Evaluation of Point Shear Wave Elastography Using Acoustic Radiation Force Impulse Imaging for Longitudinal Fibrosis Assessment in Patients with HBeAg-Negative HBV Infection.

APRI FIB-4 HBV acoustic radiation force impulse imaging fibrotest non-invasive fibrosis assessment point shear wave elastography transient elastography

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
02 Dec 2019
Historique:
received: 20 10 2019
revised: 12 11 2019
accepted: 20 11 2019
entrez: 8 12 2019
pubmed: 8 12 2019
medline: 8 12 2019
Statut: epublish

Résumé

Accurate assessment of hepatic fibrosis in patients with chronic HBeAg-negative Hepatitis B is of crucial importance not only to predict the long-term clinical course, but also to evaluate antiviral therapy indication. The aim of this study was to prospectively assess the utility of point shear wave elastography (pSWE) for longitudinal non-invasive fibrosis assessment in a large cohort of untreated patients with chronic HBeAg-negative hepatitis B virus (HBV) infection. 407 consecutive patients with HBeAg-negative HBV infection who underwent pSWE, transient elastography (TE) as well as laboratory fibrosis markers, including fibrosis index based on four factors (FIB-4), aspartate to platelet ratio index (APRI) and FibroTest, on the same day were prospectively followed up for six years. Patients were classified into one of the three groups: inactive carriers (IC; HBV-DNA <2000 IU/mL and ALT <40 U/L); grey zone group 1 (GZ-1; HBV DNA <2000 IU/mL and ALT >40 U/L); grey zone group 2 (GZ-2; HBV-DNA >2000 IU/mL and ALT <40 U/L). pSWE results were significantly correlated with TE (r = 0.29, Our data indicate that pSWE could be useful for non-invasive fibrosis assessment and follow-up in patients with HBeAg-negative chronic HBV infection.

Sections du résumé

BACKGROUND BACKGROUND
Accurate assessment of hepatic fibrosis in patients with chronic HBeAg-negative Hepatitis B is of crucial importance not only to predict the long-term clinical course, but also to evaluate antiviral therapy indication. The aim of this study was to prospectively assess the utility of point shear wave elastography (pSWE) for longitudinal non-invasive fibrosis assessment in a large cohort of untreated patients with chronic HBeAg-negative hepatitis B virus (HBV) infection.
METHODS METHODS
407 consecutive patients with HBeAg-negative HBV infection who underwent pSWE, transient elastography (TE) as well as laboratory fibrosis markers, including fibrosis index based on four factors (FIB-4), aspartate to platelet ratio index (APRI) and FibroTest, on the same day were prospectively followed up for six years. Patients were classified into one of the three groups: inactive carriers (IC; HBV-DNA <2000 IU/mL and ALT <40 U/L); grey zone group 1 (GZ-1; HBV DNA <2000 IU/mL and ALT >40 U/L); grey zone group 2 (GZ-2; HBV-DNA >2000 IU/mL and ALT <40 U/L).
RESULTS RESULTS
pSWE results were significantly correlated with TE (r = 0.29,
CONCLUSION CONCLUSIONS
Our data indicate that pSWE could be useful for non-invasive fibrosis assessment and follow-up in patients with HBeAg-negative chronic HBV infection.

Identifiants

pubmed: 31810183
pii: jcm8122101
doi: 10.3390/jcm8122101
pmc: PMC6947378
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Christiana Graf (C)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Antonia Mondorf (A)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Viola Knop (V)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Kai-Henrik Peiffer (KH)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Julia Dietz (J)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Julia Friess (J)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Heiner Wedemeyer (H)

Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, 30625 Hannover, Germany.
Department of Gastroenterology and Hepatology, University Hospital Essen, 45147 Essen, Germany.

Peter Buggisch (P)

Institute for Interdisciplinary Medicine IFI, 20099 Hamburg, Germany.

Stefan Mauss (S)

Center for HIV and Hepatogastroenterology, 40237 Düsseldorf, Germany.

Thomas Berg (T)

Department of Gastroenterology and Rheumatology, University Hospital Leipzig, 04103 Leipzig, Germany.

Michael Rausch (M)

Practice of Internal Medicine, 10777 Berlin, Germany.

Martin Sprinzl (M)

Department of Internal Medicine I, University Medical Centre of the Johannes Gutenberg-University, 55131 Mainz, Germany.

Hartwig Klinker (H)

Department of Medicine II, Division of Hepatology, University Hospital Würzburg, 97080 Würzburg, Germany.

Holger Hinrichsen (H)

Gastroenterology-Hepatology Center, 24105 Kiel, Germany.

Jean-Pierre Bronowicki (JP)

Hepato-Gastroenterology, Hopital Brabois- CHU Nancy, 54500 Vandoeuvre-les-Nancy, France.

Sebastian Haag (S)

Practice of Gastroenterology, 65189 Wiesbaden, Germany.

Dietrich Hüppe (D)

Practice of Hepatology, 44623 Herne, Germany.

Thomas Lutz (T)

Infektiologikum, 60596 Frankfurt, Germany.

Thierry Poynard (T)

BioPredictive, 75007 Paris, France.

Stefan Zeuzem (S)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Mireen Friedrich-Rust (M)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Christoph Sarrazin (C)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.
Department of Gastroenterology, St. Josefs-Hospital, 65189 Wiesbaden, Germany.

Johannes Vermehren (J)

Department of Internal Medicine 1, University Hospital Frankfurt, 60596 Frankfurt, Germany.

Classifications MeSH