Subjective cognitive decline and rates of incident Alzheimer's disease and non-Alzheimer's disease dementia

Slot, Rosalinde E.R.; Sikkes, Sietske A.M.; Berkhof, Johannes; Brodaty, Henry; Buckley, Rachel; Cavedo, Enrica; Dardiotis, Efthimios; Guillo‐Benarous, Francoise; Hampel, Harald; Kochan, Nicole A.; Lista, Simone; Luck, Tobias; Maruff, Paul; Molinuevo, José Luis; Kornhuber, Johannes; Reisberg, Barry; Riedel‐Heller, Steffi G.; Risacher, Shannon L.; Roehr, Susanne; Sachdev, Perminder S.; Scarmeas, Nikolaos; Scheltens, Philip; Shulman, Melanie B.; Saykin, Andrew J.; Verfaillie, Sander C.J.; Visser, Pieter Jelle; Vos, Stephanie J.B.; Wagner, Michael; Wolfsgruber, Steffen; Jessen, Frank; the Alzheimer's Disease Neuroimaging Initiative; the DESCRIPA working group; the INSIGHT‐preAD study group; SCD‐I working group; van der Flier, Wiesje M.

doi:10.1016/j.jalz.2018.10.003

Cited by 428Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCancer-related cognitive impairment studies

Subjective cognitive decline and rates of incident Alzheimer's disease and non-Alzheimer's disease dementia

Open access

Slot, Rosalinde E.R., Sikkes, Sietske A.M., Berkhof, Johannes, Brodaty, Henry, Buckley, Rachel, Cavedo, Enrica, Dardiotis, Efthimios, Guillo‐Benarous, Francoise +27 more·2019·Alzheimer's & Dementia

DOI 10.1016/j.jalz.2018.10.003PMC PMC6465066

Open this paper in CoChat — free account Open PDF

Abstract

INTRODUCTION: In this multicenter study on subjective cognitive decline (SCD) in community-based and memory clinic settings, we assessed the (1) incidence of Alzheimer's disease (AD) and non-AD dementia and (2) determinants of progression to dementia. METHODS: Eleven cohorts provided 2978 participants with SCD and 1391 controls. We estimated dementia incidence and identified risk factors using Cox proportional hazards models. RESULTS: In SCD, incidence of dementia was 17.7 (95% Poisson confidence interval 15.2-20.3)/1000 person-years (AD: 11.5 [9.6-13.7], non-AD: 6.1 [4.7-7.7]), compared with 14.2 (11.3-17.6) in controls (AD: 10.1 [7.7-13.0], non-AD: 4.1 [2.6-6.0]). The risk of dementia was strongly increased in SCD in a memory clinic setting but less so in a community-based setting. In addition, higher age (hazard ratio 1.1 [95% confidence interval 1.1-1.1]), lower Mini-Mental State Examination (0.7 [0.66-0.8]), and apolipoprotein E ε4 (1.8 [1.3-2.5]) increased the risk of dementia. DISCUSSION: SCD can precede both AD and non-AD dementia. Despite their younger age, individuals with SCD in a memory clinic setting have a higher risk of dementia than those in community-based cohorts.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1016/j.jalz.2018.10.003

Cites

61 of 61 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

SCD is associated with increased risks of AD biomarker abnormalities and future cognitive decline and dementia.
“SCD is postulated to manifest at a relatively late phase of preclinical AD and is associated with increased risks of AD biomarker abnormalities and future cognitive decline and dementia [2, 4, 6]”
From Neuroimaging advances regarding subjective cognitive decline in preclinical Alzheimer's disease (2020) · cites this paper as [6]
The Introduction (page unavailable) states that people with SCD have an increased risk of subsequent objective cognitive decline and dementia, and the Results report higher dementia incidence in SCD than in controls, especially in memory-clinic cohorts. The paper does not establish an increased risk of AD biomarker abnormalities; the Discussion says biomarker data were unavailable for a large part of the cohort. (LLM, conf=0.88)
Experimental — accuracy not yet measured
SCD is postulated to manifest at a relatively late phase of preclinical AD.
“SCD is postulated to manifest at a relatively late phase of preclinical AD and is associated with increased risks of AD biomarker abnormalities and future cognitive decline and dementia [2, 4, 6]”
From Neuroimaging advances regarding subjective cognitive decline in preclinical Alzheimer's disease (2020) · cites this paper as [6]
Subjective cognitive decline might be a risk factor of clinical progression, but the ability of subjective cognitive decline to predict progression to objective cognitive decline remains low (OR 1·5-3·08).
“Subjective cognitive decline might be a risk factor of clinical progression,24 but the ability of subjective cognitive decline to predict progression to objective cognitive decline (ie, mild cognitive decline, or dementia, or both) remains low (OR 1·5–3·081).”
From Clinical diagnosis of Alzheimer’s disease: Recommendations of the International Working Group (2021) · cites this paper as [81]

