此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Metabolic Syndrome and Insulin Resistance at Allina (MISURA)

2016年8月30日 更新者:Jeffery Dusek、Allina Health System

Randomized, Controlled Trial of Vitamin D Replenishment in Metabolic Syndrome

Vitamin D deficiency is widespread and appears to represent one easily and inexpensively modifiable risk factor for diabetes and cardiovascular disease. More than 40 years of data link hypovitaminosis D to metabolic syndrome, insulin resistance, hyperglycemia, type 2 diabetes and increased cardiovascular risk.

Screening for vitamin D deficiency followed by supplementation in appropriate individuals could be among the simplest and most cost-effective measures for reducing metabolic syndrome and insulin resistance in the general population.

This study will test the hypothesis that increasing vitamin D status in vitamin D deficient individuals with metabolic syndrome will:

  1. reduce multiple serum cardiometabolic risk factors for both diabetes and cardiovascular disease,
  2. stabilize or reverse the stage of pre-diabetes,
  3. improve quality of life, and,
  4. improve the ability to make health-related behavioral changes.

研究概览

详细说明

Longitudinal observational studies suggest a significant inverse association between vitamin D status and both incident and prevalent metabolic syndrome/type II diabetes. Results from small underpowered trials and post-hoc analyses of data from larger trials designed for bone-specific outcomes suggest that vitamin D may slow the progression to diabetes in adults with glucose intolerance. However, at this time, no randomized trials of sufficient size exist to assess effectiveness.

Importantly, in the investigators' own study of over 10,000 Allina employees, the investigators found that 6% of these employees had levels less than 10 ng/mL, 30% less than 20 ng/ml and 60% less than 30 ng/ml. Recently, the Intermountain Heart Collaborative Study Group reviewed 41,504 patient records with at least one measured vitamin D level. Surprisingly, both the Intermountain and the Allina Employee study demonstrate vitamin D deficiency (≤30 ng/ml) in more than 60% of people tested with only minor differences by gender or age (Plotnikoff GA, Finch M, Dusek JA. Impact of Vitamin D Deficiency on the Productivity of a Health Care Workforce. J Occup Environ Med (in press)).

Furthermore, the Intermountain group demonstrated that vitamin D levels less than 30 ng/ml, compared to levels greater than 30 ng/ml, were associated with highly significant (p <0.0001) increases in the prevalence of diabetes, hypertension, hyperlipidemia, and peripheral vascular disease. Also, those without risk factors but with severe deficiency had an increased likelihood of developing diabetes, hypertension, and hyperlipidemia. The vitamin D levels were also highly associated with coronary artery disease, myocardial infarction, heart failure, and stroke (all p <0.0001), as well as with incident death, heart failure, coronary artery disease/myocardial infarction (all p <0.0001), stroke (p = 0.003), and their composite (p <0.0001).

Numerous prevention efforts are underway to minimize the predicted economic and human burdens from these increasingly common diseases. However, few, if any, prospective clinical trials are underway with vitamin D interventions. This trial is specifically designed to prospectively test the impact of vitamin D replenishment on both metabolic syndrome and insulin resistance.

The 2011 Endocrine Society guidelines assert that vitamin D intakes above the current recommendations may be associated with better health outcomes. However, there is no consensus on the optimal 25(OH)D concentration necessary to minimize metabolic syndrome, insulin resistance and progression to diabetes. This trial is designed to prospectively identify optimal serum levels for reduction of cardiometabolic risk factors.

研究类型

介入性

注册 (实际的)

84

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Minnesota
      • Minneapolis、Minnesota、美国、55407
        • Allina Health

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Please Note: All participants must be an employee of Allina Health or the spouse of an Allina employee.

Inclusion Criteria:

  • Vitamin D deficiency, defined as 25-OH vitamin D ≤ 25 ng/ml
  • Metabolic syndrome as defined by more than three or more of the following:

Elevated waist circumference

  • Men - Equal to or greater than 40 inches
  • Women - Equal to or greater than 35 inches
  • Elevated serum triglycerides (≥150 mg/dL)
  • Men - Less than 40 mg/dL
  • Women - Less than 50 mg/dL
  • Elevated blood pressure (≥130/85 or use of medication for hypertension)
  • Elevated fasting glucose (≥100 mg/dL or use of medication for hyperglycemia)

Exclusion Criteria:

  • Known cardiovascular disease defined as current or prior coronary heart disease, stroke/transient ischemic attack, heart failure, or peripheral vascular disease.
  • During the study, addition of any medications known to change outcome measures including medications or supplements for hyperlipidemia, hypertension, weight loss, diabetes.
  • Current Vitamin D supplementation beyond that found in a multivitamin (400 IU)
  • Current calcium supplementation greater than 600 mg
  • Untreated blood pressure greater than 159/99 at baseline
  • Treated blood pressure greater than 150/90 at baseline
  • Any condition which could limit the ability to complete and comply with 6-month study
  • Unwillingness or inability to comply with study requirements
  • Known allergy to coconut or coconut oil

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
有源比较器:Regular Dose
Intervention: 600 IUs of cholecalciferol taken by mouth daily.
Active intervention: 6,000 IUs taken by mouth daily for 6 months Active Comparator: 600 IUs taken by mouth daily for 6 months
其他名称:
  • D-Drops
实验性的:High Dose D
Intervention: 6,000 IUs of cholecalciferol taken by mouth daily.
Active intervention: 6,000 IUs taken by mouth daily for 6 months Active Comparator: 600 IUs taken by mouth daily for 6 months
其他名称:
  • D-Drops

