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Available data do not allow carcinogenesis mechanisms in cirrhotic patients to be well understood in absence of studies taking into account all recognised factors. A large scale clinical, biochemical and molecular studies is potentially relevant to the understanding of nutrition, physical activity, body weight metabolic syndrome whatever the etiology of underlying cirrhosis. It will open new perspectives :
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Inclusion criteria
Cases and controls will be males and females aged 35 or older, and will give an informed consent to participate in the study.
* Hepatocellular carcinoma case:
All hepatocellular carcinoma cases evolving in cirrhotic liver, whatever the etiology of cirrhosis, will be included. Criteria for the diagnosis of hepatocellular carcinoma will be those defined by the European Association for Study of the Liver (EASL) (Bruix J, J Hepatol 2001):
Focal hepatic lesions ≥ 2cm in diameter:
Focal hepatic lesions < 2 cm in diameter:
Whatever the size of focal lesions, the diagnosis of cirrhosis will be made according to the same criteria as in the cirrhotic group control.
* Cirrhotic control patients:
All patients with cirrhosis, whatever its etiology, will be included. The diagnosis of cirrhosis will rely on:
Histological confirmation by liver biopsy or in the absence of biopsy:
And/or biological signs of hepatocellular failure (TP<70%, low albuminemia) And/or sinusoidal block assessed by liver venous gradient > 18mmHG In the present state of knowledge, a fibrotest value at 4 or a fibroscan value > 12.5 kilopascal.
Without any other clinical or biological signs will be considered as diagnosis criteria of cirrhosis only for chronic viral C hepatitis.
The lack of hepatocellular carcinoma in cirrhotic patients at inclusion will be assessed through good quality imaging examinations (abdominal US, CT scan or MRI) and AFP below 100 ng/ml.
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1,246 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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