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P143: New therapies for Alzheimer’s dementia and its implications on healthcare system: are we ready?

Published online by Cambridge University Press:  02 February 2024

M. A. Pão-Trigo
Affiliation:
Centro Hospitalar Universitário do Algarve, Department of Psychiatry and Mental Health - Faro, Faro, Portugal
J. Sá Couto
Affiliation:
Centro Hospitalar Universitário do Algarve, Department of Psychiatry and Mental Health - Faro, Faro, Portugal
B. Luz
Affiliation:
Centro Hospitalar Universitário do Algarve, Department of Psychiatry and Mental Health - Faro, Faro, Portugal
M. Mota Oliveira
Affiliation:
Centro Hospitalar Universitário do Algarve, Department of Psychiatry and Mental Health - Faro, Faro, Portugal

Abstract

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Objective:

The amyloid hypothesis suggests that errors in production, accumulation, or disposal of beta-amyloid are the primary causes of Alzheimer's disease (AD). Since this was hypothesized, there has been significant effort in developing treatments that prevent the build-up of amyloid beta (Aβ) plaques in the brain. A disease modifying therapy (DMT) changes the clinical progression of AD by interfering in its pathophysiological mechanisms.

The aim of this article is to review the current literature regarding the role of new DMTs for Alzheimer’s dementia and assess the preparedness of health care systems to implement these treatment options.

Methods:

Review of the most recent literature regarding the role of new DMTs for Alzheimer’s dementia and the challenges faced by the health care system to implement these treatment options. The research was carried out through the PubMed and UptoDate databases, using the terms “amyloid hypothesis”, “Alzheimer”, “disease modifying treatments” and “dementia”.

Results:

Research has been focusing on developing monoclonal antibodies as potential DMTs that target Aβ. Aducanumab, a human antibody, or immunotherapy, is the only disease-modifying medication currently approved to treat AD. It targets the Aβ protein and helps to reduce amyloid plaques and is currently the only FDA approved medication to slow the progression of AD. Lecanemab, a humanized IgG1 monoclonal antibody, binds to Aβ soluble protofibrils with high affinity. Even though there is considerable optimism about its potential, lecanemab will probably be more useful to patients on early stages of the disease.

Conclusion:

DMTs administration obeys to certain needs such as a vacancy in Day Hospital for infusion and regular monitorization and for lumbar punction. It demands a complex network involving general practitioner, neurologist, psychiatrist, psychologist, and social services. It also involves a genetic study and complementary diagnosis exams such as PET (Positron emission tomography) scans and MRIs (Magnetic resonance imaging), which are expensive. There is an emerging need to develop enhanced and safer treatments.

Type
Posters
Copyright
© International Psychogeriatric Association 2024