Multivariate discriminant function based on six biochemical markers in blood can predict the cirrhotic evolution of chronic hepatitis

Citation
G. Fortunato et al., Multivariate discriminant function based on six biochemical markers in blood can predict the cirrhotic evolution of chronic hepatitis, CLIN CHEM, 47(9), 2001, pp. 1696-1700
Citations number
22
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICAL CHEMISTRY
ISSN journal
00099147 → ACNP
Volume
47
Issue
9
Year of publication
2001
Pages
1696 - 1700
Database
ISI
SICI code
0009-9147(200109)47:9<1696:MDFBOS>2.0.ZU;2-N
Abstract
Background: Serologic markers have been proposed for monitoring hepatic fib rosis in chronic active liver disease. Because none of these markers, when used singly, is totally satisfactory, we developed and evaluated a multivar iate approach. Methods: We studied two cohorts of chronic hepatitis (54 patients) and cirr hosis patients (49 patients) to identify a panel of biochemical markers tha t discriminates between the two diseases. Using multivariate discriminant a nalysis, we selected a function, based on the concentrations of six biochem ical markers (fibronectin, prothrombin, pseudocholinesterase, alanine amino transferase, manganese superoxide dismutase, and N-acetyl-beta -glucosamini dase). We then prospectively validated this function on a second temporal c ohort of patients. Results: Multivariate discriminant analysis correctly classified 93.7% of p atients (94.3% of chronic hepatitis and 92.9% of cirrhosis patients) in the first cohort and 85% of patients (89.5% of chronic hepatitis patients and 81% of cirrhosis patients) in the second cohort. Conclusions: Discriminant analysis of results of six inexpensive biochemica l markers provides a high predictive value for differentiation between live r cirrhosis and chronic hepatitis. Consequently, these biochemical markers condensed into a multivariate discriminant analysis value for each patient provide information that can be contributory for subsequent options during the evolution of the natural history of chronic hepatitis. (C) 2001 America n Association for Clinical Chemistry.