Exercise and Alzheimer’s disease biomarkers in cognitively normal older adults

The Clinical Dementia Rating (CDR): Current version and scoring rules

Morris, J. C. (1993) · Neurology · doi:10.1212/wnl.43.11.2412-a · Cited by 9,882 · see citing works

Compendium of physical activities: an update of activity codes and MET intensities

AINSWORTH, B. E., HASKELL, W. L., WHITT, M. C., IRWIN, M. L., SWARTZ, A. M., STRATH, S. J., O???BRIEN, W. L., BASSETT, D. R., SCHMITZ, K. H., EMPLAINCOURT, P. O., et al. (2000) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200009001-00009 · Cited by 8,497 · see citing works

Physical Activity and Public Health: Updated Recommendation for Adults From the American College of Sports Medicine and the American Heart Association

(2007) · Circulation · doi:10.1161/circulationaha.107.185649 · Cited by 6,545 · see citing works

Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound‐B

Klunk, W. E., Engler, H., Nordberg, A., Wang, Y., Blomqvist, G., Holt, D. P., Bergström, M., Savitcheva, I., Huang, G., Estrada, S., et al. (2004) · Annals of Neurology · doi:10.1002/ana.20009 · Cited by 4,496 · see citing works

Be smart, exercise your heart: Exercise effects on brain and cognition

Hillman, C. H., Erickson, K. I., & Kramer, A. F. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2298 · Cited by 3,563 · see citing works

Physical Activity and Public Health in Older Adults

Nelson, M. E., Rejeski, W. J., Blair, S. N., Duncan, P. W., Judge, J. O., King, A. C., Macera, C. A., & Castaneda‐Sceppa, C. (2007) · Circulation · doi:10.1161/circulationaha.107.185650 · Cited by 2,991 · see citing works

Aerobic Exercise Training Increases Brain Volume in Aging Humans

Colcombe, S. J., Erickson, K. I., Scalf, P. E., Kim, J. S., Prakash, R., McAuley, E., Elavsky, S., Marquez, D. X., Hu, L., & Kramer, A. F. (2006) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/61.11.1166 · Cited by 2,134 · see citing works

Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid Aβ ₄₂ in humans

Fagan, A. M., Mintun, M. A., Mach, R. H., Lee, S., Dence, C. S., Shah, A. R., LaRossa, G. N., Spinner, M. L., Klunk, W. E., Mathis, C. A., et al. (2006) · Annals of Neurology · doi:10.1002/ana.20730 · Cited by 1,246 · see citing works

Leisure-time physical activity at midlife and the risk of dementia and Alzheimer's disease

Rovio, S., Kåreholt, I., Helkala, E.-L., Viitanen, M., Winblad, B., Tuomilehto, J., Soininen, H., Nissinen, A., & Kivipelto, M. (2005) · The Lancet Neurology · doi:10.1016/s1474-4422(05)70198-8 · Cited by 1,054 · see citing works

[ ¹¹ C]PIB in a nondemented population: Potential antecedent marker of Alzheimer disease

Mintun, M. A., LaRossa, G. N., Sheline, Y. I., Dence, C. S., Lee, S. Y., Mach, R. H., Klunk, W. E., Mathis, C. A., DeKosky, S. T., & Morris, J. C. (2006) · Neurology · doi:10.1212/01.wnl.0000228230.26044.a4 · Cited by 1,036 · see citing works

Cerebrospinal Fluid tau/β-Amyloid42 Ratio as a Prediction of Cognitive Decline in Nondemented Older Adults

Fagan, A. M., Roe, C. M., Xiong, C., Mintun, M. A., Morris, J. C., & Holtzman, D. M. (2007) · Archives of Neurology · doi:10.1001/archneur.64.3.noc60123 · Cited by 897 · see citing works

Environmental Enrichment Reduces Aβ Levels and Amyloid Deposition in Transgenic Mice

Lazarov, O., Robinson, J., Tang, Y.-P., Hairston, I. S., Korade-Mirnics, Z., Lee, V. M.-Y., Hersh, L. B., Sapolsky, R. M., Mirnics, K., & Sisodia, S. S. (2005) · Cell · doi:10.1016/j.cell.2005.01.015 · Cited by 885 · see citing works

<i>APOE</i> predicts amyloid‐beta but not tau Alzheimer pathology in cognitively normal aging

Morris, J. C., Roe, C. M., Xiong, C., Fagan, A. M., Goate, A. M., Holtzman, D. M., & Mintun, M. A. (2010) · Annals of Neurology · doi:10.1002/ana.21843 · Cited by 830 · see citing works

Voluntary Exercise Decreases Amyloid Load in a Transgenic Model of Alzheimer's Disease

Adlard, P. A., Perreau, V. M., Pop, V., & Cotman, C. W. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0496-05.2005 · Cited by 806 · see citing works

Fibrillar amyloid-β burden in cognitively normal people at 3 levels of genetic risk for Alzheimer's disease

Reiman, E. M., Chen, K., Liu, X., Bandy, D., Yu, M., Lee, W., Ayutyanont, N., Keppler, J., Reeder, S. A., Langbaum, J. B. S., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900345106 · Cited by 785 · see citing works

Physical Activity, APOE Genotype, and Dementia Risk: Findings from the Cardiovascular Health Cognition Study

Podewils, L. J. (2005) · American Journal of Epidemiology · doi:10.1093/aje/kwi092 · Cited by 675 · see citing works

Core candidate neurochemical and imaging biomarkers of Alzheimer's disease

Hampel, H. J., Bürger, K., Teipel, S. J., Bokde, A. L. W., Zetterberg, H., & Blennow, K. (2007) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2007.08.006 · Cited by 532 · see citing works

Pathologic Correlates of Nondemented Aging, Mild Cognitive Impairment, and Early-Stage Alzheimer's Disease

Morris, J. C., & Price, J. L. (2001) · Journal of Molecular Neuroscience · doi:10.1385/jmn:17:2:101 · Cited by 513 · see citing works

Simultaneous Measurement of β-Amyloid(1–42), Total Tau, and Phosphorylated Tau (Thr181) in Cerebrospinal Fluid by the xMAP Technology

Olsson, A., Vanderstichele, H., Andreasen, N., Meyer, G. D., Wallin, A., Holmberg, B., Rosengren, L., Vanmechelen, E., & Blennow, K. (2004) · Clinical Chemistry · doi:10.1373/clinchem.2004.039347 · Cited by 424 · see citing works

Cardiorespiratory fitness and brain atrophy in early Alzheimer disease.

