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dc.contributor.authorda Silva Santos, T.
dc.contributor.authorFonseca, L.
dc.contributor.authorSantos Monteiro, S.
dc.contributor.authorBorges Duarte, D.
dc.contributor.authorMartins Lopes, A.
dc.contributor.authorCouto de Carvalho, A.
dc.contributor.authorOliveira, M.J.
dc.contributor.authorBorges, T.
dc.contributor.authorLaranjeira, F.
dc.contributor.authorCouce Pico, María Luz
dc.contributor.authorCardoso, M.H.
dc.date.accessioned2025-08-26T08:48:06Z
dc.date.available2025-08-26T08:48:06Z
dc.date.issued2022
dc.identifier.citationda Silva Santos T, Fonseca L, Santos Monteiro S, Borges Duarte D, Martins Lopes A, Couto de Carvalho A, et al. MODY probability calculator utility in individuals" selection for genetic testing: Its accuracy and performance. Endocrinology, Diabetes and Metabolism. 2022;5(5).
dc.identifier.issn2398-9238
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/62e5c37be5f0e01a6a1d0bc8*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20599
dc.description.abstractIntroduction: MODY probability calculator (MPC) represents an easy-to-use tool developed by Exeter University to help clinicians prioritize which individuals should be oriented to genetic testing. We aimed to assess the utility of MPC in a Portuguese cohort with early-onset monogenic diabetes. Methods: This single-centre retrospective study enrolled 132 participants submitted to genetic testing between 2015 and 2020. Automatic sequencing and, in case of initial negative results, generation sequencing were performed. MODY probability was calculated using the probability calculator available online. Positive and negative predictive values (PPV and NPV, respectively), accuracy, sensitivity and specificity of the calculator were determined for this cohort. Results: Seventy-three individuals were included according to inclusion criteria: 20 glucokinase (GCK-MODY); 16 hepatocyte nuclear factor 1A (HNF1A-MODY); 2 hepatocyte nuclear factor 4A (HNF4A-MODY) and 35 DM individuals with no monogenic mutations found. The median probability score of MODY was significantly higher in monogenic diabetes-positive subgroup (75.5% vs. 24.2%, p <.001). The discriminative accuracy of the calculator, as expressed by area under the curve, was 75% (95% CI: 64%-85%). In our cohort, the best cut-off value for the MODY calculator was found to be 36%, with a PPV of 74.4%, NPV of 73.5% and corresponding sensitivity and specificity of 76.2% and 71.4%, respectively. Conclusions: In a highly pre-selected group of probands qualified for genetic testing, the Exeter MODY probability calculator provided a useful tool in individuals' selection for genetic testing, with good discrimination ability under an optimal probability cut-off of 36%. Further geographical and population adjustments are warranted for general use.en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleMODY probability calculator utility in individuals' selection for genetic testing: Its accuracy and performance*
dc.typeArticleen
dc.authorsophosda Silva Santos, M. H. T.
dc.authorsophosFonseca, L.
dc.authorsophosSantos Monteiro, S.
dc.authorsophosBorges Duarte, D.
dc.authorsophosMartins Lopes, A.
dc.authorsophosCouto de Carvalho, A.
dc.authorsophosOliveira, M. J.
dc.authorsophosBorges, T.
dc.authorsophosLaranjeira, F.
dc.authorsophosCouce, M. L.
dc.authorsophosCardoso
dc.identifier.doi10.1002/edm2.332
dc.identifier.sophos62e5c37be5f0e01a6a1d0bc8
dc.issue.number5
dc.journal.titleEndocrinology, Diabetes and Metabolism*
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/edm2.332;https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/edm2.332?download=truees
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Santiagoes
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number5


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