Assessment of liver fibrosis by a noninvasive method of transient elastography and biochemical markers

AIM: To assess the correlation between the fibrotic area (FA) as calculated by a digital image analysis (DIA), and to compare the diagnostic accuracy of FibroScan to the other existing Liver fibrosis (LF) markers using the receiver operating curve analysis. METHODS: We recruited 30 patients who unde...

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Veröffentlicht in:World journal of gastroenterology : WJG 2006-07, Vol.12 (27), p.4325-4330
Hauptverfasser: Kawamoto, Masaki, Mizuguchi, Toru, Katsuramaki, Tadashi, Nagayama, Minoru, Oshima, Hideki, Kawasaki, Hiroyuki, Nobuoka, Takayuki, Kimura, Yasutoshi, Hirata, Koichi
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Sprache:eng
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Zusammenfassung:AIM: To assess the correlation between the fibrotic area (FA) as calculated by a digital image analysis (DIA), and to compare the diagnostic accuracy of FibroScan to the other existing Liver fibrosis (LF) markers using the receiver operating curve analysis. METHODS: We recruited 30 patients who underwent a liver resection for three different etiologies including normal liver, hepatitis B, and hepatitis C. Liver stiffness was measured by using a FibroScan. The FA was then calculated by DIA to evaluate LF in order to avoid any sampling bias. RESULTS: The FA negatively correlated with Prothrombin time (PT), platelet count, lecithin-cholesterol acyltransferase (LCAT), and pre-albumin (ALB). On the other hand, the findings of FibroScan correlated with similar markers. The FA positively correlated with FibroScan, serum hyaluronate level, and type Ⅳ collagen level, and aspartate transaminase to platelet ratio index (APRI). The area under the receiver operating curve for FibroScan was higher than that for the other markers, even though the statistical significance was minimal. CONCLUSION: Our findings suggest that FibroScan can initially be used to assess LF as an alternative to a liver biopsy (LB) and serum diagnosis, because it is a safe method with comparable diagnostic accuracy regarding the existing LF markers.
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v12.i27.4325