Please use this identifier to cite or link to this item: https://hdl.handle.net/11000/32352
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dc.contributor.authorMiguel, Laura de-
dc.contributor.authorBallester, Purificación-
dc.contributor.authorEgoavil, Cecilia-
dc.contributor.authorSánchez-Ocaña, María Luisa-
dc.contributor.authorGarcía-Muñoz, Ana María-
dc.contributor.authorCerdá, Begoña-
dc.contributor.authorZAFRILLA, PILAR-
dc.contributor.authorRamos, Enrique-
dc.contributor.authorPeiró, Ana-
dc.contributor.otherDepartamentos de la UMH::Farmacología, Pediatría y Química Orgánicaes_ES
dc.date.accessioned2024-06-27T10:40:17Z-
dc.date.available2024-06-27T10:40:17Z-
dc.date.created2023-10-20-
dc.identifier.citationPharmaceuticals (Basel). 2023 Oct 20;16(10):1496es_ES
dc.identifier.issn1424-8247-
dc.identifier.urihttps://hdl.handle.net/11000/32352-
dc.description.abstractIntroduction: Up to 73% of individuals with autism spectrum disorder (ASD) and intellectual disability (ID) currently have prescriptions for psychotropic drugs. This is explained by a higher prevalence of medical and psychiatric chronic comorbidities, which favors polypharmacy, increasing the probability of the appearance of adverse events (AEs). These could be a preventable cause of harm to patients with ASD and an unnecessary waste of healthcare resources. Objective: To study the impact of pharmacogenetic markers on the prevention of AE appearance in a population with ASD and ID. Methods: This is a cross-sectional, observational study (n = 118, 72 participants completed all information) in the ASD population. Sociodemographic and pharmacological data were gathered. The Udvalg for Kliniske Undersøgelser Scale (UKU Scale) was used to identify AEs related to the use of psychotropic medication. Polymorphisms of DOP2, ABCB1, and COMT were genotyped and correlated with the AE to find candidate genes. Furthermore, a review of all medications assessed in a clinical trial for adults with autism was performed to enrich the search for potential pharmacogenetic markers, keeping in mind the usual medications. Results: The majority of the study population were men (75%) with multiple comorbidities and polypharmacy, the most frequently prescribed drugs were antipsychotics (69%); 21% of the participants had four or more AEs related to psychotropic drugs. The most common were “Neurological” and” Psychiatric” (both 41%). Statistical analysis results suggested a significant correlation between the neurological symptoms and the DOP2 genotype, given that they are not equally distributed among its allelic variants. The final review considered 19 manuscripts of medications for adults with ASD, and the confirmed genetic markers for those medications were consulted in databases. Conclusion: A possible correlation between neurologic AEs and polymorphisms of DOP2 was observed; therefore, studying this gene could contribute to the safety of this population’s prescriptions. The following studies are underway to maximize statistical power and have a better representation of the population.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent17es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectautismspectrumdisorderes_ES
dc.subjectpharmacogeneticses_ES
dc.subjectadverse eventses_ES
dc.subjectpolypharmacyes_ES
dc.subjectdopaminergic systemes_ES
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicina::615 - Farmacología. Terapéutica. Toxicología. Radiologíaes_ES
dc.titlePharmacogenetics May Prevent Psychotropic Adverse Events in Autism Spectrum Disorder: An Observational Pilot Studyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.contributor.instituteInstitutos de la UMH::Instituto de Bioingenieríaes_ES
dc.relation.publisherversionhttps://doi.org/10.3390/ph16101496es_ES
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Artículos Farmacología, Pediatría y Química Orgánica


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