Burns, J. M., Cronk, B. B., Anderson, H. S., Donnelly, J. E., Thomas, G. P., Harsha, A., Brooks, W. M., & Swerdlow, R. H. (2008) · Neurology · doi:10.1212/01.wnl.0000317094.86209.cb · Cited by 363 · see citing works

Decreased cerebrospinal fluid Aβ ₄₂ correlates with brain atrophy in cognitively normal elderly

Fagan, A. M., Head, D., Shah, A. R., Marcus, D., Mintun, M., Morris, J. C., & Holtzman, D. M. (2009) · Annals of Neurology · doi:10.1002/ana.21559 · Cited by 327 · see citing works

Neuropathological and Neuropsychological Changes in “Normal” Aging: Evidence for Preclinical Alzheimer Disease in Cognitively Normal Individuals

HULETTE, C. M., WELSH-BOHMER, K. A., MURRAY, M. G., SAUNDERS, A. M., MASH, D. C., & MCINTYRE, L. M. (1998) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199812000-00009 · Cited by 311 · see citing works

Cognitive Decline and Brain Volume Loss as Signatures of Cerebral Amyloid-β Peptide Deposition Identified With Pittsburgh Compound B

Storandt, M., Mintun, M. A., Head, D. M., & Morris, J. C. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.272 · Cited by 304 · see citing works

Cognitive and Physical Activity Differently Modulate Disease Progression in the Amyloid Precursor Protein (APP)-23 Model of Alzheimer’s Disease

Wolf, S. A., Kronenberg, G., Lehmann, K., Blankenship, A., Overall, R., Staufenbiel, M., & Kempermann, G. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.04.004 · Cited by 288 · see citing works

A decade of modeling Alzheimer's disease in transgenic mice

MCGOWAN, E., ERIKSEN, J., & HUTTON, M. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.03.007 · Cited by 287 · see citing works

Longitudinal course and neuropathologic outcomes in original vs revised MCI and in pre-MCI

Storandt, M., Grant, E., Miller, J. P., & Morris, J. C. (2006) · Neurology · doi:10.1212/01.wnl.0000228231.26111.6e · Cited by 285 · see citing works

Environmental Enrichment Exacerbates Amyloid Plaque Formation in a Transgenic Mouse Model of Alzheimer Disease

Jankowsky, J. L., Xu, G. M., Fromholt, D., Gonzales, V., & Borchelt, D. (2003) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/62.12.1220 · Cited by 240 · see citing works

Environmental enrichment improves cognition in aged Alzheimer's transgenic mice despite stable β-amyloid deposition

Arendash, G. W., Garcia, M. F., Costa, D. A., Cracchiolo, J. R., Wefes, I., & Potter, H. (2004) · Neuroreport · doi:10.1097/01.wnr.0000137183.68847.4e · Cited by 237 · see citing works

Exercise moderates age-related atrophy of the medial temporal lobe

Bugg, J. M., & Head, D. M. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.03.008 · Cited by 236 · see citing works

Enrichment improves cognition in AD mice by amyloid-related and unrelated mechanisms

Costa, D. A., Cracchiolo, J. R., Bachstetter, A. D., Hughes, T. F., Bales, K. R., Paul, S. M., Mervis, R. F., Arendash, G. W., & Potter, H. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.04.009 · Cited by 217 · see citing works

Cardiorespiratory Fitness and Preserved Medial Temporal Lobe Volume in Alzheimer Disease

Honea, R. A., Thomas, G., Harsha, A., Anderson, H. S., Donnelly, J. E., Brooks, W. M., & Burns, J. M. (2009) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0b013e31819cb8a2 · Cited by 214 · see citing works

Exercise improves cognition and hippocampal plasticity in <i>APOE</i> ɛ4 mice

Nichol, K., Deeny, S. P., Seif, J., Camaclang, K., & Cotman, C. W. (2009) · Alzheimer's &amp; Dementia · doi:10.1016/j.jalz.2009.02.006 · Cited by 213 · see citing works

Exercise training acts as a therapeutic strategy for reduction of the pathogenic phenotypes for Alzheimer's disease in an NSE/APPsw-transgenic model

Cho, Y. (1998) · International Journal of Molecular Medicine · doi:10.3892/ijmm_00000052 · Cited by 196 · see citing works

Enhanced cognitive activity--over and above social or physical activity--is required to protect Alzheimer's mice against cognitive impairment, reduce Abeta deposition, and increase synaptic immunoreactivity.

Cracchiolo, J. R., Mori, T., Nazian, S., Tan, J., Potter, H., & Arendash, G. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.07.007 · Cited by 161 · see citing works

Drug development for Alzheimer's disease: where are we now and where are we headed?

