Human Ketone Metabolism - Validation of 3-[11C]-OHB as a New PET Ketontracer
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 6
- 试验地点
- 1
- 主要终点
- Biodistribution of 3-[11C]-OHB
研究概览
简要总结
Ketone bodies are produced in the liver at high levels of fatty acids, and act as an important source of energy for the brain and heart during fasting. The energy production from ketone metabolism is less oxygen-demanding than both glucose and fatty acid metabolism, and ketone substances can therefore be a very energy-efficient substrate for the heart. Insulin-resistant people as well as people with heart disease have difficulty burning glucose in the heart due to the insulin resistant condition and are therefore dependent on other energy sources such as free fatty acids and ketones. Because ketones are oxygen-sparing compared to fatty acids, interventions that increase the level of ketone bodies can potentially reduce the heart's need for oxygen in patients with narrowed coronary arteries. PET/CT is a functional and non-invasive imaging modality and suitable for tracking the fate of metabolites non-invasively, as most substrates or metabolites can be labeled by a PET isotope.
The purpose of this experiment is therefore to validate a new ketone tracer called 3-[11C]-OHB. Implementation of the 3-[11C]-OHB tracer will in future allow the investigators to more directly estimate the impact of different levels of ketone bodies on organ functions by measuring tissue-specific ketone uptake, both after intravenous and oral administration.
详细描述
Background:
Ketone bodies consists of 3-hydroxybutyrat, acetoacetate, and acetone. They are produced in the liver at high levels of fatty acids, and act as an important source of energy for the heart, brain and skeletal muscle during fasting. Energy production by ketone metabolism is less oxygen-intensive than both glucose and fatty acid metabolism, and ketone substances can therefore be a highly energy-efficient substrate. Insulin resistant individuals as well as people with heart disease have difficulty utilising glucose in the heart due to the insulin resistant condition and are therefore dependent on other energy sources such as free fatty acids and ketones. Because ketones are oxygen sparing compared to fatty acids, interventions that increase the level of ketone bodies can potentially reduce the heart's need for oxygen in patients with narrowed coronary arteries. This has led to an increased focus on the potential of ketone bodies in the treatment of a number of diseases, including especially cardiovascular disease.
Our group has shown that ketone bodies are efficiently absorbed by the heart despite maximal stimulation with insulin and glucose. In the study, healthy subjects increased the level of circulating ketone bodies to approximately 4 millimolar with a continuous ketone infusion, which resulted in a 50% reduction in cardiac glucose consumption. Since the consumption of free fatty acids in the experiment was unchanged and the overall work of the heart was the same, up to 50% of the heart's energy consumption was thus covered by ketone bodies. In addition, the high levels of ketone bodies led to a marked increase in the blood flow to the heart, which could potentially further benefit patients with narrowed coronary arteries
PET/CT is a functional and non-invasive imaging modality that is well established in oncological staging and treatment monitoring. The technique is also suitable for tracking the fate of metabolites non-invasively, as most substrates or metabolites can be labeled by a suitable PET isotope. PET has sufficient spatial and temporal resolution to enable direct quantification of e.g. uptake and oxidation rates and has been successfully used by our department to assess heart efficiency, oxygen consumption and fatty acid metabolism.
Purpose With this study, the investigators want to determine the metabolism of ketone bodies in healthy individuals and validate a newly developed ketone PET tracer for use in humans called 3-[11C]-OHB. Previous studies conducted by our and others' groups have only been able to indirectly estimate the uptake of ketone bodies into the heart. With 3-[11C]-OHB, the investigators will be able to directly measure tissue-specific ketone uptake, both after intravenous and oral administration.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 50 Years 至 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age between 50-70 years
- •BMI: 20-30 kg/m^2
排除标准
- •All drugs that could affect the outcome
- •HbA1c > 48 mmol/mol
- •Known heart failure og episodes of acute myocardial infarction
- •Liver disease ALAT > higher than 3 times of the normal level
- •Kidney disease eGFR < 60 ml/min
- •Blood donation in the last 3 months before inclusion
- •Participation in other studies with radiation in the last 6 months
- •Alcohol addiction
研究组 & 干预措施
Administration of 3-[11C]-OHB
All participants will first be injected with 200 MBq 3-[11C]-OHB followed by an oral ingestion of 100 MBq 3-[11C]-OHB.
干预措施: 3-[11C]-OHB (Radiation)
结局指标
主要结局
Biodistribution of 3-[11C]-OHB
时间窗: Through study completion, an average of 6 months
The investigators will measure time activity curves by quantifying uptake of the PET ketone tracer 3-\[11C\]-OHB in kilo becquerel/ml over time (seconds).
Radiation exposure of 3-[11C]-OHB
时间窗: Through study completion, an average of 6 months
The investigators will measure radiation exposure of 3-\[11C\]-OHB in millisievert in relevant organs.
次要结局
未报告次要终点
