Glucose Metabolism Effects of Vitamin D Supplementation in Prediabetes (VitDmet)
Primary Purpose
Prediabetic State, Overweight, Obese
Status
Completed
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Vitamin D3
Placebo
Vitamin D 80
Sponsored by
About this trial
This is an interventional basic science trial for Prediabetic State focused on measuring vitamin D, cholecalciferol, supplementation, prediabetic state, obesity, glucose metabolism, gene expression, transcriptomics, epigenomics, immunological function, insulin sensitivity, peripheral mononuclear cells
Eligibility Criteria
Inclusion Criteria:
- Age 60 years or older
- Serum calcidiol <75 nmol/L
- Body mass index 25-35 kg/m2
- Impaired fasting glucose or impaired glucose tolerance (fasting glucose 5.6-7.0 mmol/L or 2h oral glucose tolerance test glucose 7.8-11.0 mmol/L)
Exclusion Criteria:
- Any chronic disease and condition, which may hamper to follow the intervention protocol (such as alcohol abuse)
- Any chronic disease or therapy which may mask or interact with the investigated effects (such as diabetes or systemic corticosteroid therapy)
- Any disease or state that raises a vitamin D related safety concern (such as chronic liver, thyroid or kidney disease, hypercalcemia, sarcoidosis or other granulomatous diseases such as active chronic tuberculosis or Wegener's granulomatosis)
- Use of supplements yielding vitamin D over 20 µg/d and unwillingness to discontinue the use.
Sites / Locations
- University of Eastern Finland, Kuopio Campus
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Vitamin D 40
Vitamin D 80
Placebo
Arm Description
Vitamin D3 40 micrograms (1600 IU) per day
Vitamin D3 80 micrograms (3200 IU) per day
Outcomes
Primary Outcome Measures
Insulin sensitivity
Change in insulin sensitivity measured by oral glucose tolerance test at baseline and after 6 months
Secondary Outcome Measures
Peripheral blood mononuclear cell gene expression
Inflammation
Change in inflammation measured as serum cytokines and adipose tissue inflammation at baseline and after 6 months
Adipose tissue gene expression
Full Information
NCT ID
NCT01479933
First Posted
August 29, 2011
Last Updated
March 3, 2013
Sponsor
University of Eastern Finland
Collaborators
Academy of Finland, Juho Vainio Foundation, Finnish Foundation for Cardiovascular Research, Diabetes Research Foundation, Finland
1. Study Identification
Unique Protocol Identification Number
NCT01479933
Brief Title
Glucose Metabolism Effects of Vitamin D Supplementation in Prediabetes
Acronym
VitDmet
Official Title
Randomized Controlled Trial of Vitamin D Supplementation on Glucose Metabolism in Subjects With Components of the Metabolic Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
March 2013
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
May 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Eastern Finland
Collaborators
Academy of Finland, Juho Vainio Foundation, Finnish Foundation for Cardiovascular Research, Diabetes Research Foundation, Finland
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Vitamin D deficiency is widespread throughout the world, and the deficiency has been associated with several chronic diseases, such as cardiovascular diseases and diabetes. In Nordic countries, like in Finland, there is a particular variation in vitamin D status, and during wintertime, when there is no exposure to ultraviolet-B light from the sun, serum concentrations of vitamin D decrease substantially. In Finland, some 40% of middle-aged men and one third of women also have some degree of impairment of glucose metabolism.
The purpose of this trial is to investigate the effects of two different daily doses of vitamin D on glucose metabolism in men 60 years of age or older and who are vitamin D deficient, have a high body mass index and at least two characteristics of cardio-metabolic syndrome.
Altogether 102 subjects with low serum calcidiol (<60 nmol/L) will be recruited and randomized to one of the three groups: 1) 40 µg/d vitamin D3, 2) 80 µg/d vitamin D3 or 3) placebo. The supplementation period will last for 6 months from September 2011 to March 2012.
The main hypotheses of the trial are: (1.) Vitamin D supplementation will improve glucose and insulin metabolism in people with a low baseline vitamin D status, in a dose-dependent manner. (2.) Vitamin D supplementation will have an effect on the expression of genes involved in glucose and insulin metabolism and inflammation. (3.) Vitamin D supplementation will have an effect on epigenetic changes in key genes participating in vitamin D metabolism.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetic State, Overweight, Obese
Keywords
vitamin D, cholecalciferol, supplementation, prediabetic state, obesity, glucose metabolism, gene expression, transcriptomics, epigenomics, immunological function, insulin sensitivity, peripheral mononuclear cells
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
73 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vitamin D 40
Arm Type
Experimental
Arm Description
Vitamin D3 40 micrograms (1600 IU) per day
Arm Title
Vitamin D 80
Arm Type
Experimental
Arm Description
Vitamin D3 80 micrograms (3200 IU) per day
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3
Intervention Description
Vitamin D3 40 micrograms (1600 IU) per day
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Inactive placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D 80
Intervention Description
Vitamin D3 80 micrograms (3200 IU) per day
Primary Outcome Measure Information:
Title
Insulin sensitivity
Description
Change in insulin sensitivity measured by oral glucose tolerance test at baseline and after 6 months
Time Frame
Six months
Secondary Outcome Measure Information:
Title
Peripheral blood mononuclear cell gene expression
Time Frame
Six months
Title
Inflammation
Description
Change in inflammation measured as serum cytokines and adipose tissue inflammation at baseline and after 6 months
Time Frame
Baseline to six months
Title
Adipose tissue gene expression
Time Frame
Six months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 60 years or older
Serum calcidiol <75 nmol/L
Body mass index 25-35 kg/m2
Impaired fasting glucose or impaired glucose tolerance (fasting glucose 5.6-7.0 mmol/L or 2h oral glucose tolerance test glucose 7.8-11.0 mmol/L)
Exclusion Criteria:
Any chronic disease and condition, which may hamper to follow the intervention protocol (such as alcohol abuse)
Any chronic disease or therapy which may mask or interact with the investigated effects (such as diabetes or systemic corticosteroid therapy)
Any disease or state that raises a vitamin D related safety concern (such as chronic liver, thyroid or kidney disease, hypercalcemia, sarcoidosis or other granulomatous diseases such as active chronic tuberculosis or Wegener's granulomatosis)
Use of supplements yielding vitamin D over 20 µg/d and unwillingness to discontinue the use.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tomi-Pekka Tuomainen, MD, PhD
Organizational Affiliation
University of Eastern Finland
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Eastern Finland, Kuopio Campus
City
Kuopio
ZIP/Postal Code
70211
Country
Finland
12. IPD Sharing Statement
Citations:
PubMed Identifier
24975273
Citation
Ryynanen J, Neme A, Tuomainen TP, Virtanen JK, Voutilainen S, Nurmi T, de Mello VD, Uusitupa M, Carlberg C. Changes in vitamin D target gene expression in adipose tissue monitor the vitamin D response of human individuals. Mol Nutr Food Res. 2014 Oct;58(10):2036-45. doi: 10.1002/mnfr.201400291. Epub 2014 Jul 28.
Results Reference
derived
Links:
URL
http://www.uef.fi
Description
University of Eastern Finland
Learn more about this trial
Glucose Metabolism Effects of Vitamin D Supplementation in Prediabetes
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