Effect of Liraglutide on Fatty Liver Content Evaluated by Proton-spectroscopy (1H-spectroscopy) and Lipoprotein Kinetic, in Patients With Type 2 Diabetes

Official Summary

Non-alcoholic fatty liver disease (NAFLD) is commonly associated with obesity, metabolic syndrome and type 2 diabetes. NAFLD, in patients with type 2 diabetes, has been shown to be associated with lipid abnormalities (such as hypertriglyceridemia and decreased HDL-cholesterol) and increased cardiovascular risk. Such lipid abnormalities (hypertriglyceridemia and decreased HDL-cholesterol) are very frequent in patients with type 2 diabetes. Moreover, NAFLD is a risk for further development of cirrhosis (estimated between 3 and 5%). Animal studies have shown that liraglutide is able to decrease liver fat content, but the effect of liraglutide on liver fat content in patients with diabetes remains unknown. In addition, human studies with liraglutide have shown significant modification of plasma lipids, such as reduction of plasma triglycerides and LDL-cholesterol. However, the mechanisms responsible for these liraglutide induced lipid modifications are not yet known. Because increased in liver fat content and hypertriglyceridemia are associated in patients with type 2 diabetes, it seems interesting to study the effect of liraglutide on both liver fat content and lipid metabolism using gold-standard methods (proton-spectroscopy for liver fat content assessment and kinetic study with stable isotope to study lipoprotein metabolism). This is a monocentric study. Fatty liver content will be performed by proton-spectroscopy in patients with type 2 diabetes (n=120) before and after a 6 month period of liraglutide therapy (1.2 mg/day). Moreover, an in vivo kinetic study will be performed with stable isotopes (13C leucine) in 10 patients among the 120 patients with type 2 diabetes (n=10) before and after a 6-month period of liraglutide (1.2 mg/day) therapy. Each kinetic study will be performed during a 2-day hospitalization For the main study, 3 visits will be performed: * a first visit at T0, before starting the treatment with liraglutide, including clinical and biologic

Study Design

• Study Type: INTERVENTIONAL
• Allocation: NA
• Model: SINGLE_GROUP
• Masking: NONE
• Enrollment: 127 participants

Interventions

• DRUG: Liraglutide
• DRUG: MRI/ MRS (Magnetic Resonance Imaging /Magnetic Resonance Spectroscopy)
• BIOLOGICAL: Blood sample
• OTHER: Kinetic substudy (10 patients)

Primary Outcomes

• Effect of liraglutide on fatty liver content evaluated by proton-spectroscopy (1H-spectroscopy and lipoprotein kinetics, in patients with type 2 diabetes (Before and after 6 month-treatment with liraglutide (1.2 mg/day))
• Effects of liraglutide on Very Low Density Lipoprotein 1 (VLDL1) apolipoprotein B (apoB) production rate (Before and after 6 month-treatment with liraglutide (1.2 mg/day))
• Effects of liraglutide on Very Low Density Lipoprotein 2 (VLDL2) apolipoprotein B (apoB) production rate (Before and after 6 month-treatment with liraglutide (1.2 mg/day))
• Effects of liraglutide on Intermediate Density Lipoprotein (IDL) apolipoprotein B (apoB) production rate (Before and after 6 month-treatment with liraglutide (1.2 mg/day))
• Effects of liraglutide on Low Density Lipoprotein (LDL) apolipoprotein B (apoB) production rate (Before and after 6 month-treatment with liraglutide (1.2 mg/day))

Secondary Outcomes

• Modification of body weight (Before and after 6 month-treatment with liraglutide (1.2 mg/day))
• Modification of subcutaneous fat by Magnetic Resonance Imaging (MRI) (Before and after 6 month-treatment with liraglutide (1.2 mg/day))
• Modification of visceral fat by Magnetic Resonance Imaging (MRI) (Before and after 6 month-treatment with liraglutide (1.2 mg/day))

Eligibility Criteria

Inclusion Criteria:

* Patients with type 2 diabetes
* Patients treated by metformin and/or sulfonylureas (or glinides) and/or acarbose and/or insulin,
* HbA1C \>= 7 %,
* Patients who gave their written consent.

For the kinetic substudy:

* Patients who have the typical features of diabetic dyslipidemia (triglycerides \>= 1.50 g/l and/or HDL\<0.50 g/l \[women\], 0.40 g/l \[men\])

Exclusion Criteria:

* Treatment with thiazolidinediones or other Glucagon-like peptide-1(GLP1) agonist.
* No treatment with a Dipeptidyl peptidase-4 (DPP4) inhibitor during the 3 previous months,
* Renal or hepatic failure,
* Contra-indication for proton-spectroscopy (pacemaker, implantable prosthesis,..),
* Pregnancy.

For the kinetic substudy:

* Patients on hypolipidemic agents

Trial Locations

• CHU de Dijon, Dijon, France

More Type 2 Diabetes Trials

View all Type 2 Diabetes clinical trials