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Synapse
September 16, 20256 citations

Review of Anti-amyloid-Beta (Aβ) monoclonal antibodies for the treatment of Alzheimer's disease.

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EFEmily FrancisSPSamantha PaylorCVCornelis Van

Key Points

  • Anti-amyloid-beta monoclonal antibodies modestly slow cognitive decline in early Alzheimer's disease, showing significant positive effects.
  • Recent therapies, such as lecanemab and donanemab, specifically bind aggregated amyloid-beta, demonstrating efficacy.
  • The review analyzes safety aspects related to amyloid-related imaging abnormalities, particularly among APOE ε4 carriers.
  • Challenges like cost and treatment burden limit the broader adoption of these new therapies for Alzheimer's disease.

Abstract

Alzheimer's disease (AD) remains a major public health challenge, with growing prevalence and limited treatment options that modify disease progression. Recent advances have led to the development and approval of Anti-amyloid-β (Aβ) monoclonal antibodies, which represent a paradigm shift from symptomatic management to targeted disease modification. Agents such as lecanemab and donanemab selectively bind aggregated forms of Aβ and have demonstrated modest but statistically significant slowing of cognitive and functional decline in early AD. However, these therapies are associated with amyloid-related imaging abnormalities (ARIA), particularly in individuals carrying the APOE ε4 allele, necessitating close monitoring and individualized risk assessment. Implementation challenges, including high treatment burden, cost, and real-world applicability, have limited broad clinical adoption. This review examines the mechanistic differences, clinical trial outcomes, and safety considerations of Aβ monoclonal antibodies, while also highlighting emerging therapies and the need for inclusive, precision-guided approaches. As research continues to evolve, balancing clinical benefit with safety and accessibility will be critical in defining the role of anti-amyloid therapies within the broader landscape of AD care.

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Cite This Study

Francis et al. (2025) studied this question.

synapsesocial.com/papers/68c93fe601120bef803bb0b3https://doi.org/10.1080/17512433.2025.2556122
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