Accuracy of controlled attenuation parameter measurement for the detection of steatosis in autoimmune liver diseases.

Autoimmune hepatitis Autoimmune liver disease Controlled attenuation parameter Inflammation Non-invasive steatosis measurement Primary biliary cholangitis Primary sclerosing cholangitis Steatosis hepatis

Journal

JHEP reports : innovation in hepatology
ISSN: 2589-5559
Titre abrégé: JHEP Rep
Pays: Netherlands
ID NLM: 101761237

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 12 02 2023
revised: 08 08 2023
accepted: 17 08 2023
medline: 13 11 2023
pubmed: 13 11 2023
entrez: 13 11 2023
Statut: epublish

Résumé

Concurrent fatty liver disease represents an emerging challenge in the care of individuals with autoimmune liver diseases (AILD). Therefore, we aimed to validate the ultrasound-based method of controlled-attenuation parameter (CAP) as a non-invasive tool to detect hepatic steatosis in individuals with AILD. The diagnostic performance of CAP to determine biopsy-proven hepatic steatosis (>5%) was assessed in individuals with AILD (autoimmune hepatitis [AIH], primary biliary cholangitis [PBC], primary biliary cholangitis [PSC], or variant syndromes) who underwent liver biopsy at the University Medical Center Hamburg-Eppendorf between 2015-2020 by calculating the area under the receiver operating characteristic (AUROC) curves. In AIH, the impact of disease activity was evaluated by assessment of CAP upon resolution of hepatic inflammation during follow-up. Overall, 433 individuals with AILD (AIH: 218, PBC: 51, PSC: 85, PBC/AIH: 63, PSC/AIH: 16) were included. Histologically proven steatosis was present in 90 individuals (20.8%). Steatosis was less frequently observed in people with PSC (14%) than in other AILD. CAP values correlated positively with grade of steatosis ( In PBC and PSC, hepatic steatosis can be reliably detected by applying disease-specific thresholds of CAP. In AIH, the diagnostic accuracy of CAP is moderate at diagnosis, but improves after acute hepatitis has resolved. Non-invasive estimation of fat content in the liver can be performed with the ultrasound-based method of controlled-attenuation parameter (CAP). Here, we showed that the presence of a concomitant fatty liver is frequent in people with autoimmune liver diseases and we determined disease-specific thresholds of CAP to best predict the presence of a fatty liver. CAP measurement was shown to be a valid tool to detect fatty liver in individuals with PSC and PBC; however, in AIH, CAP had limited accuracy especially when significant inflammatory activity was present in the liver. In the context of substantial liver inflammation, therefore, CAP values should be interpreted with caution, and measurements should be repeated after acute hepatitis has resolved.

Sections du résumé

Background & Aims UNASSIGNED
Concurrent fatty liver disease represents an emerging challenge in the care of individuals with autoimmune liver diseases (AILD). Therefore, we aimed to validate the ultrasound-based method of controlled-attenuation parameter (CAP) as a non-invasive tool to detect hepatic steatosis in individuals with AILD.
Methods UNASSIGNED
The diagnostic performance of CAP to determine biopsy-proven hepatic steatosis (>5%) was assessed in individuals with AILD (autoimmune hepatitis [AIH], primary biliary cholangitis [PBC], primary biliary cholangitis [PSC], or variant syndromes) who underwent liver biopsy at the University Medical Center Hamburg-Eppendorf between 2015-2020 by calculating the area under the receiver operating characteristic (AUROC) curves. In AIH, the impact of disease activity was evaluated by assessment of CAP upon resolution of hepatic inflammation during follow-up.
Results UNASSIGNED
Overall, 433 individuals with AILD (AIH: 218, PBC: 51, PSC: 85, PBC/AIH: 63, PSC/AIH: 16) were included. Histologically proven steatosis was present in 90 individuals (20.8%). Steatosis was less frequently observed in people with PSC (14%) than in other AILD. CAP values correlated positively with grade of steatosis (
Conclusions UNASSIGNED
In PBC and PSC, hepatic steatosis can be reliably detected by applying disease-specific thresholds of CAP. In AIH, the diagnostic accuracy of CAP is moderate at diagnosis, but improves after acute hepatitis has resolved.
Impact and implications UNASSIGNED
Non-invasive estimation of fat content in the liver can be performed with the ultrasound-based method of controlled-attenuation parameter (CAP). Here, we showed that the presence of a concomitant fatty liver is frequent in people with autoimmune liver diseases and we determined disease-specific thresholds of CAP to best predict the presence of a fatty liver. CAP measurement was shown to be a valid tool to detect fatty liver in individuals with PSC and PBC; however, in AIH, CAP had limited accuracy especially when significant inflammatory activity was present in the liver. In the context of substantial liver inflammation, therefore, CAP values should be interpreted with caution, and measurements should be repeated after acute hepatitis has resolved.

Identifiants

pubmed: 37954487
doi: 10.1016/j.jhepr.2023.100898
pii: S2589-5559(23)00229-X
pmc: PMC10632533
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100898

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest related to this manuscript. Please refer to the accompanying ICMJE disclosure forms for further details.

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Auteurs

Silja Steinmann (S)

I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.
European Reference Network for Hepatological Diseases (ERN-RARE LIVER), Hamburg, Germany.

Johannes Hartl (J)

I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.
European Reference Network for Hepatological Diseases (ERN-RARE LIVER), Hamburg, Germany.

Sören Weidemann (S)

Institute of Pathology, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.

Katja Füssel (K)

I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.

Claudia Kroll (C)

I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.

Marcial Sebode (M)

I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.
European Reference Network for Hepatological Diseases (ERN-RARE LIVER), Hamburg, Germany.

Ansgar Wilhelm Lohse (AW)

I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.
European Reference Network for Hepatological Diseases (ERN-RARE LIVER), Hamburg, Germany.
Hamburg Centre for Translational Immunology (HCTI), University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

Christoph Schramm (C)

I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany.
European Reference Network for Hepatological Diseases (ERN-RARE LIVER), Hamburg, Germany.
Hamburg Centre for Translational Immunology (HCTI), University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Martin Zeitz Center for Rare Diseases, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Classifications MeSH