Effect of Nicotinic Acid on Adipose Tissue Inflammation in Obese Subjects
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 24
- 试验地点
- 1
- 主要终点
- Comparison of changes of AT inflammation will be measured by gene expression analysis
研究概览
简要总结
Our working hypothesis postulates that lipolysis is a determinant of inflammation in adipose tissue (AT). Inhibition of lipolysis, e.g. using the oldest normolipidemic drug, nicotinic acid, has proved valuable to combat the metabolic syndrome. Our proposal will determine whether part of the beneficial effects of this antilipolytic compound is due to a diminution of AT inflammation.
To this aim, the effect of nicotinic acid or placebo will be studied in male obese subjects with or without a training program which goal is to enhance lipolysis.
详细描述
24 male obese insulin resistant subjects will receive nicotinic acid or placebo for 16 weeks. The last 8 weeks, the subjects will follow a training program calculated to optimize use of lipid. Insulin sensitivity and glucose tolerance will be assessed using, respectively, fasting-based estimates of insulin sensitivity (plasma and muscle) and oral glucose tolerance test. Plasma parameters of adipokines and, inflammatory and metabolic parameters will be determined. As an index of AT inflammation, the percentage and the phenotype of macrophages will be determined using flow cytometry of cells of the stromavascular fraction of subcutaneous AT. Macrophage infiltration will be investigated by light microscopy. The characterization of the inflammatory profile of AT will be completed by measurements of the expression of genes that are either specific markers of human AT macrophages or inflammatory and anti-inflammatory adipokines. This combination of approaches has never been carried out during a pharmacological intervention in humans. The following points will be addressed:
- determine the influence of lipolysis on AT inflammation, specifically on macrophage activation and adipokine production.
- examine the causal relationship between adipocyte FA metabolism, AT inflammation and insulin sensitivity.
- establish whether the beneficial effect of antilipolytic drugs may be attributable at least in part to a decrease in AT inflammation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Basic Science
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 25 Years 至 45 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Signature of informed consent form
- •Age 25 to 45 year-old
- •Male, insulin resistant obese subjects (30<BMI<40 kg/m2),
- •Blood arterial pressure<140/90 mmHg
排除标准
- •History of cardiovascular disease
- •Treatment with drugs which can interfere with cardiovascular system and autonomic nervous system (i.e. beta blockers).
- •Treatment with nicotinic acid
- •Treatment with fibrates, statins, cholestyramine and ezetimibe
- •Treatment with thiazidics
- •Fasted hyperglycaemia > 1,26 g/l (Diabetes)
- •Triglycerides >5 g/l
- •Blood arterial pressure > 140/90 mm Hg
研究组 & 干预措施
placebo
for 16 weeks
干预措施: training (Behavioral)
placebo
for 16 weeks
干预措施: Placebo (Drug)
nicotinic acid
for 16 weeks :
- week 1 = 375 mg per day,
- week 2 = 500 mg per day,
- week 3 = 750 mg per day,
- week 4 = 1000 mg per day,
- week 5 = 1500 mg per day,
- weeks 6 to 16 = 2000 mg per day.
干预措施: training (Behavioral)
nicotinic acid
for 16 weeks :
- week 1 = 375 mg per day,
- week 2 = 500 mg per day,
- week 3 = 750 mg per day,
- week 4 = 1000 mg per day,
- week 5 = 1500 mg per day,
- weeks 6 to 16 = 2000 mg per day.
干预措施: nicotinic acid (Drug)
结局指标
主要结局
Comparison of changes of AT inflammation will be measured by gene expression analysis
时间窗: Visit 1(T0), Visit 2 (T+8 weeks of treatment) and Visit 3 (T+16 weeks of treatment)
次要结局
- Comparison of changes in insulin sensitivity and glucose tolerance(Visit 1(T0), Visit 2 (T+8 weeks of treatment) and Visit 3 (T+16 weeks of treatment))