Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in China

ABSTRACT Background Emerging evidence suggests the presence of distinct endotypes of Type 1 diabetes mellitus (T1DM): T1DE1 in individuals diagnosed at age < 7 years in contrast to T1DE2 in those diagnosed at ≥ 13 years of age. We aimed to comprehensively explore the phenotypic heterogeneity of T...

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Main Authors: Qiaoli Zhou, Xueqin Zheng, Chenguang Ma, Wei Gu
Format: Article
Language:English
Published: Wiley 2025-06-01
Series:Journal of Diabetes
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Online Access:https://doi.org/10.1111/1753-0407.70111
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author Qiaoli Zhou
Xueqin Zheng
Chenguang Ma
Wei Gu
author_facet Qiaoli Zhou
Xueqin Zheng
Chenguang Ma
Wei Gu
author_sort Qiaoli Zhou
collection DOAJ
description ABSTRACT Background Emerging evidence suggests the presence of distinct endotypes of Type 1 diabetes mellitus (T1DM): T1DE1 in individuals diagnosed at age < 7 years in contrast to T1DE2 in those diagnosed at ≥ 13 years of age. We aimed to comprehensively explore the phenotypic heterogeneity of T1DM with respect to the age‐related endotypes. Methods This cross‐sectional study was conducted in China and involved 1204 children newly diagnosed with T1DM who were admitted to the pediatric department of a tertiary hospital from January 1, 2010 to December 31, 2023. The patients were divided into three age groups: < 7 years (T1DE1), 7–12 years, and ≥ 13 years (T1DE2). A comparison was made among the age groups regarding demographic characteristics, glucose metabolism, β‐cell autoimmunity, and metabolic decompensation. Results Patients under 7 years exhibited a shorter symptom duration before diagnosis, along with the lowest fasting and postprandial C‐peptide and C‐peptide to glucose ratio levels and the highest postprandial glucose levels. They also showed the highest insulin autoantibody positivity rate and creatine kinase‐MB levels. In contrast, patients aged 13 and older had the highest HbA1c levels and glutamate decarboxylase antibody positivity rate. In addition, this group showed the highest prevalence of TPOAb and TgAb positivity, as well as the largest proportion of abnormal liver function cases. Conclusions The study illustrates age‐specific phenotypic heterogeneity in pediatric T1DM, indicating the presence of distinct endotypes. Further investigation of these endotypes may offer more evidence for the precise treatment of T1DM.
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spelling doaj-art-5b3d4d1d9ce04983979088bd5cbab8422025-08-20T03:27:01ZengWileyJournal of Diabetes1753-03931753-04072025-06-01176n/an/a10.1111/1753-0407.70111Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in ChinaQiaoli Zhou0Xueqin Zheng1Chenguang Ma2Wei Gu3Department of Endocrinology Children's Hospital of Nanjing Medical University Nanjing ChinaDepartment of Endocrinology Children's Hospital of Nanjing Medical University Nanjing ChinaDepartment of Endocrinology Children's Hospital of Nanjing Medical University Nanjing ChinaDepartment of Endocrinology Children's Hospital of Nanjing Medical University Nanjing ChinaABSTRACT Background Emerging evidence suggests the presence of distinct endotypes of Type 1 diabetes mellitus (T1DM): T1DE1 in individuals diagnosed at age < 7 years in contrast to T1DE2 in those diagnosed at ≥ 13 years of age. We aimed to comprehensively explore the phenotypic heterogeneity of T1DM with respect to the age‐related endotypes. Methods This cross‐sectional study was conducted in China and involved 1204 children newly diagnosed with T1DM who were admitted to the pediatric department of a tertiary hospital from January 1, 2010 to December 31, 2023. The patients were divided into three age groups: < 7 years (T1DE1), 7–12 years, and ≥ 13 years (T1DE2). A comparison was made among the age groups regarding demographic characteristics, glucose metabolism, β‐cell autoimmunity, and metabolic decompensation. Results Patients under 7 years exhibited a shorter symptom duration before diagnosis, along with the lowest fasting and postprandial C‐peptide and C‐peptide to glucose ratio levels and the highest postprandial glucose levels. They also showed the highest insulin autoantibody positivity rate and creatine kinase‐MB levels. In contrast, patients aged 13 and older had the highest HbA1c levels and glutamate decarboxylase antibody positivity rate. In addition, this group showed the highest prevalence of TPOAb and TgAb positivity, as well as the largest proportion of abnormal liver function cases. Conclusions The study illustrates age‐specific phenotypic heterogeneity in pediatric T1DM, indicating the presence of distinct endotypes. Further investigation of these endotypes may offer more evidence for the precise treatment of T1DM.https://doi.org/10.1111/1753-0407.70111β‐cell autoimmunityendotypephenotypic variationpopulation heterogeneityType 1 diabetes mellitus
spellingShingle Qiaoli Zhou
Xueqin Zheng
Chenguang Ma
Wei Gu
Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in China
Journal of Diabetes
β‐cell autoimmunity
endotype
phenotypic variation
population heterogeneity
Type 1 diabetes mellitus
title Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in China
title_full Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in China
title_fullStr Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in China
title_full_unstemmed Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in China
title_short Phenotypic Spectrum at Diagnosis of Age‐Related Endotypes of Type 1 Diabetes Mellitus: A Cross‐Sectional Study in China
title_sort phenotypic spectrum at diagnosis of age related endotypes of type 1 diabetes mellitus a cross sectional study in china
topic β‐cell autoimmunity
endotype
phenotypic variation
population heterogeneity
Type 1 diabetes mellitus
url https://doi.org/10.1111/1753-0407.70111
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