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Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control

BACKGROUND AND AIMS: The relationship between vitamin D deficiency and type I DM is an ongoing area of interest. The study aims to identify the prevalence of vitamin D deficiency in children and adolescents with T1DM and to assess the impact of treatment of vitamin D deficiency on their glycaemic co...

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Autores principales: Giri, Dinesh, Pintus, Dona, Burnside, Girvan, Ghatak, Atrayee, Mehta, Fulya, Paul, Princy, Senniappan, Senthil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590233/
https://www.ncbi.nlm.nih.gov/pubmed/28882195
http://dx.doi.org/10.1186/s13104-017-2794-3
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author Giri, Dinesh
Pintus, Dona
Burnside, Girvan
Ghatak, Atrayee
Mehta, Fulya
Paul, Princy
Senniappan, Senthil
author_facet Giri, Dinesh
Pintus, Dona
Burnside, Girvan
Ghatak, Atrayee
Mehta, Fulya
Paul, Princy
Senniappan, Senthil
author_sort Giri, Dinesh
collection PubMed
description BACKGROUND AND AIMS: The relationship between vitamin D deficiency and type I DM is an ongoing area of interest. The study aims to identify the prevalence of vitamin D deficiency in children and adolescents with T1DM and to assess the impact of treatment of vitamin D deficiency on their glycaemic control. METHODS: Retrospective data was collected from 271 children and adolescents with T1DM. The vitamin D deficient (25(OH)D <30 nmol/L) and insufficient (25(OH)D 30–50 nmol/L) patients were treated with 6000 units of cholecalciferol and 400 units of cholecalciferol, once daily for 3 months respectively. HbA1c and 25(OH)D concentrations were measured before and at the end of the vitamin D treatment. RESULTS: 14.8% from the whole cohort (n = 271) were vitamin D deficient and 31% were insufficient. Among the children included in the final analysis (n = 73), the mean age and plasma 25(OH)D concentration (±SD) were 7.7 years (±4.4) and 32.2 nmol/l (±8.2) respectively. The mean 25(OH)D concentration post-treatment was 65.3 nmol/l (±9.3). The mean HbA1c (±SD) before and after cholecalciferol was 73.5 mmol/mol (±14.9) and 65 mmol/mol (±11.2) respectively (p < 0.001). Children with higher pre-treatment HbA1c had greater reduction in HbA1c (p < 0.001) and those with lower 25(OH)D concentration showed higher reduction in HbA1c (p = 0.004) after treatment. CONCLUSIONS: Low 25(OH)D concentrations are fairly prevalent in children and adolescents with T1DM, treatment of which, can potentially improve the glycaemic control.
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spelling pubmed-55902332017-09-13 Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control Giri, Dinesh Pintus, Dona Burnside, Girvan Ghatak, Atrayee Mehta, Fulya Paul, Princy Senniappan, Senthil BMC Res Notes Research Article BACKGROUND AND AIMS: The relationship between vitamin D deficiency and type I DM is an ongoing area of interest. The study aims to identify the prevalence of vitamin D deficiency in children and adolescents with T1DM and to assess the impact of treatment of vitamin D deficiency on their glycaemic control. METHODS: Retrospective data was collected from 271 children and adolescents with T1DM. The vitamin D deficient (25(OH)D <30 nmol/L) and insufficient (25(OH)D 30–50 nmol/L) patients were treated with 6000 units of cholecalciferol and 400 units of cholecalciferol, once daily for 3 months respectively. HbA1c and 25(OH)D concentrations were measured before and at the end of the vitamin D treatment. RESULTS: 14.8% from the whole cohort (n = 271) were vitamin D deficient and 31% were insufficient. Among the children included in the final analysis (n = 73), the mean age and plasma 25(OH)D concentration (±SD) were 7.7 years (±4.4) and 32.2 nmol/l (±8.2) respectively. The mean 25(OH)D concentration post-treatment was 65.3 nmol/l (±9.3). The mean HbA1c (±SD) before and after cholecalciferol was 73.5 mmol/mol (±14.9) and 65 mmol/mol (±11.2) respectively (p < 0.001). Children with higher pre-treatment HbA1c had greater reduction in HbA1c (p < 0.001) and those with lower 25(OH)D concentration showed higher reduction in HbA1c (p = 0.004) after treatment. CONCLUSIONS: Low 25(OH)D concentrations are fairly prevalent in children and adolescents with T1DM, treatment of which, can potentially improve the glycaemic control. BioMed Central 2017-09-07 /pmc/articles/PMC5590233/ /pubmed/28882195 http://dx.doi.org/10.1186/s13104-017-2794-3 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Giri, Dinesh
Pintus, Dona
Burnside, Girvan
Ghatak, Atrayee
Mehta, Fulya
Paul, Princy
Senniappan, Senthil
Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control
title Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control
title_full Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control
title_fullStr Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control
title_full_unstemmed Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control
title_short Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control
title_sort treating vitamin d deficiency in children with type i diabetes could improve their glycaemic control
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590233/
https://www.ncbi.nlm.nih.gov/pubmed/28882195
http://dx.doi.org/10.1186/s13104-017-2794-3
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