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Effects of Vitamin D3 Versus 25OHD3 on Mineral Metabolism and Immune Function

Primary Purpose

Vitamin D Deficiency

Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Vitamin D
25(OH)D3
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vitamin D Deficiency focused on measuring Hypovitaminosis D, Free 25-hydroxyvitamin D, Total 25-hydroxyvitamin D

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18
  • 25D < 20 mg/ml

Exclusion Criteria:

  • Age < 18
  • 25D > 20 ng/ml at time of screening
  • Clear signs of infection at time of screening (coughing, sneezing, wheezing, frequency, dysuria)
  • History of conditions that would influence intestinal absorption of vitamin D3 or 25OHD3 supplements
  • History of nephrolithiasis, primary hyperparathyroidism, or other metabolic bone disease
  • History of chronic kidney disease (defined as CrCl < 30 ml/min)
  • History of rheumatologic or autoimmune conditions
  • History of sarcoidosis
  • History of active or latent tuberculosis
  • History of HIV
  • History of hyperthyroidism
  • History of chronic glucocorticoid use defined as the equivalent of 5 mg of prednisone per day for more than 2 months within the last 6 months
  • History of use of medications known to affect calcium/vitamin D metabolism, bone metabolism, and immune response
  • Hypercalcemia
  • Hypercalcinuria

Sites / Locations

  • UCLA Clinical and Translational Research Center (CTRC)
  • University of California, Los Angeles

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

25(OH)D3

Vitamin D3

Arm Description

20 micrograms/day by mouth for 16 weeks

2,400 IU/day by mouth for 16 weeks

Outcomes

Primary Outcome Measures

Change in total serum 25D

Secondary Outcome Measures

Change in serum free 25D
Change in serum total 1,25D
Change in total free 1,25D
Change in serum calcium
Change in urinary calcium
Change in serum iPTH
Change in serum bone turnover markers
Change in markers of immune function

Full Information

First Posted
March 12, 2014
Last Updated
April 26, 2021
Sponsor
University of California, Los Angeles
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
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1. Study Identification

Unique Protocol Identification Number
NCT02091219
Brief Title
Effects of Vitamin D3 Versus 25OHD3 on Mineral Metabolism and Immune Function
Official Title
The Effects of Vitamin D3 Versus 25OHD3 (HyD) on Serum Vitamin D Metabolites and Markers of Mineral Metabolism and Immune Function
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
June 2014 (undefined)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
December 7, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the effects of two different forms of vitamin D supplements (vitamin D3 and 25-hyrdroxyvitamin D3 [25(OH)D3]) on vitamin D levels in the blood, and on markers of skeletal and immune health. This study is designed as a pilot study. A multi-ethnic cohort of 48 patients will be included (12 Caucasian, 12 African American, 12 Hispanic/Latino, 12 Asian/Asian American). Potential study candidates will undergo a screening visit during which a medical history will be taken, a physical exam performed, a dietary questionnaire administered, and blood collected. The purpose of the screening visit is to identify vitamin D-deficient (25-hydroxyvitamin D <20 ng/ml) individuals who are candidates for vitamin D supplementation. Eligible patients will then be randomly assigned to receive either vitamin D3 (2400 IU/day) or 25(OH)D3 (20 mcg/day) for 16 weeks. After initiating supplementation, study patients will return for follow-up visits at weeks 4, 8, and 16. At each visit, blood will be collected to assess vitamin D levels in the blood, as well as markers of skeletal and immune function. Participation in this study will therefore involve a total of 5 visits (1 screening visit, 1 randomization visit during which participants will receive their study supplements, 3 follow-up visits). After all data is collected, changes in vitamin D levels in the blood following supplementation with either vitamin D3 versus 25(OH)D3 will be determined, and correlated to markers of calcium balance and immune function. Knowledge gained from this study may have a significant impact on how vitamin D status is defined, and how vitamin D repletion is administered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Deficiency
Keywords
Hypovitaminosis D, Free 25-hydroxyvitamin D, Total 25-hydroxyvitamin D

7. Study Design

Primary Purpose
Prevention
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
35 (Actual)

8. Arms, Groups, and Interventions

Arm Title
25(OH)D3
Arm Type
Experimental
Arm Description
20 micrograms/day by mouth for 16 weeks
Arm Title
Vitamin D3
Arm Type
Experimental
Arm Description
2,400 IU/day by mouth for 16 weeks
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Other Intervention Name(s)
Cholecalciferol
Intervention Description
2400 IU/day by mouth for 16 weeks
Intervention Type
Drug
Intervention Name(s)
25(OH)D3
Other Intervention Name(s)
Calcifediol, HyD
Intervention Description
20 micrograms/day by mouth for 16 weeks
Primary Outcome Measure Information:
Title
Change in total serum 25D
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
Change in serum free 25D
Time Frame
16 weeks
Title
Change in serum total 1,25D
Time Frame
16 weeks
Title
Change in total free 1,25D
Time Frame
16 weeks
Title
Change in serum calcium
Time Frame
16 weeks
Title
Change in urinary calcium
Time Frame
16 weeks
Title
Change in serum iPTH
Time Frame
16 weeks
Title
Change in serum bone turnover markers
Time Frame
16 weeks
Title
Change in markers of immune function
Time Frame
16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 25D < 20 mg/ml Exclusion Criteria: Age < 18 25D > 20 ng/ml at time of screening Clear signs of infection at time of screening (coughing, sneezing, wheezing, frequency, dysuria) History of conditions that would influence intestinal absorption of vitamin D3 or 25OHD3 supplements History of nephrolithiasis, primary hyperparathyroidism, or other metabolic bone disease History of chronic kidney disease (defined as CrCl < 30 ml/min) History of rheumatologic or autoimmune conditions History of sarcoidosis History of active or latent tuberculosis History of HIV History of hyperthyroidism History of chronic glucocorticoid use defined as the equivalent of 5 mg of prednisone per day for more than 2 months within the last 6 months History of use of medications known to affect calcium/vitamin D metabolism, bone metabolism, and immune response Hypercalcemia Hypercalcinuria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John S Adams, MD
Organizational Affiliation
University of California, Los Angeles Department of Orhtopaedic Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA Clinical and Translational Research Center (CTRC)
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
University of California, Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
34343292
Citation
Shieh A, Lee SM, Lagishetty V, Gottleib C, Jacobs JP, Adams JS. Pilot Trial of Vitamin D3 and Calcifediol in Healthy Vitamin D Deficient Adults: Does It Change the Fecal Microbiome? J Clin Endocrinol Metab. 2021 Nov 19;106(12):3464-3476. doi: 10.1210/clinem/dgab573.
Results Reference
derived
PubMed Identifier
29931358
Citation
Shieh A, Ma C, Chun RF, Wittwer-Schegg J, Swinkels L, Huijs T, Wang J, Donangelo I, Hewison M, Adams JS. Associations Between Change in Total and Free 25-Hydroxyvitamin D With 24,25-Dihydroxyvitamin D and Parathyroid Hormone. J Clin Endocrinol Metab. 2018 Sep 1;103(9):3368-3375. doi: 10.1210/jc.2018-00515.
Results Reference
derived

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Effects of Vitamin D3 Versus 25OHD3 on Mineral Metabolism and Immune Function

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