Published online Oct 7, 2019. doi: 10.3748/wjg.v25.i37.5667
Peer-review started: July 16, 2019
First decision: August 2, 2019
Revised: August 21, 2019
Accepted: September 11, 2019
Article in press: September 11, 2019
Published online: October 7, 2019
Processing time: 76 Days and 13.5 Hours
Since hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) is a syndrome with a high short-term mortality rate, and clinically identifying those patients at a high mortality risk is of great significance.
The aim of this study was to investigate the clinical value of soluble mannose receptor (sMR) in patients with HBV-ACLF.
To investigate the clinical value of sMR for predicting 90-d mortality of patients with HBV-ACLF.
A total of 43 patients with HBV-ACLF were enrolled in this retrospective study, and their serum sMR levels were determined using an enzyme-linked immunosorbent assay. A multivariate logistic regression analysis was used to analyze the independent risk factors for mortality.
When compared with chronic hepatitis B patients and healthy controls, serum sMR level was significantly higher in HBV-ACLF patients. Serum sMR helped to distinguish the survivors from non-survivors, and it was positively correlated with model for end-stage liver disease (MELD) score, HBV-DNA level, and total bilirubin level. In addition, serum sMR level was an independent risk factor and significantly improved the performance of MELD score in predicting the prognosis of HBV-ACLF patients.
Serum sMR level is significantly elevated in patients with HBV-ACLF, and it is significantly associated with indicators of liver injury and disease severity. Additionally, sMR level is negatively correlated with patients outcome. Finally, sMR level may be a predictor of the prognosis of patients with HBV-ACLF.
Future studies are needed to investigate the mechanisms underlying the role of sMR. And it is necessary to determine the dynamic changes in serum sMR during the progression of HBV-ACLF. Multicenter trials with large sample sizes are also required to confirm the current findings.