We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress
Sign In
Advertise with Us
Abbott Diagnostics

Download Mobile App


ATTENTION: Due to the COVID-19 PANDEMIC, many events are being rescheduled for a later date, converted into virtual venues, or altogether cancelled. Please check with the event organizer or website prior to planning for any forthcoming event.
05 Sep 2020 - 09 Sep 2020
Virtual Venue

Blood Tests Predicts the Risk of Liver Cirrhosis

By LabMedica International staff writers
Posted on 15 Jul 2020
Print article
Image: High magnification photomicrograph of a liver with cirrhosis (Photo courtesy of Nephron).
Image: High magnification photomicrograph of a liver with cirrhosis (Photo courtesy of Nephron).
Fat accumulation in the liver is common and is often seen in people with obesity or diabetes. In the worst case, fatty liver can lead to cirrhosis or liver cancer. It is unusual for this to occur but in those affected, symptoms often only occur at a late stage when there is no available treatment.

The gold standard for diagnosing fibrosis is liver biopsy, which is not reasonable to use as a screening tool in larger populations, expressly in a general population or primary care setting. Several non-invasive scores have been developed to identify individuals with prevalent advanced fibrosis. The Fibrosis-4 (FIB-4) scoring system is often used to estimate the risk of advanced fibrosis in liver diseases.

Hepatology Specialists at the Karolinska University Hospital (Stockholm, Sweden) and their colleagues tested the general hypothesis that repeated measurements of the commonly used FIB-4 index (FIB-4) would improve the identification of individuals at risk of severe liver disease compared with a single measurement. The investigators used the AMORIS cohort that contains laboratory test data in a very large population, surveyed between 1985 and 1996. More than 40,000 people had blood test data for FIB-4 from several sampling occasions. They were followed in national registers to identify those who developed cirrhosis after up to 27 years.

All laboratory analyses were conducted on fresh blood serum samples (53% after overnight fasting) using a uniform and well-documented methodology. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were determined with an enzymatic UV test and Gamma-glutamyltransferase (GGT) by an enzymatic colorimetric test using a Technicon DAX 96 Multichannel Analyzer (Technicon Instruments Corp., Tarrytown, NY, USA). Glucose levels were analyzed with an enzyme colorimetric technique (glucose oxidase/peroxidase, GOD-PAP) using an AutoChemist-PRISMA automated multichannel analyzers (New Clinicon, Stockholm, Sweden).

The scientists reported that an increase of one unit in FIB-4 was associated with an elevated risk of severe liver disease (adjusted Hazard ratio [aHR] = 1.81). Transitioning from a low- or intermediate- to a high-risk group was associated with an increased risk of severe liver disease compared with those consistently in the low-risk group (aHR = 7.99 and 8.64, respectively). A particularly increased risk of severe liver disease was found in persons defined as high-risk at both tests (aHR=17.04). However, almost half of all events occurred in those consistently in the low-risk group.

Hannes Hagström, MD, PhD, a Consultant in Hepatology and lead author of the study, said, “It is difficult to predict the risk of cirrhosis, although you can get some guidance in using regular blood tests that measure liver damage. We showed that this biomarker is useful for identifying people in primary care with an increased risk of cirrhosis who may need to be more carefully investigated and to exclude people who do not need this. But the method needs to be further developed to reduce the risk of false positive findings, which can lead to unnecessary examinations in healthy people.”

The authors concluded that repeated testing of FIB-4 within five years improves the identification of individuals in the general population at an increased risk of severe liver disease. The study was published on July 1, 2020 in the Journal of Hepatology.

Related Links:
Karolinska University Hospital
Technicon Instruments Corp
New Clinicon

Print article


Molecular Diagnostics

view channel
Image: The NovaSeq 6000 Sequencing System offers high-throughput sequencing across a broad range of applications (Photo courtesy of Illumina).

Somatic Evolution Identified in Non-Neoplastic IBD-Affected Colon

Inflammatory bowel disease (IBD) is a debilitating disease characterized by repeated flares of intestinal inflammation. The two major subtypes of IBD, Crohn’s disease (CD) and ulcerative colitis (UC) are... Read more

Industry News

view channel
Image: ChemWell RPR Analyzer (Photo courtesy of Awareness Technology, Inc.)

Awareness Technology Announces ChemWell RPR Analyzer - The Most Significant Innovation in Syphilis Testing in Last 30 Years

Awareness Technology, Inc. (Palm City, FL, USA) has announced the most significant innovation in syphilis testing in the last 30 years with the launch of the ChemWell RPR automated nontreponemal analyzer... Read more
Copyright © 2000-2020 Globetech Media. All rights reserved.