Effects of cholecalciferol supplementation on serum and urinary vitamin D metabolites and binding protein in HIV-infected youth. Issue 168 (April 2017)
- Record Type:
- Journal Article
- Title:
- Effects of cholecalciferol supplementation on serum and urinary vitamin D metabolites and binding protein in HIV-infected youth. Issue 168 (April 2017)
- Main Title:
- Effects of cholecalciferol supplementation on serum and urinary vitamin D metabolites and binding protein in HIV-infected youth
- Authors:
- Eckard, Allison Ross
Thierry-Palmer, Myrtle
Silvestrov, Natalia
Rosebush, Julia C.
O'Riordan, Mary Ann
Daniels, Julie E.
Uribe-Leitz, Monika
Labbato, Danielle
Ruff, Joshua H.
Singh, Ravinder J.
Tangpricha, Vin
McComsey, Grace A. - Abstract:
- Highlights: Cholecalciferol supplementation effectively raises serum 25-hydroxyvitamin D in the majority of HIV-infected youth. Changes in vitamin D metabolites are similar between HIV-infected youth and controls with cholecalciferol supplementation. High-dose cholecalciferol raises 25-hydroxyvitamin D in HIV-infected youth regardless of efavirenz use. Abstract: Vitamin D insufficiency is widespread in HIV-infected patients. HIV and/or antiretroviral therapy (ART), particularly efavirenz (EFV), may interfere with vitamin D metabolism. However, few data from randomized, controlled trials exist. Here, we investigate changes in vitamin D metabolites and binding protein (VDBP) after 6 months of supplementation in a randomized, active-control, double-blind trial investigating 2 different monthly cholecalciferol (vitamin D3 ) doses [60, 000 (medium) or 120, 000 (high) IU/month] vs. a control arm of 18, 000 IU/month in 8–25 year old HIV-infected youth on ART with HIV-1 RNA <1000 copies/mL and baseline 25-hydroxycholecalciferol (25(OH)D3 ) ≤30 ng/mL. A matched healthy uninfected group was enrolled in a similar parallel study for comparison. Changes after 6 months were analyzed as intent-to-treat within/between groups [control group (low dose) vs. combined supplementation doses (medium + high)]. At 6 months, 55% vs. 82% of subjects in control and supplementation groups, respectively, reached 25(OH)D3 ≥30 ng/mL (P = 0.01) with no difference between medium and high doses (both 82%Highlights: Cholecalciferol supplementation effectively raises serum 25-hydroxyvitamin D in the majority of HIV-infected youth. Changes in vitamin D metabolites are similar between HIV-infected youth and controls with cholecalciferol supplementation. High-dose cholecalciferol raises 25-hydroxyvitamin D in HIV-infected youth regardless of efavirenz use. Abstract: Vitamin D insufficiency is widespread in HIV-infected patients. HIV and/or antiretroviral therapy (ART), particularly efavirenz (EFV), may interfere with vitamin D metabolism. However, few data from randomized, controlled trials exist. Here, we investigate changes in vitamin D metabolites and binding protein (VDBP) after 6 months of supplementation in a randomized, active-control, double-blind trial investigating 2 different monthly cholecalciferol (vitamin D3 ) doses [60, 000 (medium) or 120, 000 (high) IU/month] vs. a control arm of 18, 000 IU/month in 8–25 year old HIV-infected youth on ART with HIV-1 RNA <1000 copies/mL and baseline 25-hydroxycholecalciferol (25(OH)D3 ) ≤30 ng/mL. A matched healthy uninfected group was enrolled in a similar parallel study for comparison. Changes after 6 months were analyzed as intent-to-treat within/between groups [control group (low dose) vs. combined supplementation doses (medium + high)]. At 6 months, 55% vs. 82% of subjects in control and supplementation groups, respectively, reached 25(OH)D3 ≥30 ng/mL (P = 0.01) with no difference between medium and high doses (both 82% ≥30 ng/mL). There were few differences for those on EFV vs. no-EFV, except serum VDBP decreased in EFV-treated subjects (both within- and between-groups P ≤ 0.01). There were no significant differences between the HIV-infected vs. healthy uninfected groups. The major finding of the present study is that cholecalciferol supplementation (60, 000 or 120, 000 IU/month) effectively raises serum 25(OH)D3 in the majority of HIV-infected subjects, regardless of EFV use. Notably, response to supplementation was similar to that of uninfected subjects. … (more)
- Is Part Of:
- Journal of steroid biochemistry and molecular biology. Issue 168(2017)
- Journal:
- Journal of steroid biochemistry and molecular biology
- Issue:
- Issue 168(2017)
- Issue Display:
- Volume 168, Issue 168 (2017)
- Year:
- 2017
- Volume:
- 168
- Issue:
- 168
- Issue Sort Value:
- 2017-0168-0168-0000
- Page Start:
- 38
- Page End:
- 48
- Publication Date:
- 2017-04
- Subjects:
- 1, 25(OH)2D3 1, 25-dihydroxycholecalciferol -- 1, 25(OH)2D 1, 25-dihydroxyvitamin D -- 24, 25(OH)2D3 24, 25-dihydroxycholecalciferol -- 24, 25(OH)2D 24, 25-dihydroxyvitamin D -- 25(OH)D3 25-hydroxycholecalciferol -- 25(OH)D 25-hydroxyvitamin D -- vitamin D3 cholecalciferol -- VDBP vitamin D binding protein -- PTH parathyroid hormone -- cART combination antiretroviral therapy (cART) -- EFV efavirenz -- NNRTI non-nucleoside reverse transcriptase inhibitor -- PI protease inhibitor -- NRTI nucleoside reverse transcriptase inhibitor -- RCT randomized-controlled trial -- CV coefficients of variance
HIV -- Vitamin d metabolites -- Vitamin d binding protein -- Cholecalciferol supplementation -- Randomized-controlled trial -- Pediatrics and adolescents -- Vitamin D
Steroid hormones -- Periodicals
Biochemistry -- Periodicals
Hormones -- Periodicals
Molecular Biology -- Periodicals
Hormones stéroïdes -- Périodiques
Steroid hormones
Periodicals
572.579 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09600760 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jsbmb.2017.01.018 ↗
- Languages:
- English
- ISSNs:
- 0960-0760
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5066.850010
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