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Circadian Rest-Activity Pattern Changes in Aging and Preclinical Alzheimer Disease
Open accessAbstract
Importance: Circadian rhythm disturbances occur in symptomatic Alzheimer disease (AD) and have been hypothesized to contribute to disease pathogenesis. However, it is unknown whether circadian changes occur during the presymptomatic phase of the disease. Objective: To examine the associations between circadian function, aging, and preclinical AD pathology in cognitively normal adults. Design, Setting, and Participants: This cross-sectional study was conducted using community volunteers from the Knight Alzheimer's Disease Research Center at Washington University in St Louis. Cognitively normal participants (n = 205) underwent 7 to 14 days of actigraphy in their home environment between 2010 and 2012, in addition to clinical assessment, amyloid imaging with Pittsburgh Compound B (PiB), and cerebrospinal fluid biomarker collection. Data collected from 3 years before to 6 months after actigraphy were included. Sixteen participants were excluded owing to incomplete data collection. Main Outcomes and Measures: Circadian rhythm analysis was performed on actigraphy data using 3 methods: cosinor, nonparametric, and empirical mode decomposition. Preclinical AD was assessed by longitudinal clinical assessment, amyloid imaging with PiB, and cerebrospinal fluid biomarker collection. Results: Data from 189 participants were included in the analyses. The mean (SD) age was 66.6 (8.3) years, and 121 participants (64%) were women. Older age (β = .247; P = .003) and male sex (β = .170; P = .04), in the absence of amyloid pathology, were associated with a significant increase in intradaily variability, a nonparametric measure of rest-activity rhythm fragmentation, as well as decreased amplitude by several measures. After correction for age and sex, the presence of preclinical amyloid plaque pathology, assessed by positive PiB imaging (mean [SD], 0.804 [0.187] for PiB negative vs 0.875 [0.178] for PiB positive; P = .05) or increasing cerebrospinal fluid phosphorylated-tau to amyloid β 42 ratio (β = .231; P = .008), was associated with increased intradaily variability, indicating rest-activity rhythm fragmentation. Conclusions and Relevance: Preclinical AD is associated with rest-activity rhythm fragmentation, independent of age or sex. Aging was also associated with circadian dysfunction independently of preclinical AD pathology, particularly in men. The presence of circadian rhythm abnormalities in the preclinical phase of AD suggests that circadian dysfunction could contribute to early disease pathogenesis or serve as a biomarker of preclinical disease.
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“There is also some evidence of an association of Aβ accumulation with disruption of the circadian rhythm and sleep pattern in cognitively normal adults.(321)”
From Dementia prevention, intervention, and care: 2024 report of the Lancet standing Commission (2024) · cites this paper as [321]
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Citations
Cites
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
Self-citationSperling, R. A., Aisen, P. S., Beckett, L. A., Bennett, D. A., Craft, S., Fagan, A. M., Iwatsubo, T., Jack, C. R., Kaye, J., Montine, T. J., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.003 · Cited by 7,155
Hypothetical model of dynamic biomarkers of the Alzheimer's pathological cascade
