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Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus

PURPOSE: This study investigated the prevalence of islet autoantibodies in children and adults with T1DM according to their age and the duration of disease. METHODS: We measured the levels of islet autoantibodies, including antiglutamic acid decarboxylase antibody (anti-GAD Ab), and combined these w...

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Autores principales: Kong, Young Hwa, Kim, Min Sun, Lee, Dae-Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027092/
https://www.ncbi.nlm.nih.gov/pubmed/24904854
http://dx.doi.org/10.6065/apem.2013.18.2.65
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author Kong, Young Hwa
Kim, Min Sun
Lee, Dae-Yeol
author_facet Kong, Young Hwa
Kim, Min Sun
Lee, Dae-Yeol
author_sort Kong, Young Hwa
collection PubMed
description PURPOSE: This study investigated the prevalence of islet autoantibodies in children and adults with T1DM according to their age and the duration of disease. METHODS: We measured the levels of islet autoantibodies, including antiglutamic acid decarboxylase antibody (anti-GAD Ab), and combined these with anthropometric measurements and laboratory tests of 137 patients newly diagnosed with T1DM during the last 20 years. The subjects were subdivided into four groups according to their age at the onset of the disease. We then compared the prevalence of islet autoantibodies in the different age groups with the duration of disease. RESULTS: Among the 137 patients, 68.9% tested positive for islet autoantibodies (71.4% within 1 year; 67.7% after 1 year of the disease onset). Within 1 year of the onset of the disease, 66.3% of the patients were positive for the anti-GAD Ab, and 35.6% were positive for IAAs. The prevalence of islet autoantibodies was significantly higher in the prepubertal groups than in the postpubertal groups (80.0% vs. 58.3%). The rate of positive islet autoantibodies changed with the duration of disease, and it differed according to the type of autoantibody and the age of the patient. CONCLUSION: The rates of positive islet autoantibodies were significantly higher in younger than in older patients at the time of the diagnosis of the disease. The positive rates were significantly changed 1 year after the onset of the disease in the preschool and the children groups. So these findings suggest that we need to diagnose type 1B diabetes distinguished T2DM in aldolescent group, carefully.
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spelling pubmed-40270922014-06-05 Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus Kong, Young Hwa Kim, Min Sun Lee, Dae-Yeol Ann Pediatr Endocrinol Metab Original Article PURPOSE: This study investigated the prevalence of islet autoantibodies in children and adults with T1DM according to their age and the duration of disease. METHODS: We measured the levels of islet autoantibodies, including antiglutamic acid decarboxylase antibody (anti-GAD Ab), and combined these with anthropometric measurements and laboratory tests of 137 patients newly diagnosed with T1DM during the last 20 years. The subjects were subdivided into four groups according to their age at the onset of the disease. We then compared the prevalence of islet autoantibodies in the different age groups with the duration of disease. RESULTS: Among the 137 patients, 68.9% tested positive for islet autoantibodies (71.4% within 1 year; 67.7% after 1 year of the disease onset). Within 1 year of the onset of the disease, 66.3% of the patients were positive for the anti-GAD Ab, and 35.6% were positive for IAAs. The prevalence of islet autoantibodies was significantly higher in the prepubertal groups than in the postpubertal groups (80.0% vs. 58.3%). The rate of positive islet autoantibodies changed with the duration of disease, and it differed according to the type of autoantibody and the age of the patient. CONCLUSION: The rates of positive islet autoantibodies were significantly higher in younger than in older patients at the time of the diagnosis of the disease. The positive rates were significantly changed 1 year after the onset of the disease in the preschool and the children groups. So these findings suggest that we need to diagnose type 1B diabetes distinguished T2DM in aldolescent group, carefully. The Korean Society of Pediatric Endocrinology 2013-06 2013-06-30 /pmc/articles/PMC4027092/ /pubmed/24904854 http://dx.doi.org/10.6065/apem.2013.18.2.65 Text en © 2013 Annals of Pediatric Endocrinology & Metabolism http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kong, Young Hwa
Kim, Min Sun
Lee, Dae-Yeol
Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus
title Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus
title_full Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus
title_fullStr Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus
title_full_unstemmed Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus
title_short Comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus
title_sort comparison of the prevalence of islet autoantibodies according to age and disease duration in patients with type 1 diabetes mellitus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027092/
https://www.ncbi.nlm.nih.gov/pubmed/24904854
http://dx.doi.org/10.6065/apem.2013.18.2.65
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