Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/61247
Title: Hyaluronic acid: Additional biochemical marker in the diagnosis of biliary atresia
Authors: Nuthapong Ukarapol
Lumduan Wongsawasdi
Siriwan Ong-Chai
Pornthawee Riddhiputra
Prachya Kongtawelert
Keywords: Medicine
Issue Date: 1-Oct-2007
Abstract: Background: The purpose of the present paper was to evaluate the value of biochemical markers, including conventional liver function tests, γ-glutamyl transferase (GGT), and hyaluronic acid (HA), in the diagnosis of neonatal cholestasis. Methods: Infants with neonatal jaundice were consecutively enrolled during 1 year period. The patients were diagnosed as having biliary atresia (BA) if there was either bile ductular proliferation in the portal tracts, atretic common bile duct/gallbladder, or evidence of bile duct obstruction demonstrated by liver pathology or intraoperative cholangiography, respectively. Serum HA was measured using an enzyme-linked immunosorbent assay-based test. Results: A total of 25 patients diagnosed as having BA (n = 10), neonatal hepatitis (NH; n = 9), choledochal cyst (n = 3) and parenteral nutrition-induced cholestasis (n = 3), were studied. The age at diagnosis was not significantly different between groups. Only GGT and HA were significantly elevated in the patients with BA when compared to NH (P = 0.02, P = 0.03, respectively). In BA, the median value of serum HA was 514 ng/mL (range 19-4476 ng/mL), compared to 50 ng/mL (range 19-315 ng/mL) in NH. Additionally, the serum HA level was much higher in children with choledochal cyst. Conclusion: HA could be considered as a complementary biochemical marker for evaluating infants with prolonged jaundice. © 2007 Japan Pediatric Society.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34548671854&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/61247
ISSN: 1442200X
13288067
Appears in Collections:CMUL: Journal Articles

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