Published online Dec 7, 2016. doi: 10.3748/wjg.v22.i45.9880
Peer-review started: September 3, 2016
First decision: September 28, 2016
Revised: October 10, 2016
Accepted: November 15, 2016
Article in press: November 16, 2016
Published online: December 7, 2016
Processing time: 95 Days and 16.7 Hours
Chronic liver disease is a major cause of morbidity and mortality worldwide and usually develops over many years, as a result of chronic inflammation and scarring, resulting in end-stage liver disease and its complications. The progression of disease is characterised by ongoing inflammation and consequent fibrosis, although hepatic steatosis is increasingly being recognised as an important pathological feature of disease, rather than being simply an innocent bystander. However, the current gold standard method of quantifying and staging liver disease, histological analysis by liver biopsy, has several limitations and can have associated morbidity and even mortality. Therefore, there is a clear need for safe and non-invasive assessment modalities to determine hepatic steatosis, inflammation and fibrosis. This review covers key mechanisms and the importance of fibrosis and steatosis in the progression of liver disease. We address non-invasive imaging and blood biomarker assessments that can be used as an alternative to information gained on liver biopsy.
Core tip: Ongoing hepatic fibrosis and steatosis are well recognised features of chronic liver disease. Liver biopsy is currently the gold standard for assessing the disease although this has an associated but low morbidity and mortality risk. Therefore, alternative methods of non-invasive assessment of liver disease are of relevance and importance. We outline the mechanisms of hepatic fibrosis and steatosis and review uses of non-invasive imaging and blood biomarkers as an alternative to liver biopsy.