Semira Abdi Beshir, Nadia Hussain, Vineetha Bharathan Menon, Amal H I Al Haddad, Rahaf Adnan Kh Al Zeer, Asim Ahmed Elnour
{"title":"Advancements and Challenges in Antiamyloid Therapy for Alzheimer's Disease: A Comprehensive Review.","authors":"Semira Abdi Beshir, Nadia Hussain, Vineetha Bharathan Menon, Amal H I Al Haddad, Rahaf Adnan Kh Al Zeer, Asim Ahmed Elnour","doi":"10.1155/2024/2052142","DOIUrl":null,"url":null,"abstract":"<p><p>Alzheimer's disease (AD) is a progressive neurodegenerative disorder caused by the accumulation of amyloid-beta (A<i>β</i>) proteins and neurofibrillary tangles in the brain. There have been recent advancements in antiamyloid therapy for AD. This narrative review explores the recent advancements and challenges in antiamyloid therapy. In addition, a summary of evidence from antiamyloid therapy trials is presented with a focus on lecanemab. Lecanemab is the most recently approved monoclonal antibody that targets A<i>β</i> protofibrils for the treatment of patients with early AD and mild cognitive impairment (MCI). Lecanemab was the first drug shown to slow cognitive decline in patients with MCI or early onset AD dementia when administered as an infusion once every two weeks. In the Clarity AD trial, lecanemab was associated with infusion-site reactions (26.4%) and amyloid-related imaging abnormalities (12.6%). The clinical relevance and long-term side effects of lecanemab require further longitudinal observation. However, several challenges must be addressed before the drug can be routinely used in clinical practice. The drug's route of administration, need for imaging and genetic testing, affordability, accessibility, infrastructure, and potential for serious side effects are some of these challenges. Lecanemab's approval has fueled interest in the potential of other antiamyloid therapies, such as donanemab. Future research must focus on developing strategies to prevent AD; identify easy-to-use validated plasma-based assays; and discover newer user-friendly, and cost-effective drugs that target multiple pathways in AD pathology.</p>","PeriodicalId":13802,"journal":{"name":"International Journal of Alzheimer's Disease","volume":"2024 ","pages":"2052142"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11288696/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Alzheimer's Disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2024/2052142","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Neuroscience","Score":null,"Total":0}
引用次数: 0
Abstract
Alzheimer's disease (AD) is a progressive neurodegenerative disorder caused by the accumulation of amyloid-beta (Aβ) proteins and neurofibrillary tangles in the brain. There have been recent advancements in antiamyloid therapy for AD. This narrative review explores the recent advancements and challenges in antiamyloid therapy. In addition, a summary of evidence from antiamyloid therapy trials is presented with a focus on lecanemab. Lecanemab is the most recently approved monoclonal antibody that targets Aβ protofibrils for the treatment of patients with early AD and mild cognitive impairment (MCI). Lecanemab was the first drug shown to slow cognitive decline in patients with MCI or early onset AD dementia when administered as an infusion once every two weeks. In the Clarity AD trial, lecanemab was associated with infusion-site reactions (26.4%) and amyloid-related imaging abnormalities (12.6%). The clinical relevance and long-term side effects of lecanemab require further longitudinal observation. However, several challenges must be addressed before the drug can be routinely used in clinical practice. The drug's route of administration, need for imaging and genetic testing, affordability, accessibility, infrastructure, and potential for serious side effects are some of these challenges. Lecanemab's approval has fueled interest in the potential of other antiamyloid therapies, such as donanemab. Future research must focus on developing strategies to prevent AD; identify easy-to-use validated plasma-based assays; and discover newer user-friendly, and cost-effective drugs that target multiple pathways in AD pathology.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,由淀粉样β(Aβ)蛋白和神经纤维缠结在大脑中的积累引起。抗淀粉样蛋白疗法在治疗多发性硬化症方面取得了最新进展。本综述探讨了抗淀粉样蛋白疗法的最新进展和挑战。此外,还总结了抗淀粉样蛋白疗法试验的证据,重点介绍了来卡尼单抗。来卡尼单抗是最近获批的针对Aβ原纤维的单克隆抗体,用于治疗早期AD和轻度认知障碍(MCI)患者。莱卡单抗是第一种被证明能减缓 MCI 或早期 AD 痴呆症患者认知能力下降的药物,每两周输注一次。在 Clarity AD 试验中,来卡尼单抗与输液部位反应(26.4%)和淀粉样蛋白相关成像异常(12.6%)有关。莱卡奈单抗的临床意义和长期副作用需要进一步的纵向观察。然而,在将该药物常规用于临床实践之前,还必须解决几个难题。药物的给药途径、成像和基因检测的需要、可负担性、可及性、基础设施以及潜在的严重副作用就是其中的一些挑战。莱卡单抗的获批激发了人们对其他抗淀粉样蛋白疗法(如多那尼单抗)潜力的兴趣。未来的研究必须专注于开发预防渐冻人症的策略;确定易于使用的基于血浆的有效检测方法;以及发现针对渐冻人症病理中多种途径的更新、更易于使用且更具成本效益的药物。