Table 1.
Baseline characteristic | MAFLD, n (%) N = 113 (44.0) | MAFLD-HCC, n (%) N = 144 (56.0) | p value |
---|---|---|---|
Age (mean, IQR) | 53.3 (13) | 71.6 (10) | <0.001 |
Sex | |||
Male | 66 (58.4) | 107 (74.3) | 0.02 |
Female | 47 (41.6) | 37 (25.7) | |
BMI (mean, IQR) (N = 188) | 30.3 (6.1) | 31.2 (7.9) | 0.27 |
Metabolic syndrome* (present) (N = 193) | 34 (33.7) | 81 (88.8) | <0.001 |
Diabetes (present) (N = 243) | 40 (38.1) | 108 (78.3) | <0.001 |
Hypertension (present) (N = 162) | 40 (38.8) | 48 (81.4) | <0.001 |
Ethnicity** | |||
White | 57 (50.4) | 110 (76.4) | |
Asian | 18 (15.9) | 16 (11.1) | |
Black | 13 (11.5) | 3 (2.1) | <0.001 |
Middle Eastern | 4 (3.5) | 6 (4.2) | |
Chinese | 3 (2.7) | 3 (2.1) | |
Other | 18 (15.9) | 6 (4.2) | |
HBA1C (mean, IQR) (N = 116)*** | 44.0 (7.0) | 48.6 (33.8) | 0.35 |
Total cholesterol (mean, IQR) (N = 141)*** | 4.9 (1.3) | 3.9 (1.2) | <0.001 |
Triglyceride levels (mean, IQR) (N = 140)*** | 1.9 (1.1) | 1.4 (0.8) | <0.01 |
HDL levels (mean, IQR) (N = 118)*** | 1.2 (0.4) | 1.1 (0.4) | 0.47 |
Cirrhosis | |||
Absent | 89 (84.8) | 36 (25.2) | <0.001 |
Present | 16 (15.2) | 107 (74.8) | |
Child-Turcotte-Pugh class (N = 241) | |||
A | 100 (99.0) | 99 (70.7) | |
B | 1 (1.0) | 35 (25.0) | <0.001 |
C | 6 (4.3) | ||
BCLC (N = 127) | |||
A | 37 (29.1) | ||
B | 39 (30.7) | ||
C | 39 (30.7) | ||
D | 12 (9.4) | ||
Maximum tumor diameter (N = 128) | |||
≤7 cm | 92 (71.9) | ||
>7 cm | 36 (28.1) | ||
PVT (N = 127) | |||
Absent | 69 (54.3) | ||
Present | 58 (45.7) | ||
Metastases (N = 112)**** | |||
Absent | 94 (83.4) | ||
Present | 18 (16.0) | ||
Treatments, n | |||
0 | 18 (12.8) | ||
1 | 105 (72.9) | ||
2 | 4 (2.8) | ||
>3 | 7 (4.9) | ||
OS | 23.0 (17.71–28.83) |
Metabolic syndrome defined according to WHO 1999 criteria. Data regarding metabolic syndrome were not available for Mt Sinai cohort.
Other as identified by patients (N = 24).
Data pertaining for HBAIC, cholesterol, triglycerides, and HDL levels not available for Newcastle, Mt Sinai, and Bologna cohort.
Presence of extrahepatic disease not available for Sydney cohort.