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MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes

Background: Data on the course of puberty and pubertal growth in boys with Type 1 diabetes (T1D) are sparse. Objectives: To study the course of puberty, pubertal growth and final height in boys with T1D as well as possible factors affecting these. Methods: In this retrospective longitudinal study, 6...

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Autores principales: Shpitzer, Hana, Lazar, Liora, Shalitin, Shlomit, Phillip, Moshe, de Vries, Liat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207849/
http://dx.doi.org/10.1210/jendso/bvaa046.1745
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author Shpitzer, Hana
Lazar, Liora
Shalitin, Shlomit
Phillip, Moshe
de Vries, Liat
author_facet Shpitzer, Hana
Lazar, Liora
Shalitin, Shlomit
Phillip, Moshe
de Vries, Liat
author_sort Shpitzer, Hana
collection PubMed
description Background: Data on the course of puberty and pubertal growth in boys with Type 1 diabetes (T1D) are sparse. Objectives: To study the course of puberty, pubertal growth and final height in boys with T1D as well as possible factors affecting these. Methods: In this retrospective longitudinal study, 68 boys diagnosed with T1D between 1996-2009 who were pre-pubertal at diagnosis and had completed puberty served as the cohort. Collected were data on anthropometric measurements, Tanner stage, and HbA1c levels from diagnosis to final height (F-Ht). F-Ht was compared to parental height and to the data of the national health survey Results – In the study cohort final height-SDS was lower than that at diagnosis. It was similar to parental Ht-SDS as well as to that of the national health survey (p=0.126). F-Ht was inversely related to average HbA1c during puberty (R=-0.27, p=0.045). Boys who presented with diabetic ketoacidosis at diagnosis were shorter than those who did not throughout the entire follow-up. Age at onset of puberty was significantly related to the age of maternal menarche (R=0.44, p=0.01) and to HbA1c levels in the year preceding puberty onset (R=0.36, p=0.01). Total pubertal growth was inversely related to HbA1c levels in the year preceding onset of puberty (average R=-0.3, p=0.03) Conclusions: Boys with T1D diagnosed before puberty achieve final height similar to that of their parents and that of the general population. Diabetic ketoacidosis at the diagnosis is associated with diminished F-Ht. Age of pubertal onset and F-Ht are affected by genetic factors as well as by glycemic control before and during puberty. These results emphasize the importance of tight metabolic control in adolescents, to enable growth within the genetic target.
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spelling pubmed-72078492020-05-13 MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes Shpitzer, Hana Lazar, Liora Shalitin, Shlomit Phillip, Moshe de Vries, Liat J Endocr Soc Diabetes Mellitus and Glucose Metabolism Background: Data on the course of puberty and pubertal growth in boys with Type 1 diabetes (T1D) are sparse. Objectives: To study the course of puberty, pubertal growth and final height in boys with T1D as well as possible factors affecting these. Methods: In this retrospective longitudinal study, 68 boys diagnosed with T1D between 1996-2009 who were pre-pubertal at diagnosis and had completed puberty served as the cohort. Collected were data on anthropometric measurements, Tanner stage, and HbA1c levels from diagnosis to final height (F-Ht). F-Ht was compared to parental height and to the data of the national health survey Results – In the study cohort final height-SDS was lower than that at diagnosis. It was similar to parental Ht-SDS as well as to that of the national health survey (p=0.126). F-Ht was inversely related to average HbA1c during puberty (R=-0.27, p=0.045). Boys who presented with diabetic ketoacidosis at diagnosis were shorter than those who did not throughout the entire follow-up. Age at onset of puberty was significantly related to the age of maternal menarche (R=0.44, p=0.01) and to HbA1c levels in the year preceding puberty onset (R=0.36, p=0.01). Total pubertal growth was inversely related to HbA1c levels in the year preceding onset of puberty (average R=-0.3, p=0.03) Conclusions: Boys with T1D diagnosed before puberty achieve final height similar to that of their parents and that of the general population. Diabetic ketoacidosis at the diagnosis is associated with diminished F-Ht. Age of pubertal onset and F-Ht are affected by genetic factors as well as by glycemic control before and during puberty. These results emphasize the importance of tight metabolic control in adolescents, to enable growth within the genetic target. Oxford University Press 2020-05-08 /pmc/articles/PMC7207849/ http://dx.doi.org/10.1210/jendso/bvaa046.1745 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Diabetes Mellitus and Glucose Metabolism
Shpitzer, Hana
Lazar, Liora
Shalitin, Shlomit
Phillip, Moshe
de Vries, Liat
MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes
title MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes
title_full MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes
title_fullStr MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes
title_full_unstemmed MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes
title_short MON-659 Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes
title_sort mon-659 course of puberty and growth spurt in boys with type 1 diabetes
topic Diabetes Mellitus and Glucose Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207849/
http://dx.doi.org/10.1210/jendso/bvaa046.1745
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