Sabbagh, M. N. (2009) · ˜The œAmerican journal of geriatric pharmacotherapy · doi:10.1016/j.amjopharm.2009.06.003 · Cited by 147 · see citing works

Physical activity and the maintenance of cognitive function

Rockwood, K. J., & Middleton, L. E. (2007) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2007.01.003 · Cited by 135 · see citing works

Cognitive Performance in Older Women Relative to ApoE-ε4 Genotype and Aerobic Fitness

ETNIER, J. L., CASELLI, R. J., REIMAN, E. M., ALEXANDER, G. E., SIBLEY, B. A., TESSIER, D., & MCLEMORE, E. C. (2007) · Medicine &amp; Science in Sports &amp; Exercise · doi:10.1249/01.mss.0000239399.85955.5e · Cited by 124 · see citing works

CSF phosphorylated tau in the diagnosis and prognosis of mild cognitive impairment and Alzheimer's disease: a meta-analysis of 51 studies

Mitchell, A. J. (2009) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2008.167791 · Cited by 123 · see citing works

Environmental Enrichment Delays the Onset of Memory Deficits and Reduces Neuropathological Hallmarks in a Mouse Model of Alzheimer-Like Neurodegeneration

Berardi, N., Braschi, C., Capsoni, S., Cattaneo, A., & Maffei, L. (2007) · Journal of Alzheimer s Disease · doi:10.3233/jad-2007-11312 · Cited by 110 · see citing works

Exercise, APOE, and working memory: MEG and behavioral evidence for benefit of exercise in epsilon4 carriers

Deeny, S. P., Poeppel, D., Zimmerman, J. B., Roth, S. M., Brandauer, J., Witkowski, S., Hearn, J. W., Ludlow, A. T., Contreras-Vidal, J. L., Brandt, J., et al. (2008) · Biological Psychology · doi:10.1016/j.biopsycho.2008.02.007 · Cited by 107 · see citing works

Repression of tau hyperphosphorylation by chronic endurance exercise in aged transgenic mouse model of tauopathies

Leem, Y., Lim, H., Shim, S., Cho, J., Kim, B., & Han, P. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22075 · Cited by 105 · see citing works

Wheel-running in a transgenic mouse model of Alzheimer's disease: Protection or symptom?

Richter, H., Ambrée, O., Lewejohann, L., Herring, A., Keyvani, K., Paulus, W., Palme, R., Touma, C., Schäbitz, W., & Sachser, N. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.005 · Cited by 102 · see citing works

The impact of voluntary exercise on mental health in rodents: A neuroplasticity perspective

Pietropaolo, S., Sun, Y., Li, R., Brana, C., Feldon, J., & Yee, B. K. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.03.014 · Cited by 99 · see citing works

Construct Validity of Self-reported Historical Physical Activity

Bowles, H. R. (2004) · American Journal of Epidemiology · doi:10.1093/aje/kwh209 · Cited by 96 · see citing works

Use of cerebrospinal fluid biomarkers in diagnosis of dementia across Europe

Hort, J., Bartoš, A., Pirttilä, T., & Scheltens, P. (2009) · European Journal of Neurology · doi:10.1111/j.1468-1331.2009.02753.x · Cited by 73 · see citing works

Influence of Cognitive Status, Age, and APOE-4 Genetic Risk on Brain FDDNP Positron-Emission Tomography Imaging in Persons Without Dementia

Small, G. W., Siddarth, P., Burggren, A. C., Kepe, V., Ercoli, L. M., Miller, K. J., Lavretsky, H., Thompson, P. M., Cole, G. M., Huang, S. C., et al. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2008.516 · Cited by 57 · see citing works

Preclinical Alzheimer’s Disease: Definition, Natural History, and Diagnostic Criteria

Dubois, B., Hampel, H., Feldman, H. H., Scheltens, P., Aisen, P., Andrieu, S., Bakardjian, H., Benali, H., Bertram, L., Blennow, K., et al. (2016) · Alzheimer's &amp; Dementia · doi:10.1016/j.jalz.2016.02.002 · Cited by 1,925 · see citing works

The Pathobiology of Vascular Dementia

Iadecola, C. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.008 · Cited by 1,857 · see citing works

Alzheimer’s Disease: The Challenge of the Second Century

Holtzman, D. M., Morris, J. C., & Goate, A. M. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002369 · Cited by 1,424 · see citing works

Bridging animal and human models of exercise-induced brain plasticity

Voss, M. W., Vivar, C., Kramer, A. F., & van Praag, H. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.08.001 · Cited by 1,030 · see citing works

Physical Exercise as a Preventive or Disease-Modifying Treatment of Dementia and Brain Aging

Ahlskog, J. E., Geda, Y. E., Graff-Radford, N. R., & Petersen, R. C. (2011) · Mayo Clinic Proceedings · doi:10.4065/mcp.2011.0252 · Cited by 885 · see citing works

Sleep Quality and Preclinical Alzheimer Disease

Ju, Y.-E. S., McLeland, J. S., Toedebusch, C. D., Xiong, C., Fagan, A. M., Duntley, S. P., Morris, J. C., & Holtzman, D. M. (2013) · JAMA Neurology · doi:10.1001/jamaneurol.2013.2334 · Cited by 744 · see citing works

Physical exercise in the prevention and treatment of Alzheimer's disease

la Rosa, A. D., González, G. O., Arc‐Chagnaud, C., Millán-Domingo, F., Salvador‐Pascual, A., García-Lucerga, C., Blasco-Lafarga, C., García-Domínguez, E., Carretero, A., Correas, Á. G., et al. (2020) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2020.01.004 · Cited by 617 · see citing works

Exergaming and Older Adult Cognition

Anderson-Hanley, C., Arciero, P. J., Brickman, A. M., Nimon, J. P., Okuma, N., Westen, S. C., Merz, M. E., Pence, B. D., Woods, J. A., Kramer, A. F., et al. (2012) · American Journal of Preventive Medicine · doi:10.1016/j.amepre.2011.10.016 · Cited by 464 · see citing works

Cognitive Reserve and the Prevention of Dementia: the Role of Physical and Cognitive Activities

Cheng, S.-T. (2016) · Current Psychiatry Reports · doi:10.1007/s11920-016-0721-2 · Cited by 385 · see citing works

Resistance vs resilience to Alzheimer disease

Arenaza‐Urquijo, E. M., & Vemuri, P. (2018) · Neurology · doi:10.1212/wnl.0000000000005303 · Cited by 372 · see citing works

