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7.  Determination of allograft fibrosis by measurement of liver stiffness using transient elastography in children after liver transplantation at Shiraz Organ Transplant Center.

Authors:  Seyed Mohsen Dehghani; Maryam Ataollahi; Seyyed Bozorgmehr Hedayati; Fateme Parooie; Iraj Shahramian
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Review 8.  Significance of progressive liver fibrosis in pediatric liver transplants: A review of current evidence.

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Journal:  World J Gastroenterol       Date:  2020-05-07       Impact factor: 5.742

9.  TIM-4 interference in Kupffer cells against CCL4-induced liver fibrosis by mediating Akt1/Mitophagy signalling pathway.

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  9 in total

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