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临床试验/NCT01544751
NCT01544751Unknown不适用

Metformin Versus Atorvastatin in Nonalcoholic Hepatic Steatosis: a Randomized Study

Prof Antonino Belfiore1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2011年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
150
试验地点
1
主要终点
Number of Participants with improvement of liver hyperechogenicity

研究概览

简要总结

The first line approach to NAFLD is currently based on diet and lifestyle modification. Aim of our Unit is to compare the efficacy of two different doses of metformin (1 g/day and 2 g/day) with atorvastatin (20 mg/day) on amelioration of inflammatory and cardiometabolic parameters, ultrasound signs and clinical scores associated with liver fibrosis in early-stage NAFLD non-diabetic patients.

详细描述

Non alcoholic fatty liver disease (NAFLD) is a common liver disease that encompasses both simple steatosis and non alcoholic steatohepatitis (NASH.

There is currently no therapy that is of proven benefit for these liver disorders both of which are closely associated with insulin resistance and features of the metabolic syndrome such as obesity, hyperlipidaemia and type 2 diabetes mellitus. The first line approach to NAFLD is currently based on diet and lifestyle modification. However, dietary treatment is limited by the lack of compliance and the frequent regain of weight at follow-up.

Aim of our Unit is to compare the efficacy of two different doses of metformin (1 g/day and 2 g/day) with atorvastatin (20 mg/day) on amelioration of inflammatory and cardiometabolic parameters, ultrasound signs and clinical scores associated with liver fibrosis in early-stage NAFLD non-diabetic patients.

The investigators will enrol obese or overweight non-diabetic patients with ultrasonographic diagnosis of hepatic steatosis at early stage (NAFLD). The investigators will exclude from the study patients with clinical-biochemical and ultrasound markers of disease severity (age, BMI, lipid profile, AST, ALT, Angulo, BAAT and HAIR clinical fibrosis scores, signs of portal hypertension and posterior attenuation of the deep liver parenchyma at US). Patients who meet all eligibility criteria will be randomly assigned to one of three groups for 12 months of study treatment. The first group (n=50) will receive metformin (1g/day) plus dietary treatment; the second group (n=50) will be given metformin (2 g/day) and the third group (n=50) will be treated with atorvastatin (20 mg/day). All participants will be followed-up at 3, 6, 9, 12 months intervals after randomization. We will compare the effects of two doses of metformin with atorvastatin on the amelioration of both inflammatory (PCR, TNF-a , IL-6) and metabolic parameters (lipid profile, BMI, waist circumference, fasting glucose, 2-h glucose tolerance test, insulin, transaminases, adiponectin,leptin, HOMA-IR index and VAI index). Furthermore, we will assess the improvement under drug treatment of liver steatosis on the basis of US signs (liver echogenicity and stiffness) and of fibrosis scoring systems (Angulo, BAAT and HAIR scores).

In conclusion, considering the increasing prevalence of NAFLD and its strong association with cardiovascular diseases and cancer, the investigators expect to identify a safe pharmacological regimen that, in addition to dietary treatment, may ameliorate or even reverse this liver disease and the underlying risk factors. This study could have an important social impact in terms of both preventive and therapeutic interventions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age <=55
  • BMI <=40
  • Total cholesterol <=280 mg/dl
  • LDL <=180 mg/dl
  • Triglycerides <=200 mg/dl
  • AST and ALT in the normal range
  • Signs of simple liver steatosis at ultrasonorography.
  • Exclusion criteria:
  • Type 2 diabetes
  • Heart disease
  • Renal failure
  • Smoking habit
  • Alcohol intake of more than 20 g per day in the case of women and more than 30 g per day in the case of men
  • Hepatic virus infection
  • Autoimmune, metabolic or genetic liver diseases
  • Use of drugs known to induce liver steatosis

排除标准

  • 未提供

研究组 & 干预措施

Low dose Metformin

Active Comparator

500 mg twice a day for one year

干预措施: Low dose metformin (Drug)

Metformin

Active Comparator

1000 mg twice a day for one year

干预措施: Metformin (Drug)

Atorvastatin

Active Comparator

20 mg day

干预措施: Atorvastatin (Drug)

结局指标

主要结局

Number of Participants with improvement of liver hyperechogenicity

时间窗: one year

We will investigate efficacy of metformin and atorvastatin in amelioration of liver hyperechogenicity and fibrosis scores.

次要结局

  • Number of Participants with amelioration of metabolic syndrome and HOMA-Index(one years)

研究者

发起方
Prof Antonino Belfiore
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Prof Antonino Belfiore

Full Professor

University Magna Graecia

研究点 (1)

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