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How does apolipoprotein E genotype influence the relationship between physical activity and Alzheimer's disease risk? A novel integrative model
被引:13
|作者:
de Frutos Lucas, Jaisalmer
[1
,2
,3
]
Sewell, Kelsey R.
[4
]
Garcia-Colomo, Alejandra
[1
]
Markovic, Shaun
[4
,5
]
Erickson, Kirk I.
[6
,7
,8
]
Brown, Belinda M.
[2
,4
,5
,9
]
机构:
[1] Univ Complutense Madrid, Sch Psychol, Expt Psychol Cognit Proc & Logopedia Dept, Pozuelo De Alarcon 28223, Spain
[2] Edith Cowan Univ, Ctr Precis Hlth, Joondalup, WA 6027, Australia
[3] Univ Antonio Nebrija, Dept Psicol, Fac Ciencias Vida & Nat, Madrid 28015, Spain
[4] Murdoch Univ, Hlth Futures Inst, Ctr Hlth Ageing, Murdoch, WA 6150, Australia
[5] Australian Alzheimers Res Fdn, Sarich Neurosci Res Inst, Nedlands, WA 6009, Australia
[6] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15260 USA
[7] Univ Granada, Sport & Hlth Univ Res Inst iMUDS, PROFITH PROmoting FITness & Hlth Phys Act Res Grp, Dept Phys & Sports Educ,Fac Sport Sci, E-18071 Granada, Spain
[8] AdventHlth Res Inst, Orlando, FL 32804 USA
[9] Edith Cowan Univ, Sch Med & Hlth Sci, Joondalup, WA 6027, Australia
关键词:
APOE epsilon 4;
Alzheimer's disease;
Physical activity;
Amyloid pathology;
Tau pathology;
Cerebrovascular health;
Neurotrophic factors;
Neuroinflammation;
Glucose metabolism;
Mitochondrial dysfunction;
APP/PS1 MOUSE MODEL;
HUMAN APOE ISOFORMS;
GROWTH-FACTOR-I;
AMYLOID-BETA;
A-BETA;
NEUROTROPHIC FACTOR;
TREADMILL EXERCISE;
RESISTANCE EXERCISE;
GLUCOSE-METABOLISM;
BDNF LEVELS;
D O I:
10.1186/s13195-023-01170-4
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background Wide evidence suggests that physical activity (PA) confers protection against Alzheimer's disease (AD). On the other hand, the apolipoprotein E gene (APOE) epsilon 4 allele represents the greatest genetic risk factor for developing AD. Extensive research has been conducted to determine whether frequent PA can mitigate the increased AD risk associated with APOE epsilon 4. However, thus far, these attempts have produced inconclusive results. In this context, one possible explanation could be that the influence of the combined effect of PA and APOE epsilon 4 carriage might be dependent on the specific outcome measure utilised. Main body. In order to bridge these discrepancies, the aim of this theoretical article is to propose a novel model on the interactive effects of PA and APOE epsilon 4 carriage on well-established mechanisms underlying AD. Available literature was searched to investigate how PA and APOE epsilon 4 carriage, independently and in combination, may alter several molecular pathways involved in AD pathogenesis. The reviewed mechanisms include amyloid beta (A beta) and tau deposition and clearance, neuronal resilience and neurogenesis, lipid function and cerebrovascular alterations, brain immune response and glucose metabolism. Finally, combining all this information, we have built an integrative model, which includes evidence-based and theoretical synergistic interactions across mechanisms. Moreover, we have identified key knowledge gaps in the literature, providing a list of testable hypotheses that future studies need to address. ConclusionsWe conclude that PA influences a wide array of molecular targets involved in AD neuropathology. A deeper understanding of where, when and, most importantly, how PA decreases AD risk even in the presence of the APOE epsilon 4 allele will enable the creation of new protocols using exercise along pharmaceuticals in combined therapeutic approaches.
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页数:16
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