Jack, C. R., Knopman, D. S., Jagust, W. J., Shaw, L. M., Aisen, P. S., Weiner, M. W., Petersen, R. C., & Trojanowski, J. Q. (2010) · The Lancet Neurology · doi:10.1016/s1474-4422(09)70299-6 · Cited by 4,806
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
Villemagne, V. L., Burnham, S., Bourgeat, P., Brown, B., Ellis, K. A., Salvado, O., Szoeke, C., Macaulay, S. L., Martins, R., Maruff, P., et al. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70044-9 · Cited by 2,279
Central and Peripheral Circadian Clocks in Mammals
Mohawk, J. A., Green, C. B., & Takahashi, J. S. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153128 · Cited by 2,265
Circadian integration of metabolism and energetics
Bass, J., & Takahashi, J. S. (2010) · Science · doi:10.1126/science.1195027 · Cited by 1,910
Prevalence of Cerebral Amyloid Pathology in Persons Without Dementia: A Meta-analysis
Jansen, W. J., Ossenkoppele, R., Knol, D. L., Tijms, B. M., Scheltens, P., Verhey, F. R. J., Visser, P. J., Aalten, P., Aarsland, D., Alcolea, D., et al. (2015) · JAMA · doi:10.1001/jama.2015.4668 · Cited by 1,610
Self-citationAmyloid-β Dynamics Are Regulated by Orexin and the Sleep-Wake Cycle
Kang, J.-E., Lim, M. M., Bateman, R. J., Lee, J. J., Smyth, L. P., Cirrito, J. R., Fujiki, N., Nishino, S., & Holtzman, D. M. (2009) · Science · doi:10.1126/science.1180962 · Cited by 1,565
Self-citationSleep and Alzheimer disease pathology--a bidirectional relationship
Ju, Y.-E. S., Lucey, B. P., & Holtzman, D. M. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2013.269 · Cited by 996
Self-citationPost-mortem correlates of in vivo PiB-PET amyloid imaging in a typical case of Alzheimer's disease
Ikonomovic, M. D., Klunk, W. E., Abrahamson, E. E., Mathis, C. A., Price, J. C., Tsopelas, N. D., Lopresti, B. J., Ziolko, S., Bi, W., Paljug, W. R., et al. (2008) · Brain · doi:10.1093/brain/awn016 · Cited by 933
Night Shift Work, Light at Night, and Risk of Breast Cancer
Davis, S., Mirick, D. K., & Stevens, R. G. (2001) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/93.20.1557 · Cited by 930
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
Self-citationTapiola, T., Alafuzoff, I., Herukka, S.-K., Parkkinen, L., Hartikainen, P., Soininen, H., & Pirttilä, T. (2009) · Archives of Neurology · doi:10.1001/archneurol.2008.596 · Cited by 896
Mechanisms linking circadian clocks, sleep, and neurodegeneration
Musiek, E. S., & Holtzman, D. M. (2016) · Science · doi:10.1126/science.aah4968 · Cited by 878
Self-citationLim, A. S. P., Kowgier, M., Yu, L., Buchman, A. S., & Bennett, D. A. (2013) · Sleep · doi:10.5665/sleep.2802 · Cited by 793
Aton, S. J., Colwell, C. S., Harmar, A. J., Waschek, J. A., & Herzog, E. D. (2005) · Nature Neuroscience · doi:10.1038/nn1419 · Cited by 767
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
Self-citationMultimodal techniques for diagnosis and prognosis of Alzheimer's disease
Perrin, R. J., Fagan, A. M., & Holtzman, D. M. (2009) · Nature · doi:10.1038/nature08538 · Cited by 702
Self-citationNeuropathology of nondemented aging: presumptive evidence for preclinical Alzheimer disease
Price, J. L., McKeel, D. W., Buckles, V. D., Roe, C. M., Xiong, C., Grundman, M., Hansen, L. A., Petersen, R. C., Parisi, J. E., Dickson, D. W., et al. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.04.002 · Cited by 661
Self-citationAlterations in the circadian rest-activity rhythm in aging and Alzheimer's disease
