Wu Chuang-Kuo, Fuh Jong-Ling
Alzheimer's Disease and Memory Disorders Center, Department of Neurology, Brown University Health, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
J Chin Med Assoc. 2025 Jul 1;88(7):495-502. doi: 10.1097/JCMA.0000000000001252. Epub 2025 May 30.
Alzheimer's disease (AD) is a complex and progressive neurodegenerative disorder with a continuum of stages ranging from preclinical/asymptomatic phase to severe dementia. Over the past decades, significant advances in diagnostic biomarkers and disease-modifying therapies have reshaped the treatment landscape. This review provides a comprehensive overview of the current treatment paradigm for AD in 2025, incorporating the latest developments in pharmacological and non-pharmacological interventions. The advent of anti-amyloid immunotherapy, including the US Food & Drug Administration (FDA)-approved monoclonal antibodies such as lecanemab and donanemab, has proven efficacy in slowing cognitive decline in early-stage AD. These therapies mark a change in thinking in AD management, emphasizing the importance of early diagnosis and intervention. Cholinesterase inhibitors and memantine remain the standard treatments for mild, moderate to severe dementia, providing symptomatic relief and functional stabilization. Additionally, emerging strategies targeting tau pathology and neuroinflammation are under investigation, offering hope for future breakthroughs. Beyond pharmacotherapy, this review highlights the importance of personalized, multimodal treatment approaches that integrate lifestyle modifications, cognitive training, and caregiver support. The updated diagnostic framework, incorporating fluid and imaging biomarkers, enables more precise staging and individualized treatment plans. Despite these advances, challenges still lie in refining patient selection, addressing treatment-related side effects, and ensuring accessibility to appropriate therapies. As the field moves forward, ongoing clinical trials and real-world evidence will further refine treatment strategies. A proactive approach, combining early detection with disease-modifying and symptomatic therapies, is essential for improving patient outcomes and quality of life. This article synthesizes current knowledge and provides a roadmap for clinicians and researchers navigating the evolving landscape of AD treatment.
阿尔茨海默病(AD)是一种复杂的进行性神经退行性疾病,具有从临床前/无症状阶段到重度痴呆的连续阶段。在过去几十年中,诊断生物标志物和疾病修饰疗法取得了重大进展,重塑了治疗格局。本综述全面概述了2025年AD的当前治疗模式,纳入了药理学和非药理学干预的最新进展。抗淀粉样蛋白免疫疗法的出现,包括美国食品药品监督管理局(FDA)批准的单克隆抗体,如乐卡奈单抗和多奈单抗,已证明在减缓早期AD认知衰退方面有效。这些疗法标志着AD管理思维的转变,强调了早期诊断和干预的重要性。胆碱酯酶抑制剂和美金刚仍然是轻度、中度至重度痴呆的标准治疗方法,可提供症状缓解和功能稳定。此外,针对tau病理和神经炎症的新兴策略正在研究中,为未来的突破带来希望。除了药物治疗,本综述强调了个性化多模式治疗方法的重要性,该方法整合了生活方式改变、认知训练和护理人员支持。纳入血液和影像生物标志物的更新诊断框架能够实现更精确分期和个性化治疗方案。尽管取得了这些进展,但在优化患者选择、解决治疗相关副作用以及确保获得适当治疗方面仍存在挑战。随着该领域的发展,正在进行的临床试验和真实世界证据将进一步完善治疗策略。将早期检测与疾病修饰和对症治疗相结合的积极方法对于改善患者预后和生活质量至关重要。本文综合了当前知识,并为临床医生和研究人员在不断演变的AD治疗领域中导航提供了路线图。