Amyloid imaging in cognitively normal individuals, at-risk populations and preclinical Alzheimer's disease

Chételat, G., Joie, R. L., Villain, N., Perrotin, A., Sayette, V. D. L., Eustache, F., & Vandenberghe, R. R. (2013) · NeuroImage Clinical · doi:10.1016/j.nicl.2013.02.006 · Cited by 353 · see citing works

Association of Lifetime Cognitive Engagement and Low β-Amyloid Deposition

Marks, S. M. (2012) · Archives of Neurology · doi:10.1001/archneurol.2011.2748 · Cited by 342 · see citing works

Exercise benefits on Alzheimer’s disease: State-of-the-science

Valenzuela, P. L., Castillo-García, A., Morales, J. S., de la Villa, P., Hampel, H., Emanuele, E., Lista, S., & Lucia, A. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101108 · Cited by 337 · see citing works

Physical Activity, Brain Plasticity, and Alzheimer's Disease

Erickson, K. I., Weinstein, A. M., & Lopez, O. L. (2012) · Archives of Medical Research · doi:10.1016/j.arcmed.2012.09.008 · Cited by 288 · see citing works

Exercise counteracts declining hippocampal function in aging and Alzheimer's disease

Intlekofer, K. A., & Cotman, C. W. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.06.011 · Cited by 286 · see citing works

Prevention of diseases after menopause

Løbo, R. A., Davis, S. R., de Villiers, T. J., Gompel, A., Henderson, V. W., Hodis, H. N., Lumsden, M.-A., Mack, W. J., Shapiro, S., & Baber, R. (2014) · Climacteric · doi:10.3109/13697137.2014.933411 · Cited by 275 · see citing works

Untitled work

Head (2012) · doi:10.1001/archneurol.2011.845 · Cited by 267 · see citing works

Adaptive responses of neuronal mitochondria to bioenergetic challenges: Roles in neuroplasticity and disease resistance

Raefsky, S. M., & Mattson, M. P. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.045 · Cited by 274 · see citing works

Physical activity and amyloid-β plasma and brain levels: results from the Australian Imaging, Biomarkers and Lifestyle Study of Ageing

Brown, B. M., Peiffer, J. J., Taddei, K., Lui, J. K., Laws, S. M., Gupta, V. B., Taddei, T., Ward, V. K., Rodrigues, M. A., Burnham, S., et al. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.107 · Cited by 235 · see citing works

Multiple effects of physical activity on molecular and cognitive signs of brain aging: can exercise slow neurodegeneration and delay Alzheimer’s disease?

Brown, B. M., Peiffer, J. J., & Martins, R. N. (2012) · Molecular Psychiatry · doi:10.1038/mp.2012.162 · Cited by 228 · see citing works

Physical activity attenuates age-related biomarker alterations in preclinical AD

Okonkwo, O. C., Schultz, S. A., Oh, J. M., Larson, J., Edwards, D. F., Cook, D. B., Koscik, R. L., Gallagher, C. L., Dowling, N. M., Carlsson, C. M., et al. (2014) · Neurology · doi:10.1212/wnl.0000000000000964 · Cited by 227 · see citing works

Lifespan brain activity, β-amyloid, and Alzheimer's disease

Jagust, W. J., & Mormino, E. C. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.09.004 · Cited by 221 · see citing works

Alzheimer's disease: a comprehensive review of epidemiology, risk factors, symptoms diagnosis, management, caregiving, advanced treatments and associated challenges

Safiri, S., Jolfayi, A. G., Fazlollahi, A., Morsali, S., Sarkesh, A., Sorkhabi, A. D., Golabi, B., Aletaha, R., Asghari, K. M., Hamidi, S., et al. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1474043 · Cited by 242 · see citing works

Causes and Patterns of Dementia: An Update in the Era of Redefining Alzheimer's Disease

James, B. D., & Bennett, D. A. (2019) · Annual Review of Public Health · doi:10.1146/annurev-publhealth-040218-043758 · Cited by 200 · see citing works

Exercise-Induced Cognitive Plasticity, Implications for Mild Cognitive Impairment and Alzheimer’s Disease

Foster, P. P., Rosenblatt, K. P., & Kuljiš, R. O. (2011) · Frontiers in Neurology · doi:10.3389/fneur.2011.00028 · Cited by 204 · see citing works

Effect of lifestyle activities on alzheimer disease biomarkers and cognition

Vemuri, P., Lesnick, T. G., Przybelski, S. A., Knopman, D. S., Roberts, R. O., Lowe, V. J., Kantarci, K., Senjem, M. L., Gunter, J. L., Boeve, B. F., et al. (2012) · Annals of Neurology · doi:10.1002/ana.23665 · Cited by 193 · see citing works

Gains in cognition through combined cognitive and physical training: the role of training dosage and severity of neurocognitive disorder

Bamidis, P. D., Fissler, P., Papageorgiou, S. G., Zilidou, V. I., Konstantinidis, E. I., Billis, A. S., Romanopoulou, E. D., Karagianni, M. A., Beratis, I., Tsapanou, A., et al. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00152 · Cited by 186 · see citing works

Mitochondria and Ageing

Leeuwenburgh, C., Pamplona, R., & Sanz, A. (2011) · Journal of Aging Research · doi:10.4061/2011/782946 · Cited by 186 · see citing works

Nutrition and neurodegeneration: epidemiological evidence and challenges for future research

Guyonnet, S., Secher, M., & Vellas, B. J. (2013) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.12058 · Cited by 187 · see citing works

Relationships between sleep quality and brain volume, metabolism, and amyloid deposition in late adulthood

Branger, P., Arenaza-Urquijo, E. M., Tomadesso, C., Mézenge, F., André, C., de Flores, R., Mutlu, J., de La Sayette, V., Eustache, F., Chételat, G., et al. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.02.009 · Cited by 186 · see citing works

