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Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis

BACKGROUND: Diagnosis of mature-onset diabetes of the young (MODY), a non-autoimmune monogenic form of diabetes mellitus, is confirmed by genetic testing. However, a positive genetic diagnosis is achieved in only around 50% of patients with clinical characteristics of this disease. RESULTS: We evalu...

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Autores principales: Vázquez-Mosquera, María E., González-Vioque, Emiliano, Barbosa-Gouveia, Sofía, Bellido-Guerrero, Diego, Tejera-Pérez, Cristina, Martinez-Olmos, Miguel A., Fernández-Pombo, Antía, Castaño-González, Luis A., Chans-Gerpe, Roi, Couce, María L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896342/
https://www.ncbi.nlm.nih.gov/pubmed/35246208
http://dx.doi.org/10.1186/s13023-022-02263-3
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author Vázquez-Mosquera, María E.
González-Vioque, Emiliano
Barbosa-Gouveia, Sofía
Bellido-Guerrero, Diego
Tejera-Pérez, Cristina
Martinez-Olmos, Miguel A.
Fernández-Pombo, Antía
Castaño-González, Luis A.
Chans-Gerpe, Roi
Couce, María L.
author_facet Vázquez-Mosquera, María E.
González-Vioque, Emiliano
Barbosa-Gouveia, Sofía
Bellido-Guerrero, Diego
Tejera-Pérez, Cristina
Martinez-Olmos, Miguel A.
Fernández-Pombo, Antía
Castaño-González, Luis A.
Chans-Gerpe, Roi
Couce, María L.
author_sort Vázquez-Mosquera, María E.
collection PubMed
description BACKGROUND: Diagnosis of mature-onset diabetes of the young (MODY), a non-autoimmune monogenic form of diabetes mellitus, is confirmed by genetic testing. However, a positive genetic diagnosis is achieved in only around 50% of patients with clinical characteristics of this disease. RESULTS: We evaluated the diagnostic utility of transcriptomic analysis in patients with clinical suspicion of MODY but a negative genetic diagnosis. Using Nanostring nCounter technology, we conducted transcriptomic analysis of 19 MODY-associated genes in peripheral blood samples from 19 patients and 8 healthy controls. Normalized gene expression was compared between patients and controls and correlated with each patient’s biochemical and clinical variables. Z-scores were calculated to identify significant changes in gene expression in patients versus controls. Only 7 of the genes analyzed were detected in peripheral blood. HADH expression was significantly lower in patients versus controls. Among patients with suspected MODY, GLIS3 expression was higher in obese versus normal-weight patients, and in patients aged < 25 versus > 25 years at diabetes onset. Significant alteration with respect to controls of any gene was observed in 57.9% of patients. CONCLUSIONS: Although blood does not seem to be a suitable sample for transcriptomic analysis of patients with suspected MODY, in our study, we detected expression alterations in some of the genes studied in almost 58% of patients. That opens the door for future studies that can clarify the molecular cause of the clinic of these patients and thus be able to maintain a more specific follow-up and treatment in each case. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02263-3.
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spelling pubmed-88963422022-03-14 Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis Vázquez-Mosquera, María E. González-Vioque, Emiliano Barbosa-Gouveia, Sofía Bellido-Guerrero, Diego Tejera-Pérez, Cristina Martinez-Olmos, Miguel A. Fernández-Pombo, Antía Castaño-González, Luis A. Chans-Gerpe, Roi Couce, María L. Orphanet J Rare Dis Research BACKGROUND: Diagnosis of mature-onset diabetes of the young (MODY), a non-autoimmune monogenic form of diabetes mellitus, is confirmed by genetic testing. However, a positive genetic diagnosis is achieved in only around 50% of patients with clinical characteristics of this disease. RESULTS: We evaluated the diagnostic utility of transcriptomic analysis in patients with clinical suspicion of MODY but a negative genetic diagnosis. Using Nanostring nCounter technology, we conducted transcriptomic analysis of 19 MODY-associated genes in peripheral blood samples from 19 patients and 8 healthy controls. Normalized gene expression was compared between patients and controls and correlated with each patient’s biochemical and clinical variables. Z-scores were calculated to identify significant changes in gene expression in patients versus controls. Only 7 of the genes analyzed were detected in peripheral blood. HADH expression was significantly lower in patients versus controls. Among patients with suspected MODY, GLIS3 expression was higher in obese versus normal-weight patients, and in patients aged < 25 versus > 25 years at diabetes onset. Significant alteration with respect to controls of any gene was observed in 57.9% of patients. CONCLUSIONS: Although blood does not seem to be a suitable sample for transcriptomic analysis of patients with suspected MODY, in our study, we detected expression alterations in some of the genes studied in almost 58% of patients. That opens the door for future studies that can clarify the molecular cause of the clinic of these patients and thus be able to maintain a more specific follow-up and treatment in each case. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02263-3. BioMed Central 2022-03-04 /pmc/articles/PMC8896342/ /pubmed/35246208 http://dx.doi.org/10.1186/s13023-022-02263-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Vázquez-Mosquera, María E.
González-Vioque, Emiliano
Barbosa-Gouveia, Sofía
Bellido-Guerrero, Diego
Tejera-Pérez, Cristina
Martinez-Olmos, Miguel A.
Fernández-Pombo, Antía
Castaño-González, Luis A.
Chans-Gerpe, Roi
Couce, María L.
Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis
title Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis
title_full Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis
title_fullStr Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis
title_full_unstemmed Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis
title_short Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis
title_sort transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (mody) with a negative genetic diagnosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896342/
https://www.ncbi.nlm.nih.gov/pubmed/35246208
http://dx.doi.org/10.1186/s13023-022-02263-3
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