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Serum IL-6 and IL-8 in infants with biliary atresia in comparison to intrahepatic cholestasis
 
Amel AM El-Faramawy,1 Lerine BE El-Shazly,1 Amal A Abbass,2 Hend AB Ismail1
Department of Paeditrics1 and
Department of Clinical pathology,2
Faculty of Medicine,
Ain Shams University,
Cairo, Egypt


Corresponding Author
: Dr. Amel Elfaramawy
Email: amelhome4@gmail.com


Abstract

Background: Biliary atresia (BA) is an idiopathic progressive inflammation and fibrosclerosis of the extra and intrahepatic bile ducts.

 

Aim: To measure the serum levels of IL-6 and IL-8 in biliary atresia and correlate with clinical outcome.

 

Methods: Sixty children were included, 20 with BA (group 1), 20 with intrahepatic cholestasis (group 2) and 20 normal children as controls. Complete blood count (CBC), liver function tests, serum IL-6 and IL-8 were analyzed in all the three groups.

 

Results: Mean serum IL-6 and IL-8 levels were significantly higher in group 1 (394.7 + 40.2 and 111.2 + 9.7 pg/dl, respectively) than group 2 (175.5 + 33.1and 53.5 + 8.2 pg/dl, respectively) (p=0.0 for both). Both IL-6 and IL-8 were significantly higher in both the disease groups compared to controls (30.4 + 8.8 and 13.7 + 4.1 pg/dl, respectively). IL-8 showed a significant positive correlation with lymphocytes and significant negative correlation with albumin in group 1. Higher IL-6 was found in patients with BA with severe fibrosis than in patients with mild fibrosis while higher IL-8 was found in children with persistent jaundice than those free from jaundice in group 1.

 

Conclusion: Serum IL-6 and IL8 are high in patients with BA indicating ongoing inflammation. They may serve to determine disease severity and may predict the progression to liver fibrosis in these cases.