A systematic review of pharmacogenetic testing to guide antipsychotic treatment

[EN]Pharmacogenomics could optimize antipsychotic treatment by preventing adverse drug reactions, improving treatment efficacy or relieving the cost burden on the healthcare system. Here we conducted a systematic review to investigate whether pharmacogenetic testing in individuals undergoing antipsy...

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Detalles Bibliográficos
Autores: Saadullah Khani, Noushin, Hudson, Georgie, Mills, Georgina, Ramesh, Soumita, Varney, Lauren, Cotic, Marius, Abidoph, Rosemary, Richards-Belle, Alvin, Carrascal-Laso, Lorena, Franco Martín, Manuel Ángel, Kaas-Hansen, Benjamin Skov, Jürgens, Gesche, Barrett, Barbara, Jin, Huajie, Bramon, Elvira
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2024
País:España
Institución:Universidad de Salamanca (USAL)
Repositorio:GREDOS. Repositorio Institucional de la Universidad de Salamanca
OAI Identifier:oai:gredos.usal.es:10366/166772
Acceso en línea:http://hdl.handle.net/10366/166772
Access Level:acceso abierto
Palabra clave:Pharmacogenetics
Genetics research
Genetic Research
2409 Genética
farmacogenética
investigación genética
Descripción
Sumario:[EN]Pharmacogenomics could optimize antipsychotic treatment by preventing adverse drug reactions, improving treatment efficacy or relieving the cost burden on the healthcare system. Here we conducted a systematic review to investigate whether pharmacogenetic testing in individuals undergoing antipsychotic treatment influences clinical or economic outcomes. On 12 January 2024, we searched MEDLINE, EMBASE, PsycINFO and Cochrane Centrale Register of Controlled Trials. The results were summarized using a narrative approach and summary tables. In total, 13 studies were eligible for inclusion in the systematic review. The current evidence base is either in favor of pharmacogenetics-guided prescribing or showed no difference between pharmacogenetics and treatment as usual for clinical and economic outcomes. In the future, we require randomized controlled trials with sufficient sample sizes that provide recommendations for patients who take antipsychotics based on a broad, multigene panel, with consistent and comparable clinical outcomes