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
insulin resistance score by NMR lipid fractionation
大体时间:6 months
additional insulin resistance measure
6 months
Reynolds Risk Score
大体时间:6 months
The Reynolds Risk Score is designed to predict one's risk of having a future heart attack, stroke, or other major heart disease in the next 10 years. In addition to your age, blood pressure, cholesterol levels and whether you currently smoke, the Reynolds Risk Score uses information from two other risk factors, a blood test called hsCRP (a measure of inflammation) and whether or not either of your parents had a heart attack before they reached age 60 (a measure of genetic risk).
6 months
Pre-diabetes stage
大体时间:6 months
The pre-diabetes stage, a marker of progression toward type 2 diabetes mellitus, is a calculated score based upon results of fasting adiponectin, insulin and proinsulin.
6 months

次要结果测量

结果测量
措施说明
大体时间
血压
大体时间:6个月
6个月
重量
大体时间:6个月
6个月
25-OH-vitamin D
大体时间:6 months
25-OH-vitamin D is the best measure of vitamin D status.
6 months
fasting lipid profile
大体时间:6 months
6 months
adiposity markers
大体时间:6 months

Adiponectin: This adipocyte-derived protein increases hepatic and peripheral insulin sensitivity, moderates fat tissue growth, decreases lipid and glucose production in the liver and suppresses vascular inflammation. This measure declines as insulin resistance increases.

Leptin: This adipocyte-derived hormone plays a key role in regulating neuroendocrine and immune function, appetite, metabolic rate and body weight. Many overweight individuals have elevated levels and leptin resistance.

6 months
TNF-alpha
大体时间:6 months
Inflammatory markers: TNF-alpha, IL-6, IL-8. These inflammatory mediators are central to the pathophysiology of obesity and its systemic effects
6 months
PROMIS-29
大体时间:6 months
PROMIS is a questionnaire data bank developed and made available by the National Institutes of Health for research purposes. It is used to measure the core domains of physical functioning, fatigue, pain, depression, anxiety, and social role participation.
6 months
Perceived Stress Scale (PSS)
大体时间:6 months
The PSS is brief, validated and widely used psychological instrument for assessing a participant's perception of stress. The PSS-4 consists of 4 questions to measure the degree to which situations in the participant's life are perceived as stressful including questions related to perceived unpredictability and lack of control.
6 months
WPAI
大体时间:6 months
This 6 item, validated instrument measures work and general activity impairment due to health problems. It uses a seven day recall and has been adapted for use in populations with differing health problems.
6 months
PROMIS-GH
大体时间:6 months
PROMIS is a questionnaire data bank developed and made available by the National Institutes of Health for research purposes. The PROMIS-GH consists of 10 items, representing multiple domains and can be scored into a Global Physical Health component and a Global Mental Health component
6 months
International Physical Activity Questionnaire (IPAQ)
大体时间:6 months
The International Physical Activity Questionnaire (IPAQ) short form (4 generic items) versions for use by either telephone or self-administered methods are available. The purpose of the questionnaire is to provide a common instrument that can be used to obtain internationally comparable data on health related physical activity. The development of this international measure for physical activity commenced in Geneva in 1998 and was followed by extensive reliability and validity testing undertaken in 12 countries (14 sites) across 6 continents during 2000.
6 months
IL-6
大体时间:6 months
Inflammatory mediators, including IL-6, are central to the pathophysiology of obesity and its systemic effects.
6 months
IL-8
大体时间:6 months
Inflammatory mediators, inlcuding IL-8, are central to the pathophysiology of obesity and its systemic effects.
6 months
HS-CRP
大体时间:6 months
Elevated HS-CRP predicts the development of type II diabetes and is a crucial factor in calculating the Reynolds Risk Score.
6 months
Lp-PLA2 (PLAC)
大体时间:6 months
This is an enzyme produced by inflammatory cells that hydrolyzes oxidized phospholipids in HDL and catalyzes the degradation of PAF, platelet activating factor. Levels are positively correlated with increased risk of developing coronary artery disease and stroke.
6 months
PAI-1
大体时间:6 months
This is the primary inhibitor of plasminogen activation. Elevated levels predispose to clot formation by inhibiting fibrinolytic activity.
6 months
Fibrinogen
大体时间:6 months
Fibrinogen is also known as coagulation Factor I. Elevated levels are associated with cardiovascular disease. This is an acute-phase protein that is elevated in any form of inflammation.
6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Gregory Plotnikoff, MD、Allina Health
  • 研究主任:Jeffery Dusek, PhD、Allina Health
  • 研究主任:Shaina Biron、Allina Health

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2012年3月1日

初级完成 (实际的)

2014年2月1日

研究完成 (实际的)

2014年3月1日

研究注册日期

首次提交

2012年2月28日

首先提交符合 QC 标准的

2012年3月6日

首次发布 (估计)

2012年3月7日

研究记录更新

最后更新发布 (估计)

2016年9月1日

上次提交的符合 QC 标准的更新

2016年8月30日

最后验证

2016年8月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