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Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results
Objective: Increased prevalence of celiac disease (CD) and autoimmune thyroid disorders (ATD) in patients with Type 1 diabetes mellitus (T1D) has been widely reported. Such an association may lead to adverse effects on the growth, bone metabolism and fertility, and response to therapy may become dif...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Galenos Publishing
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005689/ https://www.ncbi.nlm.nih.gov/pubmed/21274314 http://dx.doi.org/10.4274/jcrpe.v2i4.151 |
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author | Ergür, Ayça Törel Öçal, Gönül Berberoğlu, Merih Adıyaman, Pelin Şıklar, Zeynep Aycan, Zehra Evliyaoğlu, Olcay Kansu, Aydan Girgin, Nurten Ensari, Arzu |
author_facet | Ergür, Ayça Törel Öçal, Gönül Berberoğlu, Merih Adıyaman, Pelin Şıklar, Zeynep Aycan, Zehra Evliyaoğlu, Olcay Kansu, Aydan Girgin, Nurten Ensari, Arzu |
author_sort | Ergür, Ayça Törel |
collection | PubMed |
description | Objective: Increased prevalence of celiac disease (CD) and autoimmune thyroid disorders (ATD) in patients with Type 1 diabetes mellitus (T1D) has been widely reported. Such an association may lead to adverse effects on the growth, bone metabolism and fertility, and response to therapy may become difficult. The aim of this study was to evaluate the clinical findings and HLA typing results in patients with T1D associated with CD or ATD. Methods: The association of CD and ATD was evaluated in 38 children with T1D aged 1.5−16.8 years who had been followed for 48.3±28 months. Diagnosis of CD was based on positivity for serum endomysial IgA antibody and histopathological findings of intestinal biopsy specimens. Thyroid autoimmunity was assessed by antithyroglobulin and antithyroid peroxidase antibodies and with diagnostic ultrasonographic findings. Results: ATD was detected in 31.5%, and CD−in 7.8% of T1D patients. Subjects with CD showed either no symptoms or suggestive problems such as short stature, hepatosteatosis, pubertal delay and difficulties in the control of diabetes. Patients with ATD had no clinical symptoms. DQ8 was the most prominent finding in CD. Conclusions: It is essential that patients with T1D, regardless of presence or absence of symptoms, should be investigated for CD and ATD. Conflict of interest:None declared. |
format | Text |
id | pubmed-3005689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-30056892011-01-27 Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results Ergür, Ayça Törel Öçal, Gönül Berberoğlu, Merih Adıyaman, Pelin Şıklar, Zeynep Aycan, Zehra Evliyaoğlu, Olcay Kansu, Aydan Girgin, Nurten Ensari, Arzu J Clin Res Pediatr Endocrinol Original Article Objective: Increased prevalence of celiac disease (CD) and autoimmune thyroid disorders (ATD) in patients with Type 1 diabetes mellitus (T1D) has been widely reported. Such an association may lead to adverse effects on the growth, bone metabolism and fertility, and response to therapy may become difficult. The aim of this study was to evaluate the clinical findings and HLA typing results in patients with T1D associated with CD or ATD. Methods: The association of CD and ATD was evaluated in 38 children with T1D aged 1.5−16.8 years who had been followed for 48.3±28 months. Diagnosis of CD was based on positivity for serum endomysial IgA antibody and histopathological findings of intestinal biopsy specimens. Thyroid autoimmunity was assessed by antithyroglobulin and antithyroid peroxidase antibodies and with diagnostic ultrasonographic findings. Results: ATD was detected in 31.5%, and CD−in 7.8% of T1D patients. Subjects with CD showed either no symptoms or suggestive problems such as short stature, hepatosteatosis, pubertal delay and difficulties in the control of diabetes. Patients with ATD had no clinical symptoms. DQ8 was the most prominent finding in CD. Conclusions: It is essential that patients with T1D, regardless of presence or absence of symptoms, should be investigated for CD and ATD. Conflict of interest:None declared. Galenos Publishing 2010-12 2010-11-03 /pmc/articles/PMC3005689/ /pubmed/21274314 http://dx.doi.org/10.4274/jcrpe.v2i4.151 Text en © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ergür, Ayça Törel Öçal, Gönül Berberoğlu, Merih Adıyaman, Pelin Şıklar, Zeynep Aycan, Zehra Evliyaoğlu, Olcay Kansu, Aydan Girgin, Nurten Ensari, Arzu Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results |
title | Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results |
title_full | Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results |
title_fullStr | Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results |
title_full_unstemmed | Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results |
title_short | Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results |
title_sort | celiac disease and autoimmune thyroid disease in children with type 1 diabetes mellitus: clinical and hla−genotyping results |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005689/ https://www.ncbi.nlm.nih.gov/pubmed/21274314 http://dx.doi.org/10.4274/jcrpe.v2i4.151 |
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