Effect of Vitamin D3 Supplementation on Insulin Resistance and Cardiovascular Risk Factors in Obese Adolescents
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Purpose
The prevalence of obesity has reached epidemic proportions nationally as well as internationally. Currently, 16 % of American adolescents are obese. In adults, obesity is a risk factor for vitamin D insufficiency and up to 80% of obese adults have been noted to vitamin D insufficient. In adults, low vitamin D status appears to be associated with the development of type 2 diabetes and metabolic syndrome. There is little information on the prevalence of vitamin D insufficiency and its implications in obese adolescents. Additionally, it is unknown whether treatment of vitamin D insufficiency in adolescents might result in improvement in insulin resistance, lipids and cardiovascular risk markers.
We hypothesize that vitamin D insufficiency correlates positively with insulin resistance and cardiovascular risk in obese adolescents and that vitamin D3 supplementation improves insulin resistance and cardiovascular risk factors in this population. The purpose of the study is to determine the impact of vitamin D3 supplementation on various parameters of insulin secretion, insulin action, lipids and C-reactive protein in obese adolescents.
| Condition | Intervention | Phase |
|---|---|---|
|
Obesity |
Dietary Supplement: Vitamin D3 |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Significance of Vitamin D Status in Obese Adolescents- A Pilot Study to Examine the Effect of Vitamin D3 Supplementation on Insulin Resistance and Cardiovascular Risk Factors |
- Assesment of insulin sensitivity before and after vitamin D3 supplementation index [ Time Frame: 12 weeks ] [ Designated as safety issue: Yes ]
- Monitor effect of vitamin D supplementation with 400 and 2,000 IU/day for 12 weeks on lipids and c-reactive protein. [ Time Frame: 12 weeks ] [ Designated as safety issue: Yes ]
| Enrollment: | 55 |
| Study Start Date: | April 2009 |
| Study Completion Date: | December 2012 |
| Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Vitamin D3-low dose
Vitamin D3 400 IU/once daily
|
Dietary Supplement: Vitamin D3
One arm would receive vitamin D3 at a dose of 400 IU by mouth once daily for 12 weeks and the other arm would receive vitamin D3 as a single oral daily dose of 2000 IU for 12 weeks.
|
|
Experimental: vitamin D3-high dose
Vitamin D3 2000 IU/capsule, once capsule once daily
|
Dietary Supplement: Vitamin D3
One arm would receive vitamin D3 at a dose of 400 IU by mouth once daily for 12 weeks and the other arm would receive vitamin D3 as a single oral daily dose of 2000 IU for 12 weeks.
|
Detailed Description:
The problem of childhood obesity has reached epidemic proportions both nationally and internationally. The prevalence of obesity has tripled in the last three decades and currently 16 % of American adolescents are obese. Nearly 30% of obese adolescents demonstrate a metabolic syndrome characterized by insulin resistance and dyslipidemia. These abnormalities lead to the development of type 2 diabetes mellitus and to increased cardiovascular morbidity and mortality. Obesity is a well-known risk factor for vitamin D insufficiency and up to 80% of obese adults have been found to be insufficient in vitamin D. Observational studies in adults have shown consistent associations between low vitamin D status and prevalence of type 2 diabetes mellitus and metabolic syndrome. There is paucity of data on the prevalence of vitamin D insufficiency and its implications in obese adolescents. It is also not known whether treatment of vitamin D insufficiency in children or adults might result in improvement in insulin resistance and cardiovascular risk factors.
Hypotheses: We hypothesize that vitamin D insufficiency correlates positively with insulin resistance and cardiovascular risk in obese adolescents and that vitamin D3 supplementation decreases insulin resistance and cardiovascular risk factors in this population.
Objectives:
- Determine if there is any correlation between serum 25(OH)D levels and HOMA-IR, HDL cholesterol and C-reactive protein, in obese adolescents.
- Study the impact of vitamin D3 supplementation on various parameters reflecting insulin action, secretion, lipids and C-reactive protein in obese adolescents.
Eligibility| Ages Eligible for Study: | 12 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Age between 12-18 years
- BMI is at or greater than the 95th percentile for age and gender
Exclusion Criteria:
- Subjects with 25 (OH)- D levels >100 ng/mL
- Serum calcium >10.8 mg/dL
- Current cancer
- Those taking a multivitamin supplementation
- Hepatic or renal disorders
- Type 1 or type 2 diabetes mellitus.
Those receiving insulin, metformin or oral hypoglycemic medications
- Use of glucocorticoids and anti-seizure medications in the previous 6 months
- Malabsorption syndromes such as celiac disease
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Seema Kumar, M.D., Mayo Clinic |
| ClinicalTrials.gov Identifier: | NCT00858247 History of Changes |
| Other Study ID Numbers: | 08-008743, 1624 |
| Study First Received: | March 5, 2009 |
| Last Updated: | February 26, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Mayo Clinic:
|
vitamin D Obesity Insulin sensitivity Adolescent Obesity |
Additional relevant MeSH terms:
|
Insulin Resistance Obesity Hyperinsulinism Glucose Metabolism Disorders Metabolic Diseases Overnutrition Nutrition Disorders Overweight Body Weight Signs and Symptoms Cholecalciferol |
Vitamin D Ergocalciferols Vitamins Insulin Micronutrients Growth Substances Physiological Effects of Drugs Pharmacologic Actions Bone Density Conservation Agents Hypoglycemic Agents |
ClinicalTrials.gov processed this record on May 19, 2013