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. 2013 Feb 25;2013:168012. doi: 10.1155/2013/168012

Table 2.

Comparison of clinicopathological characteristics between patients who had developed hepatocellular carcinoma (HCC) and those who had not developed HCC at follow-up.

Overall Female
Patients who had developed HCC at follow-up Patients who had not developed HCC at follow-up P Patients who had developed HCC at follow-up Patients who had not developed HCC at follow-up P
Number of patients 13 166 11 144
Number of male patients 2 22 0.687 NA NA NA
Age of Dx of PBC (years)* 63 (46–77) 56 (22–85) 0.072 63 (46–77) 56 (24–85) 0.049
PBC Stage at Dx of PBC (I/II/III/IV) 2/4/3/4 99/38/16/13 0.004 2/3/3/3 86/34/14/10 0.011
Number of symptomatic patients 8 45 0.022 7 42 0.037
 Pruritus 4 33 0.474 4 32 0.282
 Jaundice 1 8 0.501 1 6 0.409
 Ascites 0 3 1 0 3 1
 Varices 5 12 0.003 4 11 0.013
Biochemical data
 AST (IU/L)* 78 (30–231) 46 (16–258) 0.088 77 (30–231) 46 (16–258) 0.15
 ALT (IU/L)* 51 (22–319) 45 (10–329) 0.644 47.5 (22–319) 41 (10–329) 0.761
 ALP (IU/L)* 402.5 (175–1185) 543.5 (94–2985) 0.314 402.5 (175–1185) 543.5 (112–2985) 0.489
γGTP (IU/L)* 174.5 (16–470) 173.5 (13–1349) 0.285 114 (16–470) 173.5 (13–1004) 0.181
 lgG (mg/dL)* 2165 (1030–4532) 1655 (778–3900) 0.021 2165 (1030–4532) 1660 (778–3900) 0.049
 lgM (mg/dL)* 405 (136–918) 351.5 (48–1660) 0.364 359.5 (136–918) 336 (48–1660) 0.352
 Alb (g/dL)* 3.7 (1.9–4.6) 4.2 (2.0–5.1) 0.016 4.0 (1.9–4.6) 4.2 (2.0–5.0) 0.085
 T-Bil (mg/dL)* 0.7 (0.3–2.5) 0.7 (0.1–6.3) 0.925 0.7 (0.3–2.5) 0.7 (0.1–6.3) 0.888
 Plt (×104/μL)* 12.4 (5.3–24.4) 21.4 (5.3–58.1) 0.001 12.3 (5.3–21.8) 21.0 (5.3–48.6) 0.001
 PT (%)* 96.5 (57.0–117.0) 100.9 (44.0–139.0) 0.204 93.0 (57.0–117.0) 100.9 (44.0–139.0) 0.123
ANA positive 7 106 0.658 6 98 0.579
Brinkman index* 0 (0–400) 0 (0–1575) 0.175 0 (0-0) 0 (0–940) 0.12
Number of patients with a history of blood transfusion 3 20 0.415 3 17 0.285
Number of patients with a history of drinking 0 11 1 0 7 1
Number of patients with a familial history of malignancy 3 61 0.359 2 56 0.261
Number of patients with a familial history of liver disease 1 25 0.764 0 24 0.337
Number of patients with DM 2 17 0.632 2 14 0.317
Number of patients with HT 5 27 0.059 4 22 0.09
Number of patients with HL 3 40 1 3 34 0.725
Number of patients with autoimmune disease 5 53 0.759 5 51 0.528
 Sjogren's syndrome 2 24 1 2 24 1
 Hashimoto's disease 3 15 0.128 3 15 0.12
 Rheumatoid arthritis 1 15 1 1 14 1
 Scleroderma 0 15 0.606 0 15 0.602
 Systemic lupus erythematosus 0 2 1 0 1 1
BMI* 24.3 (13.8–27.4) 22.6 (14.3–33.1) 0.341 24.3 (15.8–27.4) 22.6 (16.0–32.5) 0.536
Number of patients with medications
 UDCA/BF/UDCA + BF/none 13/0/0/0 131/1/29/5 0.388 11/0/0/0 116/1/22/5 0.512
Number of patients with biochemical response to UDCA and of those with medications
 Responder/non-responder/BF only/no
 medication (Rotterdam)
11/2/0/0 141/19/1/5 0.911 9/2/0/0 123/15/1/5 0.696
 Responder/non-responder/BF only/no
 medication (Barcelona)
9/4/0/0 80/80/1/5 0.701 7/4/0/0 67/71/1/5 0.816
 Responder/non-responder/BF only/no
 medication (Paris)
12/1/0/0 134/26/1/5 0.832 10/1/0/0 119/19/1/5 0.905
 Responder/non-responder/BF only/no
 medication (Toronto)
11/2/0/0 130/30/1/5 0.914 9/2/0/0 113/25/1/5 0.928
Modalities (US/CT/MRI/US-CT/US-MRI/CT-MRI/US-CT-MRI) 12/0/0/1/0/0/0 129/10/0/22/3/1/1 0.96 10/0/0/1/0/0/0 114/7/0/18/3/1/1 0.985
HCC screening interval (months) 9 (6–12) 6 (6–12) 0.435 12 (6–12) 6 (6–12) 0.413

*Data expressed as median (range); Alb: albumin; ALP: alkaline phosphatase; AMA: anti-mitochondrial antibody; ANA: antinuclear antibody; ALT: alanine aminotransferase; AST: aspartate aminotransferase; BF: bezafibrate; BMI: body mass index; CT: computer tomography; DM: diabetes mellitus; Dx: diagnosis; γ-GTP: γ-glutamyltranspeptidase; HCC: hepatocellular carcinoma; HT: hypertension; HL: hyperlipidemia; MRI: magnetic resonance imaging; NA: not applcable; PBC: primary biliary cirrhosis; Plt: platelet; PT: prothrombin time; T-Bil: total bilirubin; UDCA: ursodeoxycholic acid; US: ultrasonography. Responses were defined as biochemical response to UDCA according to the Barcelona, Paris, Rotterdam, and Toronto definitions. These modalities were alternately applied to the patients.