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

“Mini-mental state”
Folstein, M. F., Folstein, S. E., & McHugh, P. R. (1975) · Journal of Psychiatric Research · doi:10.1016/0022-3956(75)90026-6 · Cited by 88,282 · see citing works
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS‐ADRDA Work Group* under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D., & Stadlan, E. M. (1984) · Neurology · doi:10.1212/wnl.34.7.939 · Cited by 27,915 · see citing works
[Japanese version of the Neuropsychiatric Inventory--a scoring system for neuropsychiatric disturbance in dementia patients].
Hirono, N., Mori, E., Ikejiri, Y., Imamura, T., Shimomura, T., Hashimoto, M., Yamashita, H., & Ikeda, M. (1997) · PubMed · Cited by 21,010 · see citing works
Special Care Units and Traditional Care in Dementia: Relationship with Behavior, Cognition, Functional Status and Quality of Life - A Review
Kok, J. S., Berg, I. J., & Scherder, E. J. A. (2013) · Dementia and Geriatric Cognitive Disorders Extra · doi:10.1159/000353441 · Cited by 20,589 · see citing works
Older Adults' Reasons for Using Technology while Aging in Place
Peek, S. T. M., Luijkx, K. G., Rijnaard, M. D., Nieboer, M. E., van der Voort, C. S., Aarts, S., van Hoof, J., Vrijhoef, H. J., & Wouters, E. (2015) · Gerontology · doi:10.1159/000430949 · Cited by 19,803 · see citing works
Sensitivity and False Alarm Rate of a Fall Sensor in Long-Term Fall Detection in the Elderly
Kangas, M., Korpelainen, R., Vikman, I., Nyberg, L., & Jämsä, T. J. (2014) · Gerontology · doi:10.1159/000362720 · Cited by 19,003 · see citing works
The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
McKhann, G. M., Knopman, D. S., Chertkow, H., Hyman, B. T., Jack, C. R., Kawas, C. H., Klunk, W. E., Koroshetz, W. J., Manly, J. J., Mayeux, R., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.005 · Cited by 18,657 · see citing works
The diagnosis of mild cognitive impairment due to Alzheimer's disease: Recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
Albert, M. S., DeKosky, S. T., Dickson, D., Dubois, B., Feldman, H. H., Fox, N. C., Gamst, A., Holtzman, D. M., Jagust, W. J., Petersen, R. C., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.008 · Cited by 10,152 · see citing works
Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families
Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., & Pericak-Vance, M. A. (1993) · Science · doi:10.1126/science.8346443 · Cited by 9,429 · see citing works
Toward defining the preclinical stages of Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease
Sperling, 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 · see citing works
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Rascovsky, K., Hodges, J. R., Knopman, D., Mendez, M. F., Kramer, J. H., Neuhaus, J., van Swieten, J. C., Seelaar, H., Dopper, E. G. P., Onyike, C. U., et al. (2011) · Brain · doi:10.1093/brain/awr179 · Cited by 5,221 · see citing works
Diagnosis and management of dementia with Lewy bodies: Third report of the DLB consortium
McKeith, I. G., Dickson, D. W., Lowe, J., Emre, M., O'Brien, J. T., Feldman, H., Cummings, J., Duda, J. E., Lippa, C., Perry, E. K., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000187889.17253.b1 · Cited by 5,105 · see citing works
Tracking pathophysiological processes in Alzheimer's disease: an updated hypothetical model of dynamic biomarkers
Jack, C. R., Knopman, D. S., Jagust, W. J., Petersen, R. C., Weiner, M. W., Aisen, P. S., Shaw, L. M., Vemuri, P., Wiste, H. J., Weigand, S. D., et al. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(12)70291-0 · Cited by 4,396 · see citing works
Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy
Liu, C.-C., Kanekiyo, T., Xu, H., & Bu, G. (2013) · Nature Reviews Neurology · doi:10.1038/nrneurol.2012.263 · Cited by 3,459 · see citing works
Alzheimer’s Disease
Scheltens, P., Blennow, K., Breteler, M. M. B., de Strooper, B., Frisoni, G. B., Salloway, S., & Van der Flier, W. M. (2016) · The Lancet · doi:10.1016/s0140-6736(15)01124-1 · Cited by 3,125 · see citing works
A conceptual framework for research on subjective cognitive decline in preclinical Alzheimer's disease
Jessen, F., Amariglio, R. E., van Boxtel, M., Breteler, M., Ceccaldi, M., Chételat, G., Dubois, B., Dufouil, C., Ellis, K. A., van der Flier, W. M., et al. (2014) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2014.01.001 · Cited by 3,014 · see citing works
The Determinants of Quality of Life of Nursing Home Residents with Young-Onset Dementia and the Differences between Dementia Subtypes
Appelhof, B., Bakker, C., den IJssel, J. C. L. V. D., Zwijsen, S. A., Smalbrugge, M., Verhey, F. R. J., de Vugt, M. E., Zuidema, S. U., & Koopmans, R. T. C. M. (2017) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000477087 · Cited by 2,773 · see citing works
The Diagnosis of Mild Cognitive Impairment due to Alzheimer’s Disease: Recommendations from the National Institute on Aging-Alzheimer’s Association Workgroups on Diagnostic Guidelines for Alzheimer’s Disease
Albert, M., DeKosky, S. T., Dickson, D. W., Dubois, B., Feldman, H., Fox, N. C., Gamst, A. C., Holtzman, D. M., Jagust, W. J., Petersen, R. C., et al. (2013) · FOCUS The Journal of Lifelong Learning in Psychiatry · doi:10.1176/appi.focus.11.1.96 · Cited by 2,630 · see citing works
Risk of dementia and mild cognitive impairment in older people with subjective memory complaints: meta-analysis
Mitchell, A. J., Beaumont, H., Ferguson, D. Y., Yadegarfar, M., & Stubbs, B. (2014) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12336 · Cited by 1,171 · see citing works
Frontotemporal dementia
Bang, J., Spina, S., & Miller, B. L. (2015) · The Lancet · doi:10.1016/s0140-6736(15)00461-4 · Cited by 1,144 · see citing works
Vascular dementia
O'Brien, J. T., & Thomas, A. (2015) · The Lancet · doi:10.1016/s0140-6736(15)00463-8 · Cited by 1,136 · see citing works
The Australian Imaging, Biomarkers and Lifestyle (AIBL) study of aging: methodology and baseline characteristics of 1112 individuals recruited for a longitudinal study of Alzheimer's disease
