Biomarkers for liver fibrosis: advances, advantages and disadvantages

被引:20
作者
Cequera, A. [1 ]
de Leon Mendez, M. C. Garcia [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Unidad Invest Med Expt, Mexico City, DF, Mexico
来源
REVISTA DE GASTROENTEROLOGIA DE MEXICO | 2014年 / 79卷 / 03期
关键词
Fibrosis biomarkers; Liver cirrhosis; Liver biopsy; Fibrotest; FibroScan; Elastography;
D O I
10.1016/j.rgmx.2014.05.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver cirrhosis in Mexico is one of the most important causes of death in persons between the ages of 25 and 50 years. One of the reasons for therapeutic failure is the lack of knowledge about the molecular mechanisms that cause liver disorder and make it irreversible. One of its prevalent anatomical characteristics is an excessive deposition of fibrous tissue that takes different forms depending on etiology and disease stage. Liver biopsy, traditionally regarded as the gold standard of fibrosis staging, has been brought into question over the past decade, resulting in the proposal for developing non-invasive technologies based on different, but complementary, approaches: a biological one that takes the serum levels of products arising from the fibrosis into account, and a more physical one that evaluates scarring of the liver by methods such as ultrasound and magnetic resonance elastography; some of the methods were originally studied and validated in patients with hepatitis C. There is great interest in determining non-invasive markers for the diagnosis of liver fibrosis, since at present there is no panel or parameter efficient and reliable enough for diagnostic use. In this paper, we describe the biomarkers that are currently being used for studying liver fibrosis in humans, their advantages and disadvantages, as well as the implementation of new-generation technologies and the evaluation of their possible use in the diagnosis of fibrosis. (C) 2014 Asociacion Mexicana de Gastroenterologia. Published by Masson Doyma Mexico S.A. All rights reserved.
引用
收藏
页码:187 / 199
页数:13
相关论文
共 83 条
[1]   Hepascore: An accurate validated predictor of liver fibrosis in chronic hepatitis C infection [J].
Adams, LA ;
Bulsara, M ;
Rossi, E ;
Deboer, B ;
Speers, D ;
George, J ;
Kench, J ;
Farrell, G ;
McCaughan, GW ;
Jeffrey, GP .
CLINICAL CHEMISTRY, 2005, 51 (10) :1867-1873
[2]   Complex non-invasive fibrosis models are more accurate than simple models in non-alcoholic fatty liver disease [J].
Adams, Leon A. ;
George, Jacob ;
Bugianesi, Elisabetta ;
Rossi, Enrico ;
De Boer, W. Bastiaan ;
van der Poorten, David ;
Ching, Helena L. I. ;
Bulsara, Max ;
Jeffrey, Gary P. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2011, 26 (10) :1536-1543
[3]   A brief review on molecular, genetic and imaging techniques for HCV fibrosis evaluation [J].
Ahmad, Waqar ;
Ijaz, Bushra ;
Gull, Sana ;
Asad, Sultan ;
Khaliq, Saba ;
Jahan, Shah ;
Sarwar, Muhammad T. ;
Kausar, Humera ;
Sumrin, Aleena ;
Shahid, Imran ;
Hassan, Sajida .
VIROLOGY JOURNAL, 2011, 8
[4]   Non-Invasive markers for hepatic fibrosis [J].
Baranova, Ancha ;
Lal, Priyanka ;
Birerdinc, Aybike ;
Younossi, Zobair M. .
BMC GASTROENTEROLOGY, 2011, 11
[5]   Liver extracellular matrix in health and disease [J].
Bedossa, P ;
Paradis, V .
JOURNAL OF PATHOLOGY, 2003, 200 (04) :504-515
[6]   An algorithm for the grading of activity in chronic hepatitis C [J].
Bedossa, P ;
Poynard, T .
HEPATOLOGY, 1996, 24 (02) :289-293
[7]   Sampling variability of liver fibrosis in chronic hepatitis C [J].
Bedossa, P ;
Dargère, D ;
Paradis, V .
HEPATOLOGY, 2003, 38 (06) :1449-1457
[8]   Alteration of protein glycosylation in liver diseases [J].
Blomme, Bram ;
Van Steenkiste, Christophe ;
Callewaert, Nico ;
Van Vlierberghe, Hans .
JOURNAL OF HEPATOLOGY, 2009, 50 (03) :592-603
[9]   Noninvasive diagnosis of liver cirrhosis using DNA sequencer-based total serum protein glycomics [J].
Callewaert, N ;
Van Vlierberghe, H ;
Van Hecke, A ;
Laroy, W ;
Delanghe, J ;
Contreras, R .
NATURE MEDICINE, 2004, 10 (04) :429-434
[10]   Noninvasive Methods to Assess Liver Disease in Patients With Hepatitis B or C [J].
Castera, Laurent .
GASTROENTEROLOGY, 2012, 142 (06) :1293-+