|
|
||||||||
1-Acid Glycoprotein Fucosylation for Liver Cirrhosis in Patients Undergoing Hepatic Biopsy
1 Department of Clinical Chemistry, Kalmar County Hospital, SE 39185 Kalmar, Sweden.
2 Division of Clinical Chemistry, Department of Biomedicine and Surgery, Linköping University, SE 58185 Linköping, Sweden.
3 Gastroenterology-Hepatology Division, Department of Medicine, Malmö University Hospital, SE 20502 Malmö, Sweden.
aAuthor for correspondence. Fax 46-480-81025; e-mail ingvar.ryden{at}telia.com.
Background: Increased fucosylation of serum glycoproteins has previously been reported in patients with liver disease. We analyzed
1-acid glycoprotein (AGP) fucosylation in serum samples from patients investigated for suspected liver disease to evaluate its value as a biochemical marker for liver cirrhosis.
Methods: We used a novel lectin immunoassay adapted to the AutoDELFIA system to analyze AGP fucosylation in 261 consecutive patients admitted for liver biopsy at Malmö University Hospital in Southern Sweden. The results were compared with histopathologic findings. In addition, AGP fucosylation was compared with other biochemical markers described as useful in the diagnosis of liver cirrhosis. The biochemical markers were compared by ROC curve analysis.
Results: AGP fucosylation was significantly (P <0.05) higher in patients with liver cirrhosis (n = 65) than in healthy controls (n = 72), patients with normal histology (n = 29), patients with steatosis only (n = 38), patients with viral or chronic hepatitis without cirrhosis (n = 71), and patients with other liver diseases without histologic signs of cirrhosis (n = 58). By calculating the AGP fucosylation index (AGP-FI = AGP fucosylation/AGP serum concentration), we obtained a high diagnostic accuracy. The areas under the ROC curves for AGP-FI were 0.83 and 0.74 for men and women, respectively, compared with 0.82 for hyaluronic acid and 0.77 for the aspartate aminotransferase/alanine aminotransferase ratio in both men and women.
Conclusions: AGP fucosylation appears to be useful in identifying patients with liver cirrhosis among patients investigated for liver disease. The lectin immunoassay showed satisfactory reproducibility and is suitable for routine use in a clinical laboratory.
The following articles in journals at HighWire Press have cited this article:
![]() |
R. K.T. Kam, T. C.W. Poon, H. L.Y. Chan, N. Wong, A. Y. Hui, and J. J.Y. Sung High-Throughput Quantitative Profiling of Serum N-Glycome by MALDI-TOF Mass Spectrometry and N-Glycomic Fingerprint of Liver Fibrosis Clin. Chem., July 1, 2007; 53(7): 1254 - 1263. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Sawa, T.-L. Hsu, T. Itoh, M. Sugiyama, S. R. Hanson, P. K. Vogt, and C.-H. Wong Glycoproteomic probes for fluorescent imaging of fucosylated glycans in vivo PNAS, August 15, 2006; 103(33): 12371 - 12376. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Morelle, C. Flahaut, J.-C. Michalski, A. Louvet, P. Mathurin, and A. Klein Mass spectrometric approach for screening modifications of total serum N-glycome in human diseases: application to cirrhosis Glycobiology, April 1, 2006; 16(4): 281 - 293. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Lumbreras-Lacarra, J. M. Ramos-Rincon, and I. Hernandez-Aguado Methodology in Diagnostic Laboratory Test Research in Clinical Chemistry and Clinical Chemistry and Laboratory Medicine Clin. Chem., March 1, 2004; 50(3): 530 - 536. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |