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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


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