Pharmacogenetic interventions improve the clinical outcome of treatment-resistant autistic spectrum disorder sufferers

BACKGROUND: Autistic spectrum disorders (ASD) are severe neurodevelopmental alterations characterised by deficits in social communication and repetitive and restricted behaviours. About a third of patients receive pharmacological treatment for comorbid symptoms. However, 30–50% do not respond adequa...

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Detalles Bibliográficos
Autores: Arranz, Maria J, Salazar, Juliana, Bote, Valentin, Artigas-Baleri, Alícia, Serra-Llovich, Alexandre, Triviño, Emma, Roige, Jordi, Lombardia, Carlos, Cancino, Martha, Hernández Hernández, Marta, Cendros, Marc, Duran-Tauleria, Enric, Maraver, Natalia, Hervas, Amaia
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:20.500.14342/3725
Acceso en línea:http://hdl.handle.net/20.500.14342/3725
https://doi.org/10.3390/pharmaceutics14050999
Access Level:acceso abierto
Palabra clave:Infants autistes
Autisme
ASD
Farmacogenètica
Farmacologia
Antipsicòtics
Antidepressius
Tranquil·lizants
615
616.89
Descripción
Sumario:BACKGROUND: Autistic spectrum disorders (ASD) are severe neurodevelopmental alterations characterised by deficits in social communication and repetitive and restricted behaviours. About a third of patients receive pharmacological treatment for comorbid symptoms. However, 30–50% do not respond adequately and/or present severe and long-lasting side effects. METHODS: Genetic variants in CYP1A2, CYP2C19, CYP2D6 and SLC6A4 were investigated in N = 42 ASD sufferers resistant to pharmacological treatment. Clinical recommendations based on their pharmacogenetic profiles were provided within 24–48 h of receiving a biological sample. RESULTS: A total of 39 participants (93%) improved after the pharmacogenetic intervention according to their CGI scores (difference in basal-final scores: 2.26, SD 1.55) and 37 participants (88%) according to their CGAS scores (average improvement of 20.29, SD 11.85). Twenty-three of them (55%) achieved symptom stability (CGI ≤ 3 and CGAS improvement ≥ 20 points), requiring less frequent visits to their clinicians and hospital stays. Furthermore, the clinical improvement was higher than that observed in a control group (N = 62) with no pharmacogenetic interventions, in which 66% responded to treatment (difference in CGI scores: −0.87, SD 9.4, p = 1 × 10−5; difference in CGAS scores: 6.59, SD 7.76, p = 5 × 10−8). CONCLUSIONS: The implementation of pharmacogenetic interventions has the potential to significantly improve the clinical outcomes in severe comorbid ASD populations with drug treatment resistance and poor prognosis.