Developing tomorrow’s antipsychotics: the need for a more personalised approach

R. Hunter
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引用次数: 3

Abstract

There has been little pharmacological advance in the treatment of schizophrenia since the introduction of chlorpromazine in the 1950s. This may be set to change as recent advances in molecular biology offer the prospect of a better understanding of the pathophysiology of the disorder and allow investigation of the complex interplay of genetic and environmental risk factors. In this review I discuss future approaches to antipsychotic drug development, highlighting the need to better define symptom areas and develop drugs based on an understanding of neurobiological mechanisms. The development of biomarkers has the potential in future to improve differential diagnosis and help predict response to treatment. These developments herald the possibility of a more integrated drug discovery approach and the subsequent provision of more stratified healthcare, and hopefully significant improvements in patient care and improved long-term outcomes.
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开发未来的抗精神病药物:需要更个性化的方法
自20世纪50年代氯丙嗪问世以来,精神分裂症的药理学治疗几乎没有什么进展。随着分子生物学的最新进展为更好地理解这种疾病的病理生理学提供了前景,并允许对遗传和环境风险因素的复杂相互作用进行调查,这种情况可能会发生变化。在这篇综述中,我讨论了抗精神病药物开发的未来途径,强调需要更好地定义症状区域,并在理解神经生物学机制的基础上开发药物。生物标志物的发展在未来有潜力改善鉴别诊断和帮助预测对治疗的反应。这些发展预示着一种更综合的药物发现方法和随后提供更分层的医疗保健的可能性,并有望显著改善患者护理和改善长期结果。
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