Pilar Zafrilla

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Articles (18)

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Introduction: 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.

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Collaborators (10)

Thierry Durand

Head of Department

CNRS Délégation Languedoc-Roussillon

FRANCE
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Débora Villaño Valencia

Profesor Ayudante Doctor

Universidad de Navarra

SPAIN
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Desirée Victoria-Montesinos

Professor and researcher

Universidad Católica San Antonio de Murcia

SPAIN
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Ana Mª García-Muñoz

Universidad Católica de Murcia (UCAM)

SPAIN
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Angel Gil-Izquierdo

-

SPAIN
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Sonia Medina

-

SPAIN
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Ana M. Peiró

-

SPAIN
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Cerdá Begoña

Profesor Contratado Doctor

Universidad Católica San Antonio de Murcia

SPAIN
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Pura Ballester

Universidad de Alcalá de Henares Facultad de Medicina y Ciencias de la Salud

SPAIN
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Raúl Arcusa

Universidad Católica San Antonio de Murcia

SPAIN
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