INFLAMMATION AND DRUG METABOLISM - Does the Effect of Drugs Decrease When Patients With Type 2 Diabetes Initiate Antidiabetic Treatment?
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- Change from Baseline in Metabolic Rate of Midazolam (CYP3A4) at Week 3.
研究概览
简要总结
Type 2 diabetes is a major public health concern. It is widely established that type 2 diabetes in linked to activated innate immunity and increased levels of C-reactive protein and interleukin-6 (IL-6) in plasma. Studies in humans and in liver cells has shown that IL-6 downregulates important drug metabolizing enzymes in the liver (cytochrome P450 (CYP) enzymes). More than half of the most prescribed drugs are eliminated by biotransformation of these enzymes.
The investigators have previously shown that initiating glucose-lowering treatment (e.g. metformin, sulphonylureas and insulin) leads to decreased therapeutic efficacy of the blood-thinning vitamin-K antagonist warfarin. Due to the non-specific effect of glucose lowering drugs, the investigators hypothesize that this is caused by the glucose-lowering effect rather than drug-drug interactions caused by the individual drugs.
Based on the proposal that reversal of increased plasma glucose affects drug metabolism, the investigators will perform a clinical pharmacokinetic trial. The purpose of the study is to elucidate whether initiation of glucose-lowering treatment causes altered drug metabolism among patients with type 2 diabetes. The study will include newly diagnosed and untreated type 2 diabetes patients who will ingest a 6-drug cocktail consisting of probes for specific CYP enzymes. Plasma and urine will be drawn over 6 hours to determine concentrations of the drugs and their metabolites. Patients will then initiate metformin treatment and to assess both short- and long-term impact of glucose-lowering, the same 6-drug cocktail will be ingested, and concentrations measured, after three weeks and three months. To help understand the mechanism and the putative involvement of inflammation, markers of inflammation such as cytokines, transcription factors, etc. will also be assesses.
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
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Type 2 diabetes, not treated metformin.
- •Hemoglobin 1Ac (HbA1c): ≥48 mmol/mol
- •Age: 18-75 years
- •Body Mass Index (BMI) ≤ 40 kg/m2
- •Estimated Glomerular Filtration Rate (eGFR) > 60 mL/min
- •Alanine Aminotransferase (ALAT), bilirubin and hemoglobin within reference range or clinically insignificant differ from this.
排除标准
- •Acute or chronic infection or inflammation
- •Active cancer
- •Glutamic acid decarboxylase (GAD)-antibodies
- •Known hypersensitivity to one or several of the drugs
- •Intake of medications which can influence the safety of the patient or the results of the study
- •Alcohol consumption above the limits recommended by the Danish Health Authorities (Men 14 units/week, women 7 units/week)
- •Participation in other trials with interventions.
- •Women: Positive pregnancy test at inclusion or on one of the test-days.
研究组 & 干预措施
Metformin
Patients will receive metformin 1000-2000 mg daily for 12 weeks.
干预措施: Metformin (Drug)
Metformin
Patients will receive metformin 1000-2000 mg daily for 12 weeks.
干预措施: Caffeine (Drug)
Metformin
Patients will receive metformin 1000-2000 mg daily for 12 weeks.
干预措施: Efavirenz (Drug)
Metformin
Patients will receive metformin 1000-2000 mg daily for 12 weeks.
干预措施: Losartan (Drug)
Metformin
Patients will receive metformin 1000-2000 mg daily for 12 weeks.
干预措施: Omeprazol (Drug)
Metformin
Patients will receive metformin 1000-2000 mg daily for 12 weeks.
干预措施: Metoprolol (Drug)
Metformin
Patients will receive metformin 1000-2000 mg daily for 12 weeks.
干预措施: Midazolam (Drug)
结局指标
主要结局
Change from Baseline in Metabolic Rate of Midazolam (CYP3A4) at Week 3.
时间窗: Baseline and Week 3.
Change in activity of the drug metabolizing enzyme CYP3A4 following treatment with the glucose lowering drug metformin in 3 weeks. Assessment of the change is based on a change in the metabolic rate, which is the ratio between the concentration of midazolam and its primary metabolite is plasma (Probe drug for CYP3A4).
Change from Baseline in Metabolic Rate of Midazolam (CYP3A4) at Week 12.
时间窗: Baseline and Week 12.
Change in activity of the drug metabolizing enzyme CYP3A4 following treatment with the glucose lowering drug metformin in 12 weeks. Assessment of the change is based on a change in the metabolic rate, which is the ratio between the concentration of midazolam and its primary metabolite is plasma (Probe drug for CYP3A4).
次要结局
- Change from Baseline in Interleukin-6 at Week 3.(Baseline and Week 3.)
- Change from Baseline in Metabolic Rate of Caffeine (CYP1A2) at Week 3.(Baseline and Week 3.)
- Change from Baseline in Metabolic Rate of Caffeine (CYP1A2) at Week 12.(Baseline and Week 12.)
- Change from Baseline in Metabolic Rate of Efavirenz (CYP2B6) at Week 3.(Baseline and Week 3.)
- Change from Baseline in Metabolic Rate of Losartan (CYP2C9) at Week 3.(Baseline and Week 3.)
- Change from Baseline in HbA1c at Week 3.(Baseline and Week 3.)
- Change from Baseline in Metabolic Rate of Efavirenz (CYP2B6) at Week 12.(Baseline and Week 12.)
- Change from Baseline in Metabolic Rate of Losartan (CYP2C9) at Week 12.(Baseline and Week 12.)
- Change from Baseline in Metabolic Rate of Metoprolol (CYP2D6) at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interleukin-1-B at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interferon-y at Week 3.(Baseline and Week 3.)
- Change from Baseline in Interferon-y at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interleukin-6 at Week 12.(Baseline and Week 12.)
- Change from Baseline in Metabolic Rate of Omeprazole (CYP2C19) at Week 3.(Baseline and Week 3.)
- Change from Baseline in Metabolic Rate of Omeprazole (CYP2C19) at Week 12.(Baseline and Week 12.)
- Change from Baseline in insulin resistance at Week 3.(Baseline and Week 3.)
- Change from Baseline in insulin resistance at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interferon-a at Week 3.(Baseline and Week 3.)
- Change from Baseline in Metabolic Rate of Metoprolol (CYP2D6) at Week 3.(Baseline and Week 3.)
- Change from Baseline in HbA1c at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interleukin-2 at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interferon-a at Week 12.(Baseline and Week 12.)
- Change from Baseline in Tumor Necrosis Factor-a at Week 12.(Baseline and Week 12.)
- Change from Baseline in High Sensitivity C-Reactive Protein at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interleukin-1-B at Week 3.(Baseline and Week 3.)
- Change from Baseline in Interleukin-2 at Week 3.(Baseline and Week 3.)
- Change from Baseline in Interleukin-10 at Week 3.(Baseline and Week 3.)
- Change from Baseline in Interferon-B at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interleukin-10 at Week 12.(Baseline and Week 12.)
- Change from Baseline in Interferon-B at Week 3.(Baseline and Week 3.)
- Change from Baseline in Tumor Necrosis Factor-a at Week 3.(Baseline and Week 3.)
- Change from Baseline in High Sensitivity C-Reactive Protein at Week 3.(Baseline and Week 3.)
研究者
Ann-Cathrine Dunvald
Principal Investigator
University of Southern Denmark