Witting, W., Kwa, I. H., Eikelenboom, P., Mirmiran, M., & Swaab, D. F. (1990) · Biological Psychiatry · doi:10.1016/0006-3223(90)90523-5 · Cited by 621
Someren, E. J. W. V., Swaab, D. F., Colenda, C. C., Cohen, W., McCall, W. V., & Rosenquist, P. B. (1999) · Chronobiology International · doi:10.3109/07420529908998724 · Cited by 616
SIRT1 Mediates Central Circadian Control in the SCN by a Mechanism that Decays with Aging
Chang, H.-C., & Guarente, L. (2013) · Cell · doi:10.1016/j.cell.2013.05.027 · Cited by 615
Slow wave sleep disruption increases cerebrospinal fluid amyloid-β levels
Ju, Y.-E. S., Ooms, S. J., Sutphen, C., Macauley, S. L., Zangrilli, M. A., Jerome, G., Fagan, A. M., Mignot, E., Zempel, J. M., Claassen, J. A. H. R., et al. (2017) · Brain · doi:10.1093/brain/awx148 · Cited by 604
Self-citationPreclinical Alzheimer's disease and its outcome: a longitudinal cohort study
Vos, S. J., Xiong, C., Visser, P. J., Jasielec, M. S., Hassenstab, J., Grant, E. A., Cairns, N. J., Morris, J. C., Holtzman, D. M., & Fagan, A. M. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70194-7 · Cited by 564 · cited 1×
“Cerebrospinal fluid was obtained by fasted lumbar puncture at 8AM andprocessed aspreviouslydescribed.(38) Cerebrospinal fluid amyloid β 42 (Aβ42) and phosphorylated tau181 (pTau) were measured by the Alzheimer Disease ResearchCenter Biomarker Coreusing enzyme-linked immunosorbant assay (INNOTEST; Innogenetics) in 155…”
MethodSelf-citationDisruption of circadian clocks has ramifications for metabolism, brain, and behavior
Karatsoreos, I. N., Bhagat, S., Bloss, E. B., Morrison, J. H., & McEwen, B. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018375108 · Cited by 547
Tranah, G. J., Blackwell, T., Stone, K. L., Ancoli‐Israel, S., Paudel, M. L., Ensrud, K. E., Cauley, J. A., Redline, S., Hillier, T. A., Cummings, S. R., et al. (2011) · Annals of Neurology · doi:10.1002/ana.22468 · Cited by 525
Circadian clock proteins regulate neuronal redox homeostasis and neurodegeneration
Musiek, E. S., Lim, M. M., Yang, G., Bauer, A. Q., Qi, L., Lee, Y., Roh, J. H., Ortiz-Gonzalez, X., Dearborn, J. T., Culver, J. P., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci70317 · Cited by 524
Self-citationAssociation Between Rotating Night Shift Work and Risk of Coronary Heart Disease Among Women
Vetter, C., Devore, E. E., Wegrzyn, L. R., Massa, J., Speizer, F. E., Kawachi, I., Rosner, B., Stampfer, M. J., & Schernhammer, E. S. (2016) · JAMA · doi:10.1001/jama.2016.4454 · Cited by 517
Peter‐Derex, L., Yammine, P., Bastuji, H., & Croisile, B. (2014) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2014.03.007 · Cited by 489
Ooms, S., Overeem, S., Besse, K., Rikkert, M. O., Verbeek, M., & Claassen, J. A. H. R. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2014.1173 · Cited by 438
On the computational complexity of the empirical mode decomposition algorithm
Wang, Y.-H., Yeh, C.-H., Young, H.-W. V., Hu, K., & Lo, M. (2014) · Physica A Statistical Mechanics and its Applications · doi:10.1016/j.physa.2014.01.020 · Cited by 417
Melanopsin retinal ganglion cell loss in A lzheimer disease
Morgia, C. L., Ross‐Cisneros, F. N., Koronyo, Y., Hannibal, J., Gallassi, R., Cantalupo, G., Sambati, L., Pan, B. X., Tozer, K. R., Barboni, P., et al. (2015) · Annals of Neurology · doi:10.1002/ana.24548 · Cited by 400
Age-Related Decline in Circadian Output
Nakamura, T. J., Nakamura, W., Yamazaki, S., Kudo, T., Cutler, T., Colwell, C. S., & Block, G. D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0451-11.2011 · Cited by 386
