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Metabolic Syndrome and Insulin Resistance at Allina (MISURA)

Primary Purpose

Metabolic Syndrome

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
vitamin D3 (cholecalciferol)
Sponsored by
Allina Health System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Metabolic Syndrome focused on measuring Metabolic syndrome, Insulin resistance, Vitamin D deficiency

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Allina Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Regular Dose

High Dose D

Arm Description

Intervention: 600 IUs of cholecalciferol taken by mouth daily.

Intervention: 6,000 IUs of cholecalciferol taken by mouth daily.

Outcomes

Primary Outcome Measures

insulin resistance score by NMR lipid fractionation
additional insulin resistance measure
Reynolds Risk Score
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).
Pre-diabetes stage
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.

Secondary Outcome Measures

25-OH-vitamin D
25-OH-vitamin D is the best measure of vitamin D status.
fasting lipid profile
adiposity markers
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.
TNF-alpha
Inflammatory markers: TNF-alpha, IL-6, IL-8. These inflammatory mediators are central to the pathophysiology of obesity and its systemic effects
weight
blood pressure
PROMIS-29
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.
Perceived Stress Scale (PSS)
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.
WPAI
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.
PROMIS-GH
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
International Physical Activity Questionnaire (IPAQ)
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.
IL-6
Inflammatory mediators, including IL-6, are central to the pathophysiology of obesity and its systemic effects.
IL-8
Inflammatory mediators, inlcuding IL-8, are central to the pathophysiology of obesity and its systemic effects.
HS-CRP
Elevated HS-CRP predicts the development of type II diabetes and is a crucial factor in calculating the Reynolds Risk Score.
Lp-PLA2 (PLAC)
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.
PAI-1
This is the primary inhibitor of plasminogen activation. Elevated levels predispose to clot formation by inhibiting fibrinolytic activity.
Fibrinogen
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.

Full Information

First Posted
February 28, 2012
Last Updated
August 30, 2016
Sponsor
Allina Health System
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1. Study Identification

Unique Protocol Identification Number
NCT01545830
Brief Title
Metabolic Syndrome and Insulin Resistance at Allina
Acronym
MISURA
Official Title
Randomized, Controlled Trial of Vitamin D Replenishment in Metabolic Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
March 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Allina Health System

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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: reduce multiple serum cardiometabolic risk factors for both diabetes and cardiovascular disease, stabilize or reverse the stage of pre-diabetes, improve quality of life, and, improve the ability to make health-related behavioral changes.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome
Keywords
Metabolic syndrome, Insulin resistance, Vitamin D deficiency

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
84 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Regular Dose
Arm Type
Active Comparator
Arm Description
Intervention: 600 IUs of cholecalciferol taken by mouth daily.
Arm Title
High Dose D
Arm Type
Experimental
Arm Description
Intervention: 6,000 IUs of cholecalciferol taken by mouth daily.
Intervention Type
Dietary Supplement
Intervention Name(s)
vitamin D3 (cholecalciferol)
Other Intervention Name(s)
D-Drops
Intervention Description
Active intervention: 6,000 IUs taken by mouth daily for 6 months Active Comparator: 600 IUs taken by mouth daily for 6 months
Primary Outcome Measure Information:
Title
insulin resistance score by NMR lipid fractionation
Description
additional insulin resistance measure
Time Frame
6 months
Title
Reynolds Risk Score
Description
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).
Time Frame
6 months
Title
Pre-diabetes stage
Description
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.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
25-OH-vitamin D
Description
25-OH-vitamin D is the best measure of vitamin D status.
Time Frame
6 months
Title
fasting lipid profile
Time Frame
6 months
Title
adiposity markers
Description
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.
Time Frame
6 months
Title
TNF-alpha
Description
Inflammatory markers: TNF-alpha, IL-6, IL-8. These inflammatory mediators are central to the pathophysiology of obesity and its systemic effects
Time Frame
6 months
Title
weight
Time Frame
6 months
Title
blood pressure
Time Frame
6 months
Title
PROMIS-29
Description
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.
Time Frame
6 months
Title
Perceived Stress Scale (PSS)
Description
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.
Time Frame
6 months
Title
WPAI
Description
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.
Time Frame
6 months
Title
PROMIS-GH
Description
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
Time Frame
6 months
Title
International Physical Activity Questionnaire (IPAQ)
Description
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.
Time Frame
6 months
Title
IL-6
Description
Inflammatory mediators, including IL-6, are central to the pathophysiology of obesity and its systemic effects.
Time Frame
6 months
Title
IL-8
Description
Inflammatory mediators, inlcuding IL-8, are central to the pathophysiology of obesity and its systemic effects.
Time Frame
6 months
Title
HS-CRP
Description
Elevated HS-CRP predicts the development of type II diabetes and is a crucial factor in calculating the Reynolds Risk Score.
Time Frame
6 months
Title
Lp-PLA2 (PLAC)
Description
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.
Time Frame
6 months
Title
PAI-1
Description
This is the primary inhibitor of plasminogen activation. Elevated levels predispose to clot formation by inhibiting fibrinolytic activity.
Time Frame
6 months
Title
Fibrinogen
Description
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.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gregory Plotnikoff, MD
Organizational Affiliation
Allina Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jeffery Dusek, PhD
Organizational Affiliation
Allina Health
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Shaina Biron
Organizational Affiliation
Allina Health
Official's Role
Study Director
Facility Information:
Facility Name
Allina Health
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55407
Country
United States

12. IPD Sharing Statement

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Metabolic Syndrome and Insulin Resistance at Allina

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