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Simple blood test could vastly improve detection rates of severe liver disease

Date:
October 6, 2016
Source:
Cardiff University
Summary:
A new non-invasive method of predicting the risk of developing a severe form of liver disease could ensure patients receive early and potentially life-saving medical intervention before irreversible damage is done, report researchers.
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A new non-invasive method of predicting the risk of developing a severe form of liver disease could ensure patients receive early and potentially life-saving medical intervention before irreversible damage is done.

Using information collected in a liver biopsy study, researchers at Cardiff University have developed a method of determining the onset of non-alcoholic steatohepatitis (NASH) through the analysis of lipids, metabolites and clinical markers in blood.

NASH is the most extreme form of non-alcoholic fatty liver disease (NAFLD) -- a range of conditions caused by a build-up of fat in the liver. With NASH, inflammation of the liver damages the cells, potentially causing scarring and cirrhosis.

Currently, the diagnosis of NASH can only be done with a liver biopsy -- an invasive and costly procedure. The new research could lead to a simple blood test that could catch the onset of NASH before inflammation damages the liver.

Dr You Zhou from Cardiff University's Systems Immunity Research Institute said: "Many people with non-alcoholic steatohepatitis do not have symptoms and are not aware they are developing a serious liver problem. As such, diagnosis often comes after irreversible damage is done. Our quicker and less invasive method of diagnosis could mean that more people with non-alcoholic fatty liver disease could be easily tested to determine whether they are progressing to non-alcoholic steatohepatitis, the more severe form of the disease."

A healthy liver should contain little or no fat. It's estimated that around 20% of people in the UK have early stages of NAFLD where there are small amounts of fat in their liver. NASH is estimated to affect up to 5% of the UK population and is now considered to be one of the main causes of cirrhosis -- a condition where irregular bumps replace the smooth liver tissue, making it harder and decreasing the amount of healthy cells to support normal functions. This can lead to complete liver failure.

Common risk factors for both NAFLD and NASH are obesity, lack of physical exercise and insulin resistance. But if detected and managed at an early stage, it's possible to stop both NAFLD and NASH from getting worse.

The new method of NASH diagnosis will undergo further investigation with a view to developing a simple blood test that can be used by clinicians to provide effective medical care for patients at high risk of the disease.

The study "Noninvasive Detection of Nonalcoholic Steatohepatitis Using Clinical Markers and Circulating Levels of Lipids and Metabolites" is published in Clinical Gastroenterology and Hepatology.


Story Source:

Materials provided by Cardiff University. Note: Content may be edited for style and length.


Journal Reference:

  1. You Zhou, Matej Orešič, Marja Leivonen, Peddinti Gopalacharyulu, Jenni Hyysalo, Johanna Arola, An Verrijken, Sven Francque, Luc Van Gaal, Tuulia Hyötyläinen, Hannele Yki-Järvinen. Noninvasive Detection of Nonalcoholic Steatohepatitis Using Clinical Markers and Circulating Levels of Lipids and Metabolites. Clinical Gastroenterology and Hepatology, 2016; 14 (10): 1463 DOI: 10.1016/j.cgh.2016.05.046

Cite This Page:

Cardiff University. "Simple blood test could vastly improve detection rates of severe liver disease." ScienceDaily. ScienceDaily, 6 October 2016. <www.sciencedaily.com/releases/2016/10/161006115316.htm>.
Cardiff University. (2016, October 6). Simple blood test could vastly improve detection rates of severe liver disease. ScienceDaily. Retrieved April 17, 2024 from www.sciencedaily.com/releases/2016/10/161006115316.htm
Cardiff University. "Simple blood test could vastly improve detection rates of severe liver disease." ScienceDaily. www.sciencedaily.com/releases/2016/10/161006115316.htm (accessed April 17, 2024).

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