PET amyloid-beta imaging in preclinical Alzheimer's disease

Vlassenko, A. G., Benzinger, T. L. S., & Morris, J. C. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.11.005 · Cited by 173 · see citing works

Type 2 Diabetes, Cognition, and Dementia in Older Adults: Toward a Precision Health Approach

Cholerton, B., Baker, L. D., Montine, T. J., & Craft, S. (2016) · Diabetes Spectrum · doi:10.2337/ds16-0041 · Cited by 171 · see citing works

Therapeutic approaches targeting Apolipoprotein E function in Alzheimer’s disease

Williams, T., Borchelt, D., & Chakrabarty, P. (2020) · Molecular Neurodegeneration · doi:10.1186/s13024-020-0358-9 · Cited by 166 · see citing works

Cognitive and behavioural effects of physical exercise in psychiatric patients

Knöchel, C., Oertel‐Knöchel, V., O’Dwyer, L., Prvulovic, D., Alves, G. S., Kollmann, B., & Hampel, H. J. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.11.007 · Cited by 164 · see citing works

Cognitive reserve and lifestyle: moving towards preclinical Alzheimer’s disease

Arenaza-Urquijo, E., Wirth, M., & Chételat, G. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00134 · Cited by 153 · see citing works

Insulin resistance and pathological brain ageing

Cholerton, B., Baker, L. D., & Craft, S. (2011) · Diabetic Medicine · doi:10.1111/j.1464-5491.2011.03464.x · Cited by 160 · see citing works

Distinctive Effects of Aerobic and Resistance Exercise Modes on Neurocognitive and Biochemical Changes in Individuals with Mild Cognitive Impairment

Tsai, C., Pai, M., Ukropec, J., & Ukropcová, B. (2019) · Current Alzheimer Research · doi:10.2174/1567205016666190228125429 · Cited by 160 · see citing works

Insulin and Alzheimer's Disease: Untangling the Web

Craft, S., Cholerton, B., & Baker, L. D. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2012-129042 · Cited by 157 · see citing works

Associations of Physical Activity and β-Amyloid With Longitudinal Cognition and Neurodegeneration in Clinically Normal Older Adults

Rabin, J. S., Klein, H., Kirn, D. R., Schultz, A. P., Yang, H., Hampton, O. L., Jiang, S., Buckley, R. F., Viswanathan, A., Hedden, T., et al. (2019) · JAMA Neurology · doi:10.1001/jamaneurol.2019.1879 · Cited by 155 · see citing works

A review of cardiorespiratory fitness-related neuroplasticity in the aging brain

Hayes, S. M., Hayes, J. P., Cadden, M., & Verfaellie, M. (2013) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2013.00031 · Cited by 154 · see citing works

Running exercise delays neurodegeneration in amygdala and hippocampus of Alzheimer’s disease (APP/PS1) transgenic mice

Lin, T.-W., Shih, Y.-H., Chen, S.-J., Lien, C.-H., Chang, C.-Y., Huang, T.-Y., Chen, S.-H., Jen, C. J., & Kuo, Y.-M. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.12.005 · Cited by 153 · see citing works

Physical Exercise in the Oldest Old

Valenzuela, P. L., Castillo‐García, A., Morales, J. S., Izquierdo, M., Serra‐Rexach, J. A., Santos‐Lozano, A., & Lucia, A. (2019) · Comprehensive Physiology · doi:10.1002/cphy.c190002 · Cited by 152 · see citing works

MEDITERRANEAN DIET AND MAGNETIC RESONANCE IMAGING-ASSESSED BRAIN ATROPHY IN COGNITIVELY NORMAL INDIVIDUALS AT RISK FOR ALZHEIMER’S DISEASE

Mosconi, L., Murray, J., Tsui, W. H., Li, Y., Davies, M., Williams, S., Pirraglia, E., Spector, N. C., Osorio, R. S., Glodzik, L., et al. (2014) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2014.17 · Cited by 140 · see citing works

Physical Exercise Enhances Neuroplasticity and Delays Alzheimer’s Disease

Lin, T.-W., Tsai, S., & Kuo, Y. (2018) · Brain Plasticity · doi:10.3233/bpl-180073 · Cited by 146 · see citing works

Intense physical activity is associated with cognitive performance in the elderly

Brown, B. M., Peiffer, J. J., Sohrabi, H. R., Mondal, A., Gupta, V. B., Rainey‐Smith, S. R., Taddei, K., Burnham, S. C., Ellis, K. A., Szoeke, C. E. I., et al. (2012) · Translational Psychiatry · doi:10.1038/tp.2012.118 · Cited by 136 · see citing works

The brain-derived neurotrophic factor val66met polymorphism moderates an effect of physical activity on working memory performance

Erickson, K. I., Banducci, S. E., Weinstein, A. M., MacDonald, A. W., Ferrell, R. E., Halder, I., Flory, J. D., & Manuck, S. B. (2013) · Psychological Science · doi:10.1177/0956797613480367 · Cited by 134 · see citing works

Gene-Environment Interactions: Lifetime Cognitive Activity, APOE Genotype, and Beta-Amyloid Burden

Wirth, M., Villeneuve, S., Joie, R. L., Marks, S. M., & Jagust, W. J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4612-13.2014 · Cited by 131 · see citing works

Exercise Intervention Associated with Cognitive Improvement in Alzheimer’s Disease

Cui, M. Y., Lin, Y., Sheng, J. Y., Zhang, X., & Cui, R. (2018) · Neural Plasticity · doi:10.1155/2018/9234105 · Cited by 128 · see citing works

Neuroprotective pathways: lifestyle activity, brain pathology, and cognition in cognitively normal older adults

Wirth, M., Haase, C. M., Villeneuve, S., Vogel, J. W., & Jagust, W. J. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.02.015 · Cited by 127 · see citing works

Exploring the relationship between physical activity, beta-amyloid and tau: A narrative review

