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. 2022 Apr 11;9:301–313. doi: 10.2147/JHC.S355540

Table 1.

Baseline Characteristics of Study Subjects and Main Outcomes

Variables Entire Cohort (N=2385) No. of Participants (%) Case-Cohort Study (N=961) No. of Participants (%)
Age (years)
 30–39 829 (34.8) 315 (32.8)
 40–49 894 (37.5) 376 (39.1)
 50–59 400 (16.8) 162 (16.9)
 ≥60 262 (11.0) 108 (11.2)
ALT≥ 40 U/La 214 (9.0) 84 (8.8)
History of liver disease 169 (7.1) 70 (7.3)
First-degree family history of HCCa 156 (6.5) 72 (7.5)
Obesity (BMI ≥25 kg/m2) 724 (30.4) 292 (30.4)
Diabetes mellitus 51 (2.1) 23 (2.4)
PNPLA3a
 II 940 (39.5) 381 (39.8)
 MI 1103 (46.3) 442 (46.2)
 MM 337 (14.2) 134 (14.0)
Cigarette smoking 730 (30.6) 297 (30.9)
Alcohol consumption 473 (19.8) 205 (21.3)
Heavy alcohol consumption (≥210 gram of ethanol per week)a 121 (5.1) 55 (5.8)
Ultrasonography
 Hepatic steatosis 1092 (45.8) 419 (43.6)
 Liver cirrhosis 114 (4.8) 57 (5.9)
Viral markers
 HBeAg positivea 97 (10.3)
 HBV DNA ≥ 4 log copies/mL 484 (50.4)
 HBV genotypea
  B or B+C 790 (83.2)
  C 159 (16.8)
 BCP double mutationsa 311 (33.5)
Follow-up
 HBsAg seroclearance 628 (26.3) 254 (26.4)
 Incident HCC 217 (9.1) 113 (11.8)

Notes: aData not available for all participants. Missing data in the entire cohort: ALT (n=6), HCC family history (n=1), PNPLA3 genotype (n=5), and amount of alcohol consumed (n=17); missing data in the case-cohort sample: ALT (n=3), PNPLA3 genotype (n=4), amount of alcohol consumed (n=10), HBeAg (n=23), HBV genotype (n=12), and BCP double mutations (n=34).

Abbreviations: ALT, alanine aminotransferase; BCP, basal core promoter; HCC, hepatocellular carcinoma.