TY - JOUR
T1 - How Do Modifiable Risk Factors Affect Alzheimer's Disease Pathology or Mitigate Its Effect on Clinical Symptom Expression?
AU - Ourry, Valentin
AU - Binette, Alexa Pichet
AU - St-Onge, Frédéric
AU - Strikwerda-Brown, Cherie
AU - Chagnot, Audrey
AU - Poirier, Judes
AU - Breitner, John
AU - Arenaza-Urquijo, Eider M.
AU - Rabin, Jennifer S.
AU - Buckley, Rachel
AU - Gonneaud, Julie
AU - Marchant, Natalie L.
AU - Villeneuve, Sylvia
N1 - Funding Information:
This work was supported by the Canadian Institutes of Health Research (to SV) , the Fonds de Recherche du Québec - Santé (to SV, VQ) , and the J.-Louis Lévesque Foundation (to SV) .
Funding Information:
This work was supported by the Canadian Institutes of Health Research (to SV), the Fonds de Recherche du Québec - Santé (to SV, VQ), and the J.-Louis Lévesque Foundation (to SV). We thank Alfonso Fajardo-Valdez, Amélie Metz, Bery Mohammediyan, Claire André, Jonathan Gallego Rudolf, Jordana Remz, Mohammadali Javanray, Ting Qiu, and Yara Yakoub for helpful discussions and feedback during the draft of this review. The authors refer interested readers to the following papers of special interest (articles: 27,57,88,91,111,162,193; reviews: 1,15,40,62,100,117,122,128,129,192,194,195). The authors report no biomedical financial interests or potential conflicts of interest.
Publisher Copyright:
© 2023 Society of Biological Psychiatry
PY - 2024/6/1
Y1 - 2024/6/1
N2 - Epidemiological studies show that modifiable risk factors account for approximately 40% of the population variability in risk of developing dementia, including sporadic Alzheimer's disease (AD). Recent findings suggest that these factors may also modify disease trajectories of people with autosomal-dominant AD. With positron emission tomography imaging, it is now possible to study the disease many years before its clinical onset. Such studies can provide key knowledge regarding pathways for either the prevention of pathology or the postponement of its clinical expression. The former “resistance pathway” suggests that modifiable risk factors could affect amyloid and tau burden decades before the appearance of cognitive impairment. Alternatively, the resilience pathway suggests that modifiable risk factors may mitigate the symptomatic expression of AD pathology on cognition. These pathways are not mutually exclusive and may appear at different disease stages. Here, in a narrative review, we present neuroimaging evidence that supports both pathways in sporadic AD and autosomal-dominant AD. We then propose mechanisms for their protective effect. Among possible mechanisms, we examine neural and vascular mechanisms for the resistance pathway. We also describe brain maintenance and functional compensation as bases for the resilience pathway. Improved mechanistic understanding of both pathways may suggest new interventions.
AB - Epidemiological studies show that modifiable risk factors account for approximately 40% of the population variability in risk of developing dementia, including sporadic Alzheimer's disease (AD). Recent findings suggest that these factors may also modify disease trajectories of people with autosomal-dominant AD. With positron emission tomography imaging, it is now possible to study the disease many years before its clinical onset. Such studies can provide key knowledge regarding pathways for either the prevention of pathology or the postponement of its clinical expression. The former “resistance pathway” suggests that modifiable risk factors could affect amyloid and tau burden decades before the appearance of cognitive impairment. Alternatively, the resilience pathway suggests that modifiable risk factors may mitigate the symptomatic expression of AD pathology on cognition. These pathways are not mutually exclusive and may appear at different disease stages. Here, in a narrative review, we present neuroimaging evidence that supports both pathways in sporadic AD and autosomal-dominant AD. We then propose mechanisms for their protective effect. Among possible mechanisms, we examine neural and vascular mechanisms for the resistance pathway. We also describe brain maintenance and functional compensation as bases for the resilience pathway. Improved mechanistic understanding of both pathways may suggest new interventions.
KW - Alzheimer disease
KW - Amyloid
KW - Modifiable risk factors
KW - Positron emission tomography
KW - Prevention
KW - Tau
UR - http://www.scopus.com/inward/record.url?scp=85177032226&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2023.09.003
DO - 10.1016/j.biopsych.2023.09.003
M3 - Review article
C2 - 37689129
AN - SCOPUS:85177032226
SN - 0006-3223
VL - 95
SP - 1006
EP - 1019
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 11
ER -