Background/purpose of the study: Mac-2-binding protein glycosylation isomer (M2BPGi), a biomarker for liver fibrosis, is influenced by various etiologies. Here, we aimed to investigate clinical factors that improve the accuracy of liver cirrhosis (LC) diagnosis based on quantitative M2BPGi (M2BPGi-Qt), regardless of etiology.
Methods: In total, 1,373 patients with chronic liver disease (CLD) were recruited. Weassessed the correlation between fibrosis stage and M2BPGi-Qt levels among CLD etiologies. If there was no correlation between the fibrosis stage and M2BPGi level in a specific etiology of CLD, we evaluated the clinical factors influencing the M2BPGi-Qt level in that specific etiology. Subsequently, we created an algorithm to detect LC based on M2BPGi-Qt, considering an influencing factor other than fibrosis.
Results: In virus hepatitis, non-alcoholic fatty liver disease, and primary biliary cholangitis, the M2BPGi-Qt levels increased liver fibrosis progression. In autoimmune hepatitis, no significant association was observed between the fibrosis stage and M2BPGi-Qt level. However, liver inflammation positively correlated with the M2BPGi-Qt levels. Considering liver inflammation, we established an algorithm, M2BPGi-Qt, to determine the alanine aminotransferase-to-platelet ratio (MAP-R) in LC. The area under the receiver operating characteristic curve (AUC) of the MAP-R index was 0.840. The AUC of MAP-R was higher than that of the M2BPGi-Qt for detecting LC.
Conclusions: New quantitative measurement system for M2BPGi reveals liver inflammation complicates liver cirrhosis diagnosis. The algorithm based on the M2BPGi-Qt level demonstrates a high accuracy for LC diagnosis.