Ellis, K. A., Bush, A. I., Darby, D., Fazio, D. D., Foster, J. K., Hudson, P. J., Lautenschlager, N. T., Lenzo, N. P., Martins, R. N., Maruff, P. T., et al. (2009) · International Psychogeriatrics · doi:10.1017/s1041610209009405 · Cited by 970 · see citing works
Recent global trends in the prevalence and incidence of dementia, and survival with dementia
Prince, M., Ali, G.-C., Guerchet, M., Prina, A. M., Albanese, E., & Wu, Y.-T. (2016) · Alzheimer's Research & Therapy · doi:10.1186/s13195-016-0188-8 · Cited by 876 · see citing works
Quantification of Five Neuropsychological Approaches to Defining Mild Cognitive Impairment
Jak, A. J., Bondi, M. W., Delano-Wood, L., Wierenga, C., Corey-Bloom, J., Salmon, D. P., & Delis, D. C. (2009) · The American Journal of Geriatric Psychiatry · doi:10.1097/jgp.0b013e31819431d5 · Cited by 823 · see citing works
The question of familial meningiomas and schwannomas:
King, A. A., & Gutmann, D. H. (2000) · Neurology · doi:10.1212/wnl.54.1.4 · Cited by 814 · see citing works
Untitled work
(2000) · PubMed · Cited by 683 · see citing works
Prediction of Dementia by Subjective Memory Impairment Effects of Severity and Temporal Association With Cognitive Impairment Dementia and Subjective Memory Impairment
Jessen, F. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.30 · Cited by 681 · see citing works
Implementation of subjective cognitive decline criteria in research studies
Molinuevo, J. L., Rabin, L. A., Amariglio, R., Buckley, R., Dubois, B., Ellis, K. A., Ewers, M., Hampel, H., Klöppel, S., Rami, L., et al. (2017) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2016.09.012 · Cited by 575 · see citing works
Outcome over seven years of healthy adults with and without subjective cognitive impairment
Reisberg, B., Shulman, M. B., Torossian, C., Leng, L., & Zhu, W. (2010) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2009.10.002 · Cited by 568 · see citing works
Self-citation
Association Between Memory Complaints and Incident Alzheimer’s Disease in Elderly People With Normal Baseline Cognition
Geerlings, M. I., Jonker, C., Bouter, L. M., Adèr, H. J., & Schmand, B. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.4.531 · Cited by 487 · see citing works
Subjective Cognitive Decline in Older Adults: An Overview of Self-Report Measures Used Across 19 International Research Studies
Rabin, L. A., Initiative, T. A. D. N., Smart, C. M., Crane, P. K., Amariglio, R. E., Berman, L., Boada, M., Buckley, R. F., Chételat, G., Dubois, B., et al. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150154 · Cited by 472 · see citing works
Optimizing Patient Care and Research: The Amsterdam Dementia Cohort
van der Flier, W. M., Pijnenburg, Y. A. L., Prins, N. D., Lemstra, A. W., Bouwman, F. H., Teunissen, C. E., van Berckel, B. N. M., Stam, C. J., Barkhof, F., Visser, P. J., et al. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-132306 · Cited by 400 · see citing works
Prevalence of dementia and major subtypes in Europe:A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group
Lobo, A., Launer, L. J., Fratiglioni, L., Andersen, K., Di Carlo, A., Breteler, M. M. B., Copeland, J., Dartigues, J. F., Jagger, C., Martinez-Lage, J., et al. (2000) · University of Southern Denmark Research Portal (University of Southern Denmark) · Cited by 388 · see citing works
Amsterdam Dementia Cohort: Performing Research to Optimize Care
van der Flier, W. M., & Scheltens, P. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-170850 · Cited by 379 · see citing works
The Sydney Memory and Ageing Study (MAS): methodology and baseline medical and neuropsychiatric characteristics of an elderly epidemiological non-demented cohort of Australians aged 70–90 years
Sachdev, P. S., Brodaty, H., Reppermund, S., Kochan, N. A., Trollor, J. N., Draper, B., Slavin, M. J., Crawford, J., Kang, K., Broe, G. A., et al. (2010) · International Psychogeriatrics · doi:10.1017/s1041610210001067 · Cited by 373 · see citing works
Subjective memory complaints may announce dementia
Schmand, B. A., Jonker, C., Hooijer, C., & Lindeboom, J. (1996) · Neurology · doi:10.1212/wnl.46.1.121 · Cited by 344 · see citing works
Cognitive and neuroimaging features and brain β-amyloidosis in individuals at risk of Alzheimer's disease (INSIGHT-preAD): a longitudinal observational study
Dubois, B., Epelbaum, S., Nyasse, F., Bakardjian, H., Gagliardi, G. P., Uspenskaya, O., Houot, M., Lista, S., Cacciamani, F., Potier, M., et al. (2018) · The Lancet Neurology · doi:10.1016/s1474-4422(18)30029-2 · Cited by 239 · see citing works
Subjective Cognitive Concerns and Neuropsychiatric Predictors of Progression to the Early Clinical Stages of Alzheimer Disease
Donovan, N. J., Amariglio, R. E., Zoller, A. S., Rudel, R. K., Gómez‐Isla, T., Blacker, D., Hyman, B. T., Locascio, J. J., Johnson, K. A., Sperling, R. A., et al. (2014) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2014.02.007 · Cited by 228 · see citing works
Islington study of dementia subtypes in the community
Stevens, T., Livingston, G., Kitchen, G., Manela, M., Walker, Z., & Katona, C. (2002) · The British Journal of Psychiatry · doi:10.1192/bjp.180.3.270 · Cited by 211 · see citing works
Cerebrospinal fluid Aβ42 is the best predictor of clinical progression in patients with subjective complaints
van Harten, A. C., Visser, P. J., Pijnenburg, Y. A. L., Teunissen, C. E., Blankenstein, M. A., Scheltens, P., & van der Flier, W. M. (2013) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2012.08.004 · Cited by 197 · see citing works
Self-citation
Toward defining the preclinical stages of Alzheimer's disease: Recommendations from the National Institute on Aging and the Alzheimer's Association workgroup
Sperling, R. A., Aisen, P. S. S., Beckett, L. A., Bennett, D. A., Craft, S., Fagan, A. M., Iwatsubo, T., Jack, C. R., Kaye, J. A., Montine, T. J., et al. (2011) · Cited by 197 · see citing works
APOE effect on Alzheimer's disease biomarkers in older adults with significant memory concern
Risacher, S. L., Kim, S., Nho, K. T., Foroud, T., Shen, L., Petersen, R. C., Jack, C. R., Beckett, L. A., Aisen, P. S. S., Koeppe, R. A., et al. (2015) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2015.03.003 · Cited by 186 · see citing works
