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Ensayo controlado aleatorizado2013

25-Hydroxyvitamin D response to graded vitamin D₃ supplementation among obese adults

Drincic A, Fuller E, Heaney RP, Armas LA

The Journal of clinical endocrinology and metabolism · 91 citas

Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación independiente
Universidad u hospital
Creighton University

Según 1 financiador declarado.

Publicación

Publicado
2013-09-14 · J Clin Endocrinol Metab · vol. 98 · número 12 · págs. 4845–4851
Editorial
Oxford University Press
Citado
139 citas · más que el 98% de estudios similares · 7.3× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
25 trabajos
Acceso
De pago
Áreas de investigación
Vitamin D Research Studies · Parathyroid Disorders and Treatments · Nutrition and Health Studies
Palabras clave
vitamin D3 supplementation, vitamin D3, 25-hydroxyvitamin D, dose-response relationship, obesity, vitamin D deficiency, body size, hypercalciuria, hypercalcemia
MeSH
humans, vitamin d deficiency, obesity, calcium, cholecalciferol, calcifediol, parathyroid hormone, body mass index, cohort studies, single-blind method, seasons, kinetics, models, biological, dietary supplements, adult, middle aged, nebraska, female, male, recommended dietary allowances

4 autores

  • Andjela Drincic🇺🇸 · autor de correspondenciaNebraska Medical Center; University of Nebraska Medical Center
  • EE Fuller🇺🇸Creighton University; University of Nebraska Medical Center
  • Robert P. Heaney🇺🇸Creighton University; University of Nebraska Medical Center
  • Laura A. G. Armas🇺🇸Creighton University

Resumen

El texto original del estudio, en el idioma en que se publicó.

Context

Guidelines have suggested that obese adults need 2 to 3 times more vitamin D than lean adults to treat vitamin D deficiency, but few studies have evaluated the vitamin D dose response in obese subjects.

Objective

The purpose of this study was to characterize the pharmacokinetics of 25-hydroxyvitamin D [25(OH)D] response to 3 different doses of vitamin D₃ (cholecalciferol) in a group of obese subjects and to quantify the 25(OH)D dose-response relationship. DESIGN, SETTING, INTERVENTION, PATIENTS: This was a randomized, single-blind study of 3 doses of oral vitamin D₃ (1000, 5000, or 10,000 IU) given daily to 67 obese subjects for 21 weeks during the winter months.

Main outcome measures

Serum 25(OH)D levels were measured at baseline and after vitamin D replacement, and 25(OH)D pharmacokinetic parameters were determined, fitting the 25(OH)D concentrations to an exponential model.

Results

Mean measured increments in 25(OH)D at week 21 were 12.4 ± 9.7 ng/mL in the 1000 IU/d group, 27.8 ± 10.2 ng/mL in the 5000 IU/d group, and 48.1 ± 19.6 ng/mL in the 10,000 IU/d group. Steady-state increments computed from the model were 20.6 ± 17.1, 35.2 ± 14.6, and 51.3 ± 22.0 ng/mL, respectively. There were no hypercalcuria or hypercalcemia events during the study.

Conclusion

Our data show that in obese people, the 25(OH)D response to vitamin D₃ is directly related to dose and body size with ∼2.5 IU/kg required for every unit increment in 25(OH)D (nanograms per milliliter).

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