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Relationship between portal chronic inflammation and disease severity in paediatric non-alcoholic fatty liver disease

Anna Alisia1, Giorgio Bedognibc1, Rita De Vitod, Donatella Comparcolaa, Melania Mancoe, Valerio NobiliaCorresponding Author Informationemail addressemail address

Received 18 January 2010; accepted 8 May 2010. published online 28 June 2010.
Corrected Proof

Abstract 

Background

The non-alcoholic steato-hepatitis Clinical Research Network has recently shown that portal chronic inflammation is associated with liver fibrosis in American children with non-alcoholic fatty liver disease.

Aim

We tested whether the portal chronic inflammation-fibrosis association was present in a series of Italian children with non-alcoholic fatty liver disease.

Methods

We re-assessed the liver biopsies of 144 consecutive Italian children with non-alcoholic fatty liver disease aged 3–18 years and followed at the “Bambino Gesù” Paediatric Hospital. Non-alcoholic fatty liver disease and portal chronic inflammation were diagnosed using the non-alcoholic steato-hepatitis Clinical Research Network criteria. Anthropometry, body composition, liver enzymes, metabolic parameters and blood pressure were measured in all children.

Results

Two children had no portal chronic inflammation, 84 had mild and 58 more than mild portal chronic inflammation according to the non-alcoholic steato-hepatitis Clinical Research Network criteria. Children with no or mild portal chronic inflammation had the same clinical features of those with more than mild portal chronic inflammation except for insulin resistance, which was greater. There was no association between steatosis, lobular inflammation, ballooning, fibrosis and portal chronic inflammation.

Conclusion

We were not able to confirm the existence of a clinico-pathological association between portal chronic inflammation and disease severity in a series of Italian children with non-alcoholic fatty liver disease. Some clinico-pathological correlates of paediatric non-alcoholic fatty liver disease may be population-specific.

a Liver Unit, Pediatric Hospital “Bambino Gesù”, IRCCS, Rome, Italy

b Clinical Epidemiology Unit, Liver Research Center, Basovizza, Trieste, Italy

c Department of Maternal and Pediatric Sciences, University of Milan, Fondazione IRCCS Cà Granda - Ospedale Maggiore Policlinico, Milan, Italy

d Laboratory of Pathology, Pediatric Hospital “Bambino Gesù”, IRCCS, Rome, Italy

e Scientific Directorate, Pediatric Hospital “Bambino Gesù”, IRCCS, Rome, Italy

Corresponding Author InformationCorresponding author at: Liver Unit, Pediatric Hospital “Bambino Gesù”, Via S. Onofrio 4, 00165 Rome, Italy. Tel.: +39 06 68 59 22 43; fax: +39 06 68 59 21 92.

1 These authors contributed equally to this work.

PII: S1590-8658(10)00171-4

doi:10.1016/j.dld.2010.05.007