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How Does Magnesium Status Influence Calcium Homeostasis?

Phase 4
Completed
Conditions
Magnesium Deficiency
Calcium Metabolism Disorders
Interventions
Dietary Supplement: vitamin D3
Registration Number
NCT01593501
Lead Sponsor
University of Wisconsin, Madison
Brief Summary

The investigators aim to recruit 60 women who have agreed to participate in an existing randomized, double-blind, placebo-controlled trial (Treatment of Vitamin D Insufficiency, HSC 2009-0055). In this trial, the investigators propose to evaluate the associations between magnesium intake, magnesium stores, fractional magnesium absorption and calcium homeostasis. The investigators will stratify 60 subjects in the sub-study, ensuring that approximately 20 subjects are randomized into each treatment arm (placebo, low-dose and high-dose vitamin D). The investigators already assess calcium homeostasis throughout the study by measuring bone mineral density, fractional calcium absorption, serum and urine calcium levels, among other tests. In the sub-study of 60 women, the investigators will evaluate whether habitually higher magnesium intake increases or decreases fractional calcium absorption. The investigators will evaluate the interplay between magnesium stores, vitamin D levels and serum parathyroid hormone levels. The investigators will directly assess magnesium stores using serum magnesium and 24-hour urine magnesium levels, and will measure magnesium absorption using the dual stable isotope approach.

Detailed Description

Use of serum magnesium isotopes to measure fractional magnesium absorption Four day food diaries to assess magnesium intake Standard urine and serum chemistries for remaining labs as noted above

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
39
Inclusion Criteria
  • participants eligible for the study "Treatment of vitamin D insufficiency" are eligible for participation in the current sub-study
Exclusion Criteria
  • identical to those covered in HSC #2009-0055

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
High dose vitamin Dvitamin D350,000 IU vitamin D3 every 15 days, with a loading dose of 50,000 IU per day for the first 15 days of an approximate 365-day treatment.
Low dose vitamin Dvitamin D3800 IU vitamin D3 every day of an approximate 365-day treatment.
Placebovitamin D3A pill that looks like the low/high dose vitamin D pills, but contains no vitamin D. Given to preserve the double-blind nature of the study.
Primary Outcome Measures
NameTimeMethod
Evaluate the associations between magnesium intake, magnesium stores, fractional magnesium absorption and calcium homeostasis.0-12 months

To evaluate relationships between magnesium intake and fractional magnesium absorption at baseline and 12 months, among 60 women participating in HSC Protocol 2009-0055, and to assess whether vitamin D therapy influences magnesium absorption among these women. We will also evaluate whether data collected from less than 72 hours of urine following tracer administration permits accurate assessment of fractional magnesium absorption.

Secondary Outcome Measures
NameTimeMethod
Assessing relationships between magnesium status and bone mineral density.0-12 months
Evaluate how magnesium status impacts the relationship between vitamin D levels and parathyroid hormone levels.0-12 months
Does vitamin D therapy have a differential impact on calcium absorption that is dependent on magnesium stores?0-12 months

To assess whether vitamin D therapy has a differential impact on calcium absorption, depending on magnesium stores. We will use data from all subjects participating in HSC Protocol 2009-0055 to evaluate whether magnesium status is a co-factor in the change in calcium absorption that occurs with vitamin D therapy.

Trial Locations

Locations (1)

University of Wisconsin-Madison Hospital, Clinical Research Unit, Osteoporosis Research Center

🇺🇸

Madison, Wisconsin, United States

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