Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps

Purpose Type 1 diabetes (T1D) is the most common type of diabetes in children, but the frequency of type 2 diabetes (T2D) is increasing rapidly. Classification of diabetes is based on a constellation of features that vary by type. We aimed to compare demographic, clinical, and laboratory characteris...

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Main Authors: Teresa Nieto, Beatriz Castillo, Jacobo Nieto, Maria J. Redondo
Format: Article
Language:English
Published: Korean Society of Pediatric Endocrinology 2021-10-01
Series:Annals of Pediatric Endocrinology & Metabolism
Subjects:
Online Access:http://e-apem.org/upload/pdf/apem-2142170-085.pdf
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author Teresa Nieto
Beatriz Castillo
Jacobo Nieto
Maria J. Redondo
author_facet Teresa Nieto
Beatriz Castillo
Jacobo Nieto
Maria J. Redondo
author_sort Teresa Nieto
collection DOAJ
description Purpose Type 1 diabetes (T1D) is the most common type of diabetes in children, but the frequency of type 2 diabetes (T2D) is increasing rapidly. Classification of diabetes is based on a constellation of features that vary by type. We aimed to compare demographic, clinical, and laboratory characteristics at diagnosis of pediatric T1D and T2D. Methods We studied children who visited a large academic hospital in Houston, Texas (USA) with a new diagnosis of T2D (n=753) or T1D (n=758). We compared age, sex, race/ethnicity, presence of obesity, glucose, hemoglobin A1c, islet autoantibody positivity, C-peptide, and presence of diabetic ketoacidosis (DKA) at diabetes diagnosis. Results At diagnosis, children with T2D, compared with those with T1D, were older (13.6 years vs. 9.7 years), more likely female (63.2% vs. 47.8%), of racial/ethnic minority (91.1% vs. 42.3%), and obese (90.9% vs. 19.4%) and were less likely to have DKA (7.8% vs. 35.0%) and diabetes autoantibodies (5.5% vs. 95.4%). Children with T2D also had significantly lower glucose, lower hemoglobin A1c and lower C-peptide level (all comparisons, P<0.0001). In multiple logistic regression analysis, older age, racial/ethnic minority, obesity, higher C-peptide, and negative islet autoantibodies were independently associated with T2D (all, P<0.05), while sex, glucose, hemoglobin A1c, and DKA were not (model P<0.0001). Conclusions There are important demographic, clinical, and laboratory differences between T1D and T2D in children. However, none of the characteristics were unique to either diabetes type, which poses challenges to diabetes classification at diagnosis.
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spelling doaj.art-a123a290edc741178ba3ef640a8a46122022-12-22T02:29:16ZengKorean Society of Pediatric EndocrinologyAnnals of Pediatric Endocrinology & Metabolism2287-10122287-12922021-10-0127212112510.6065/apem.2142170.085894Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlapsTeresa Nieto0Beatriz Castillo1Jacobo Nieto2Maria J. Redondo3 St. Agnes Academy, Houston, TX, USA Baylor College of Medicine, School of Medicine, Houston, TX, USA Rice University, Houston, TX, USA Baylor College of Medicine, Texas Children’s Hospital, Houston, TX, USAPurpose Type 1 diabetes (T1D) is the most common type of diabetes in children, but the frequency of type 2 diabetes (T2D) is increasing rapidly. Classification of diabetes is based on a constellation of features that vary by type. We aimed to compare demographic, clinical, and laboratory characteristics at diagnosis of pediatric T1D and T2D. Methods We studied children who visited a large academic hospital in Houston, Texas (USA) with a new diagnosis of T2D (n=753) or T1D (n=758). We compared age, sex, race/ethnicity, presence of obesity, glucose, hemoglobin A1c, islet autoantibody positivity, C-peptide, and presence of diabetic ketoacidosis (DKA) at diabetes diagnosis. Results At diagnosis, children with T2D, compared with those with T1D, were older (13.6 years vs. 9.7 years), more likely female (63.2% vs. 47.8%), of racial/ethnic minority (91.1% vs. 42.3%), and obese (90.9% vs. 19.4%) and were less likely to have DKA (7.8% vs. 35.0%) and diabetes autoantibodies (5.5% vs. 95.4%). Children with T2D also had significantly lower glucose, lower hemoglobin A1c and lower C-peptide level (all comparisons, P<0.0001). In multiple logistic regression analysis, older age, racial/ethnic minority, obesity, higher C-peptide, and negative islet autoantibodies were independently associated with T2D (all, P<0.05), while sex, glucose, hemoglobin A1c, and DKA were not (model P<0.0001). Conclusions There are important demographic, clinical, and laboratory differences between T1D and T2D in children. However, none of the characteristics were unique to either diabetes type, which poses challenges to diabetes classification at diagnosis.http://e-apem.org/upload/pdf/apem-2142170-085.pdftype 1 diabetestype 2 diabetespediatricdiagnosisoverlapclassificationautoimmunitymetabolicdemographicheterogeneity
spellingShingle Teresa Nieto
Beatriz Castillo
Jacobo Nieto
Maria J. Redondo
Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps
Annals of Pediatric Endocrinology & Metabolism
type 1 diabetes
type 2 diabetes
pediatric
diagnosis
overlap
classification
autoimmunity
metabolic
demographic
heterogeneity
title Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps
title_full Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps
title_fullStr Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps
title_full_unstemmed Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps
title_short Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps
title_sort demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes differences and overlaps
topic type 1 diabetes
type 2 diabetes
pediatric
diagnosis
overlap
classification
autoimmunity
metabolic
demographic
heterogeneity
url http://e-apem.org/upload/pdf/apem-2142170-085.pdf
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