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Evidence that calcium modulates circulating 25-hydroxyvitamin D in man
1Veterans Administration Medical Center, Charleston, SC 29403.
Summary
Increased calcium intake significantly blunts the rise in serum 25-hydroxyvitamin D (25-OHD) levels after vitamin D supplementation in healthy individuals. This suggests a role for calcium in modulating vitamin D metabolism.
Area of Science:
- Endocrinology
- Nutritional Science
- Human Physiology
Background:
- 1,25-dihydroxyvitamin D3 (1,25(OH)2D) previously shown to prevent vitamin D-induced increases in serum 25-hydroxyvitamin D (25-OHD) in normal subjects.
- Understanding the interplay between vitamin D, calcium, and their metabolites is crucial for maintaining mineral homeostasis and bone health.
Purpose of the Study:
- To investigate whether increased calcium intake alters the serum 25-hydroxyvitamin D (25-OHD) response to vitamin D challenge in healthy individuals.
- To explore the impact of combined vitamin D and calcium administration on serum mineral levels and vitamin D metabolites.
Main Methods:
- Eight healthy subjects participated in a controlled study.
- Vitamin D (100,000 U/d for 4 days) was administered alone (control) and in combination with calcium (2,000 mg/d for 4 days).
- Serum levels of 25-OHD, calcium, ionized calcium, phosphorus, creatinine, and 1,25(OH)2D were measured.
Main Results:
- Vitamin D alone significantly increased serum 25-OHD by 133% (24 ng/ml).
- Combined vitamin D and calcium administration resulted in a significantly smaller increase in serum 25-OHD (63%, 12 ng/ml) compared to vitamin D alone (p < 0.02).
- Concurrent administration of vitamin D and calcium led to significant increases in serum calcium and ionized calcium, and a significant decrease in serum 1,25(OH)2D.
Conclusions:
- Increased calcium intake significantly attenuates the rise in serum 25-hydroxyvitamin D following vitamin D supplementation.
- This finding suggests that calcium plays a role in modulating the vitamin D endocrine system's response.
- Further research is warranted to elucidate the precise mechanisms underlying this interaction and its clinical implications.