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布雷哌唑用于治疗阿尔茨海默病所致痴呆相关的激越症状。

Brexpiprazole for Agitation Associated With Dementia Due to Alzheimer's Disease.

作者信息

Lee Daniel, Clark Emily D, Antonsdottir Inga M, Porsteinsson Anton P

机构信息

Alzheimer's Disease Care, Research and Education (AD-CARE), Department of Psychiatry, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.

Johns Hopkins School of Nursing, Baltimore, MD, USA; Department of Psychiatry and Behavioral Sciences, Richman Family Precision Medicine Center of Excellence in Alzheimer's Disease, Johns Hopkins Bayview, Johns Hopkins Medicine, Baltimore, MD, USA.

出版信息

J Am Med Dir Assoc. 2024 Oct;25(10):105173. doi: 10.1016/j.jamda.2024.105173. Epub 2024 Jul 22.

Abstract

Alzheimer's disease (AD) is a prevalent neurodegenerative disease characterized by progressive cognitive and functional decline. Nearly all patients with AD develop neuropsychiatric symptoms (NPSs). Agitation is one of the most distressing and challenging NPS. Brexpiprazole is an oral antipsychotic and is the first approved pharmacologic agent in the United States for the treatment of agitation associated with dementia due to AD. Its effect is thought to be from its partial serotonin 5-HT and dopamine D receptor agonist activity and serotonin 5-HT receptor antagonism. Brexpiprazole is a maintenance medication, and it should not be used "as needed" or as a "PRN" treatment for breakthrough agitation. Brexpiprazole is a major substrate of CYP2D6 and CYP3A4. Dose adjustments may be required for drug interactions or impaired renal or hepatic function. Clinical trials found brexpiprazole 2 to 3 mg/d demonstrated significant improvements in agitation, with brexpiprazole showing an approximate 5-point greater reduction on change in the Cohen-Mansfield Agitation Inventory total score at week 12 from baseline compared with placebo. Brexpiprazole is generally well tolerated and safe, and common adverse reactions when used for this indication include dizziness, headaches, insomnia, nasopharyngitis, somnolence, and urinary tract infections. Like other antipsychotics used for agitation in AD, brexpiprazole is associated with higher mortality rates compared with placebo. In a long-term care setting, there are several considerations for its use. Benefits include an oral agent that is well tolerated and clinical data showing statistically significant effects on agitation. However, brexpiprazole has not been studied in head-to-head clinical trials against other antipsychotics, and there are differing opinions if the agitation score reductions translate to a clinically meaningful difference. The approval of brexpiprazole signals favorably for upcoming agents for this indication, including escitalopram and dextromethorphan-bupropion. Both escitalopram and dextromethorphan-bupropion are currently undergoing clinical trials.

摘要

阿尔茨海默病(AD)是一种常见的神经退行性疾病,其特征为进行性认知和功能衰退。几乎所有AD患者都会出现神经精神症状(NPSs)。激越状态是最令人痛苦且具有挑战性的NPS之一。布雷哌唑是一种口服抗精神病药物,是美国首个获批用于治疗与AD所致痴呆相关激越状态的药物。其作用被认为源于其部分5-羟色胺(5-HT)和多巴胺D受体激动剂活性以及5-HT受体拮抗作用。布雷哌唑是一种维持性药物,不应“按需”使用或作为突破性激越状态的“必要时”治疗药物。布雷哌唑是细胞色素P450 2D6(CYP2D6)和细胞色素P450 3A4(CYP3A4)的主要底物。因药物相互作用或肾功能或肝功能受损可能需要调整剂量。临床试验发现,每日服用2至3毫克布雷哌唑可显著改善激越状态,与安慰剂相比,在第12周时,布雷哌唑使科恩-曼斯菲尔德激越量表总分较基线变化的降幅大约多5分。布雷哌唑总体耐受性良好且安全,用于该适应证时的常见不良反应包括头晕、头痛、失眠、鼻咽炎、嗜睡和尿路感染。与其他用于AD激越状态的抗精神病药物一样,与安慰剂相比,布雷哌唑与更高的死亡率相关。在长期护理环境中,使用该药有几个需要考虑的方面。益处包括一种耐受性良好的口服药物以及显示对激越状态有统计学显著效果的临床数据。然而,尚未针对布雷哌唑与其他抗精神病药物进行头对头临床试验,而且对于激越评分降低是否转化为具有临床意义的差异存在不同观点。布雷哌唑的获批对该适应证的后续药物,包括艾司西酞普兰和右美沙芬-安非他酮,发出了有利信号。艾司西酞普兰和右美沙芬-安非他酮目前都在进行临床试验。

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