Factors Affecting Resilience and Prevention of Alzheimer's Disease and Related Dementias

Author:

Masurkar Arjun V.123,Marsh Karyn12,Morgan Brianna4,Leitner Dominique125ORCID,Wisniewski Thomas1267ORCID

Affiliation:

1. Department of Neurology New York University Grossman School of Medicine New York NY USA

2. Center for Cognitive Neurology New York University Grossman School of Medicine New York NY USA

3. Department of Neuroscience and Physiology New York University Grossman School of Medicine New York NY USA

4. Department of Medicine New York University Grossman School of Medicine New York NY USA

5. Comprehensive Epilepsy Center New York University Grossman School of Medicine New York NY USA

6. Department of Pathology New York University Grossman School of Medicine New York NY USA

7. Department of Psychiatry New York University Grossman School of Medicine New York NY USA

Abstract

Alzheimer's disease (AD) is a devastating, age‐associated neurodegenerative disorder and the most common cause of dementia. The clinical continuum of AD spans from preclinical disease to subjective cognitive decline, mild cognitive impairment, and dementia stages (mild, moderate, and severe). Neuropathologically, AD is defined by the accumulation of amyloid β (Aβ) into extracellular plaques in the brain parenchyma and in the cerebral vasculature, and by abnormally phosphorylated tau that accumulates intraneuronally forming neurofibrillary tangles (NFTs). Development of treatment approaches that prevent or even reduce the cognitive decline because of AD has been slow compared to other major causes of death. Recently, the United States Food and Drug Administration gave full approval to 2 different Aβ‐targeting monoclonal antibodies. However, this breakthrough disease modifying approach only applies to a limited subset of patients in the AD continuum and there are stringent eligibility criteria. Furthermore, these approaches do not prevent progression of disease, because other AD‐related pathologies, such as NFTs, are not directly targeted. A non‐mutually exclusive alternative is to address lifestyle interventions that can help reduce the risk of AD and AD‐related dementias (ADRD). It is estimated that addressing such modifiable risk factors could potentially delay up to 40% of AD/ADRD cases. In this review, we discuss some of the many modifiable risk factors that may be associated with prevention of AD/ADRD and/or increasing brain resilience, as well as other factors that may interact with these modifiable risk factors to influence AD/ADRD progression. ANN NEUROL 2024

Publisher

Wiley

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