Brown, B. M., Peiffer, J. J., & Rainey‐Smith, S. R. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.01.003 · Cited by 125 · see citing works

Oxidative Stress Is a Central Target for Physical Exercise Neuroprotection Against Pathological Brain Aging

García‐Mesa, Y., Colié, S., Corpas, R., Cristòfol, R. M., Comellas, F., Nebreda, Á. R., Giménez‐Llort, L., & Sanfeliu, C. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv005 · Cited by 124 · see citing works

Volumetric Feature-Based Alzheimer’s Disease Diagnosis From sMRI Data Using a Convolutional Neural Network and a Deep Neural Network

Basher, A., Kim, B. C., Lee, K. H., & Jung, H. Y. (2021) · IEEE Access · doi:10.1109/access.2021.3059658 · Cited by 122 · see citing works

Molecular Mechanisms Underlying the Beneficial Effects of Exercise on Brain Function and Neurological Disorders

Nay, K., Smiles, W. J., Kaiser, J., McAloon, L. M., Loh, K., Galić, S., Oakhill, J. S., Gundlach, A. L., & Scott, J. W. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084052 · Cited by 108 · see citing works

Cardiorespiratory fitness is associated with atrophy in Alzheimer's and aging over 2 years

Vidoni, E. D., Honea, R. A., Billinger, S. A., Swerdlow, R. H., & Burns, J. M. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.03.016 · Cited by 105 · see citing works

Effect of Early Adult Patterns of Physical Activity and Television Viewing on Midlife Cognitive Function

Hoang, T. D. M., Reis, J. P., Zhu, N., Jacobs, D. R., Launer, L. J., Whitmer, R. A., Sidney, S. S., & Yaffe, K. S. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.2468 · Cited by 99 · see citing works

Association between educational attainment and amyloid deposition across the spectrum from normal cognition to dementia: neuroimaging evidence for protection and compensation

Arenaza‐Urquijo, E. M., Bejanin, A., Gonneaud, J., Wirth, M., Joie, R. L., Mutlu, J., Gaubert, M., Landeau, B., Sayette, V. D. L., Eustache, F., et al. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.06.016 · Cited by 94 · see citing works

Neuroprotective Effects of Exercise Treatments after Injury: The Dual Role of Neurotrophic Factors

Cobianchi, S., Arbat-Plana, A., Lopez-Alvarez, V. M., & Navarro, X. (2017) · Current Neuropharmacology · doi:10.2174/1570159x14666160330105132 · Cited by 94 · see citing works

Effect of aerobic exercise on amyloid accumulation in preclinical Alzheimer’s: A 1-year randomized controlled trial

Vidoni, E. D., Morris, J. K., Watts, A. S., Perry, M., Clutton, J., Sciver, A. R. V., Kamat, A., Mahnken, J. D., Hunt, S. L., Townley, R. A., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0244893 · Cited by 94 · see citing works

3xTgAD mice exhibit altered behavior and elevated Aβ after chronic mild social stress

Rothman, S. M., Herdener, N. D., Camandola, S., Texel, S. J., Mughal, M. R., Cong, W., Martin, B., & Mattson, M. P. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.07.005 · Cited by 95 · see citing works

Preventive effects of regular physical exercise against cognitive decline and the risk of dementia with age advancement

Paillard, T. (2015) · Sports Medicine - Open · doi:10.1186/s40798-015-0016-x · Cited by 90 · see citing works

Moderate intensity physical activity associates with CSF biomarkers in a cohort at risk for Alzheimer's disease

Law, L. L., Rol, R. N., Schultz, S. A., Dougherty, R. J., Edwards, D. F., Koscik, R. L., Gallagher, C. L., Carlsson, C. M., Bendlin, B. B., Zetterberg, H., et al. (2018) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1016/j.dadm.2018.01.001 · Cited by 88 · see citing works

Exercise Training in Amnestic Mild Cognitive Impairment: A One-Year Randomized Controlled Trial

Tarumi, T., Rossetti, H. C., Thomas, B. P., Harris, T. S., Tseng, B. Y., Turner, M., Wang, C., German, Z., Martin‐Cook, K., Stowe, A. M., et al. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-181175 · Cited by 87 · see citing works

The long-term association between physical activity and risk of dementia in the community: the Hisayama Study

Kishimoto, H., Ohara, T., Hata, J., Ninomiya, T., Yoshida, D., Mukai, N., Nagata, M., Ikeda, F., Fukuhara, M., Kumagai, S., et al. (2016) · European Journal of Epidemiology · doi:10.1007/s10654-016-0125-y · Cited by 87 · see citing works

Effects of physical exercise on Alzheimer's disease biomarkers: a systematic review of intervention studies

Frederiksen, K. S., Gjerum, L., Waldemar, G., & Hasselbalch, S. G. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170567 · Cited by 86 · see citing works

Motoric Cognitive Risk Syndrome: Prevalence and Risk Factors in Japanese Seniors

Doi, T., Verghese, J., Shimada, H., Makizako, H., Tsutsumimoto, K., Hotta, R., Nakakubo, S., & Suzuki, T. (2015) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2015.09.003 · Cited by 86 · see citing works

The early contribution of cerebrovascular factors to the pathogenesis of Alzheimer’s disease

Pimentel‐Coelho, P. M., & Rivest, S. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08126.x · Cited by 85 · see citing works

Lifestyle and vascular risk effects on MRI-based biomarkers of Alzheimer’s disease: a cross-sectional study of middle-aged adults from the broader New York City area

Mosconi, L., Walters, M., Sterling, J. L., Quinn, C. G., McHugh, P. F., Andrews, R. D., Matthews, D. C., Ganzer, C. A., Osorio, R. S., Isaacson, R., et al. (2018) · BMJ Open · doi:10.1136/bmjopen-2017-019362 · Cited by 82 · see citing works

Impact of Diet and Exercise Interventions on Cognition and Brain Health in Older Adults: A Narrative Review

Key, M. N., & Szabo‐Reed, A. N. (2023) · Nutrients · doi:10.3390/nu15112495 · Cited by 85 · see citing works

Physical Exercise-Induced Myokines in Neurodegenerative Diseases

Lee, B., Shin, M., Park, Y., Won, S.-Y., & Cho, K. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115795 · Cited by 79 · see citing works

Can exercise training teach us how to treat Alzheimer's disease?

