| Literature DB >> 34537988 |
Pere Ginès1,2,3,4, Laurent Castera5,6,7, Frank Lammert8,9,10, Isabel Graupera1,2,3,4, Miquel Serra-Burriel11, Alina M Allen12, Vincent Wai-Sun Wong13, Phillipp Hartmann14, Maja Thiele15, Llorenç Caballeria16, Robert J de Knegt17, Ivica Grgurevic18, Salvador Augustin3,19,20, Emmanuel A Tsochatzis21, Jörn M Schattenberg22, Indra Neil Guha23, Andrea Martini24, Rosa M Morillas3,20,25, Montserrat Garcia-Retortillo26, Harry J de Koning27, Núria Fabrellas2,28, Judit Pich29, Ann T Ma1,2,4, M Alba Diaz30, Dominique Roulot31, Philip N Newsome32,33, Michael Manns8, Patrick S Kamath12, Aleksander Krag15.
Abstract
Cirrhosis, highly prevalent worldwide, develops after years of hepatic inflammation triggering progressive fibrosis. Currently, the main etiologies of cirrhosis are non-alcoholic fatty liver disease and alcohol-related liver disease, although chronic hepatitis B and C infections are still major etiological factors in some areas of the world. Recent studies have shown that liver fibrosis can be assessed with relatively high accuracy noninvasively by serological tests, transient elastography, and radiological methods. These modalities may be utilized for screening for liver fibrosis in at-risk populations. Thus far, a limited number of population-based studies using noninvasive tests in different areas of the world indicate that a significant percentage of subjects without known liver disease (around 5% in general populations and a higher rate -18% to 27%-in populations with risk factors for liver disease) have significant undetected liver fibrosis or established cirrhosis. Larger international studies are required to show the harms and benefits before concluding that screening for liver fibrosis should be applied to populations at risk for chronic liver diseases. Screening for liver fibrosis has the potential for changing the current approach from diagnosing chronic liver diseases late when patients have already developed complications of cirrhosis to diagnosing liver fibrosis in asymptomatic subjects providing the opportunity of preventing disease progression.Entities:
Mesh:
Year: 2021 PMID: 34537988 DOI: 10.1002/hep.32163
Source DB: PubMed Journal: Hepatology ISSN: 0270-9139 Impact factor: 17.425