How Do Modifiable Risk Factors Affect Alzheimer's Disease Pathology or Mitigate Its Effect on Clinical Symptom Expression?

被引:4
|
作者
Ourry, Valentin [1 ,2 ]
Binette, Alexa Pichet [1 ,2 ,3 ]
St-Onge, Frederic [1 ,2 ,4 ]
Strikwerda-Brown, Cherie [1 ,2 ,5 ]
Chagnot, Audrey [6 ,7 ]
Poirier, Judes [1 ,2 ]
Breitner, John [1 ,2 ]
Arenaza-Urquijo, Eider M. [8 ,9 ]
Rabin, Jennifer S. [10 ,11 ,12 ]
Buckley, Rachel [13 ,14 ,15 ,16 ]
Gonneaud, Julie [17 ]
Marchant, Natalie L. [18 ]
Villeneuve, Sylvia [1 ,2 ,19 ]
机构
[1] McGill Univ, Fac Med, Dept Psychiat, Montreal, PQ, Canada
[2] Douglas Mental Hlth Univ Inst, Montreal, PQ, Canada
[3] Lund Univ, Dept Clin Sci, Clin Memory Res Unit, Malmo, Sweden
[4] McGill Univ, Fac Med, Integrated Program Neurosci, Montreal, PQ, Canada
[5] Univ Western Australia, Sch Psychol Sci, Perth, WA, Australia
[6] Univ Edinburgh, UK Dementia Res Inst, Edinburgh Med Sch, Edinburgh, Scotland
[7] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh, Scotland
[8] Barcelona Inst Global Hlth ISGlobal, Environm & Hlth Lifecourse Programme, Barcelona, Spain
[9] Mayo Clin, Dept Radiol, Rochester, MN USA
[10] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Med, Div Neurol, Toronto, ON, Canada
[11] Univ Toronto, Sunnybrook Res Inst, Harquail Ctr Neuromodulat, Hurvitz Brain Sci Program, Toronto, ON, Canada
[12] Univ Toronto, Rehabil Sci Inst, Toronto, ON, Canada
[13] Univ Melbourne, Melbourne Sch Psychol Sci, Parkville, Vic, Australia
[14] Massachusetts Gen Hosp, Dept Neurol, Boston, MA USA
[15] Harvard Med Sch, Boston, MA USA
[16] Brigham & Womens Hosp, Ctr Alzheimer Res & Treatment, Dept Neurol, Boston, MA USA
[17] Normandie Univ, Inst Blood & Brain Caen Normandie, UNICAEN, INSERM,U1237,GIP Cyceron,PhIND Physiopathol & Imag, Caen, France
[18] UCL, Div Psychiat, London, England
[19] McGill Univ, Montreal Neurol Inst, McConnell BrainImaging Ctr, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
POSITRON-EMISSION-TOMOGRAPHY; FUNCTIONAL BRAIN CONNECTIVITY; BETA-AMYLOID ACCUMULATION; APOLIPOPROTEIN-E GENOTYPE; PITTSBURGH COMPOUND-B; LIFE-STYLE ACTIVITIES; NORMAL OLDER-ADULTS; COGNITIVE DECLINE; DEPRESSIVE SYMPTOMS; PHYSICAL-ACTIVITY;
D O I
10.1016/j.biopsych.2023.09.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:1006 / 1019
页数:14
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