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MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases

Background: Autoimmune thyroid disease (ATD) share common pathophysiology pathways with several other autoimmune diseases. It can be a first manifestation of an immunoregulatory diathesis, leading to a cluster of associated autoimmunities. Aim: The present study aimed to evaluate and compare the fre...

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Autores principales: Lopes, Fernanda, Almeida, Maria Aparecida, Oliveira, Renata, Pratesi, Riccardo, Castro, Luiz Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550611/
http://dx.doi.org/10.1210/js.2019-MON-596
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author Lopes, Fernanda
Almeida, Maria Aparecida
Oliveira, Renata
Pratesi, Riccardo
Castro, Luiz Claudio
author_facet Lopes, Fernanda
Almeida, Maria Aparecida
Oliveira, Renata
Pratesi, Riccardo
Castro, Luiz Claudio
author_sort Lopes, Fernanda
collection PubMed
description Background: Autoimmune thyroid disease (ATD) share common pathophysiology pathways with several other autoimmune diseases. It can be a first manifestation of an immunoregulatory diathesis, leading to a cluster of associated autoimmunities. Aim: The present study aimed to evaluate and compare the frequency of Type 1 diabetes (T1DM) and celiac disease (CD) related antibodies among pediatric and adult patients with Hashimoto’s thyroiditis (HT) and Graves’ disease (GD). Methods: A total of 145 individuals, aged 2 to 50 years (114 females; 89 pediatric patients) were included in a cross-sectional descriptive study (74 HT). Determination of antibodies related to T1DM (GADA(65) and IA2), CD (tTG-IgA and EMA-IgA) and Anti-Saccharomyces Cerevisiae (ASCA) were performed. Results: Non-thyroidal autoimmune diseases (NTAID) was found in 8.3% of individuals. Males presented a 3.2-time higher risk for a second NTAID (p=0.004) and a 4-time higher risk for a third NTAID (p=0.017). The pediatric group had 53% higher risk for developing a second NTAID (p=0.042). GADA(65), IA2 and ASCA-IgG positivity were found in 11%, 2.7% and 14.4% of the individuals, respectively. CD-related antibodies were found in a ratio of 1:48 patients. Conclusion: Individuals with ATD present high rates of T1DM and CD-related antibodies. The male group, regardless of age, has a higher rate of CD-related antibodies and also higher risk for developing two or more NTAIDs. The pediatric population with ATD presents a higher rate of AID clustering than adults. A closer surveillance for associated NTAID throughout follow-up should be performed, mainly in young male group.
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spelling pubmed-65506112019-06-13 MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases Lopes, Fernanda Almeida, Maria Aparecida Oliveira, Renata Pratesi, Riccardo Castro, Luiz Claudio J Endocr Soc Thyroid Background: Autoimmune thyroid disease (ATD) share common pathophysiology pathways with several other autoimmune diseases. It can be a first manifestation of an immunoregulatory diathesis, leading to a cluster of associated autoimmunities. Aim: The present study aimed to evaluate and compare the frequency of Type 1 diabetes (T1DM) and celiac disease (CD) related antibodies among pediatric and adult patients with Hashimoto’s thyroiditis (HT) and Graves’ disease (GD). Methods: A total of 145 individuals, aged 2 to 50 years (114 females; 89 pediatric patients) were included in a cross-sectional descriptive study (74 HT). Determination of antibodies related to T1DM (GADA(65) and IA2), CD (tTG-IgA and EMA-IgA) and Anti-Saccharomyces Cerevisiae (ASCA) were performed. Results: Non-thyroidal autoimmune diseases (NTAID) was found in 8.3% of individuals. Males presented a 3.2-time higher risk for a second NTAID (p=0.004) and a 4-time higher risk for a third NTAID (p=0.017). The pediatric group had 53% higher risk for developing a second NTAID (p=0.042). GADA(65), IA2 and ASCA-IgG positivity were found in 11%, 2.7% and 14.4% of the individuals, respectively. CD-related antibodies were found in a ratio of 1:48 patients. Conclusion: Individuals with ATD present high rates of T1DM and CD-related antibodies. The male group, regardless of age, has a higher rate of CD-related antibodies and also higher risk for developing two or more NTAIDs. The pediatric population with ATD presents a higher rate of AID clustering than adults. A closer surveillance for associated NTAID throughout follow-up should be performed, mainly in young male group. Endocrine Society 2019-04-30 /pmc/articles/PMC6550611/ http://dx.doi.org/10.1210/js.2019-MON-596 Text en Copyright © 2019 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Thyroid
Lopes, Fernanda
Almeida, Maria Aparecida
Oliveira, Renata
Pratesi, Riccardo
Castro, Luiz Claudio
MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases
title MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases
title_full MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases
title_fullStr MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases
title_full_unstemmed MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases
title_short MON-596 Male Individuals with Autoimmune Thyroid Disease Present Higher Risk for Clustering Other Non-Thyroidal Autoimmune Diseases
title_sort mon-596 male individuals with autoimmune thyroid disease present higher risk for clustering other non-thyroidal autoimmune diseases
topic Thyroid
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550611/
http://dx.doi.org/10.1210/js.2019-MON-596
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