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. 2020 Jun 15;26(3):261–279. doi: 10.3350/cmh.2020.0032

Table 2.

Clinical applications of M2BPGi in CHB patients

Category Finding M2BPGi level (C.O.I.) and point Reference
Liver fibrosis Significant fibrosis (≥F2) in CHB ≥1.06 C.O.I. (AUC, 0.753) [73]
HCC occurrence/recurrence Higher risk of HCC development in CHB patients ≥1.8 C.O.I. for patients without cirrhosis (P<0.001) [78]
≥1.8 C.O.I. for patients with cirrhosis (P=0.073)
Low risk of HCC in HBeAg-negative patients ≤0.68 C.O.I. at baseline [81]
Risk for HCC development in CHB patients with cirrhosis treated with NAs M2BPGi-based score* ≥652.5 at baseline [83]
Risk for HCC development in CHB patients treated with NAs ≥1.215 C.O.I. at 48 weeks [84]
HCC development in CHB patients ≥0.69 C.O.I. at baseline [85]

M2BPGi, Mac-2 binding protein glycosylation isomer; CHB, chronic hepatitis B; C.O.I., cut-off index; AUC, area under the curve; HCC, hepatocellular carcinoma; HBeAg, hepatitis B envelope antigen; NAs, nucleos(t)ide analogues.

*

M2BPGi-based score, 8 × age (years) + 7 × baseline M2BPGi (COI) + 10 × body mass index (kg/m2). The score was calculable in 171 CHB patients with cirrhosis with a median of 652.5 (IQR, 581.3, 709.4) point.