Pharmacogenetic Interventions Improve the Clinical Outcome of Treatment-Resistant Autistic Spectrum Disorder Sufferers

被引:12
作者
Arranz, Maria J. [1 ,2 ]
Salazar, Juliana [3 ]
Bote, Valentin [4 ]
Artigas-Baleri, Alicia [5 ]
Serra-LLovich, Alexandre [1 ]
Trivino, Emma [6 ]
Roige, Jordi [6 ]
Lombardia, Carlos [6 ]
Cancino, Martha [4 ]
Hernandez, Marta [1 ,7 ]
Cendros, Marc [1 ,8 ]
Duran-Tauleria, Enric [9 ]
Maraver, Natalia [9 ]
Hervas, Amaia [4 ,9 ]
机构
[1] Fundacio Docencia & Recerca Mutua Terrassa, Terrassa 08221, Spain
[2] Ctr Invest Biomed Red Salud Mental CIBERSAM, Madrid 28029, Spain
[3] Inst Recerca Biomed St Pau IIB St Pau, Translat Med Oncol Lab, Barcelona 08041, Spain
[4] Hosp Univ Mutua Terrassa, Dept Child Psychiat, Terrassa 08221, Spain
[5] Hosp Santa Creu & Sant Pau, Genet Dept, Barcelona 08025, Spain
[6] Genet Dept, Catlab, Barcelona 08232, Spain
[7] Univ Ramon Llull, Sch Hlth Sci Blanquerna, Barcelona 08024, Spain
[8] EUGENOMIC Genom & Farmacogenet, Barcelona 08029, Spain
[9] Inst Global Atencio Integral Neurodesenvolupament, Barcelona 08007, Spain
关键词
ASD; pharmacogenetic intervention; pharmacotherapy; personalisation of treatment; antipsychotics; antidepressants; anxiolytics; SEROTONIN TRANSPORTER GENE; ASSOCIATION; POLYMORPHISM; METAANALYSIS; ESCITALOPRAM; RISPERIDONE; VALIDITY; CHILDREN;
D O I
10.3390/pharmaceutics14050999
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 x 10(-5); difference in CGAS scores: 6.59, SD 7.76, p = 5 x 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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页数:12
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