Non-Invasive Indirect Markers of Liver Fibrosis after Interferon-Free Treatment for Hepatitis C.

3D regimen HCV eradication hepatitis C non-invasive fibrosis markers

Journal

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

Informations de publication

Date de publication:
31 Aug 2021
Historique:
received: 14 07 2021
revised: 26 08 2021
accepted: 28 08 2021
entrez: 10 9 2021
pubmed: 11 9 2021
medline: 11 9 2021
Statut: epublish

Résumé

The effectiveness of interferon-free therapy during the course of HCV infection has already been confirmed. Liver fibrosis can be assessed in several ways, from biopsies to imaging tests. The present study evaluates the usefulness of non-invasive indirect biomarkers of liver fibrosis (APRI, GAPRI, FORNS, FIB-4, the AP index and HUI score) as markers of the effective treatment of HCV with the 3D regimen. Blood samples were collected from 70 patients suffering from chronic hepatitis C. Patients received the 3D AbbVie regimen for hepatitis C. All patients had HCV genotype 1b. The APRI, GAPRI, FIB-4, FORNS, HUI and AP index (age-platelet score) values were calculated with their respective algorithms. The stage of fibrosis was evaluated on the basis of a liver biopsy and confirmed by FibroScan-based transient elastography. An undetectable level of HCV RNA after 12 weeks of treatment with the 3D regimen indicates 100% eradication of hepatitis C virus. After the treatment, non-invasive indirect markers of liver fibrosis achieved levels below the limit for significant fibrosis, Thus, non-invasive indirect biomarkers of hepatic fibrosis failed to detect the presence of significant fibrosis, which was proved in histopathological examination. However, the eradication of hepatitis C virus by means of the 3D regimen treatment does not mean that patients were completely cured.

Identifiants

pubmed: 34501398
pii: jcm10173951
doi: 10.3390/jcm10173951
pmc: PMC8432198
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Dagmara Przekop (D)

Diagnostics-Experimental Center of Sexually Transmissible Diseases, 15-879 Bialystok, Poland.

Jakub Klapaczynski (J)

Department of Internal Diseases and Hepatology, Central Clinical Hospital of Ministry of Home Affairs and Administration, 02-507 Warszawa, Poland.

Agnieszka Grytczuk (A)

Department of Laboratory Diagnostics, University Clinical Hospital in Bialystok, 15-540 Bialystok, Poland.

Ewa Gruszewska (E)

Department of Biochemical Diagnostics, Medical University of Bialystok, 15-269 Bialystok, Poland.

Andrzej Gietka (A)

Department of Internal Diseases and Hepatology, Central Clinical Hospital of Ministry of Home Affairs and Administration, 02-507 Warszawa, Poland.

Anatol Panasiuk (A)

Department of Internal Diseases and Gastroenterology, Provincial Welded Hospital in Bialystok, 15-950 Bialystok, Poland.
Department of Clinical Medicine, Medical University of Bialystok, 15-254 Bialystok, Poland.

Slawomir Golaszewski (S)

Department of General, Minimally Invasive and Oncological Surgery, Provincial Welded Hospital in Bialystok, 15-950 Bialystok, Poland.

Bogdan Cylwik (B)

Department of Pediatric Laboratory Diagnostics, Medical University of Bialystok, 15-274 Bialystok, Poland.

Lech Chrostek (L)

Department of Biochemical Diagnostics, Medical University of Bialystok, 15-269 Bialystok, Poland.

Classifications MeSH