Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/handle/10553/139838
Campo DC Valoridioma
dc.contributor.authorFerrera Alayón, Lauraen_US
dc.contributor.authorSalas-Salas, Barbaraen_US
dc.contributor.authorPalmas-Candia, Fiorella Ximenaen_US
dc.contributor.authorCabrera Díaz-Saavedra, Raquelen_US
dc.contributor.authorRamos Ortiz, Anaïsen_US
dc.contributor.authorLara Jiménez, Pedro Carlosen_US
dc.contributor.authorLloret Sáez-Bravo, Martaen_US
dc.date.accessioned2025-06-10T13:59:42Z-
dc.date.available2025-06-10T13:59:42Z-
dc.date.issued2025en_US
dc.identifier.issn1699-048Xen_US
dc.identifier.otherScopus-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/139838-
dc.description.abstractPurpose: Oropharyngeal dysphagia is a common and debilitating condition in head and neck cancer (HNC) patients. This study aimed to evaluate the relationship between tongue muscle composition (quantity and quality) and the risk of dysphagia in non-surgically treated HNC patients, using artificial intelligence (AI) analysis of pretreatment computed tomography (CT) scans. Methods: A prospective analysis was conducted on 41 non-surgically treated HNC patients under-going curative radiotherapy. Tongue muscle quantity was measured as cross-sectional area (cm2) and as a percentage of body composition using AI-based segmentation of CT images. Muscle quality was assessed through Hounsfield Units (HU), representing muscle density. Dysphagia risk was evaluated with the validated EAT-10 questionnaire, considering scores ≥ 3 as indicative of increased risk. Results: A significant association was found between EAT-10 categorical scores and dysphagia risk (Chi2 = 26.07, p < 0.0001). However, no significant correlation was observed between the percentage of tongue muscle and density (R = 0.081, p = 0.07). Patients with EAT-10 scores ≥ 3 had significantly larger percentages of tongue muscle area (mean 61.17 ± 10.44 cm2) compared to those with EAT-10 < 3 (mean 56.58 ± 5.77 cm2; p = 0.004). Additionally, higher tongue muscle density (HU) was associated with increased dysphagia risk (p = 0.046). A significant association was also observed between pre-treatment and post-treatment dysphagia, with patients who reported pre-treatment dysphagia (EAT-10 ≥ 3) continuing to experience higher post-treatment dysphagia (p = 0.009, R = 0.411). Biologically Effective Dose (BED) (p = 0.0042), advanced tumor stage (p = 0.004), and systemic treatment (p = 0.027) were further associated with increased post-treatment dysphagia risk. Conclusions: The study demonstrates that non-surgically treated HNC patients with increased tongue area percentages and higher muscle density are at greater risk of dysphagia. Additionally, pre-treatment dysphagia was found to be a strong predictor of post-treatment dysphagia. The use of AI-based CT analysis provides a precise method for identifying patients at risk, allowing for timely interventions to improve swallowing function and quality of life.en_US
dc.languageengen_US
dc.relation.ispartofClinical and Translational Oncologyen_US
dc.sourceClinical and Translational Oncology[ISSN 1699-048X], (Enero 2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320713 Oncologíaen_US
dc.subject120304 Inteligencia artificialen_US
dc.subject.otherArtificial Intelligenceen_US
dc.subject.otherDeglutition Disordersen_US
dc.subject.otherHead And Neck Neoplasmsen_US
dc.subject.otherMuscleen_US
dc.subject.otherRadiotherapyen_US
dc.subject.otherSkeletalen_US
dc.subject.otherTomographyen_US
dc.subject.otherTongueen_US
dc.titleArtificial intelligence in dysphagia assessment: evaluating lingual muscle composition in head and neck canceren_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s12094-025-03900-6en_US
dc.identifier.scopus105000847458-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0003-1709-6232-
dc.contributor.orcidNO DATA-
dc.contributor.authorscopusid57209144026-
dc.contributor.authorscopusid57209142019-
dc.contributor.authorscopusid57194164384-
dc.contributor.authorscopusid58926431500-
dc.contributor.authorscopusid59706725100-
dc.contributor.authorscopusid7004374085-
dc.contributor.authorscopusid57211187914-
dc.identifier.eissn1699-3055-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.date.coverdateEnero 2025en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,837
dc.description.jcr2,8
dc.description.sjrqQ2
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds10,8
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.fullNameCabrera Díaz-Saavedra, Raquel-
crisitem.author.fullNameRamos Ortiz, Anaïs-
crisitem.author.fullNameLara Jiménez, Pedro Carlos-
crisitem.author.fullNameLloret Sáez-Bravo, Marta-
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