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Development and prognostic relevance of a histologic grading and staging system for alcohol-related liver disease.
Lackner, Carolin; Stauber, Rudolf E; Davies, Susan; Denk, Helmut; Dienes, Hans Peter; Gnemmi, Viviane; Guido, Maria; Miquel, Rosa; Paradis, Valerie; Schirmacher, Peter; Terracciano, Luigi; Berghold, Andrea; Pregartner, Gudrun; Binder, Lukas; Douschan, Philipp; Rainer, Florian; Sygulla, Stephan; Jager, Marion; Rautou, Pierre-Emmanuel; Bumbu, Andreea; Horhat, Adelina; Rusu, Ioana; Stefanescu, Horia; Detlefsen, Sönke; Krag, Aleksander; Thiele, Maja; Cortez-Pinto, Helena; Moreno, Christophe; Gouw, Annette S H; Tiniakos, Dina G.
Afiliação
  • Lackner C; Institute of Pathology, Medical University of Graz, Austria. Electronic address: karoline.lackner@medunigraz.at.
  • Stauber RE; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Davies S; Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Denk H; Institute of Pathology, Medical University of Graz, Austria.
  • Dienes HP; Department of Pathology, Medical University of Vienna, Vienna, Austria.
  • Gnemmi V; Université Lille, Canther, Inserm, UMR-S 1277, CHU Lille, Service de Pathologie, Lille, France.
  • Guido M; Department of Medicine - DIMED, University of Padova, Padova, Italy.
  • Miquel R; Liver Histopathology Laboratory, Institute of Liver Studies, King's College Hospital, London, United Kingdom.
  • Paradis V; Assistance Publique-Hôpitaux de Paris, Service d'Anatomie et de Cytologie Pathologiques, Hôpital Universitaire Beaujon, France; Université Paris Diderot, CNRS, Centre de Recherche sur l'Inflammation (CRI), Paris, France; Département Hospitalo-Universitaire (DHU) UNITY, Clichy, France.
  • Schirmacher P; Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
  • Terracciano L; Anatomic Pathology Institute, Humanitas University Research Hospital, Rozzano, Milano, Italy.
  • Berghold A; Institute for Medical Informatics, Statistics and Documentation, Medical University of Graz, Graz, Austria.
  • Pregartner G; Institute for Medical Informatics, Statistics and Documentation, Medical University of Graz, Graz, Austria.
  • Binder L; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Douschan P; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Rainer F; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Sygulla S; Institute of Pathology, Medical University of Graz, Austria.
  • Jager M; Université de Paris, AP-HP, Hôpital Beaujon, Service d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de recherche sur l'inflammation, Inserm, UMR 1149, Paris, France.
  • Rautou PE; Université de Paris, AP-HP, Hôpital Beaujon, Service d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de recherche sur l'inflammation, Inserm, UMR 1149, Paris, France.
  • Bumbu A; Liver Unit, Regional Institute of Gastroenterology and Hepatology, Cluj-Napoca, Romania; Liver Research Club, Cluj-Napoca, Romania.
  • Horhat A; Liver Unit, Regional Institute of Gastroenterology and Hepatology, Cluj-Napoca, Romania; Liver Research Club, Cluj-Napoca, Romania.
  • Rusu I; University of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
  • Stefanescu H; Liver Unit, Regional Institute of Gastroenterology and Hepatology, Cluj-Napoca, Romania; Liver Research Club, Cluj-Napoca, Romania.
  • Detlefsen S; Department of Pathology, Odense University Hospital, Odense C, Denmark; Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense C, Denmark.
  • Krag A; Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense C, Denmark; Department of Gastroenterology and Hepatology and OPEN, Odense Patient data Explorative Network, Odense University Hospital, Odense C, Denmark.
  • Thiele M; Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense C, Denmark; Department of Gastroenterology and Hepatology and OPEN, Odense Patient data Explorative Network, Odense University Hospital, Odense C, Denmark.
  • Cortez-Pinto H; Clínica Universitária de Gastrenterologia, Laboratório de Nutrição, Faculdade de Medicina, Universidade de Lisboa, Portugal.
  • Moreno C; Department of Gastroenterology, Hepatopancreatology and Digestive Oncology, CUB Hôpital Erasme, Université Libre de Bruxelles, Bruxelles, Belgium.
  • Gouw ASH; Department of Pathology and Medical Biology, University Medical Center Groningen, Groningen, Netherlands.
  • Tiniakos DG; Transitional and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK; Department of Pathology, Aretaieio Hospital, Medical School, National & Kapodistrian University of Athens, Athens 11528, Greece.
J Hepatol ; 75(4): 810-819, 2021 10.
Article em En | MEDLINE | ID: mdl-34126105
ABSTRACT
BACKGROUND &

AIMS:

The SALVE Histopathology Group (SHG) developed and validated a grading and staging system for the clinical and full histological spectrum of alcohol-related liver disease (ALD) and evaluated its prognostic utility in a multinational cohort of 445 patients.

METHODS:

SALVE grade was described by semiquantitative scores for steatosis, activity (hepatocellular injury and lobular neutrophils) and cholestasis. The histological diagnosis of steatohepatitis due to ALD (histological ASH, hASH) was based on the presence of hepatocellular ballooning and lobular neutrophils. Fibrosis staging was adapted from the Clinical Research Network staging system for non-alcoholic fatty liver disease and the Laennec staging system and reflects the pattern and extent of ALD fibrosis. There are 7 SALVE fibrosis stages (SFS) ranging from no fibrosis to severe cirrhosis.

RESULTS:

Interobserver κ-value for each grading and staging parameter was >0.6. In the whole study cohort, long-term outcome was associated with activity grade and cholestasis, as well as cirrhosis with very broad septa (severe cirrhosis) (p <0.001 for all parameters). In decompensated ALD, adverse short-term outcome was associated with activity grade, hASH and cholestasis (p = 0.038, 0.012 and 0.001, respectively), whereas in compensated ALD, hASH and severe fibrosis/cirrhosis were associated with decompensation-free survival (p = 0.011 and 0.001, respectively). On multivariable analysis, severe cirrhosis emerged as an independent histological predictor of long-term survival in the whole study cohort. Severe cirrhosis and hASH were identified as independent predictors of short-term survival in decompensated ALD, and also as independent predictors of decompensation-free survival in compensated ALD.

CONCLUSION:

The SALVE grading and staging system is a reproducible and prognostically relevant method for the histological assessment of disease activity and fibrosis in ALD. LAY

SUMMARY:

Patients with alcohol-related liver disease (ALD) may undergo liver biopsy to assess disease severity. We developed a system to classify ALD under the microscope by grading ALD activity and staging the extent of liver scarring. We validated the prognostic performance of this system in 445 patients from 4 European centers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prognóstico / Projetos de Pesquisa / Hepatopatia Gordurosa não Alcoólica / Histologia / Fígado Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prognóstico / Projetos de Pesquisa / Hepatopatia Gordurosa não Alcoólica / Histologia / Fígado Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article