Department of Gastroenterology, Shanghai Children′s Medical Center, School of Medicine, Shanghai Jiaotong University, Shanghai 200127, China. Email:13901730330@139.com
Abstract OBJECTIVE: This study aimed to investigate the value of the liver function test in the differential diagnosis of infantile hepatitis syndrome (IHS) and biliary atresia (BA) by analyzing seven conventional serological markers in this test using receiver operating characteristic (ROC) curves. METHODS: Serum levels of seven conventional serological markers: alanine aminotransferase (ALT), aspartate aminotransferase (AST), γ-glutamyl transpeptidase (γ-GT), alkaline phosphatase (ALP), total bilirubin (TB), conjugated bilirubin (CB) and serum albumin (ALB) were measured in 103 children with IHS and 60 children with BA. ROC curves were used to evaluate the sensitivity, specificity, positive and predictive values and optimal cut-off. The united tests (parallel test and serial test) of γ-GT, TB and CB were performed to elevate diagnostic efficiency. RESULTS: Compared with the IHS group, the BA group had significantly increased serum ALT, AST, γ-GT, TB and CB levels (P<0.01). The area under ROC (AUCROC) of AST, γ-GT, CB and TB was 0.77, 0.881, 0.841 and 0.87, respectively. γ-GT showed the highest AUCROC, specificity, positive predictive value and positive likelihood ratio in the diagnosis of BA, followed by CB, TB and AST in turn. The negative predictive value of CB was the highest, followed by TB. The negative likelihood ratio of CB was the lowest but its Youden index was the highest. The Youden index of γ-GT and TB was lower than that of CB. After the parallel tests, the sensitivity and negative predictive value of γ-GT, CB and TB increased to 100%. After the serial tests, the specificity of γ-GT, CB and TB increased to 90.4% and the positive predictive value increased to 87.5%. CONCLUSIONS: The measurement of γ-GT, TB and CB levels are valuable in the differential diagnosis of BA and IHS. An imaging examination is required in the parallel test positive patients.[Chin J Contemp Pediatr, 2009, 11 (12):953-956]
CHU Bo,JIANG Li-Rong,ZHOU Sha et al. Value of the liver function test in differential diagnosis of infantile hepatitis syndrome and biliary atresia[J]. 中国当代儿科杂志, 2009, 11(12): 953-956.
CHU Bo,JIANG Li-Rong,ZHOU Sha et al. Value of the liver function test in differential diagnosis of infantile hepatitis syndrome and biliary atresia[J]. CJCP, 2009, 11(12): 953-956.
[3]Fischler B, Woxenius S, Nemeth A, Papadogiannakis N. Immunoglobulin deposits in liver tissue from infants with biliary atresia and the correlation to cytomegalovirus infection[J]. J Pediatr Surg, 2005, 40(3):541-546.
[4]Shimadera S, Iwai N, Deguchi E, Kimura O, Ono S, Fumino S, et al. Significance of ductal plate malformation in the postoperative clinical course of biliary atresia[J]. J Pediatr Surg, 2008, 43(2):304-307.
[5]Haber BA, Erlichman J, Loomes KM.Recent advances in biliary atresia:prospects for novel therapies[J]. Expert Opin Investig Drugs, 2008, 17(12):1911-1924.
[6]Serinet MO, Wildhaber BE, Brone P, Lachaux A, Sarles J, Jacquemin E, et al.Impact of age at kasai operation on its results in late childhood and adolescence:a rational basis for biliary atresia screening[J].Pediatrics, 2009, 123(5):1280-1286.
[7]Tang KS, Huang LT, Huang YH, Lai CY, Wu CH, Wang SM, et al. Gamma-glutamyl transferase in the diagnosis of biliary atresia[J]. Acta Paediatr Taiwan, 2007, 48(4):196-200.
[8]Sucky FJ, Sokol RJ, Balistreri WF. Liver disease in children[M].Philadelphia: Lippincott Williams & Wilkins, 2001, 155-169.
[9]Poddar U, Thapa BR, Das A, Bhattacharya A, Rao KN, Singh K. Neonatal cholestasis:differentiation of biliary atresia from neonatal hepatitis in a developing country[J]. Acta Paediatr, 2009, 98(8):1260-1264.