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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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (実際)

84

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Minnesota
      • Minneapolis、Minnesota、アメリカ、55407
        • Allina Health

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ: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
他の名前:
  • D-Drops
実験的: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
他の名前:
  • D-Drops

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
insulin resistance score by NMR lipid fractionation
時間枠:6 months
additional insulin resistance measure
6 months
Reynolds Risk Score
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
血圧
時間枠:6ヵ月
6ヵ月
重さ
時間枠:6ヵ月
6ヵ月
25-OH-vitamin D
時間枠:6 months
25-OH-vitamin D is the best measure of vitamin D status.
6 months
fasting lipid profile
時間枠:6 months
6 months
adiposity markers
時間枠: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
時間枠: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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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)
時間枠: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
時間枠:6 months
Inflammatory mediators, including IL-6, are central to the pathophysiology of obesity and its systemic effects.
6 months
IL-8
時間枠:6 months
Inflammatory mediators, inlcuding IL-8, are central to the pathophysiology of obesity and its systemic effects.
6 months
HS-CRP
時間枠: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)
時間枠: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
時間枠:6 months
This is the primary inhibitor of plasminogen activation. Elevated levels predispose to clot formation by inhibiting fibrinolytic activity.
6 months
Fibrinogen
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Gregory Plotnikoff, MD、Allina Health
  • スタディディレクター:Jeffery Dusek, PhD、Allina Health
  • スタディディレクター:Shaina Biron、Allina Health

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2012年3月1日

一次修了 (実際)

2014年2月1日

研究の完了 (実際)

2014年3月1日

試験登録日

最初に提出

2012年2月28日

QC基準を満たした最初の提出物

2012年3月6日

最初の投稿 (見積もり)

2012年3月7日

学習記録の更新

投稿された最後の更新 (見積もり)

2016年9月1日

QC基準を満たした最後の更新が送信されました

2016年8月30日

最終確認日

2016年8月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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