Optimizing Vitamin D Nutrition in Healthy Adults

NYU Langone Hospitals

Status

Completed

Conditions

Vitamin D Deficiency

Treatments

Drug: Oral Vitamin D Supplementation

Study type

Interventional

Funder types

Other

Identifiers

NCT00327847

IRB Protocol #04037

Details and patient eligibility

About

The purpose of this study is to determine the average dosage of oral vitamin D supplementation to maintain optimal vitamin D levels in the body and to see if there are differences in the response to oral vitamin D supplementation between African-American and Caucasian subjects.

Full description

There is ample evidence that improvement in vitamin D nutrition retards bone loss and prevents fractures in the elderly. It is clear that many people living in areas of northern latitude have less than optimal levels of vitamin D. The current recommendations for vitamin D intake are not enough to bring a large majority of the population to the desired adequate level. Furthermore, differences have been observed in the amount of Vitamin D produced in the skin in whites and blacks.

Based on the evidence from literature and our experience from prior studies we hypothesize that:

the dose of oral vitamin D3 supplement exceeds current recommendations to achieve adequate desired level;
there may be differences in the dose-response to vitamin D supplement between Blacks and Whites; and
vitamin D supplementation that produces serum 25-hydroxyvitamin D (25-OHD) levels in the range proposed is safe.

The aims for this pilot study are to determine:

the average dose of vitamin D3 needed to attain 25-OHD levels between 80-140 nmol/L in a healthy population of mixed races; and
if there are differences in response to vitamin D3 supplementation between African American and Caucasians subjects.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy African-American and Caucasian adults aged 18-65 years.

Exclusion criteria

Subjects who are not either African-American or Caucasian. The investigators plan to examine racial differences in response to oral vitamin D dosing and, therefore, have chosen the most affected (African-American) and the least affected (Caucasian) racial groups. Including other racial/ethnic groups may confound the results unless they are studied as separate groups.
Any chronic medical illness including diabetes mellitus, history of myocardial infarction or heart failure, malignancy, hypertension (systolic blood pressure [SBP] > 140), obesity (body mass index [BMI] > 35 kg/m2), history of anemia, leukemia, or other hematologic abnormalities, lupus, rheumatoid arthritis, or other rheumatologic disease, or kidney disease of any kind as determined by history and physical examination.
Subjects with osteoporosis or taking medications for osteoporosis such as bisphosphonates.
Pregnancy.
Use of medication that influences bone metabolism (i.e. anticonvulsant medications, steroids, diuretics).
Significant deviation from normal in either history, physical examination, or laboratory tests, as evaluated by the primary investigator.
Patients with a history of hypercalciuria, hypercalcemia, nephrolithiasis, and active sarcoidosis.
Participation in another investigational trial in the past 30 days prior to the screening evaluation.
Unexplained weight loss of > 15% during the previous year or history of anorexia nervosa.
Medications that interfere with vitamin D metabolism. Oral contraceptive use will be allowed, but will be appropriately documented.
Smokers greater than 1 pack per day.
Patients reporting alcohol intake greater than 2 drinks daily.
Subjects with baseline 25-OHD level greater than 80 nmol/L or less than 20 nmol/L.