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Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes

OBJECTIVE: To study body mass index (BMI) changes and metabolic control in children and adolescents during the first year following the diagnosis of type 1 diabetes. RESEARCH DESIGN AND METHODS: 200 children and adolescents (<18 years) diagnosed with type 1 diabetes, started on multiple injection...

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Autores principales: Grönberg, Annika, Swenne, Ingemar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964219/
https://www.ncbi.nlm.nih.gov/pubmed/27547411
http://dx.doi.org/10.1136/bmjdrc-2016-000209
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author Grönberg, Annika
Swenne, Ingemar
author_facet Grönberg, Annika
Swenne, Ingemar
author_sort Grönberg, Annika
collection PubMed
description OBJECTIVE: To study body mass index (BMI) changes and metabolic control in children and adolescents during the first year following the diagnosis of type 1 diabetes. RESEARCH DESIGN AND METHODS: 200 children and adolescents (<18 years) diagnosed with type 1 diabetes, started on multiple injection treatment and followed up for 1 year were studied with respect to metabolic control and weight change. Growth curves preceding the onset of diabetes were procured from the school health services. BMI was recalculated into BMI SD scores (BMISDS). RESULTS: Glycated hemoglobin (HbA1c) at 1 year was 6.7±1.3% (50±10 mmol/mol). HbA1c was positively correlated with daily insulin dose (R(2)=0.13; p<0.001), negatively correlated with age (R(2)=0.03; p<0.05) but not related to gender, BMISDS at 1 year, HbA1c at presentation, or ketoacidosis at presentation. Prior to the onset of diabetes, BMISDS was 0.41±1.20 and decreased to −0.63±1.25 at presentation. BMISDS at 1 year was 0.54±0.97 and not different from the premorbid value (p>0.05). In a multiple regression analysis, BMISDS at 1 year was directly proportional to and highly predicted by BMISDS prior to onset of diabetes (R(2)=0.57; p<0.001). BMISDS at 1 year was also inversely correlated with age (R(2)=0.03; p<0.001) but could not be predicted by gender, daily insulin dose, HbA1c at 1 year, HbA1c at presentation, or by ketoacidosis at presentation. CONCLUSIONS: During the first year of treatment of type 1 diabetes in children and adolescents, it is possible to achieve good metabolic control without excess weight gain.
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spelling pubmed-49642192016-08-19 Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes Grönberg, Annika Swenne, Ingemar BMJ Open Diabetes Res Care Clinical Care/Education/Nutrition/Psychosocial Research OBJECTIVE: To study body mass index (BMI) changes and metabolic control in children and adolescents during the first year following the diagnosis of type 1 diabetes. RESEARCH DESIGN AND METHODS: 200 children and adolescents (<18 years) diagnosed with type 1 diabetes, started on multiple injection treatment and followed up for 1 year were studied with respect to metabolic control and weight change. Growth curves preceding the onset of diabetes were procured from the school health services. BMI was recalculated into BMI SD scores (BMISDS). RESULTS: Glycated hemoglobin (HbA1c) at 1 year was 6.7±1.3% (50±10 mmol/mol). HbA1c was positively correlated with daily insulin dose (R(2)=0.13; p<0.001), negatively correlated with age (R(2)=0.03; p<0.05) but not related to gender, BMISDS at 1 year, HbA1c at presentation, or ketoacidosis at presentation. Prior to the onset of diabetes, BMISDS was 0.41±1.20 and decreased to −0.63±1.25 at presentation. BMISDS at 1 year was 0.54±0.97 and not different from the premorbid value (p>0.05). In a multiple regression analysis, BMISDS at 1 year was directly proportional to and highly predicted by BMISDS prior to onset of diabetes (R(2)=0.57; p<0.001). BMISDS at 1 year was also inversely correlated with age (R(2)=0.03; p<0.001) but could not be predicted by gender, daily insulin dose, HbA1c at 1 year, HbA1c at presentation, or by ketoacidosis at presentation. CONCLUSIONS: During the first year of treatment of type 1 diabetes in children and adolescents, it is possible to achieve good metabolic control without excess weight gain. BMJ Publishing Group 2016-07-26 /pmc/articles/PMC4964219/ /pubmed/27547411 http://dx.doi.org/10.1136/bmjdrc-2016-000209 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Clinical Care/Education/Nutrition/Psychosocial Research
Grönberg, Annika
Swenne, Ingemar
Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes
title Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes
title_full Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes
title_fullStr Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes
title_full_unstemmed Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes
title_short Recovery of premorbid BMI trajectory without overshoot during the first year of treatment of children with type 1 diabetes
title_sort recovery of premorbid bmi trajectory without overshoot during the first year of treatment of children with type 1 diabetes
topic Clinical Care/Education/Nutrition/Psychosocial Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964219/
https://www.ncbi.nlm.nih.gov/pubmed/27547411
http://dx.doi.org/10.1136/bmjdrc-2016-000209
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