Published online Aug 7, 2016. doi: 10.3748/wjg.v22.i29.6663
Peer-review started: March 18, 2016
First decision: May 12, 2016
Revised: May 30, 2016
Accepted: June 15, 2016
Article in press: June 15, 2016
Published online: August 7, 2016
Processing time: 135 Days and 8.3 Hours
There are approximately 240 million patients with chronic hepatitis B virus (HBV) infection worldwide. Up to 40% of HBV-infected patients can progress to liver cirrhosis, hepatocellular carcinoma or chronic end-stage liver disease during their lifetime. This, in turn, is responsible for around 650000 deaths annually worldwide. Repeated hepatitis flares may increase the progression of liver fibrosis, making the accurate diagnosis of the stage of liver fibrosis critical in order to make antiviral therapeutic decisions for HBV-infected patients. Liver biopsy remains the “gold standard” for diagnosing liver fibrosis. However, this technique has recently been challenged by the development of several novel noninvasive tests to evaluate liver fibrosis, including serum markers, combined models and imaging techniques. In addition, the cost and accessibility of imaging techniques have been suggested as additional limitations for invasive assessment of liver fibrosis in developing countries. Therefore, a noninvasive assessment model has been suggested to evaluate liver fibrosis, specifically in HBV-infected patients, owing to its high applicability, inter-laboratory reproducibility, wide availability for repeated assays and reasonable cost. The current review aims to present the status of knowledge in this new and exciting field, and to highlight the key points in HBV-infected patients for clinicians.
Core tip: An accurate diagnosis of liver fibrosis is essential to make therapeutic decisions in patients with chronic hepatitis B (CHB). However, liver biopsy, the “gold standard” for assessing the degree of liver fibrosis, has been limited by its complications. Although noninvasive models composed with serum biomarkers were applied to assess fibrosis in patients with CHB, they have been suggested owing to their high applicability, inter-laboratory reproducibility, wide availability for repeated assays and cost. Previous data presented on the noninvasive models for assessing liver fibrosis from different levels of alanine aminotransferase have been limited.