Subjective cognitive decline in cognitively normal elders from the community or from a memory clinic: Differential affective and imaging correlates
Perrotin, A., La Joie, R., de La Sayette, V., Barré, L., Mézenge, F., Mutlu, J., Guilloteau, D., Egret, S., Eustache, F., & Chételat, G. (2017) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2016.08.011 · Cited by 179 · see citing works
Cognitive performance before and after the onset of subjective cognitive decline in old age
Koppara, A., Wagner, M., Lange, C., Ernst, A., Wiese, B., König, H., Brettschneider, C., Riedel-Heller, S. G., Luppa, M., Weyerer, S. B., et al. (2015) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1016/j.dadm.2015.02.005 · Cited by 167 · see citing works
Prevalence of dementia according to DSM–III–R and ICD–10
Riedel-Heller, S. G., Busse, A., Aurich, C., Matschinger, H., & Angermeyer, M. C. (2001) · The British Journal of Psychiatry · doi:10.1192/bjp.179.3.250 · Cited by 149 · see citing works
The Cognitive Change Index as a Measure of Self and Informant Perception of Cognitive Decline: Relation to Neuropsychological Tests
Rattanabannakit, C., Risacher, S. L., Gao, S., Lane, K. A., Brown, S. A., McDonald, B. C., Unverzagt, F. W., Apostolova, L. G., Saykin, A. J., & Farlow, M. R. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-150729 · Cited by 146 · see citing works
Risk of progression from subjective cognitive decline to mild cognitive impairment: The role of study setting
Snitz, B. E., Wang, T., Cloonan, Y. K., Jacobsen, E. P., Chang, C. H., Hughes, T. F., Kamboh, M. I., & Ganguli, M. (2018) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2017.12.003 · Cited by 139 · see citing works
The Hellenic Longitudinal Investigation of Aging and Diet (HELIAD): Rationale, Study Design, and Cohort Description
Dardiotis, E., Kosmidis, M. H., Yannakoulia, M., Hadjigeorgiou, G. M., & Scarmeas, N. (2014) · Neuroepidemiology · doi:10.1159/000362723 · Cited by 135 · see citing works
Incidence and subtypes of early-onset dementia in a geographically defined general population
Garre‐Olmo, J., Batlle, D. G., Fernández, M., Daniel, F. M., Huélamo, R. D. E., Casadevall, T., Recio, J. T., Estrada, A. T., & Pousa, S. L. (2010) · Neurology · doi:10.1212/wnl.0b013e3181f5d4c4 · Cited by 134 · see citing works
Subjective Cognitive Impairment Cohort (SCIENCe): study design and first results
Slot, R. E. R., Verfaillie, S. C. J., Overbeek, J. M., Timmers, T., Wesselman, L. M. P., Teunissen, C. E., Dols, A., Bouwman, F. H., Prins, N. D., Barkhof, F., et al. (2018) · Alzheimer s Research & Therapy · doi:10.1186/s13195-018-0390-y · Cited by 132 · see citing works
Dementia UK: Second Edition - Overview
Prince, M. J., Knapp, M. R. J., Guerchet, M., McCrone, P., Prina, M. A., Comas‐Herrera, A., Wittenberg, R., Adelaja, B., Hu, B., King, D., et al. (2014) · Research Portal (King's College London) · Cited by 114 · see citing works
Interpreting Biomarker Results in Individual Patients With Mild Cognitive Impairment in the Alzheimer’s Biomarkers in Daily Practice (ABIDE) Project
van Maurik, I. S., Zwan, M. D., Tijms, B. M., Bouwman, F. H., Teunissen, C. E., Scheltens, P., Wattjes, M. P., Barkhof, F., Berkhof, J. H., van der Flier, W. M., et al. (2017) · JAMA Neurology · doi:10.1001/jamaneurol.2017.2712 · Cited by 89 · see citing works
Development of Screening Guidelines and Clinical Criteria for Predementia Alzheimer’s Disease
Visser, P. J., Verhey, F. R. J., Boada, M., Bullock, R. M., Deyn, P. P. D., Frisoni, G. B., Frölich, L., Hampel, H. J., Jolles, J., Jones, R. W., et al. (2008) · Neuroepidemiology · doi:10.1159/000135644 · Cited by 84 · see citing works
Early and Differential Diagnosis of Dementia and Mild Cognitive Impairment
Kornhuber, J., Schmidtke, K., Frölich, L., Perneczky, R., Wolf, S., Hampel, H. J., Jessen, F., Heuser, I., Peters, O., Weih, M., et al. (2009) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000210388 · Cited by 82 · see citing works
Subjective Cognitive Decline from a Phenomenological Perspective: A Review of the Qualitative Literature
Buckley, R. F., Saling, M. M., Frommann, I., Wolfsgruber, S., & Wagner, M. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150095 · Cited by 71 · see citing works
Influence of Sampling and Recruitment Methods in Studies of Subjective Cognitive Decline
Rodríguez‐Gómez, O., Ruiz, C. A., Jessen, F., Valero, S., & Boada, M. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150189 · Cited by 57 · see citing works
Impact of Recruitment Methods in Subjective Cognitive Decline
Ruiz, C. A., Rodríguez‐Gómez, O., Alegret, M., Valero, S., Moreno–Grau, S., Sanabria, Á., Hernández, I., Rosende‐Roca, M., Vargas, L., Mauleón, A., et al. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-160915 · Cited by 42 · see citing works
Differential longitudinal decline on the mini-mental state examination in frontotemporal lobar degeneration and Alzheimer disease
Tan, K. S., Libon, D. J., Rascovsky, K., Grossman, M., & Xie, S. X. (2013) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0b013e31827bdc6f · Cited by 36 · see citing works
Effect of Alzheimer's disease risk and protective factors on cognitive trajectories in subjective memory complainers: An INSIGHT‐preAD study
Teipel, S. J., Cavedo, E., Lista, S., Habert, M., Potier, M., Grothe, M. J., Epelbaum, S., Sambati, L., Gagliardi, G. P., Toschi, N., et al. (2018) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2018.04.004 · Cited by 29 · see citing works
Subjective Memory Complaints: Symptoms and Outcome in Different Research Settings
Archer, H. A., Newson, M., & Coulthard, E. J. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150108 · Cited by 26 · see citing works
A memory clinic v. traditional community mental health team service: comparison of costs and quality
Rubinsztein, J. S., van Rensburg, M. J., Al‐Salihy, Z., Girling, D. M., Lafortune, L., Radhakrishnan, M., & Brayne, C. (2015) · BJPsych Bulletin · doi:10.1192/pb.bp.113.044263 · Cited by 20 · see citing works

