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临床试验/NCT00392717
NCT00392717已完成3 期

Effect of Atorvastatin and Fish Oils on Lipoprotein Metabolism in Visceral Obesity

The University of Western Australia2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 1998年2月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
48
试验地点
2
主要终点
Fractional catabolic rate of apoB, apoA, apoC-III and chylomicron remnants (before and after 6 week treatments)

研究概览

简要总结

Visceral obesity is strongly associated with dyslipidaemia (hypertriglyceridaemia, low HDL-cholesterol and mildly elevated LDL-cholesterol) and insulin resistance, key characteristics of metabolic syndrome (MetS). Recent evidence has clearly established that the risk of CVD is increased in subjects with the MetS. The precise reason for this remains unclear, but appears to be closely related with dyslipidaemia. Effective management of dyslipidaemia is important to reduce the risk of CVD in these subjects.

Hypothesis: Inhibition of hepatic cholesterol synthesis by statins and triglyceride synthesis by fish oils improve lipoprotein metabolism in visceral obese men.

详细描述

The study employed a factorial study design, stable isotopy and mathematical modelling to examine the independent and combined effects of decreasing cholesterol substrate availability with atorvastatin and decreasing triglyceride substrate availability with fish oils on lipoprotien kinetics (apoB, apoA, apoC-III and chylomicron remnants) in insulin-resistant men with visceral obesity.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double

入排标准

年龄范围
20 Years 至 70 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Obesity was defined as a waist circumference >100 cm, waist:hip ratio >0.97 and BMI >29 kg/m
  • Subjects were selected for having insulin-resistance, defined as a homostasis model assessment (HOMA) score (21) >5.1 (i.e. one SD above the mean for a reference population of 22 lean, normolipidemic healthy males of similar age).
  • All subjects had plasma triglyceride >1.2 mmol/L and cholesterol >5.2 mmol/L at screening while consuming ad libitum, weight-maintaining diets

排除标准

  • diabetes mellitus, apolipoprotein E2/E2 genotype, macroproteinuria, creatinemia, hypothyrodism, or abnormal liver enzymes.
  • Subjects did not consume fish oil supplements or drank more than 30g alcohol/day.
  • None reported a history of CVD, or was taking medication or other agents known to affect lipid metabolism.

结局指标

主要结局

Fractional catabolic rate of apoB, apoA, apoC-III and chylomicron remnants (before and after 6 week treatments)

Production rate of apoB, apoA, apoC-III and chylomicron remnants (before and after 6 week treatments)

次要结局

  • Cholesterol
  • Genetic polymorphisms
  • LDL-cholesterol
  • Triglyceride
  • Adipocytokines

研究者

申办方类型
Other

研究点 (2)

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Regulation of Lipoprotein Metabolism in Obese Men | 临床试验