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A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents

BACKGROUND: Type 2 diabetes (T2D) in youth is increasing in prevalence. Diabetes screening is recommended for at-risk youth but best-practice strategies for management of pediatric prediabetes are unknown. This study leverages a pediatric prediabetes clinic to assess identification of high-risk pati...

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Autores principales: Lawson, Chelsea, Ahmed, S Naseeruddin, Brady, Cassandra, Shoemaker, Ashley H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085182/
https://www.ncbi.nlm.nih.gov/pubmed/32215353
http://dx.doi.org/10.1210/jendso/bvaa008
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author Lawson, Chelsea
Ahmed, S Naseeruddin
Brady, Cassandra
Shoemaker, Ashley H
author_facet Lawson, Chelsea
Ahmed, S Naseeruddin
Brady, Cassandra
Shoemaker, Ashley H
author_sort Lawson, Chelsea
collection PubMed
description BACKGROUND: Type 2 diabetes (T2D) in youth is increasing in prevalence. Diabetes screening is recommended for at-risk youth but best-practice strategies for management of pediatric prediabetes are unknown. This study leverages a pediatric prediabetes clinic to assess identification of high-risk patients, the rate of clinic follow-up and progression to T2D in youth over time. METHODS: Retrospective chart review of children referred to a single center for evaluation of prediabetes over a 3-year period. Measurements included hemoglobin A1c (HbA1C) and oral glucose tolerance testing. Patients were classified as normal glucose tolerance (NGT), impaired glucose tolerance (IGT) or T2D based on 2019 American Diabetes Association criteria. Patients classified as IGT/T2D were prescribed metformin. RESULTS: Of the 254 patients included; 25.6% had IGT and 6.7% had T2D. The IGT/T2D groups were older and more obese than the NGT group. There was a moderate correlation between HbA1C and fasting glucose (r = 0.59, P < 0.001); HbA1C and 2-hour glucose (r = 0.63, P < 0.001). Over the 3-year study, 52 of 82 patients with IGT/T2D (63%) returned for follow-up. Four patients regained NGT; 3 of those had isolated impaired fasting glucose (100 to 102 mg/dL). Three patients (4.6%) progressed from IGT to T2D over an average of 13 ± 6.2 months. In those patients, body mass index had increased 1.7 ± 2.3 kg/m(2) from baseline. CONCLUSIONS: A pediatric prediabetes clinic may allow for identification of high-risk youth but lost to follow-up rates are high. Continued weight gain is a risk factor for progression to T2D and effective weight management programs are needed.
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spelling pubmed-70851822020-03-25 A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents Lawson, Chelsea Ahmed, S Naseeruddin Brady, Cassandra Shoemaker, Ashley H J Endocr Soc Clinical Research Article BACKGROUND: Type 2 diabetes (T2D) in youth is increasing in prevalence. Diabetes screening is recommended for at-risk youth but best-practice strategies for management of pediatric prediabetes are unknown. This study leverages a pediatric prediabetes clinic to assess identification of high-risk patients, the rate of clinic follow-up and progression to T2D in youth over time. METHODS: Retrospective chart review of children referred to a single center for evaluation of prediabetes over a 3-year period. Measurements included hemoglobin A1c (HbA1C) and oral glucose tolerance testing. Patients were classified as normal glucose tolerance (NGT), impaired glucose tolerance (IGT) or T2D based on 2019 American Diabetes Association criteria. Patients classified as IGT/T2D were prescribed metformin. RESULTS: Of the 254 patients included; 25.6% had IGT and 6.7% had T2D. The IGT/T2D groups were older and more obese than the NGT group. There was a moderate correlation between HbA1C and fasting glucose (r = 0.59, P < 0.001); HbA1C and 2-hour glucose (r = 0.63, P < 0.001). Over the 3-year study, 52 of 82 patients with IGT/T2D (63%) returned for follow-up. Four patients regained NGT; 3 of those had isolated impaired fasting glucose (100 to 102 mg/dL). Three patients (4.6%) progressed from IGT to T2D over an average of 13 ± 6.2 months. In those patients, body mass index had increased 1.7 ± 2.3 kg/m(2) from baseline. CONCLUSIONS: A pediatric prediabetes clinic may allow for identification of high-risk youth but lost to follow-up rates are high. Continued weight gain is a risk factor for progression to T2D and effective weight management programs are needed. Oxford University Press 2020-03-21 /pmc/articles/PMC7085182/ /pubmed/32215353 http://dx.doi.org/10.1210/jendso/bvaa008 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 Clinical Research Article
Lawson, Chelsea
Ahmed, S Naseeruddin
Brady, Cassandra
Shoemaker, Ashley H
A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents
title A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents
title_full A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents
title_fullStr A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents
title_full_unstemmed A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents
title_short A Clinic-based Approach to Diagnosis and Management of Prediabetes in High-risk Children and Adolescents
title_sort clinic-based approach to diagnosis and management of prediabetes in high-risk children and adolescents
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085182/
https://www.ncbi.nlm.nih.gov/pubmed/32215353
http://dx.doi.org/10.1210/jendso/bvaa008
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