Flagged first, then by citations

Sorted by citations

The characterisation of subjective cognitive decline
Jessen, F., Amariglio, R. E., Buckley, R. F., van der Flier, W. M., Han, Y., Molinuevo, J. L., Rabin, L., Rentz, D. M., Rodriguez-Gomez, O., Saykin, A. J., et al. (2020) · The Lancet Neurology · doi:10.1016/s1474-4422(19)30368-0 · Cited by 1,389 · see citing works
Clinical diagnosis of Alzheimer’s disease: Recommendations of the International Working Group
Dubois, B., Villain, N., Frisoni, G. B., Rabinovici, G. D., Sabbagh, M., Cappa, S., Bejanin, A., Bombois, S., Epelbaum, S., Teichmann, M., et al. (2021) · The Lancet Neurology · doi:10.1016/s1474-4422(21)00066-1 · Cited by 1,051 · see citing works
Amyloid-PET and 18F-FDG-PET in the diagnostic investigation of Alzheimer's disease and other dementias
Chételat, G., Arbizu, J., Barthel, H., Garibotto, V., Law, I., Morbelli, S., van de Giessen, E., Agosta, F., Barkhof, F., Brooks, D. J., et al. (2020) · The Lancet Neurology · doi:10.1016/s1474-4422(20)30314-8 · Cited by 526 · see citing works
The China Alzheimer Report 2022
Ren, R., Qi, J., Lin, S., Liu, X., Yin, P., Wang, Z., Tang, R., Wang, J., Huang, Q., Li, J., et al. (2022) · General Psychiatry · doi:10.1136/gpsych-2022-100751 · Cited by 356 · see citing works
Neuroimaging advances regarding subjective cognitive decline in preclinical Alzheimer's disease
Wang, X., Huang, W., Su, L., Xing, Y., Jessen, F., Sun, Y., Shu, N., & Han, Y. (2020) · Molecular Neurodegeneration · doi:10.1186/s13024-020-00395-3 · Cited by 265 · see citing works
Functional cognitive disorders: a systematic review
McWhirter, L., Ritchie, C., Stone, J., & Carson, A. (2020) · The Lancet Psychiatry · doi:10.1016/s2215-0366(19)30405-5 · Cited by 240 · see citing works
Serum markers glial fibrillary acidic protein and neurofilament light for prognosis and monitoring in cognitively normal older people: a prospective memory clinic-based cohort study
Verberk, I. M. W., Laarhuis, M. B., van den Bosch, K. A., Ebenau, J. L., van Leeuwenstijn, M. S. S. A., Prins, N. D., Scheltens, P., Teunissen, C. E., & van der Flier, W. M. (2021) · The Lancet Healthy Longevity · doi:10.1016/s2666-7568(20)30061-1 · Cited by 203 · see citing works
ATN classification and clinical progression in subjective cognitive decline: The SCIENCe project
Ebenau, J. L., Timmers, T., Wesselman, L. M. P., Verberk, I. M. W., Verfaillie, S. C. J., Slot, R. E. R., van Harten, A. C., Teunissen, C. E., Barkhof, F., van den Bosch, K. A., et al. (2020) · Neurology · doi:10.1212/wnl.0000000000009724 · Cited by 191 · see citing works
Estimating prevalence of subjective cognitive decline in and across international cohort studies of aging: a COSMIC study
(2020) · doi:10.1186/s13195-020-00734-y · Cited by 172 · see citing works
Burden of Illness in People with Alzheimer's Disease: A Systematic Review of Epidemiology, Comorbidities and Mortality
Lanctôt, K. L., Hahn‐Pedersen, J. H., Eichinger, C. S., Freeman, C. S., Clark, A., Tarazona, L. R. S., & Cummings, J. L. (2023) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2023.61 · Cited by 159 · see citing works
Abnormal white matter changes in Alzheimer's disease based on diffusion tensor imaging: A systematic review
Chen, Y., Wang, Y., Song, Z., Fan, Y., Gao, T., & Tang, X. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101911 · Cited by 152 · see citing works
Diagnostic contribution and therapeutic perspectives of transcranial magnetic stimulation in dementia
Lazzaro, V. D., Bella, R., Benussi, A., Bologna, M., Borroni, B., Capone, F., Chen, K.-H. S., Chen, R. E., Chistyakov, A. V., Claßen, J., et al. (2021) · Clinical Neurophysiology · doi:10.1016/j.clinph.2021.05.035 · Cited by 161 · see citing works
BG-3DM2F: Bidirectional gated 3D multi-scale feature fusion for Alzheimer’s disease diagnosis
Bakkouri, I., Afdel, K., Benois‐Pineau, J., & Catheline, G. (2022) · Multimedia Tools and Applications · doi:10.1007/s11042-022-12242-2 · Cited by 142 · see citing works
Minor neuropsychological deficits in patients with subjective cognitive decline
Wolfsgruber, S., Kleineidam, L., Guski, J., Polcher, A. A., Frommann, I., Roeske, S., Spruth, E. J., Franke, C., Priller, J., Kilimann, I., et al. (2020) · Neurology · doi:10.1212/wnl.0000000000010142 · Cited by 117 · see citing works
Diagnostic Value of the CSF α-Synuclein Real-Time Quaking-Induced Conversion Assay at the Prodromal MCI Stage of Dementia With Lewy Bodies
Rossi, M., Baiardi, S., Teunissen, C. E., Quadalti, C., Beek, M. H. C. T. V., Mammana, A., Maserati, M. S., van der Flier, W. M., Sambati, L., Zenesini, C., et al. (2021) · Neurology · doi:10.1212/wnl.0000000000012438 · Cited by 111 · see citing works
Efficacy of Bifidobacterium longum alone or in multi-strain probiotic formulations during early life and beyond
Mills, S., Yang, B. K., Smith, G., Stanton, C., & Ross, R. P. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2186098 · Cited by 106 · see citing works
Subjective cognitive decline and stage 2 of Alzheimer disease in patients from memory centers
Jessen, F., Wolfsgruber, S., Kleineidam, L., Spottke, A. E., Altenstein, S., Bartels, C., Berger, M., Brosseron, F., Daamen, M., Dichgans, M., et al. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12674 · Cited by 100 · see citing works
Apolipoprotein E4 and meningeal lymphatics in Alzheimer disease: a conceptual framework
Mentis, A. A., Dardiotis, E., & Chrousos, G. P. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0731-7 · Cited by 82 · see citing works
Highly specific and ultrasensitive plasma test detects Abeta(1–42) and Abeta(1–40) in Alzheimer’s disease
Thijssen, E. H., Verberk, I. M. W., Vanbrabant, J., Koelewijn, A., Heijst, H., Scheltens, P., van der Flier, W. M., Vanderstichele, H., Stoops, E., & Teunissen, C. E. (2021) · Scientific Reports · doi:10.1038/s41598-021-89004-x · Cited by 85 · see citing works
Precision prevention of Alzheimer's and other dementias: Anticipating future needs in the control of risk factors and implementation of disease‐modifying therapies
Frisoni, G. B., Molinuevo, J. L., Altomare, D., Carrera, E., Barkhof, F., Berkhof, J., Delrieu, J., Dubois, B., Kivipelto, M., Nordberg, A., et al. (2020) · Alzheimer's & Dementia · doi:10.1002/alz.12132 · Cited by 78 · see citing works
Self-citation
Trajectories of subjective cognitive decline, and the risk of mild cognitive impairment and dementia
Liew, T. M. (2020) · Alzheimer s Research & Therapy · doi:10.1186/s13195-020-00699-y · Cited by 79 · see citing works
Association of Subjective Cognitive Decline with Risk of Cognitive Impairment and Dementia: A Systematic Review and Meta-Analysis of Prospective Longitudinal Studies
Wang, X., Wang, Z.-T., Hu, H., Qu, Y., Wang, M.-M., Shen, X., Xu, W., Dong, Q., Tan, L., & Yu, J.-T. (2021) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2021.27 · Cited by 77 · see citing works
Ethical issues when using digital biomarkers and artificial intelligence for the early detection of dementia
