25-Hydroxylation of vitamin D3: Relation to circulating vitamin D3 under various input conditions

Robert P. Heaney, Laura A G Armas, Judith R. Shary, Norman H. Bell, Neil Binkley, Bruce W. Hollis

Research output: Contribution to journalArticle

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Abstract

Background: Neither the efficiency of the 25-hydroxylation of vitamin D nor the steady state relation between vitamin D3 and 25-hydroxyvitamin D [25(OH)D] has been studied in humans. Objective: We aimed to examine the relation between serum vitamin D3 and 25(OH)D in normal subjects after either oral administration of vitamin D3 or ultraviolet-B radiation across a broad range of inputs. Design: Values for serum vitamin D3 and (OH)D3 were aggregated from 6 studies - 1 acute and 5 near-steady state - at various vitamin D3 inputs. In 3 of the steady state studies, vitamin D3 had been administered for 18-26 wk in doses of 0 to 11 000 IU/d; in 2 studies, subjects had received solar or ultraviolet-B irradiation. Results: In the acute study, subjects receiving a single 100 000-IU dose of vitamin D3 had a rise in serum cholecalciferol to a mean of 521 nmol/L at 1 d and then a fall to near-baseline values by 7-14 d. Serum 25(OH)D peaked at 103 nmol/L on day 7 and fell slowly to baseline by day 112. In the 5 steady state studies, the relation of serum 25(OH)D to serum vitamin D3 was biphasic and was well described by a combined exponential and linear function: Y = 0.433X + 87.81[1-exp (-0.468X)], with R2 = 0.448. Conclusions: At physiologic inputs, there is rapid conversion of precursor to product at low vitamin D3 concentrations and a much slower rate of conversion at higher concentrations. These data suggest that, at typical vitamin D3 inputs and serum concentrations, there is very little native cholecalciferol in the body, and 25(OH)D constitutes the bulk of vitamin D reserves. However, at supraphysiologic inputs, large quantities of vitamin D3 are stored as the native compound, presumably in body fat, and are slowly released to be converted to 25(OH)D.

Original languageEnglish
Pages (from-to)1738-1742
Number of pages5
JournalAmerican Journal of Clinical Nutrition
Volume87
Issue number6
StatePublished - Jun 1 2008

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cholecalciferol
Cholecalciferol
hydroxylation
Hydroxylation
Serum
vitamin D
Vitamin D
ultraviolet radiation
dosage
normal values
oral administration
body fat
Oral Administration
Adipose Tissue
irradiation

All Science Journal Classification (ASJC) codes

  • Medicine (miscellaneous)
  • Food Science

Cite this

Heaney, R. P., Armas, L. A. G., Shary, J. R., Bell, N. H., Binkley, N., & Hollis, B. W. (2008). 25-Hydroxylation of vitamin D3: Relation to circulating vitamin D3 under various input conditions. American Journal of Clinical Nutrition, 87(6), 1738-1742.

25-Hydroxylation of vitamin D3 : Relation to circulating vitamin D3 under various input conditions. / Heaney, Robert P.; Armas, Laura A G; Shary, Judith R.; Bell, Norman H.; Binkley, Neil; Hollis, Bruce W.

In: American Journal of Clinical Nutrition, Vol. 87, No. 6, 01.06.2008, p. 1738-1742.

