Smoller Charles, Schiller Emily, Yamashita Kyla, Silverglate Bret David, Grossberg George Thomas
Division of Geriatric Psychiatry, Department of Psychiatry and Behavioral Neuroscience, Saint Louis University School of Medicine, 1438 S. Grand Boulevard, St. Louis, MO, 63104, USA.
Department of Psychiatry, Northern Light Health, Bangor, ME, USA.
Drugs. 2025 Sep 6. doi: 10.1007/s40265-025-02227-4.
This narrative review explores current pharmacological treatments for agitation in Alzheimer's disease (AD). Agitation, a common and difficult-to-manage symptom in AD, often requires targeted intervention. While nonpharmacological methods, such as behavioral therapy and environmental modifications, are considered first line, they may not always be effective. In cases where these approaches fail, pharmacological treatment can become a necessary component of care. Historically, antipsychotics have been the mainstay of pharmacological treatment for agitation in AD; however, safety and efficacy concerns have prompted exploration into alternative treatments. The purpose of this narrative review is to synthesize current literature on pharmacological treatments for agitation in AD with a focus on new and repurposed drugs. It also examines agents that have failed to demonstrate clinical benefit, offering insights into the ongoing challenges of drug development in this area. This review synthesizes recent findings on various drug classes, including anticonvulsants, antipsychotics, selective serotonin reuptake inhibitors (SSRIs), atypical antidepressants, sedatives, anti-dementia drugs, dextromethorphan, and cannabinoids. Both brexpiprazole and risperidone have demonstrated efficacy and received approval from government agencies, including brexpiprazole in the USA and risperidone in parts of Europe. Despite these advances, concerns remain regarding their long-term use and safety profiles. As a result, multiple other therapies are currently being studied as possible alternative solutions. However, no other pharmacological agents are currently approved, underscoring the need for further research on safe and effective options for this vulnerable population.
本叙述性综述探讨了目前用于治疗阿尔茨海默病(AD)激越症状的药物治疗方法。激越是AD中常见且难以管理的症状,通常需要针对性干预。虽然非药物方法,如行为疗法和环境调整,被视为一线治疗,但它们可能并不总是有效。在这些方法失败的情况下,药物治疗可能成为护理的必要组成部分。从历史上看,抗精神病药物一直是AD激越药物治疗的主要手段;然而,对安全性和有效性的担忧促使人们探索替代治疗方法。本叙述性综述的目的是综合当前关于AD激越药物治疗的文献,重点关注新的和重新利用的药物。它还研究了未能证明临床益处的药物,深入了解该领域药物开发中持续存在的挑战。本综述综合了关于各种药物类别的最新研究结果,包括抗惊厥药、抗精神病药、选择性5-羟色胺再摄取抑制剂(SSRI)、非典型抗抑郁药、镇静剂、抗痴呆药、右美沙芬和大麻素。布雷哌唑和利培酮均已证明有效,并获得了政府机构的批准,包括美国的布雷哌唑和欧洲部分地区的利培酮。尽管取得了这些进展,但对它们的长期使用和安全性仍存在担忧。因此,目前正在研究多种其他疗法作为可能的替代解决方案。然而,目前尚无其他药物获得批准,这突出了对这一脆弱人群安全有效的治疗方案进行进一步研究的必要性。