Ford, E. M., Milne, R., & Curlewis, K. (2023) · Wiley Interdisciplinary Reviews Data Mining and Knowledge Discovery · doi:10.1002/widm.1492 · Cited by 80 · see citing works
To Keto or Not to Keto? A Systematic Review of Randomized Controlled Trials Assessing the Effects of Ketogenic Therapy on Alzheimer Disease
Grammatikopoulou, M. G., Goulis, D. G., Gkiouras, K., Theodoridis, X., Gkouskou, K. K., Evangeliou, A., Dardiotis, E., & Bogdanos, D. P. (2020) · Advances in Nutrition · doi:10.1093/advances/nmaa073 · Cited by 77 · see citing works
The role of depression and anxiety in the relationship between poor sleep quality and subjective cognitive decline in Chinese elderly: Exploring parallel, serial, and moderated mediation
Xu, W., Lin, L., Ding, K., Ke, Y.-F., Huang, J.-H., Hou, C., Jia, F., & Wang, S. (2021) · Journal of Affective Disorders · doi:10.1016/j.jad.2021.07.063 · Cited by 71 · see citing works
Predictors of progression from subjective cognitive decline to objective cognitive impairment: A systematic review and meta-analysis of longitudinal studies
An, R., Gao, Y., Huang, X., Yang, Y., Yang, C., & Wan, Q. (2023) · International Journal of Nursing Studies · doi:10.1016/j.ijnurstu.2023.104629 · Cited by 71 · see citing works
A Narrative Review of Alzheimer’s Disease Stigma
Rosin, E. R., Blasco, D., Pilozzi, A. R., Yang, L. H., & Huang, X. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200932 · Cited by 69 · see citing works
Late-onset Cognitive Impairment and Modifiable Risk Factors in Adult Childhood Cancer Survivors
Phillips, N. S., Stratton, K. L., Williams, A. M., Ahles, T. A., Ness, K. K., Cohen, H. J., Edelstein, K., Yasui, Y., Oeffinger, K. C., Chow, E. J., et al. (2023) · JAMA Network Open · doi:10.1001/jamanetworkopen.2023.16077 · Cited by 68 · see citing works
Mild Cognitive Impairment in Relation to Alzheimer’s Disease: An Investigation of Principles, Classifications, Ethics, and Problems
Lee, J. (2023) · Neuroethics · doi:10.1007/s12152-023-09522-5 · Cited by 67 · see citing works
Amyloid-β Load Is Related to Worries, but Not to Severity of Cognitive Complaints in Individuals With Subjective Cognitive Decline: The SCIENCe Project
Verfaillie, S. C. J., Timmers, T., Slot, R. E. R., van der Weijden, C. W. J., Wesselman, L. M. P., Prins, N. D., Sikkes, S. A. M., Yaqub, M., Dols, A., Lammertsma, A. A., et al. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00007 · Cited by 63 · see citing works
Self-citation
Sum of boxes of the clinical dementia rating scale highly predicts conversion or reversion in predementia stages
Tzeng, R.-C., Yang, Y., Hsu, K.-C., Chang, H.-T., & Chiu, P. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1021792 · Cited by 62 · see citing works
Beneficial effect of computer-based multidomain cognitive training in patients with mild cognitive impairment
Νούσια, Α., Μαρτζούκου, Μ., Siokas, V., Aretouli, E., Aloizou, A., Folia, V., Peristeri, E., Messinis, L., Nasios, G., & Dardiotis, E. (2019) · Applied Neuropsychology Adult · doi:10.1080/23279095.2019.1692842 · Cited by 61 · see citing works
Progression of Subjective Cognitive Decline to MCI or Dementia in Relation to Biomarkers for Alzheimer Disease
Rostamzadeh, A., Bohr, L., Wagner, M., Baethge, C., & Jessen, F. (2022) · Neurology · doi:10.1212/wnl.0000000000201072 · Cited by 61 · see citing works
Decline in cognitively complex everyday activities accelerates along the Alzheimer’s disease continuum
Dubbelman, M. A., Jutten, R. J., Farias, S. T., Amariglio, R. E., Buckley, R. F., Visser, P. J., Rentz, D. M., Johnson, K. A., Properzi, M. J., Schultz, A. P., et al. (2020) · Alzheimer s Research & Therapy · doi:10.1186/s13195-020-00706-2 · Cited by 58 · see citing works
Characteristics of subjective cognitive decline associated with amyloid positivity
Janssen, O., Jansen, W. J., Vos, S. J. B., Boada, M., Parnetti, L., Gabryelewicz, T., Fladby, T., Molinuevo, J. L., Villeneuve, S., Hort, J., et al. (2021) · Alzheimer s & Dementia · doi:10.1002/alz.12512 · Cited by 58 · see citing works
Association between retinal thickness and β-amyloid brain accumulation in individuals with subjective cognitive decline: Fundació ACE Healthy Brain Initiative
on behalf of the FACEHBI study group, Marquié, M., Valero, S., Castilla-Marti, M., Martínez, J., Rodríguez‐Gómez, O., Sanabria, Á., Tartari, J. P., Monté, G. C., Sotolongo‐Grau, Ó., et al. (2020) · Alzheimer s Research & Therapy · doi:10.1186/s13195-020-00602-9 · Cited by 57 · see citing works
Plasma amyloid is associated with the rate of cognitive decline in cognitively normal elderly: the SCIENCe project
Verberk, I. M. W., Hendriksen, H. M. A., van Harten, A. C., Wesselman, L. M. P., Verfaillie, S. C. J., van den Bosch, K. A., Slot, R. E. R., Prins, N. D., Scheltens, P., Teunissen, C. E., et al. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.01.007 · Cited by 57 · see citing works
Alzheimer’s Disease: An Overview of Major Hypotheses and Therapeutic Options in Nanotechnology
Agarwal, M., Alam, R., Haider, M. K., Malik, M. Z., & Kim, D.-K. (2020) · Nanomaterials · doi:10.3390/nano11010059 · Cited by 53 · see citing works
Brain Health Services: organization, structure, and challenges for implementation. A user manual for Brain Health Services—part 1 of 6
Altomare, D., Molinuevo, J. L., Ritchie, C. W., Ribaldi, F., Carrera, E., Dubois, B., Jessen, F., McWhirter, L., Scheltens, P., van Duijn, C. M., et al. (2021) · Alzheimer s Research & Therapy · doi:10.1186/s13195-021-00827-2 · Cited by 53 · see citing works
Subjective Cognitive Decline Plus and Longitudinal Assessment and Risk for Cognitive Impairment
Kang, M.-I., Li, C., Mahajan, A., Spat‐Lemus, J., Durape, S., Chen, J., Gurnani, A. S., Devine, S., Auerbach, S. H., Ang, T. F. A., et al. (2024) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2024.1678 · Cited by 54 · see citing works
International Nuclear Medicine Consensus on the Clinical Use of Amyloid Positron Emission Tomography in Alzheimer’s Disease
Tian, M., Zuo, C., Civelek, A. C., Carrió, I., Watanabe, Y., Kang, K. W., Murakami, K., Garibotto, V., Prior, J. O., Barthel, H., et al. (2022) · Phenomics · doi:10.1007/s43657-022-00068-9 · Cited by 52 · see citing works
High amyloid burden is associated with fewer specific words during spontaneous speech in individuals with subjective cognitive decline
Verfaillie, S. C. J., Witteman, J., Slot, R. E. R., Pruis, I. J., Vermaat, L. E. W., Prins, N. D., Schiller, N. O., van de Wiel, M. A., Scheltens, P., van Berckel, B. N. M., et al. (2019) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2019.05.006 · Cited by 51 · see citing works
Cross-sectional and longitudinal characterization of SCD patients recruited from the community versus from a memory clinic: subjective cognitive decline, psychoaffective factors, cognitive performances, and atrophy progression over time
