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Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders

Adequate vitamin D and calcium are essential for optimal adolescent skeletal development. Adolescent vitamin D insufficiency/deficiency and poor calcium intake have been reported worldwide. Heavy alcohol use impacts negatively on skeletal health, which is concerning since heavy adolescent drinking i...

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Autores principales: Naude, Celeste E., Carey, Paul D., Laubscher, Ria, Fein, George, Senekal, Marjanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448088/
https://www.ncbi.nlm.nih.gov/pubmed/23016133
http://dx.doi.org/10.3390/nu4081076
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author Naude, Celeste E.
Carey, Paul D.
Laubscher, Ria
Fein, George
Senekal, Marjanne
author_facet Naude, Celeste E.
Carey, Paul D.
Laubscher, Ria
Fein, George
Senekal, Marjanne
author_sort Naude, Celeste E.
collection PubMed
description Adequate vitamin D and calcium are essential for optimal adolescent skeletal development. Adolescent vitamin D insufficiency/deficiency and poor calcium intake have been reported worldwide. Heavy alcohol use impacts negatively on skeletal health, which is concerning since heavy adolescent drinking is a rising public health problem. This study aimed to examine biochemical vitamin D status and dietary intakes of calcium and vitamin D in 12–16 year-old adolescents with alcohol use disorders (AUD), but without co-morbid substance use disorders, compared to adolescents without AUD. Substance use, serum 25-hydroxyvitamin D (s-25(OH)D) concentrations, energy, calcium and vitamin D intakes were assessed in heavy drinkers (meeting DSM-IV criteria for AUD) (n = 81) and in light/non-drinkers without AUD (non-AUD) (n = 81), matched for age, gender, language, socio-economic status and education. Lifetime alcohol dose was orders of magnitude higher in AUD adolescents compared to non-AUD adolescents. AUD adolescents had a binge drinking pattern and “weekends-only” style of alcohol consumption. Significantly lower (p = 0.038) s-25(OH)D (adjusted for gender, smoking, vitamin D intake) were evident in AUD adolescents compared to non-AUD adolescents. High levels of vitamin D insufficiency/deficiency (s-25(OH)D < 29.9 ng/mL) were prevalent in both groups, but was significantly higher (p = 0.013) in the AUD group (90%) compared to the non-AUD group (70%). All participants were at risk of inadequate calcium and vitamin D intakes (Estimated Average Requirement cut-point method). Both groups were at risk of inadequate calcium intake and had poor biochemical vitamin D status, with binge drinking potentially increasing the risk of the latter. This may have negative implications for peak bone mass accrual and future osteoporosis risk, particularly with protracted binge drinking.
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spelling pubmed-34480882012-09-26 Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders Naude, Celeste E. Carey, Paul D. Laubscher, Ria Fein, George Senekal, Marjanne Nutrients Article Adequate vitamin D and calcium are essential for optimal adolescent skeletal development. Adolescent vitamin D insufficiency/deficiency and poor calcium intake have been reported worldwide. Heavy alcohol use impacts negatively on skeletal health, which is concerning since heavy adolescent drinking is a rising public health problem. This study aimed to examine biochemical vitamin D status and dietary intakes of calcium and vitamin D in 12–16 year-old adolescents with alcohol use disorders (AUD), but without co-morbid substance use disorders, compared to adolescents without AUD. Substance use, serum 25-hydroxyvitamin D (s-25(OH)D) concentrations, energy, calcium and vitamin D intakes were assessed in heavy drinkers (meeting DSM-IV criteria for AUD) (n = 81) and in light/non-drinkers without AUD (non-AUD) (n = 81), matched for age, gender, language, socio-economic status and education. Lifetime alcohol dose was orders of magnitude higher in AUD adolescents compared to non-AUD adolescents. AUD adolescents had a binge drinking pattern and “weekends-only” style of alcohol consumption. Significantly lower (p = 0.038) s-25(OH)D (adjusted for gender, smoking, vitamin D intake) were evident in AUD adolescents compared to non-AUD adolescents. High levels of vitamin D insufficiency/deficiency (s-25(OH)D < 29.9 ng/mL) were prevalent in both groups, but was significantly higher (p = 0.013) in the AUD group (90%) compared to the non-AUD group (70%). All participants were at risk of inadequate calcium and vitamin D intakes (Estimated Average Requirement cut-point method). Both groups were at risk of inadequate calcium intake and had poor biochemical vitamin D status, with binge drinking potentially increasing the risk of the latter. This may have negative implications for peak bone mass accrual and future osteoporosis risk, particularly with protracted binge drinking. MDPI 2012-08-20 /pmc/articles/PMC3448088/ /pubmed/23016133 http://dx.doi.org/10.3390/nu4081076 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Naude, Celeste E.
Carey, Paul D.
Laubscher, Ria
Fein, George
Senekal, Marjanne
Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders
title Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders
title_full Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders
title_fullStr Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders
title_full_unstemmed Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders
title_short Vitamin D and Calcium Status in South African Adolescents with Alcohol Use Disorders
title_sort vitamin d and calcium status in south african adolescents with alcohol use disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448088/
https://www.ncbi.nlm.nih.gov/pubmed/23016133
http://dx.doi.org/10.3390/nu4081076
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