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Pharmacogenetic Interventions Improve the Clinical Outcome of Treatment-Resistant Autistic Spectrum Disorder Sufferers.
Arranz, Maria J; Salazar, Juliana; Bote, Valentin; Artigas-Baleri, Alicia; Serra-LLovich, Alexandre; Triviño, Emma; Roige, Jordi; Lombardia, Carlos; Cancino, Martha; Hernandez, Marta; Cendros, Marc; Duran-Tauleria, Enric; Maraver, Natalia; Hervas, Amaia.
Afiliación
  • Arranz MJ; Fundació Docència i Recerca Mútua Terrassa, 08221 Terrassa, Spain.
  • Salazar J; Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), 28029 Madrid, Spain.
  • Bote V; Translational Medical Oncology Laboratory, Institut de Recerca Biomèdica Sant Pau (IIB-Sant Pau), 08041 Barcelona, Spain.
  • Artigas-Baleri A; Department of Child Psychiatry, Hospital Universitari Mútua Terrassa, 08221 Terrassa, Spain.
  • Serra-LLovich A; Genetics Department, Hospital de la Santa Creu i Sant Pau, 08025 Barcelona, Spain.
  • Triviño E; Fundació Docència i Recerca Mútua Terrassa, 08221 Terrassa, Spain.
  • Roige J; Genetics Department, Catlab, Viladecavalls, 08232 Barcelona, Spain.
  • Lombardia C; Genetics Department, Catlab, Viladecavalls, 08232 Barcelona, Spain.
  • Cancino M; Genetics Department, Catlab, Viladecavalls, 08232 Barcelona, Spain.
  • Hernandez M; Department of Child Psychiatry, Hospital Universitari Mútua Terrassa, 08221 Terrassa, Spain.
  • Cendros M; Fundació Docència i Recerca Mútua Terrassa, 08221 Terrassa, Spain.
  • Duran-Tauleria E; School of Health Sciences Blanquerna, University Ramon Llull, 08024 Barcelona, Spain.
  • Maraver N; Fundació Docència i Recerca Mútua Terrassa, 08221 Terrassa, Spain.
  • Hervas A; EUGENOMIC Genómica y Farmacogenética, 08029 Barcelona, Spain.
Pharmaceutics ; 14(5)2022 May 06.
Article en En | MEDLINE | ID: mdl-35631585
ABSTRACT

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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Guideline / Prognostic_studies Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Guideline / Prognostic_studies Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article País de afiliación: España