Research output: Contribution to journalArticle

Heaney, RP, Armas, LAG, Shary, JR, Bell, NH, Binkley, N & Hollis, BW 2008, '25-Hydroxylation of vitamin D3: Relation to circulating vitamin D3 under various input conditions', American Journal of Clinical Nutrition, vol. 87, no. 6, pp. 1738-1742.
Heaney RP, Armas LAG, Shary JR, Bell NH, Binkley N, Hollis BW. 25-Hydroxylation of vitamin D3: Relation to circulating vitamin D3 under various input conditions. American Journal of Clinical Nutrition. 2008 Jun 1;87(6):1738-1742.
Heaney, Robert P. ; Armas, Laura A G ; Shary, Judith R. ; Bell, Norman H. ; Binkley, Neil ; Hollis, Bruce W. / 25-Hydroxylation of vitamin D3 : Relation to circulating vitamin D3 under various input conditions. In: American Journal of Clinical Nutrition. 2008 ; Vol. 87, No. 6. pp. 1738-1742.
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abstract = "Background: Neither the efficiency of the 25-hydroxylation of vitamin D nor the steady state relation between vitamin D3 and 25-hydroxyvitamin D [25(OH)D] has been studied in humans. Objective: We aimed to examine the relation between serum vitamin D3 and 25(OH)D in normal subjects after either oral administration of vitamin D3 or ultraviolet-B radiation across a broad range of inputs. Design: Values for serum vitamin D3 and (OH)D3 were aggregated from 6 studies - 1 acute and 5 near-steady state - at various vitamin D3 inputs. In 3 of the steady state studies, vitamin D3 had been administered for 18-26 wk in doses of 0 to 11 000 IU/d; in 2 studies, subjects had received solar or ultraviolet-B irradiation. Results: In the acute study, subjects receiving a single 100 000-IU dose of vitamin D3 had a rise in serum cholecalciferol to a mean of 521 nmol/L at 1 d and then a fall to near-baseline values by 7-14 d. Serum 25(OH)D peaked at 103 nmol/L on day 7 and fell slowly to baseline by day 112. In the 5 steady state studies, the relation of serum 25(OH)D to serum vitamin D3 was biphasic and was well described by a combined exponential and linear function: Y = 0.433X + 87.81[1-exp (-0.468X)], with R2 = 0.448. Conclusions: At physiologic inputs, there is rapid conversion of precursor to product at low vitamin D3 concentrations and a much slower rate of conversion at higher concentrations. These data suggest that, at typical vitamin D3 inputs and serum concentrations, there is very little native cholecalciferol in the body, and 25(OH)D constitutes the bulk of vitamin D reserves. However, at supraphysiologic inputs, large quantities of vitamin D3 are stored as the native compound, presumably in body fat, and are slowly released to be converted to 25(OH)D.",
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N2 - Background: Neither the efficiency of the 25-hydroxylation of vitamin D nor the steady state relation between vitamin D3 and 25-hydroxyvitamin D [25(OH)D] has been studied in humans. Objective: We aimed to examine the relation between serum vitamin D3 and 25(OH)D in normal subjects after either oral administration of vitamin D3 or ultraviolet-B radiation across a broad range of inputs. Design: Values for serum vitamin D3 and (OH)D3 were aggregated from 6 studies - 1 acute and 5 near-steady state - at various vitamin D3 inputs. In 3 of the steady state studies, vitamin D3 had been administered for 18-26 wk in doses of 0 to 11 000 IU/d; in 2 studies, subjects had received solar or ultraviolet-B irradiation. Results: In the acute study, subjects receiving a single 100 000-IU dose of vitamin D3 had a rise in serum cholecalciferol to a mean of 521 nmol/L at 1 d and then a fall to near-baseline values by 7-14 d. Serum 25(OH)D peaked at 103 nmol/L on day 7 and fell slowly to baseline by day 112. In the 5 steady state studies, the relation of serum 25(OH)D to serum vitamin D3 was biphasic and was well described by a combined exponential and linear function: Y = 0.433X + 87.81[1-exp (-0.468X)], with R2 = 0.448. Conclusions: At physiologic inputs, there is rapid conversion of precursor to product at low vitamin D3 concentrations and a much slower rate of conversion at higher concentrations. These data suggest that, at typical vitamin D3 inputs and serum concentrations, there is very little native cholecalciferol in the body, and 25(OH)D constitutes the bulk of vitamin D reserves. However, at supraphysiologic inputs, large quantities of vitamin D3 are stored as the native compound, presumably in body fat, and are slowly released to be converted to 25(OH)D.

AB - Background: Neither the efficiency of the 25-hydroxylation of vitamin D nor the steady state relation between vitamin D3 and 25-hydroxyvitamin D [25(OH)D] has been studied in humans. Objective: We aimed to examine the relation between serum vitamin D3 and 25(OH)D in normal subjects after either oral administration of vitamin D3 or ultraviolet-B radiation across a broad range of inputs. Design: Values for serum vitamin D3 and (OH)D3 were aggregated from 6 studies - 1 acute and 5 near-steady state - at various vitamin D3 inputs. In 3 of the steady state studies, vitamin D3 had been administered for 18-26 wk in doses of 0 to 11 000 IU/d; in 2 studies, subjects had received solar or ultraviolet-B irradiation. Results: In the acute study, subjects receiving a single 100 000-IU dose of vitamin D3 had a rise in serum cholecalciferol to a mean of 521 nmol/L at 1 d and then a fall to near-baseline values by 7-14 d. Serum 25(OH)D peaked at 103 nmol/L on day 7 and fell slowly to baseline by day 112. In the 5 steady state studies, the relation of serum 25(OH)D to serum vitamin D3 was biphasic and was well described by a combined exponential and linear function: Y = 0.433X + 87.81[1-exp (-0.468X)], with R2 = 0.448. Conclusions: At physiologic inputs, there is rapid conversion of precursor to product at low vitamin D3 concentrations and a much slower rate of conversion at higher concentrations. These data suggest that, at typical vitamin D3 inputs and serum concentrations, there is very little native cholecalciferol in the body, and 25(OH)D constitutes the bulk of vitamin D reserves. However, at supraphysiologic inputs, large quantities of vitamin D3 are stored as the native compound, presumably in body fat, and are slowly released to be converted to 25(OH)D.

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