Evaluation of 3-V Bioscience-2640, a FASN Inhibitor, to Reduce de Novo Lipogenesis in Subjects With Characteristics of the Metabolic Syndrome
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Change in Hepatic Lipogenesis
研究概览
简要总结
Metabolic syndrome increases the risk for development of heart disease. Another condition associated with metabolic syndrome is fatty liver disease which is also referred to as nonalcoholic fatty liver disease (NAFLD). Recently, drugs that block fatty acid synthesis have been developed to treat cancer. These drugs are now being considered for the treatment of NAFLD. A research test designed to measure liver fatty acid synthesis involves consumption of a sugary solution and measurement of blood fats over a six-hour period. The present study will test the drug 3-V Bioscience-2640 in healthy subjects with characteristics of the metabolic syndrome before and after 10 days of treatment to determine if 50 mg/d significantly reduces liver fat synthesis and lowers liver fat storage.
详细描述
The drug 3-V Bioscience-2640 has been tested previously in subjects with cancer because the lipogenesis pathway is important to the control of some cancer progression. Palmitate (C16:0), a saturated, 16-carbon fatty acid is a biomarker of lipogenesis present in blood triglyceride (TG), was found to be reduced significantly. A second biomarker of lipogenesis, malonyl carnitine, was significantly increased in patients as expected. The present study will test a lower dose (50 mg/d) than the maximum dose previously administered. Here, the subjects will be men with characteristics of the metabolic syndrome, who are otherwise healthy. The focus on subjects with metabolic syndrome is based on the fact that the future use of the drug will be in patients with NAFLD who will likely have metabolic syndrome characteristics.
In humans, the primary organ that synthesizes fatty acids is the liver, and this process occurs when simple sugars are consumed in the diet. The carbons in the sugars clear to the liver and become the molecule acetyl-Coenzyme A, which is the building block of fatty acids. The Laboratory of Elizabeth Parks, co-investigator, has developed an oral sugars tolerance test (OSTT) to determine the magnitude of liver stimulation of fatty acid synthesis when an individual consumes an oral bolus of sugars. This test involves the subject undergoing IV infusion with the stable (non-radioactive) isotope (13C1-acetate). The isotope gets incorporated into fatty acids that are being synthesized during the course of the infusion and when sugars stimulate lipogenesis, the label is more abundance. Those labeled fatty acids are detected as present in the blood very low-density lipoprotein (VLDL) component.
In the present study, the investigators will use this protocol to determine whether 10 days of drug treatment (one dose per day) will significantly reduce fasting and fructose-stimulated lipogenesis. The study is divided into 3 parts which will support the plan for minor adjustments in the dose of drug after the results from the first two research subjects are available in order to optimize the suppression of lipogenesis, while also minimizing any side effects the drug might have. The study is a repeated-measures design, with each subject serving as his own control. The study will be unblinded with respect to the research staff working directly with the subjects. However, laboratory personnel who will be running the biochemical analyses will be blinded as to whether they are analyzing baseline or post-treatment samples.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
盲法说明
There is only one treatment arm in this study and the subjects are all aware that they are on active treatment. The outcomes assessor will be masked as to which data are from the baseline visit and which are from the follow-up visit. In other words, data will be analyzed in the lab in a blinded fashion as to whether the samples are from before or after treatment.
入排标准
- 年龄范围
- 35 Years 至 60 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Men with characteristics of metabolic syndrome
- •Waist circumference greater than 40 in (102 cm)
- •Plasma TG greater than 150 mg/dL
- •HDL cholesterol less than 40 mg/dL
- •Blood pressure greater than or equal to 130/85 mmHg
- •Fasting plasma glucose greater than 100 mg/dL but less than 126 mg/dL
- •Fasting insulin great than 10 microunits/mL
- •35-60 years of age
- •Overweight/obese subjects with BMI 27.1 - 35.0 kg/m2
- •Family history of cardiovascular disease or diabetes
- •Habitual diets containing ≥ 5.0% of energy from added sugars
- •Creatinine clearance of ≥80 mL/min
排除标准
- •Diagnosed cardiovascular disease (unstable angina, New York Heart Association angina > Grade 2), abnormal thyroid function or liver/kidney disease, renal dysfunction (defined by a glomerular filtration rate <80 mL/min)
- •Chronic skin disorder or treatment for acne
- •History of clinically significant dry eye or eye diseases such as glaucoma
- •Diabetes defined as fasting glucose ≥ 125 mg/dL or HbA1c ≥ 6.5%
- •Habitual diets with low content of added sugars (<5% of total energy)
- •Any tobacco use
- •Elevated liver enzymes ≥ 3x normal (regional norms Alanine transaminase <42 U/L, aspartate aminotransferase <40 U/L, and gamma-glutamyl transferase 8-61 U/L)
- •Contraindications of MRI
- •Alcohol intake weekly greater than 56 g/week (4 standard drinks/wk).
- •Major surgery or donation of blood of >500 mL within the past 8 wks.
- •Patients with uncontrolled hypertension, i.e. ≥160/95 mmHg.
- •Patients with known cardiac abnormalities.
研究组 & 干预措施
3-V Bioscience-2640
Subjects will take a singly daily dose of 3-V Bioscience-2640 before bedtime or 22:30, whichever comes first, for 10 days.
干预措施: 3-V Bioscience-2640 (Drug)
结局指标
主要结局
Change in Hepatic Lipogenesis
时间窗: Baseline and after 10 days of treatment
Subject undergoes a stable isotope infusion followed by blood draws. Plasma lipid samples are measured by gas chromatography/mass spectrophotometry.
次要结局
- Change in Liver Fat Measured by MRI(Baseline and 10 days of treatment)
- Change in Skin Sebum Production(Baseline and 10 days of treatment)
研究者
Elizabeth Jane Parks
Professor, Nutrition & Exercise Physiology-MED
University of Missouri-Columbia