Cushing's Syndrome is a rare disease resulting from prolonged exposure to high levels of circulating cortisol. Clinical manifestations are variable but many patients present a metabolic syndrome (abdominal obesity, insulin resistance, dyslipidemia, hypertension). With regard to the liver, experimental data have shown that excess cortisol leads in an increase in lipogenesis and a reduction in the oxidation of fatty acids. This, in association with an accumulation of visceral adipose tissue and deregulation of adipokines, may contribute to the development of hepatic steatosis in animals. However, few data is available in humans with only one study of 50 patients with Cushing's syndrome estimating the prevalence of hepatic steatosis at 20%. NAFLD (Non-Alcoholic Fatty Liver Disease), is defined as the presence of hepatic steatosis in the absence of secondary causes of intrahepatic fat accumulation. It is a heterogeneous disease ranging from simple liver steatosis, whose prognosis is generally considered to be benign, to inflammation (NASH, Non-Alcoholic Steato-Hepatitis) which may progress to fibrosis, cirrhosis and an increased risk of hepatocellular carcinoma. The prognosis for NAFLD is mainly related to the severity of hepatic fibrosis. In Cushing's syndrome, normalization of cortisol production is the most effective strategy to improve co-morbidities associated with hypercortisolism. However, some of these complications, especially the metabolic co morbidities, could not be completely reversible and no data is available about resolution of hepatic steatosis.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
100
Quantification of hepatic steatosis with RMI at the diagnosis (T0) and one year after remission (T1). The percentage of patients with complete resolution of hepatic steatosis on MRI will be determined.
University Hospital, Angers
Angers, France
RECRUITINGUniversity Hospital, Bordeaux
Bordeaux, France
RECRUITINGUniversity Hospital, Brest
Brest, France
RECRUITINGUniversity Hospital, Grenoble
Grenoble, France
RECRUITINGUniversity Hospital, Lille
Lille, France
RECRUITINGUniversity Hospital, Nantes
Nantes, France
RECRUITINGUniversity Hospital, Nancy
Vandœuvre-lès-Nancy, France
RECRUITINGFrequency of resolution of hepatic steatosis
To evaluate the frequency of complete resolution of hepatic steatosis in patients with cushing syndrome after remission of hypercortisolism
Time frame: 2 years
Prevalence of steatosis at diagnosis of Cushing
to assess the prevalence of hepatic steatosis at the diagnosis of Cushing's syndrome.
Time frame: 2 years
Prevalence of steatosis at diagnosis of Cushing
to evaluate the prevalence of steatosis
Time frame: 2 years
Fatty Liver Index (non-invasive biomarkers of hepatic steatosis )
to evaluate the non-invasive biomarkers of hepatic steatosis (Fatty Liver Index)
Time frame: 2 years
FIB-4 (non-invasive biomarkers advanced hepatic fibrosis)
to evaluate the non-invasive biomarkers advanced hepatic fibrosis (FIB-4)
Time frame: 2 years
e-LIFT (non-invasive biomarkers advanced hepatic fibrosis)
to evaluate the non-invasive biomarkers advanced hepatic fibrosis ( e-LIFT, NAFLD Fibrosis Score)
Time frame: 2 years
NAFLD Fibrosis Score (non-invasive biomarkers advanced hepatic fibrosis)
to evaluate the non-invasive biomarkers advanced hepatic fibrosis (NAFLD Fibrosis Score)
Time frame: 2 years
Prevalence of steatosis at diagnosis of Cushing
4\. To assess the performance of CAP (Controlled Attenuation Parameter) in the diagnosis of hepatic steatosis in Cushing's syndrome.
Time frame: 2 years
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