Sundowning and Circadian Rhythms in Alzheimer’s Disease
Volicer, L., Harper, D. G., Manning, B. C., Goldstein, R., & Satlin, A. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.5.704 · Cited by 382
Changes in the Sleep and Waking EEGs of Nondemented and Demented Elderly Subjects
Prinz, P. N., Peskind, E. R., VITALIANO, P. P., Raskind, M. A., Eisdorfer, C., ZEMCUZNIKOV, H. N., & Gerber, C. J. (1982) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1982.tb01279.x · Cited by 367
Hatfield, C. F. (2004) · Brain · doi:10.1093/brain/awh129 · Cited by 323
Ancoli‐Israel, S., Klauber, M. R., Jones, D. W., Kripke, D. F., Martin, J. L., Mason, W. J., Pat‐Horenczyk, R., & Fell, R. L. (1997) · SLEEP · doi:10.1093/sleep/20.1.18 · Cited by 302
Effect of Light Treatment on Sleep and Circadian Rhythms in Demented Nursing Home Patients
Ancoli‐Israel, S., Martin, J. L., Kripke, D. F., Marler, M., & Klauber, M. R. (2002) · Journal of the American Geriatrics Society · doi:10.1046/j.1532-5415.2002.50060.x · Cited by 297
Exposure to light in healthy elderly subjects and alzheimer's patients
Campbell, S. S., Kripke, D. F., Gillin, J. C., & Hrubovcak, J. C. (1988) · Physiology & Behavior · doi:10.1016/0031-9384(88)90289-2 · Cited by 277
Melatonin rhythmicity: effect of age and Alzheimer's disease
Skene, D. J. (2003) · Experimental Gerontology · doi:10.1016/s0531-5565(02)00198-5 · Cited by 273
Mishima, K., Tozawa, T., Satoh, K., Matsumoto, Y., Hishikawa, Y., & Okawa, M. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(97)00510-6 · Cited by 269
VIP neurons in the human SCN in relation to sex, age, and Alzheimer's disease
Zhou, J. (1995) · Neurobiology of Aging · doi:10.1016/0197-4580(95)00043-e · Cited by 243
Circadian locomotor activity and core-body temperature rhythms in Alzheimer's disease
Satlin, A., Volicer, L., Stopa, E. G., & Harper, D. G. (1995) · Neurobiology of Aging · doi:10.1016/0197-4580(95)00059-n · Cited by 232
Amyloid imaging and CSF biomarkers in predicting cognitive impairment up to 7.5 years later
Roe, C. M., Fagan, A. M., Grant, E. A., Hassenstab, J., Moulder, K. L., Maue Dreyfus, D., Sutphen, C. L., Benzinger, T. L. S., Mintun, M. A., Holtzman, D. M., et al. (2013) · Neurology · doi:10.1212/wnl.0b013e3182918ca6 · Cited by 222
Self-citationSuprachiasmatic neuron numbers and rest–activity circadian rhythms in older humans
Wang, J. L., Lim, A. S., Chiang, W., Hsieh, W., Lo, M., Schneider, J. A., Buchman, A. S., Bennett, D. A., Hu, K., & Saper, C. B. (2015) · Annals of Neurology · doi:10.1002/ana.24432 · Cited by 217 · cited 2×
“Advancing age has been associated with declining circadian function, both in rodents and humans, although the mechanisms remain unknown.(9,46,49)While the prevalence of preclinicalADpathology increasesdramaticallywithage,(23)we found that increasing agewas significantly associatedwithdiminished amplitude and increased…”
BackgroundDi Meco, A., Joshi, Y. B., & Praticò, D. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.02.011 · Cited by 205
Disturbance of Endogenous Circadian Rhythm in Aging and Alzheimer Disease
Harper, D. G., Volicer, L., Stopa, E. G., McKee, A. C., Nitta, M., & Satlin, A. (2005) · American Journal of Geriatric Psychiatry · doi:10.1176/appi.ajgp.13.5.359 · Cited by 199
Luik, A. I., Zuurbier, L. A., Albert Hofman, D., Someren, E. J. W. V., & Tiemeier, H. W. (2013) · Chronobiology International · doi:10.3109/07420528.2013.813528 · Cited by 197