Huuha, A. M., Norevik, C. S., Moreira, J. B. N., Kobro-Flatmoen, A., Scrimgeour, N., Kivipelto, M., Van Praag, H., Ziaei, M., Sando, S. B., Wisløff, U., et al. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101559 · Cited by 79 · see citing works

Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's disease

Müller, S., Preische, O., Sohrabi, H. R., Gräber, S., Jucker, M., Ringman, J. M., Martins, R. N., McDade, E., Schofield, P. R., Ghetti, B. F., et al. (2018) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2018.06.3059 · Cited by 77 · see citing works

Cardiorespiratory fitness is associated with white matter integrity in aging

Hayes, S. M., Salat, D. H., Forman, D. E., Sperling, R. A., & Verfaellie, M. (2015) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.204 · Cited by 75 · see citing works

The Link Between Physical Activity and Cognitive Dysfunction in Alzheimer Disease

Phillips, C., Baktir, M. A., Das, D., Lin, B., & Salehi, A. (2015) · Physical Therapy · doi:10.2522/ptj.20140212 · Cited by 74 · see citing works

Voluntary Wheel Running Reverses Age-Induced Changes in Hippocampal Gene Expression

Kohman, R. A., Rodriguez‐Zas, S. L., Southey, B. R., Kelley, K. W., Dantzer, R., & Rhodes, J. S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022654 · Cited by 73 · see citing works

Treadmill Exercise Ameliorates Spatial Learning and Memory Deficits Through Improving the Clearance of Peripheral and Central Amyloid-Beta Levels

Khodadadi, D., Gharakhanlou, R., Naghdi, N., Salimi, M., Azimi, M., Shahed, A., & Heysieattalab, S. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2571-2 · Cited by 71 · see citing works

Obstructive Sleep Apnea and Cognitive Decline: A Review of Potential Vulnerability and Protective Factors

Legault, J., Thompson, C., Martineau‐Dussault, M., André, C., Baril, A., Villar, G. M., Carrier, J., & Gosselin, N. (2021) · Brain Sciences · doi:10.3390/brainsci11060706 · Cited by 74 · see citing works

Association between Lifetime Physical Activity and Cognitive Functioning in Middle-Aged and Older Community Dwelling Adults: Results from the Brain in Motion Study

Gill, S. J., Friedenreich, C. M., Sajobi, T. T., Longman, R. S., Drogos, L. L., Davenport, M. H., Tyndall, A. V., Eskes, G. A., Hogan, D. B., Hill, M. D., et al. (2015) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617715000880 · Cited by 73 · see citing works

Physical Activity, Mediterranean Diet and Biomarkers-Assessed Risk of Alzheimer’s: A Multi-Modality Brain Imaging Study

Matthews, D. C., Davies, M., Murray, J., Williams, S., Tsui, W. H., Li, Y., Andrews, R. D., Lukic, A., McHugh, P. F., Vallabhajosula, S., et al. (2014) · Advances in Molecular Imaging · doi:10.4236/ami.2014.44006 · Cited by 70 · see citing works

Physical activity, body mass index, and brain atrophy in Alzheimer's disease

Boyle, C. P., Raji, C. A., Erickson, K. I., López, O. L., Becker, J. T., Gach, H. M., Longstreth, W. T., Teverovskiy, L., Kuller, L. H., Carmichael, O. T., et al. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.05.036 · Cited by 70 · see citing works

Physical Exercise and Brain Functions in Older Adults

Bherer, L., Erickson, K. I., & Liu-Ambrose, T. Y. L. (2013) · Journal of Aging Research · doi:10.1155/2013/197326 · Cited by 67 · see citing works

Preventive Strategies for Cognitive Decline and Dementia: Benefits of Aerobic Physical Activity, Especially Open-Skill Exercise

Yamasaki, T. (2023) · Brain Sciences · doi:10.3390/brainsci13030521 · Cited by 64 · see citing works

Interaction between years of education and APOE ε4 status on frontal and temporal metabolism

Arenaza‐Urquijo, E. M., Gonneaud, J., Fouquet, M., Perrotin, A., Mézenge, F., Landeau, B., Egret, S., Sayette, V. D. L., Desgranges, B., & Chételat, G. (2015) · Neurology · doi:10.1212/wnl.0000000000002034 · Cited by 64 · see citing works

Cardiorespiratory Fitness Attenuates the Influence of Amyloid on Cognition

Schultz, S. A., Boots, E. A., Almeida, R. P., Oh, J. M., Einerson, J. A., Korcarz, C. E., Edwards, D. F., Koscik, R. L., Dowling, N. M., Gallagher, C. L., et al. (2015) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617715000843 · Cited by 63 · see citing works

Physical activity, inflammation, and volume of the aging brain

Braskie, M. N., Boyle, C. P., Rajagopalan, P., Gutman, B. A., Toga, A. W., Raji, C. A., Tracy, R. P., Kuller, L. H., Becker, J. T., López, O. L., et al. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.05.005 · Cited by 64 · see citing works

Habitual exercise levels are associated with cerebral amyloid load in presymptomatic autosomal dominant Alzheimer's disease

Brown, B. M., Sohrabi, H. R., Taddei, K., Gardener, S. L., Rainey‐Smith, S. R., Peiffer, J. J., Xiong, C., Fagan, A. M., Benzinger, T. L. S., Buckles, V., et al. (2017) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2017.03.008 · Cited by 63 · see citing works

Prevention and Treatment of Alzheimer’s Disease: Biological Mechanisms of Exercise

McGurran, H., Glenn, J. M., Madero, E. N., & Bott, N. T. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-180958 · Cited by 63 · see citing works

The benefits of staying active in old age: Physical activity counteracts the negative influence of PICALM, BIN1, and CLU risk alleles on episodic memory functioning.

