TY - JOUR
T1 - Diagnostic usefulness of acute-phase protein measurement in hepatocellular carcinoma
AU - Fabris, Carlo
AU - Pirisi, Mario
AU - Soardo, Giorgio
AU - Toniutto, Pierluigi
AU - Falleti, Edmondo
AU - Vitulli, Daniela
AU - Pezzetta, Francesca
AU - Gonano, Fabio
AU - Bartoli, Ettore
PY - 1996
Y1 - 1996
N2 - To compare the diagnostic usefulness as markers of hepatocellular carcinoma (HCC) of α1-antitrypsin, C-reactive protein, and α1-acid glycoprotein (all determined by nephelometric methods), we studied 132 subjects (74 male, 58 female): 43 had mild chronic liver disease, 32 cirrhosis, 24 HCC; 33 were controls. A total of 29.2% of the patients with HCC had α1-acid glycoprotein > 100 mg/dl, 75.0% had α1-antitrypsin > 220 mg/dl, 70.8% had C-reactive protein > 5 mg/L. In cirrhotics, frequencies were 3.1, 50.0 and 59.4%, respectively; in patients with mild chronic liver disease, 14.0, 11.6, and 32.6% (χ2 12.3; p < 0.01; χ2 47.3, p < 0.0001; χ2 38.0, p < 0.0001, respectively). α1-fetoprotein performed better than all acute-phase proteins. We conclude that, due to their low specificity and/or sensitivity, none of the three acute-phase reactants tested can be recommended for diagnostic use as biological markers of HCC in Western patients.
AB - To compare the diagnostic usefulness as markers of hepatocellular carcinoma (HCC) of α1-antitrypsin, C-reactive protein, and α1-acid glycoprotein (all determined by nephelometric methods), we studied 132 subjects (74 male, 58 female): 43 had mild chronic liver disease, 32 cirrhosis, 24 HCC; 33 were controls. A total of 29.2% of the patients with HCC had α1-acid glycoprotein > 100 mg/dl, 75.0% had α1-antitrypsin > 220 mg/dl, 70.8% had C-reactive protein > 5 mg/L. In cirrhotics, frequencies were 3.1, 50.0 and 59.4%, respectively; in patients with mild chronic liver disease, 14.0, 11.6, and 32.6% (χ2 12.3; p < 0.01; χ2 47.3, p < 0.0001; χ2 38.0, p < 0.0001, respectively). α1-fetoprotein performed better than all acute-phase proteins. We conclude that, due to their low specificity and/or sensitivity, none of the three acute-phase reactants tested can be recommended for diagnostic use as biological markers of HCC in Western patients.
UR - http://www.scopus.com/inward/record.url?scp=0029871056&partnerID=8YFLogxK
U2 - 10.3109/07357909609018884
DO - 10.3109/07357909609018884
M3 - Article
SN - 0735-7907
VL - 14
SP - 103
EP - 108
JO - Cancer Investigation
JF - Cancer Investigation
IS - 2
ER -