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临床试验/NCT00819338
NCT00819338已完成2 期

The Effect of n-3 Polyunsaturated Fatty Acid Supplementation in Patients With Non-alcoholic Fatty Liver Disease

University of Nottingham2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2009年1月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
58
试验地点
2
主要终点
Reduction of intrahepatic fat content as determined by magnetic resonance spectroscopy

研究概览

简要总结

The principal purpose of this study is to determine whether increased intakes of n-3 polyunsaturated (omega-3) fatty acids will reduce the amount of fat stored in the liver in patients with non-alcoholic fatty liver disease.

详细描述

Non-alcoholic fatty liver disease (NAFLD) is present in 10-24% of the general adult population. The first step of NAFLD involves the accumulation of fat within the liver (steatosis). Steatosis occurs either due to defective generation, metabolism or excretion of fatty acids by the liver. The next step in NAFLD progression is inflammation, which commonly occurs due to pro-inflammatory stimuli. Persistent inflammation results in end-stage liver disease. NAFLD is associated with the metabolic syndrome, which is characterised by central obesity, insulin resistance, raised triglycerides and hypertension. With the current obesity epidemic, there is predicted to be greater numbers of patients with NAFLD in the future.

Polyunsaturated fatty acids (PUFAs) are essential components of our diet, though standard Western intakes are lower than the recommended amounts. Supplementing the long chain n-3 PUFAs (commonly termed omega-3), EPA and DHA, improves many of the metabolic syndrome features. They lower plasma triglycerides, and may improve insulin resistance.

The diet of NAFLD patients tends to be deficient in n-3 PUFAs and have an excessive intake of the harmful n-6 PUFAs. This pattern is mirrored in their liver lipid content as assessed at biopsy.

Currently there is no proven treatment for NAFLD. Animal studies and limited studies in patients have been supportive of a benefit with n-3 polyunsaturated fatty acids. This needs to be further assessed.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Age greater than 18 years
  • Liver biopsy diagnosis of NAFLD

排除标准

  • Excessive alcohol intake - > 21 units per week in men and > 14 in women
  • A further liver disease diagnosis
  • Poorly controlled diabetes - HbA1c > 8.0%, or use of insulin sensitisers
  • Contraindications to MR scanning - pacemaker or metallic foreign body etc.
  • Changes in the dose or initiation of lipid altering medication within the preceding three months, such as statins, fibrates or systemic steroids
  • Use of n-3 PUFA supplements within the prior 4 months, an adequate washout period
  • Significant co-morbid inflammatory illnesses as determined by research team

结局指标

主要结局

Reduction of intrahepatic fat content as determined by magnetic resonance spectroscopy

时间窗: 3 months

次要结局

  • Insulin resistance as assessed by HOMA-IR and Adipose Tissue Insulin Resistance Index(3 months)
  • Liver saturated, monounsaturated and polyunsaturated fatty acid indexes as assessed by MR spectroscopy(3 months)
  • Serum liver function tests, lipids, free fatty acids(3 months)
  • Visceral obesity as quantified by MRI, and the adipose derived serum leptin and adiponectin(3 months)
  • Primary assessment of the fibrotic and inflammatory status of the liver with serum TGF beta, TNF a, IL-6, IL-8, IL-8, IL-10(3 months)
  • Further informative cytokine analyses: GM-CSF, IFN-G, IL-1B, IL-1RA, IL-2, IL-4, IL-5, MCP1(3 months)
  • Compliance assessed by serum phospholipid fatty acids(3 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard Johnston

Doctor

University of Nottingham

研究点 (2)

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