TY - JOUR
T1 - Circulating standard CD44 isoform in patients with liver disease
T2 - Relationship with other soluble adhesion molecules and evaluation of diagnostic usefulness
AU - Falleti, Edmondo
AU - Pirisi, Mario
AU - Fabris, Carlo
AU - Bortolotti, Nadia
AU - Soardo, Giorgio
AU - Gonano, Fabio
AU - Bartoli, Ettore
PY - 1997/2
Y1 - 1997/2
N2 - Objectives: To verify the diagnostic usefulness of soluble CD44 (sCD44) in liver diseases. Methods: We studied 142 subjects (90 male, 52 female): 14 had acute hepatitis (AH); 45, noncirrhotic chronic liver disease (CLD); 34, cirrhosis; 35 had extrahepatic diseases (EHD); and 14 were healthy controls. sCD44, soluble intercellular adhesion molecule-1 (sICAM-1) and soluble vascular cell adhesion molecule-1 (sVCAM-1) were measured immunoenzymatically. Results: Patients with AH or cirrhosis had higher sCD44 in comparison to CLD, EHD, and controls (p < 0.01). On univariate analysis, sCD44 was associated with sVCAM-1, sICAM-1, bilirubin, cholinesterase, aspartate aminotransferase, and alkaline phosphatase (p < 0.001). By stepwise discriminant analysis, a set of variables, including sCD44 and sVCAM-1, were entered into a model that allocated correctly 79% of observations (p < 0.0001). However, when adhesion molecules were excluded, the model could still allocate correctly 72% of observations. Conclusion: Although sCD44 concentration increases during severe acute or chronic liver disease, its measurement adds little to the clinical information provided by traditional liver biochemistry.
AB - Objectives: To verify the diagnostic usefulness of soluble CD44 (sCD44) in liver diseases. Methods: We studied 142 subjects (90 male, 52 female): 14 had acute hepatitis (AH); 45, noncirrhotic chronic liver disease (CLD); 34, cirrhosis; 35 had extrahepatic diseases (EHD); and 14 were healthy controls. sCD44, soluble intercellular adhesion molecule-1 (sICAM-1) and soluble vascular cell adhesion molecule-1 (sVCAM-1) were measured immunoenzymatically. Results: Patients with AH or cirrhosis had higher sCD44 in comparison to CLD, EHD, and controls (p < 0.01). On univariate analysis, sCD44 was associated with sVCAM-1, sICAM-1, bilirubin, cholinesterase, aspartate aminotransferase, and alkaline phosphatase (p < 0.001). By stepwise discriminant analysis, a set of variables, including sCD44 and sVCAM-1, were entered into a model that allocated correctly 79% of observations (p < 0.0001). However, when adhesion molecules were excluded, the model could still allocate correctly 72% of observations. Conclusion: Although sCD44 concentration increases during severe acute or chronic liver disease, its measurement adds little to the clinical information provided by traditional liver biochemistry.
KW - CD44
KW - adhesion molecules
KW - liver disease
KW - liver function tests
UR - http://www.scopus.com/inward/record.url?scp=0031027562&partnerID=8YFLogxK
U2 - 10.1016/S0009-9120(96)00135-X
DO - 10.1016/S0009-9120(96)00135-X
M3 - Article
SN - 0009-9120
VL - 30
SP - 69
EP - 73
JO - Clinical Biochemistry
JF - Clinical Biochemistry
IS - 1
ER -