Clinical Research
Copyright ©2008 The WJG Press and Baishideng Publishing. All rights reserved.
World J Gastroenterol. Aug 14, 2008; 14(30): 4745-4752
Published online Aug 14, 2008. doi: 10.3748/wjg.14.4745
Revaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome
Alessia Riva, Paola Trombini, Raffaella Mariani, Alessandra Salvioni, Sabina Coletti, Silvia Bonfadini, Valentina Paolini, Matteo Pozzi, Rita Facchetti, Giorgio Bovo, Alberto Piperno
Alessia Riva, Paola Trombini, Raffaella Mariani, Alessandra Salvioni, Sabina Coletti, Silvia Bonfadini, Valentina Paolini, Matteo Pozzi, Alberto Piperno, Department of Clinical Medicine, University of Milano-Bicocca, San Gerardo Hospital, Monza 20052, Italy
Rita Facchetti, Department of Clinical and Preventive Medicine, University of Milano-Bicocca, Monza 20052, Italy
Giorgio Bovo, Department of Clinical Pathology, San Gerardo Hospital, University of Milano-Bicocca, Monza 20052, Italy
Author contributions: Riva A, Trombini P and Piperno A conceived of and designed the research; Mariani R, Salvioni A, Coletti S, Bonfadini S, Paolini V and Pozzi M collected and tabulated clinical, biochemical and histological data; Bovo G performed histological evaluation; Riva A, Trombini P and Facchetti R performed the statistical analyses; Riva A, Trombini P and Piperno A wrote the paper. All authors contributed to the interpretation of data and to the preparation of the final manuscript.
Supported by Grant from the Association for the Study of Hemochromatosis and Iron Overload Disorders-ONLUS (P.T.), Monza
Correspondence to: Alberto Piperno, Professor, Clinica Medica, Azienda Ospedaliera San Gerardo, Via Pergolesi 33, Monza 20052, Italy. alberto.piperno@unimib.it
Telephone: +39-39-2339555 Fax: +39-39-322274
Received: May 7, 2008
Revised: June 16, 2008
Accepted: June 23, 2008
Published online: August 14, 2008
Abstract

AIM: To re-evaluate the diagnostic criteria of insulin resistance hepatic iron overload based on clinical, biochemical and histopathological findings.

METHODS: We studied 81 patients with hepatic iron overload not explained by known genetic and acquired causes. The metabolic syndrome (MS) was defined according to ATPIII criteria. Iron overload was assessed by liver biopsy. Liver histology was evaluated by Ishak’s score and iron accumulation by Deugnier’s score; steatosis was diagnosed when present in ≥ 5% of hepatocytes.

RESULTS: According to transferrin saturation levels, we observed significant differences in the amount of hepatic iron overload and iron distribution, as well as the number of metabolic abnormalities. Using Receiving Operating Curve analysis, we found that the presence of two components of the MS differentiated two groups with a statistically significant different hepatic iron overload (P < 0.0001). Patients with ≥ 2 metabolic alterations and steatosis had lower amount of hepatic iron, lower transferrin saturation and higher sinusoidal iron than patients with < 2 MS components and absence of steatosis.

CONCLUSION: In our patients, the presence of ≥ 2 alterations of the MS and hepatic steatosis was associated with a moderate form of iron overload with a prevalent sinusoidal distribution and a normal transferrin saturation, suggesting the existence of a peculiar pathogenetic mechanism of iron accumulation. These patients may have the typical dysmetabolic iron overload syndrome. By contrast, patients with transferrin saturation ≥ 60% had more severe iron overload, few or no metabolic abnormalities and a hemochromatosis-like pattern of iron overload.

Keywords: Iron overload; Hepatic iron distribution; Transferrin saturation; Metabolic syndrome; Hepatic steatosis