Gibson, E. M., Wang, C., Tjho, S., Khattar, N., & Kriegsfeld, L. J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015267 · Cited by 196
Nonparametric methods in actigraphy: An update
Gonçalves, B. S. B., Cavalcanti, P., Tavares, G. R., Campos, T. F., & Araújo, J. F. (2014) · Sleep Science · doi:10.1016/j.slsci.2014.09.013 · Cited by 195
Okawa, M., Mishima, K., Hishikawa, Y., Hozumi, S., Hori, H., & Takahashi, K. (1991) · SLEEP · doi:10.1093/sleep/14.6.478 · Cited by 184
Shift work and diabetes – A systematic review
Knutsson, A., & Kempe, A. (2014) · Chronobiology International · doi:10.3109/07420528.2014.957308 · Cited by 178
Rothman, S. M., Herdener, N., Frankola, K. A., Mughal, M. R., & Mattson, M. P. (2013) · Brain Research · doi:10.1016/j.brainres.2013.07.010 · Cited by 172
Hu, K., Someren, E. J. W. V., Shea, S. A., & Scheer, F. A. J. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806087106 · Cited by 171
Visinin‐like protein‐1: Diagnostic and prognostic biomarker in Alzheimer disease
Tarawneh, R. M., D’Angelo, G., Macy, E., Xiong, C., Carter, D. R., Cairns, N. J., Fagan, A. M., Head, D. M., Mintun, M. A., Ladenson, J. H., et al. (2011) · Annals of Neurology · doi:10.1002/ana.22448 · Cited by 169
Self-citationAβ-induced degradation of BMAL1 and CBP leads to circadian rhythm disruption in Alzheimer’s disease
Song, H., Moon, M., Choe, H. K., Han, D.-H., Jang, C., Kim, A., Cho, S., Kim, K., & Mook‐Jung, I. (2015) · Molecular Neurodegeneration · doi:10.1186/s13024-015-0007-x · Cited by 160
Bianchetti, A., Scuratti, A., Zanetti, O. O., Binetti, G. G., Frisoni, G. B., Magni, E., & Trabucchi, M. (1995) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000106930 · Cited by 145
Cronin, P., McCarthy, M. J., Lim, A. S. P., Salmon, D. P., Galasko, D. R., Masliah, E., Jager, P. L. D., Bennett, D. A., & Desplats, P. (2016) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2016.10.003 · Cited by 143
Alzheimer’s Disease: Sleep and Sleep/Wake Patterns
Vitiello, M. V., & Prinz, P. N. (1989) · Clinics in Geriatric Medicine · doi:10.1016/s0749-0690(18)30679-7 · Cited by 139
Circadian Misalignment and Sleep Disruption in Mild Cognitive Impairment
Naismith, S. L., Hickie, I. B., Terpening, Z., Rajaratnam, S. M. W., Hodges, J. R., Bolitho, S., Rogers, N. L., & Lewis, S. J. G. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-131217 · Cited by 139
Daily rhythm of serum melatonin in patients with dementia of the degenerate type
Uchida, K., Okamoto, N., Ohara, K., & Morita, Y. (1996) · Brain Research · doi:10.1016/0006-8993(96)00086-8 · Cited by 138
Outcomes after diagnosis of mild cognitive impairment in a large autopsy series
Abner, E. L., Kryscio, R. J., Schmitt, F. A., Fardo, D. W., Moga, D. C., Ighodaro, E. T., Jicha, G. A., Yu, L., Dodge, H. H., Xiong, C., et al. (2017) · Annals of Neurology · doi:10.1002/ana.24903 · Cited by 111
Imaging and cerebrospinal fluid biomarkers in early preclinical alzheimer disease
Vlassenko, A. G., McCue, L., Jasielec, M. S., Su, Y., Gordon, B. A., Xiong, C., Holtzman, D. M., Benzinger, T. L. S., Morris, J. C., & Fagan, A. M. (2016) · Annals of Neurology · doi:10.1002/ana.24719 · Cited by 106
Self-citationAmyloid Burden in Obstructive Sleep Apnea
Yun, C., Lee, H., Lee, S. K., Kim, H., Seo, H. S., Bang, S. A., Kim, S. E., Greve, D. N., Au, R., Shin, C., et al. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-161047 · Cited by 105
Prevalence of cerebral amyloid pathology in persons without dementia: A meta-analysis
