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Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation

Monogenic diabetes is a rare form of diabetes, accounting for approximately 1% to 6% of pediatric diabetes patients. Some types of monogenic diabetes can be misdiagnosed as type 1 diabetes in children or adolescents because of similar clinical features. Identification of the correct etiology of diab...

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Autores principales: Lezzi, Marilea, Aloi, Concetta, Salina, Alessandro, Fragola, Martina, Bassi, Marta, Strati, Marina Francesca, d’Annunzio, Giuseppe, Minuto, Nicola, Maghnie, Mohamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235348/
https://www.ncbi.nlm.nih.gov/pubmed/35769090
http://dx.doi.org/10.3389/fendo.2022.894878
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author Lezzi, Marilea
Aloi, Concetta
Salina, Alessandro
Fragola, Martina
Bassi, Marta
Strati, Marina Francesca
d’Annunzio, Giuseppe
Minuto, Nicola
Maghnie, Mohamad
author_facet Lezzi, Marilea
Aloi, Concetta
Salina, Alessandro
Fragola, Martina
Bassi, Marta
Strati, Marina Francesca
d’Annunzio, Giuseppe
Minuto, Nicola
Maghnie, Mohamad
author_sort Lezzi, Marilea
collection PubMed
description Monogenic diabetes is a rare form of diabetes, accounting for approximately 1% to 6% of pediatric diabetes patients. Some types of monogenic diabetes can be misdiagnosed as type 1 diabetes in children or adolescents because of similar clinical features. Identification of the correct etiology of diabetes is crucial for clinical, therapeutic, and prognostic issues. Our main objective was to determine the prevalence of monogenic diabetes in patients with diabetes mellitus, diagnosed in childhood or in adolescence, and negative autoimmunity. We retrospectively analyzed clinical data of 275 patients diagnosed with insulin-dependent diabetes at age <18yr in the last 10 years. 8.4% of subjects has negative autoimmunity. Their DNA was sequenced by NGS custom panel composed by 45 candidate genes involved in glucose metabolism disorder. Two novel heterozygous pathogenic or likely pathogenic variants (10,5% of autoantibody negative subjects) were detected: the frameshift variant c.617_618insA in NEUROD1 exon 2 and the missense change c.116T>C in INS exon 2. Our study corroborates previous results of other reports in literature. NGS assays are useful methods for a correct diagnosis of monogenic diabetes, even of rarest forms, highlighting mechanisms of pediatric diabetes pathogenesis.
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spelling pubmed-92353482022-06-28 Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation Lezzi, Marilea Aloi, Concetta Salina, Alessandro Fragola, Martina Bassi, Marta Strati, Marina Francesca d’Annunzio, Giuseppe Minuto, Nicola Maghnie, Mohamad Front Endocrinol (Lausanne) Endocrinology Monogenic diabetes is a rare form of diabetes, accounting for approximately 1% to 6% of pediatric diabetes patients. Some types of monogenic diabetes can be misdiagnosed as type 1 diabetes in children or adolescents because of similar clinical features. Identification of the correct etiology of diabetes is crucial for clinical, therapeutic, and prognostic issues. Our main objective was to determine the prevalence of monogenic diabetes in patients with diabetes mellitus, diagnosed in childhood or in adolescence, and negative autoimmunity. We retrospectively analyzed clinical data of 275 patients diagnosed with insulin-dependent diabetes at age <18yr in the last 10 years. 8.4% of subjects has negative autoimmunity. Their DNA was sequenced by NGS custom panel composed by 45 candidate genes involved in glucose metabolism disorder. Two novel heterozygous pathogenic or likely pathogenic variants (10,5% of autoantibody negative subjects) were detected: the frameshift variant c.617_618insA in NEUROD1 exon 2 and the missense change c.116T>C in INS exon 2. Our study corroborates previous results of other reports in literature. NGS assays are useful methods for a correct diagnosis of monogenic diabetes, even of rarest forms, highlighting mechanisms of pediatric diabetes pathogenesis. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9235348/ /pubmed/35769090 http://dx.doi.org/10.3389/fendo.2022.894878 Text en Copyright © 2022 Lezzi, Aloi, Salina, Fragola, Bassi, Strati, d’Annunzio, Minuto and Maghnie https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Lezzi, Marilea
Aloi, Concetta
Salina, Alessandro
Fragola, Martina
Bassi, Marta
Strati, Marina Francesca
d’Annunzio, Giuseppe
Minuto, Nicola
Maghnie, Mohamad
Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation
title Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation
title_full Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation
title_fullStr Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation
title_full_unstemmed Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation
title_short Diabetes Mellitus Diagnosed in Childhood and Adolescence With Negative Autoimmunity: Results of Genetic Investigation
title_sort diabetes mellitus diagnosed in childhood and adolescence with negative autoimmunity: results of genetic investigation
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235348/
https://www.ncbi.nlm.nih.gov/pubmed/35769090
http://dx.doi.org/10.3389/fendo.2022.894878
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