Vitamin D Deficiency, Insulin Resistance and FGF-23

Not Applicable

Completed

Conditions: Vitamin D Deficiency

Interventions: Dietary Supplement: Ergocalciferol placebo
Dietary Supplement: Ergocalciferol

Registration Number: NCT00491322

Lead Sponsor: Massachusetts General Hospital

Brief Summary: The purpose of this project is to determine if treating vitamin D deficiency decreases insulin resistance and improves insulin secretion in healthy volunteers. Additionally, this project will investigate if treating vitamin D deficiency affects a new phosphate-regulating hormone called FGF-23.

Detailed Description: Vitamin D deficiency or hypovitaminosis D, defined as serum 25 hydroxyvitamin D \< or = 20 ng/mL, is prevalent in several populations in the United States, specifically minorities and the elderly. Causes of vitamin D deficiency include lack of exposure to sunlight, malnutrition, and drugs that alter vitamin D metabolism and absorption.

Vitamin D is an essential factor for many organ systems. Data suggest that vitamin D is required for normal insulin secretion by the pancreas. Specifically, animal studies demonstrate that treatment of vitamin D deficiency improves insulin secretion. In humans, there is less consensus about the impact of vitamin D deficiency on insulin resistance. In one study of middle-aged patients with Type 2 diabetes mellitus, no association was seen between serum 25 hydroxyvitamin D levels and a measure of insulin resistance. However, in a larger study of younger glucose tolerant subjects, serum 25 hydroxyvitamin D levels were associated with both insulin secretion and insulin resistance. These data suggest that treatment of vitamin D deficiency may delay or prevent the development of insulin resistance, and thus diabetes mellitus type 2. Repletion of this common vitamin deficiency could therefore have major public health implications for the prevention of diabetes mellitus.

Fibroblast growth factor 23 (FGF-23) is a newly discovered phosphaturic hormone that is regulated by both dietary and serum phosphate. Hormonal regulation of FGF-23, however, is largely unknown. Recent data suggest that vitamin D plays an important role in the regulation of FGF-23. Some groups have shown that inactivation of the vitamin D receptor gene decreases serum FGF-23 levels in mice; administration of 1,25 dihydroxyvitamin D stimulates the transcription of the FGF-23 gene in vitro. Little is known, however, about the regulation of FGF-23 by vitamin D in humans.

Phosphate is critical for bone mineralization, muscle function, signal transduction, and the creation and utilization of energy. Vitamin D deficiency can result in phosphate malabsorption, osteomalacia and increased risk of fractures. Enhanced understanding of the regulation of this new phosphate-regulating hormone, FGF-23, will advance the field of phosphate metabolism.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 92

Inclusion Criteria

Age 18 to 45 yrs
Serum 25-OHD < or = 20 ng/mL
At least 1 menses in the last 3 months (females) and normal serum testosterone (males)

Exclusion Criteria

Significant cardiac, hepatic, oncologic, or psychiatric disease
History of diabetes mellitus, malabsorption, kidney stones, or recent alcohol excess/abuse (15 drinks per week in the last month)
Fasting glucose > 126 mg/dl or 2 hour OGTT > 200 mg/dl
Use of medications known to affect serum phosphate levels including phosphate-binding antacids, sodium etidronate, calcitonin, excessive doses of vitamin D (> 1000 units per day), excessive doses of vitamin A (> 20,000 units/day), calcitriol, growth hormone, or anti-convulsants
Use of metformin or insulin sensitizing agents
Serum calcium < 8 or > 11 mg/dL, creatinine > 1.5 mg/dL, or Hgb < 11 gm/dL
Liver function tests > 2 times the upper limit of normal
TSH < 0.1 or > 7 uU/mL
WBC < 2,000 or > 15,000/cmm
Platelet count < 100,000 or > 500,000/cum
Hormone replacement therapy or testosterone use
Urine uhCG positive (females), testosterone < 270 ng/dL (males)

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Ergocalciferol Placebo group	Ergocalciferol placebo	Matching placebo once a week for 12 weeks
Ergocalciferol group	Ergocalciferol	Ergocalciferol 50000 international units once a week for 12 weeks

Primary Outcome Measures

Name	Time	Method
Fibroblast Growth Factor 23 (FGF23) After 12 Weeks of Weekly Ergocalciferol 50000 Units	12 weeks	Fibroblast growth factor 23 (FGF23) is a phosphate and vitamin D regulating hormone.

Secondary Outcome Measures