Kuhn, E., Moulinet, I., Perrotin, A., La Joie, R., Landeau, B., Tomadesso, C., Bejanin, A., Sherif, S., De La Sayette, V., Desgranges, B., et al. (2019) · Alzheimer's Research & Therapy · doi:10.1186/s13195-019-0514-z · Cited by 51 · see citing works
Subjective Cognitive Decline, Cognitive Reserve Indicators, and the Incidence of Dementia
Jia, F., Li, Y., Li, M., & Cao, F. (2020) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2020.08.005 · Cited by 52 · see citing works
Brief Cognitive Tests Used in Primary Care Cannot Accurately Differentiate Mild Cognitive Impairment from Subjective Cognitive Decline
Petrazzuoli, F., Vestberg, S., Midlöv, P., Thulesius, H. O., Stomrud, E., & Palmqvist, S. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-191191 · Cited by 49 · see citing works
Disrupted Patterns of Rich-Club and Diverse-Club Organizations in Subjective Cognitive Decline and Amnestic Mild Cognitive Impairment
Xue, C., Sun, H., Hu, G., Qi, W., Yue, Y., Rao, J., Yang, W., Xiao, C., Chen, J., & Initiative, T. A. D. N. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.575652 · Cited by 49 · see citing works
Personalized risk for clinical progression in cognitively normal subjects-the ABIDE project
Initiative, F. T. A. D. N., van Maurik, I. S., Slot, R. E. R., Verfaillie, S. C. J., Zwan, M. D., Bouwman, F. H., Prins, N. D., Teunissen, C. E., Scheltens, P., Barkhof, F., et al. (2019) · Alzheimer's Research & Therapy · doi:10.1186/s13195-019-0487-y · Cited by 47 · see citing works
Subjective Cognitive Decline Among Sexual and Gender Minorities: Results from a U.S. Population-Based Sample
Brown, M. J., & Patterson, R. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190869 · Cited by 47 · see citing works
Subjective cognitive decline and subsequent dementia: a nationwide cohort study of 579,710 people aged 66 years in South Korea
Lee, Y. C., Kang, J. M., Lee, H., Kim, K., Kim, S., Yu, T. Y., Lee, E. M., Kim, C. T., Kim, D. K., Lewis, M., et al. (2020) · Alzheimer s Research & Therapy · doi:10.1186/s13195-020-00618-1 · Cited by 46 · see citing works
Trajectory of Unawareness of Memory Decline in Individuals With Autosomal Dominant Alzheimer Disease
Vannini, P., Hanseeuw, B. J., Gatchel, J. R., Sikkes, S. A. M., Alzate, D., Zuluaga, Y., Moreno, S., Méndez, L., Baena, A. Y., Ospina-Lopera, P., et al. (2020) · JAMA Network Open · doi:10.1001/jamanetworkopen.2020.27472 · Cited by 44 · see citing works
Late-life depression, subjective cognitive decline, and their additive risk in incidence of dementia: A nationwide longitudinal study
Wang, S., Han, K., Kim, N.-Y., Um, Y. H., Kang, D. W., Na, H.-R., Lee, C., & Lim, H. K. (2021) · PLoS ONE · doi:10.1371/journal.pone.0254639 · Cited by 44 · see citing works
Protective factors for subjective cognitive decline individuals: trajectories and changes in a longitudinal study with Italian elderly
Mondini, S., Pucci, V., Montemurro, S., & Rumiati, R. I. (2021) · European Journal of Neurology · doi:10.1111/ene.15183 · Cited by 43 · see citing works
Factors associated with subjective cognitive decline in dementia‐free older adults—A population‐based study
Zullo, L., Clark, C., Gholam‐Rezaee, M., Castelao, E., von Gunten, A., Preisig, M., & Popp, J. (2021) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.5509 · Cited by 43 · see citing works
Regional [18F]flortaucipir PET is more closely associated with disease severity than CSF p-tau in Alzheimer’s disease
Wolters, E. E., Ossenkoppele, R., Verfaillie, S. C. J., Coomans, E. M., Timmers, T., Visser, D., Tuncel, H., Golla, S. S. V., Windhorst, A. D., Boellaard, R., et al. (2020) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-020-04758-2 · Cited by 43 · see citing works
Alterations in resting-state network dynamics along the Alzheimer’s disease continuum
Puttaert, D., Coquelet, N., Wens, V., Peigneux, P., Fery, P., Rovaï, A., Trotta, N., Sadeghi, N., Coolen, T., Bier, J. C., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-76201-3 · Cited by 43 · see citing works
Disability trajectories and mortality in older adults with different cognitive and physical profiles
Grande, G., Vetrano, D. L., Fratiglioni, L., Marseglia, A., Vanacore, N., Laukka, E. J., Welmer, A., & Rizzuto, D. (2019) · Aging Clinical and Experimental Research · doi:10.1007/s40520-019-01297-1 · Cited by 40 · see citing works
Brain connectivity and metacognition in persons with subjective cognitive decline (COSCODE): rationale and study design
Ribaldi, F., Chicherio, C., Altomare, D., Martins, M., Tomczyk, S., Jelescu, I., Maturana, E., Scheffler, M., Haller, S., Lövblad, K., et al. (2021) · Alzheimer s Research & Therapy · doi:10.1186/s13195-021-00846-z · Cited by 40 · see citing works
Disrupted Dynamic Functional Connectivity in Distinguishing Subjective Cognitive Decline and Amnestic Mild Cognitive Impairment Based on the Triple-Network Model
Xue, C., Qi, W., Yuan, Q., Hu, G., Ge, H., Rao, J., Xiao, C., & Chen, J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.711009 · Cited by 40 · see citing works
Analysis of Psychological Symptoms Following Disclosure of Amyloid–Positron Emission Tomography Imaging Results to Adults With Subjective Cognitive Decline
Caprioglio, C., Ribaldi, F., Visser, L. N. C., Minguillón, C., Collij, L. E., Grau‐Rivera, O., Zeyen, P., Molinuevo, J. L., Gispert, J. D., Garibotto, V., et al. (2023) · JAMA Network Open · doi:10.1001/jamanetworkopen.2022.50921 · Cited by 39 · see citing works
On Disharmony in Batch Normalization and Dropout Methods for Early Categorization of Alzheimer’s Disease
Tufail, A. B., Ullah, I., Rehman, A. U., Khan, R. A., Khan, M. A., Ma, Y., Khokhar, N. H., Sadiq, M. T., Khan, R., Shafiq, M., et al. (2022) · Sustainability · doi:10.3390/su142214695 · Cited by 38 · see citing works
fNIRS as a biomarker for individuals with subjective memory complaints and MCI
Lee, T., Guo, L., & Chan, A. S.-Y. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.13897 · Cited by 38 · see citing works
Population measures of subjective cognitive decline: A means of advancing public health policy to address cognitive health
Olivari, B. S., Baumgart, M., Taylor, C. A., & McGuire, L. C. (2021) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.12142 · Cited by 38 · see citing works
Longitudinal Cognitive Profiles by Anxiety and Depressive Symptoms in American Older Adults With Subjective Cognitive Decline
Ahn, S., Mathiason, M. A., & Yu, F. (2021) · Journal of Nursing Scholarship · doi:10.1111/jnu.12692 · Cited by 36 · see citing works
Sleep Biomarkers for Predicting Cognitive Decline and Alzheimer’s Disease: A Systematic Review of Longitudinal Studies
Carpi, M., Fernandes, M., Mercuri, N. B., & Liguori, C. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230933 · Cited by 36 · see citing works
Neuropsychiatric symptoms in at-risk groups for AD dementia and their association with worry and AD biomarkers—results from the DELCODE study
Sannemann, L., Schild, A., Altenstein, S., Bartels, C., Brosseron, F., Büerger, K., Cosma, N. C., Fließbach, K., Freiesleben, S. D., Glanz, W., et al. (2020) · Alzheimer s Research & Therapy · doi:10.1186/s13195-020-00701-7 · Cited by 36 · see citing works
