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. 2013 Aug 27;109(6):1657–1665. doi: 10.1038/bjc.2013.481

Table 1. Distribution of each variable in 1351 patients with non-malignant chronic liver diseases and HCC in the estimation group.

 
Non-malignant chronic liver diseases (n=1124)
 
Variablesa F0c (N=107) F1–F3c (N=676) F4c (N=341) HCC (N=227) P-valueb
Age (years)
37.2±8.7
42.7±7.9
46.1±7.6
59±10.3
<0.0001
AST (U l−1)
34.6±14.2
41.9±26.6
71±43
128± 109
<0.0001
ALT (U l−1)
40.2±23.1
49.6± 34.7
77.6±53.6
67.6±61.0
0.31
AAR
0.85±0.44
0.97±0.47
1.1±0.45
1.9±1.53
<0.0001
ALP (U l−1)
87.1±47
83.8±47.6
94±40
260±227
<0.0001
Albumin (g l−1)
43.9±3.5
42.7± 3.7
38±4.2
29 ±5.9
<0.0001
Total bilirubin (mg dl−1)
0.84±0.38
0.83±0.33
1.11±0.68
4.1±2.9
<0.0001
Platelet count ( × 109 l−1)
238±56
195±54
155±53
135±92
0.75
Prothrombin-INR
1.10±0.12
1.20±0.20
1.23±0.15
1.30±0.20
0.06
α-Fetoprotein (U l−1)
2.3±1.1
0.58±0.44
38.8±21.2
32341±10109
<0.0001
Log α-fetoprotein (U l−1) 0.31±0.23 0.49±0.3 1.1±0.44 2.7±1.38 <0.0001

Abbreviations: AAR=AST/ALT ratio; ALP=alkaline phosphatase; ALT=alanine aminotransferase; AST=aspartate aminotransferase; HCC=hepatocellular carcinoma; INR=international normalised ratio.

a

Normal values: AST up to 40 U l−1; ALT up to 45 U lL−1; ALP 22–92 U l−1; albumin 38–54 g l−1; total bilirubin up to 1 mg% platelet count 150–400 ( × 109 l−1); and α-fetoprotein up to 10 U l−1.

b

P>0.05 is considered nonsignificant and P<0.05 is considered significant; the reference groups for P-values were HCC vs F4.

c

METAVIR score was used to stage fibrosis (F0–F3) and liver cirrhosis (F4).