Mostrar el registro sencillo del ítem

dc.contributor.authorVázquez Mosquera, María Eugenia 
dc.contributor.authorGonzález-Vioque, E.
dc.contributor.authorBarbosa Gouveia, Sofía
dc.contributor.authorBellido Guerrero, Diego 
dc.contributor.authorTejera Pérez, Cristina 
dc.contributor.authorMartínez Olmos, Miguel Ángel 
dc.contributor.authorFernández Pombo, Antía
dc.contributor.authorCastaño-González, L.A.
dc.contributor.authorChans Gerpe, Roi
dc.contributor.authorCouce Pico, María Luz
dc.date.accessioned2025-05-14T17:06:57Z
dc.date.available2025-05-14T17:06:57Z
dc.date.issued2022
dc.identifier.issn1750-1172
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20006
dc.description.abstract[EN] 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.
dc.language.isoenes
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleTranscriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis
dc.typeJournal Articlees
dcterms.bibliographicCitationVázquez-Mosquera ME, González-Vioque E, Barbosa-Gouveia S, Bellido-Guerrero D, Tejera-Pérez C, Martinez-Olmos MA, et al. Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis. Orphanet journal of rare diseases. 2022;17(1):105.
dc.authorsophosVázquez-Mosquera, M. L. M. E.;González-Vioque, E.;Barbosa-Gouveia, S.;Bellido-Guerrero, D.;Tejera-Pérez, C.;Martinez-Olmos, M. A.;Fernández-Pombo, A.;Castaño-González, L. A.;Chans-Gerpe, R.;Couce
dc.identifier.doi10.1186/S13023-022-02263-3
dc.identifier.sophos622d65c28ab9f76b45130694
dc.issue.number1
dc.journal.titleOrphanet journal of rare diseases
dc.page.initial105
dc.relation.publisherversionhttps://ojrd.biomedcentral.com/counter/pdf/10.1186/s13023-022-02263-3;https://ojrd.biomedcentral.com/counter/pdf/10.1186/s13023-022-02263-3.pdfes
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Santiagoes
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.subject.keywordINIBICes
dc.subject.keywordAS Ferroles
dc.subject.keywordCHUFes
dc.volume.number17


Ficheros en el ítem

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Atribución 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución 4.0 Internacional