Jansen, W., Ossenkoppele, R., Knol, D., Tijms, B., Scheltens, P., Fr, V., Visser, P. J., Amyloid Biomarker Study Group, Aalten, P., Aarsland, D., et al. (2015) · Archive ouverte UNIGE (University of Geneva) · Cited by 94
Self-citationDirection-dependent effects of chronic “jet-lag” on hippocampal neurogenesis
Kott, J., Leach, G., & Yan, L. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.03.048 · Cited by 58
Oyegbami, O., Collins, H. M., Pardon, M., Ebling, F. J. P., Heery, D. M., & Moran, P. M. (2017) · Current Alzheimer Research · doi:10.2174/1567205014666170317113159 · Cited by 38
Villemagne, V. L., Burnham, S., Bourgeat, P., Brown, B. M., Ellis, K. A., Salvado, O., Szoeke, C. E. I., Macaulay, S. L., Martins, R. N., Maruff, P. T., et al. (2013) · Research Bank (Australian Catholic University) · Cited by 31
Price (1999) · doi:10.1002/1531-8249(199903)45:3
Self-citation
Flagged first, then by citations
Research works printed but not linked: 2
- [20]20. Peter-Derex L, Yammine P, Bastuji H, Croisile B. Sleep and Alzheimer's disease. Sleep Med Rev. 2015; 19:29-38.
- [55]55. La Morgia C, Ross-Cisneros FN, Koronyo Y, et al. Melanopsin retinal ganglion cell loss in Alzheimer disease. Ann Neurol. 2016;79(1):90-109.
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Association between circadian rhythms and neurodegenerative diseases
Leng, Y., Musiek, E. S., Hu, K., Cappuccio, F. P., & Yaffe, K. S. (2019) · The Lancet Neurology · doi:10.1016/s1474-4422(18)30461-7 · Cited by 677
Self-citationAssociation of sleep duration in middle and old age with incidence of dementia
Sabia, S., Fayosse, A., Dumurgier, J., van Hees, V. T., Paquet, C., Sommerlad, A., Kivimäki, M., Dugravot, A., & Singh-Manoux, A. (2021) · Nature Communications · doi:10.1038/s41467-021-22354-2 · Cited by 628
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Metadata
- Authors
- Musiek, E. S., Bhimasani, M., Zangrilli, M. A., Morris, J. C., Holtzman, D. M., & Ju, Y.-E. S.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Ju, Yo-El S.
- Venue
- JAMA Neurology
- Publisher
- American Medical Association (AMA)
- Published
- 2018-05-01
- Volume
- 75
- Issue
- 5
- Pages
- 582
- ISSN
- 2168-6149 (ISSN-L)
- PMC
- PMC5885197
- OpenAlex
- W2792021696
- Cited by
- 465
- References
- 70
- Citations by year
- 2026: 59 · 2025: 75 · 2024: 64 · 2023: 52 · 2022: 50 · 2021: 58 · 2020: 57 · 2019: 32 · 2018: 18
- FWCI
- 23.17
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- JAMA Neurology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (KL2TR000450, UL1TR002345, KL2TR002346)
- National Institute on Aging (P50AG005681, P01AG003991, P01AG026276)
- National Institute of Neurological Disorders and Stroke (K23NS089922, K08NS079405, P01NS074969)
- National Center for Research Resources (UL1RR024992)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Keywords
- circadian rhythm, preclinical Alzheimer's disease, aging, actigraphy, intradaily variability, Pittsburgh compound B, amyloid-beta 42, circadian dysfunction, sex differences, cognitive aging, empirical mode decomposition, cosinor analysis, nonparametric statistics, sleep-wake cycle
- MeSH terms
- Aged, Aging, Alzheimer Disease, Aniline Compounds, Cross-Sectional Studies, Female, Humans, Longitudinal Studies, Male, Middle Aged, Peptide Fragments, Thiazoles, Amyloid beta-Peptides, tau Proteins, Statistics, Nonparametric, Chronobiology Disorders, Positron-Emission Tomography, Actigraphy
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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