Ferencz, B., Laukka, E. J., Welmer, A., Kalpouzos, G., Angleman, S. B., Keller, L., Graff, C., Lövdén, M., & Bäckman, L. (2014) · Psychology and Aging · doi:10.1037/a0035465 · Cited by 60 · see citing works

Role of Sleep Disturbance in the Trajectory of Alzheimer’s Disease

Kang, D. W., Lee, C. U., & Lim, H. K. (2017) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2017.15.2.89 · Cited by 60 · see citing works

Cognitive activity relates to cognitive performance but not to Alzheimer disease biomarkers

Gidicsin, C. M., Maye, J. E., Locascio, J. J., Pepin, L. C., Philiossaint, M., Becker, J. A., Younger, A. P., Dekhtyar, M., Schultz, A. P., Amariglio, R. E., et al. (2015) · Neurology · doi:10.1212/wnl.0000000000001704 · Cited by 56 · see citing works

The Effect of Chair Yoga in Older Adults with Moderate and Severe Alzheimer’s Disease

McCaffrey, R. G., Park, J., Newman, D., & Hagen, D. (2014) · Research in Gerontological Nursing · doi:10.3928/19404921-20140218-01 · Cited by 54 · see citing works

Clinical Application of APOE in Alzheimer's Prevention: A Precision Medicine Approach

Berkowitz, C. L., Mosconi, L., Rahman, A., Scheyer, O., Hristov, H., & Isaacson, R. (2018) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2018.35 · Cited by 53 · see citing works

Physical activity as a modifiable risk factor in preclinical Alzheimer’s disease

Yau, W. W., Kirn, D. R., Rabin, J. S., Properzi, M. J., Schultz, A. P., Shirzadi, Z., Palmgren, K. A., Matos, P., Maa, C., Pruzin, J. J., et al. (2025) · Nature Medicine · doi:10.1038/s41591-025-03955-6 · Cited by 53 · see citing works

High-Intensity Physical Activity Modulates Diet Effects on Cerebrospinal Amyloid-β Levels in Normal Aging and Mild Cognitive Impairment

Baker, L. D., Bayer-Carter, J. L., Skinner, J. S., Montine, T. J., Cholerton, B., Callaghan, M., Leverenz, J. B., Walter, B. K., Tsai, E. C., Postupna, N. O., et al. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-111076 · Cited by 54 · see citing works

Physical Activity in Preventing Alzheimer’s Disease and Cognitive Decline: A Narrative Review

Brini, S., Sohrabi, H. R., Peiffer, J. J., Karrasch, M., Hämäläinen, H., Martins, R. N., & Fairchild, T. J. (2017) · Sports Medicine · doi:10.1007/s40279-017-0787-y · Cited by 53 · see citing works

Neuroinflammation

Mukhara, D., Oh, U., & Neigh, G. N. (2020) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64123-6.00017-5 · Cited by 58 · see citing works

Exercise, Arterial Stiffness, and Cerebral Vascular Function: Potential Impact on Brain Health

Barnes, J. N., Pearson, A. G., Corkery, A. T., Eisenmann, N. A., & Miller, K. B. (2021) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617721000394 · Cited by 54 · see citing works

Self-Reported Physical Activity is Associated with Tau Burden Measured by Positron Emission Tomography

Brown, B. M., Rainey‐Smith, S. R., Doré, V., Peiffer, J. J., Burnham, S. C., Laws, S. M., Taddei, K., Ames, D. J., Masters, C. L., Rowe, C. C., et al. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-170998 · Cited by 52 · see citing works

Neuroimaging in aging and neurologic diseases

Risacher, S. L., & Saykin, A. J. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804766-8.00012-1 · Cited by 54 · see citing works

Active Life for Brain Health: A Narrative Review of the Mechanism Underlying the Protective Effects of Physical Activity on the Brain

Umegaki, H., Sakurai, T., & Arai, H. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.761674 · Cited by 51 · see citing works

The moderating role of exercise on stress-related effects on the hippocampus and memory in later adulthood.

Head, D. M., Singh, T., & Bugg, J. M. (2012) · Neuropsychology · doi:10.1037/a0027108 · Cited by 51 · see citing works

The impact of exercise on blood-based biomarkers of Alzheimer’s disease in cognitively unimpaired older adults

Sewell, K. R., Rainey‐Smith, S. R., Pedrini, S., Peiffer, J. J., Sohrabi, H. R., Taddei, K., Markovic, S. J., Martins, R. N., & Brown, B. M. (2024) · GeroScience · doi:10.1007/s11357-024-01130-2 · Cited by 25 · see citing works

Effects of aerobic exercise on plasma AT(N) biomarkers

Yu, F., Han, S., Salisbury, D. L., Pruzin, J. J., Geda, Y. E., Caselli, R. J., & Li, D. (2023) · Alzheimer s & Dementia · doi:10.1002/alz.060868

Novel Alzheimer’s disease blood‐based biomarkers in exercise trials

Karikari, T. K., Erickson, K. I., & Esteban‐Cornejo, I. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.088042

Physical Exercise and Longitudinal Trajectories in Alzheimer Disease Biomarkers and Cognitive Functioning

Stojanovic, M., Jin, Y., Fagan, A. M., Benzinger, T. L. S., Hassenstab, J. J., Cruchaga, C., Morris, J. C., & Head, D. M. (2020) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0000000000000385 · Cited by 22 · see citing works

Resistance exercise and Alzheimer’s disease blood‐based biomarkers in European cognitively healthy older adults

Esteban‐Cornejo, I. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.088043