chronic active liver disease
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2020 ◽  
Vol 46 (9) ◽  
pp. 1240-1242
Author(s):  
Steven E. Eilers ◽  
Richard Torbeck ◽  
Shalini Krishnasamy ◽  
Hooman Khorasani

2015 ◽  
pp. 177-182
Author(s):  
N. Tygstrup ◽  
G. H�ybye ◽  
M. Hilden ◽  
O. Dietrichson ◽  
P. Winkel ◽  
...  

2008 ◽  
Vol 9 (1) ◽  
pp. 36-40 ◽  
Author(s):  
Gerhard Opelz ◽  
Arnold J. M. Vogten ◽  
William H. J. Summerskill ◽  
Solko W. Schalm ◽  
Paul I. Terasaki

2001 ◽  
Vol 47 (9) ◽  
pp. 1696-1700 ◽  
Author(s):  
Giuliana Fortunato ◽  
Giuseppe Castaldo ◽  
Giovannangelo Oriani ◽  
Raimondo Cerini ◽  
Mariano Intrieri ◽  
...  

Abstract Background: Serologic markers have been proposed for monitoring hepatic fibrosis in chronic active liver disease. Because none of these markers, when used singly, is totally satisfactory, we developed and evaluated a multivariate approach. Methods: We studied two cohorts of chronic hepatitis (54 patients) and cirrhosis patients (49 patients) to identify a panel of biochemical markers that discriminates between the two diseases. Using multivariate discriminant analysis, we selected a function, based on the concentrations of six biochemical markers (fibronectin, prothrombin, pseudocholinesterase, alanine aminotransferase, manganese superoxide dismutase, and N-acetyl-β-glucosaminidase). We then prospectively validated this function on a second temporal cohort of patients. Results: Multivariate discriminant analysis correctly classified 93.7% of patients (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 biochemical markers provides a high predictive value for differentiation between liver 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.


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