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临床试验/NCT01950039
NCT01950039已完成2 期

Bedside to Bench and Back: Cardiometabolic Effects of Betaine Supplementation

Joslin Diabetes Center1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2014年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
28
试验地点
1
主要终点
Endothelial Function

研究概览

简要总结

Betaine is important in cellular metabolic pathways. Few epidemiologic studies link betaine levels to diabetes and cardiovascular disease. Small human studies suggest benefit for non-alcoholic liver disease. In this study we will determine if administration of betaine improves metabolic measures, liver fat and/or endothelial function in humans with glucose intolerance who are overweight.

详细描述

This study is a single site, prospective, randomized (1:1), double masked, placebo controlled trial to assess metabolic effects of betaine compared to placebo on glycemia and insulin sensitivity, liver fat and endothelial function.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women aged 21-65 years old;
  • Dysglycemia/prediabetes is defined as impaired fasting glucose (≥100 mg/dl), impaired glucose tolerance (2 hour post 75 g oral glucose load 140-200 mg/dl) or HbA1c 5.7-6.5%);
  • overweight to grade 3 obesity (BMI 25 to 45 kg/m2).

排除标准

  • cystathionine beta-synthase (CBS deficiency);
  • Presence of liver disease other than NAFLD;
  • Use of medications causing steatosis;
  • Known alcohol consumption ≥ 2 drink per day;
  • Use of medications known to cause insulin resistance;
  • Use of weight loss drugs (or program) within 3 months of screening;
  • Treatment with any experimental drug within the past 6 months;
  • Subjects must be willing to abstain from use of phosphodiesterase type 5 (PDE-5) inhibitors;
  • Pregnancy or lactation, and women of child bearing potential must use adequate contraception;
  • Surgery within 30 days of screening;
  • Heart disease defined as New York Heart Association Class III or IV cardiac status or hospitalization for congestive heart failure, unstable angina, myocardial infarction, cerebrovascular accident, transient ischemic attack or any revascularization within 6 months;
  • Uncontrolled hypertension;
  • eGFR <60; 14) History of acquired immune deficiency syndrome;
  • History of malignancy within 5 years;
  • Hemoglobin <12 g/dL (males), <10 g/dL (females);
  • Triglycerides (TG) >500 mg/dL;
  • Poor mental function or any other reason to expect patient difficulty in complying with study requirements;
  • Metal clips or implants that preclude magnetic resonance imaging.

研究组 & 干预措施

Betaine

Active Comparator

干预措施: Betaine (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Endothelial Function

时间窗: baseline and 12 weeks

Brachial artery reactivity to flow and nitroglycerin stimuli, assessed as percent change from baseline

Hepatic Fat, Change From Baseline

时间窗: baseline and 12 weeks

Intrahepatic triglyceride levels were assessed by magnetic resonance imaging (MRI) and magnetic resonance spectroscopy (Siemens 3T TIM Skyra, software version VD13; Siemens, Erlangen, Germany).

Insulin Sensitivity

时间窗: Baseline and 12 weeks

Euglycemic hyperinsulinemic clamp at baseline and at end of study (12 weeks) for assessment of: 1. glucose disposal (M) at low (25 mU/m2/min) and high (180 mU/m2/min) insulin infusion rates, reported as raw data 2. measurement of endogenous glucose production at basal and low insulin infusion (25 mU/m2/min), reported as change from measures at baseline of individual study days

Fasting and 2 Hour Glucose Levels, Comparing Baseline and 12 Weeks.

时间窗: baseline and 12 weeks

Glucose levels were analyzed in the fasting state and two hours after glucose load, comparing baseline to 12 weeks.

Change in Glucose AUC at 12 Weeks From Baseline (Glucose Tolerance)

时间窗: baseline and 12 weeks

Glucose tolerance was assessed by oral glucose tolerance, assessed using the change from baseline for fasting and 2 hour glucose, and change in Glucose AUC at 12 weeks from baseline was measured.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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