Subjective cognitive decline and objective cognition among diverse U.S. Hispanics/Latinos: Results from the Study of Latinos‐Investigation of Neurocognitive Aging (SOL‐INCA)
Zlatar, Z. Z., Tarraf, W., González, K. A., Vásquez, P. M., Marquine, M. J., Lipton, R. B., Gallo, L. C., Khambaty, T., Zeng, D., Youngblood, M., et al. (2021) · Alzheimer s & Dementia · doi:10.1002/alz.12381 · Cited by 34 · see citing works
Subjective cognitive decline in idiopathic Parkinson´s disease: A systematic review
Oedekoven, C., Egeri, L., Jessen, F., Wagner, M., & Dodel, R. C. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101508 · Cited by 36 · see citing works
Association between living arrangements and cognitive decline in older adults: A nationally representative longitudinal study in China
Yu, Y., Lv, J., Liu, J., Chen, Y., Chen, K., & Yang, Y. (2022) · BMC Geriatrics · doi:10.1186/s12877-022-03473-x · Cited by 35 · see citing works
Subjective cognitive decline symptoms and its association with socio-demographic characteristics and common chronic diseases in the southern Chinese older adults
Lin, L., Wang, S., Xu, W., Hu, Q., Zhang, P., Ke, Y.-F., Huang, J.-H., Ding, K., Li, X., Hou, C., et al. (2022) · BMC Public Health · doi:10.1186/s12889-022-12522-4 · Cited by 35 · see citing works
Structural and Functional Disruption of Salience Network in Distinguishing Subjective Cognitive Decline and Amnestic Mild Cognitive Impairment
Xue, C., Sun, H., Yue, Y., Wang, S., Qi, W., Hu, G., Ge, H., Yuan, Q., Rao, J., Tian, L., et al. (2021) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.1c00051 · Cited by 34 · see citing works
Subjective cognitive complaints at age 70: associations with amyloid and mental health
Pavisic, I. M., Lu, K., Keuss, S. E., James, S., Lane, C., Parker, T. D., Keshavan, A., Buchanan, S. M., Murray‐Smith, H., Cash, D. M., et al. (2021) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2020-325620 · Cited by 34 · see citing works
Subjective cognitive decline is a better marker for future cognitive decline in females than in males
Oliver, M., Morrison, C., Kamal, F., Graham, J., & Dadar, M. (2022) · Alzheimer's Research & Therapy · doi:10.1186/s13195-022-01138-w · Cited by 42 · see citing works
A Neuropsychological Perspective on Defining Cognitive Impairment in the Clinical Study of Alzheimer’s Disease: Towards a More Continuous Approach
Jutten, R. J., Thompson, L., Sikkes, S. A. M., Maruff, P., Molinuevo, J. L., Zetterberg, H., Alber, J., Faust, D., Gauthier, S. G., Gold, M., et al. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-215098 · Cited by 32 · see citing works
Longitudinal Relationships Between Subjective Cognitive Decline and Objective Memory: Depressive Symptoms Mediate Between-Person Associations
Hill, N. L., Bhargava, S., Bratlee‐Whitaker, E., Turner, J. R., Brown, M. J., & Mogle, J. A. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210230 · Cited by 32 · see citing works
The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort
Jutten, R. J., Harrison, J., Brunner, A., Vreeswijk, R., van Deelen, R. A. J., de Jong, F. J., Opmeer, E. M., Ritchie, C. W., Aleman, A., Scheltens, P., et al. (2020) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.12020 · Cited by 31 · see citing works
Overall and sex-specific risk factors for subjective cognitive decline: findings from the 2015–2018 Behavioral Risk Factor Surveillance System Survey
Schliep, K. C., Barbeau, W. A., Lynch, K. E., Sorweid, M. K., Varner, M. W., Foster, N. L., & Qeadan, F. (2022) · Biology of Sex Differences · doi:10.1186/s13293-022-00425-3 · Cited by 34 · see citing works
Protocols for cognitive enhancement. A user manual for Brain Health Services—part 5 of 6
Guevara, A. B., Bieler-Aeschlimann, M., Altomare, D., Berthier, M. L., Csajka, C., Dautricourt, S., Démonet, J., Dodich, A., Frisoni, G. B., Miniussi, C., et al. (2021) · Alzheimer s Research & Therapy · doi:10.1186/s13195-021-00844-1 · Cited by 29 · see citing works
Effect of Alzheimer's disease risk and protective factors on cognitive trajectories in subjective memory complainers: An INSIGHT‐preAD study
Teipel, S. J., Cavedo, E., Lista, S., Habert, M., Potier, M., Grothe, M. J., Epelbaum, S., Sambati, L., Gagliardi, G. P., Toschi, N., et al. (2018) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2018.04.004 · Cited by 29 · see citing works
Clinical Characteristics in Subjective Cognitive Decline with and without Worry: Baseline Investigation of the SILCODE Study
Chen, G., Yang, K. Y., Du, W., Hu, X., & Han, Y. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190501 · Cited by 29 · see citing works
Disclosure of Amyloid Status for Risk of Alzheimer Disease to Cognitively Normal Research Participants With Subjective Cognitive Decline: A Longitudinal Study
Wake, T., Tabuchi, H., Funaki, K., Ito, D., Yamagata, B., Yoshizaki, T., Nakahara, T., Jinzaki, M., Yoshimasu, H., Tanahashi, I., et al. (2020) · American Journal of Alzheimer s Disease & Other Dementias® · doi:10.1177/1533317520904551 · Cited by 28 · see citing works
Mental Fatigue Is Associated with Subjective Cognitive Decline among Older Adults
Zhang, Q., Sun, M., Sun, Q., Mei, H., Rao, H., & Liu, J. (2023) · Brain Sciences · doi:10.3390/brainsci13030376 · Cited by 31 · see citing works
Relevance of Minor Neuropsychological Deficits in Patients With Subjective Cognitive Decline
Stark, M., Wolfsgruber, S., Kleineidam, L., Frommann, I., Altenstein, S., Bartels, C., Brosseron, F., Büerger, K., Burow, L., Butryn, M., et al. (2023) · Neurology · doi:10.1212/wnl.0000000000207844 · Cited by 28 · see citing works
Biomarker-based signature of alzheimer's disease in pre-MCI individuals
Chipi, E., Salvadori, N., Farotti, L., & Parnetti, L. (2019) · Brain Sciences · doi:10.3390/brainsci9090213 · Cited by 27 · see citing works
Eugenol relieves the pathological manifestations of Alzheimer's disease in 5×FAD mice
Jung, M., Kim, N., Jeon, S. H., Gee, M. S., Kim, J., & Lee, J. K. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154930 · Cited by 28 · see citing works
Association of adverse childhood experiences with subjective cognitive decline in adulthood: Findings from a population-based study
Baiden, P., Cassidy, J., Panisch, L. S., LaBrenz, C. A., & Onyeaka, H. (2021) · Aging & Mental Health · doi:10.1080/13607863.2021.2017848 · Cited by 27 · see citing works
Altered limbic functional connectivity in individuals with subjective cognitive decline: Converging and diverging findings across Chinese and German cohorts
Jiang, X., Hu, X., Daamen, M., Wang, X., Fan, C., Meiberth, D. U., Spottke, A. E., Roeske, S., Fließbach, K., Spruth, E. J., et al. (2023) · Alzheimer s & Dementia · doi:10.1002/alz.13068 · Cited by 27 · see citing works
Performance of a [ 18 F]Flortaucipir PET Visual Read Method Across the Alzheimer Disease Continuum and in Dementia With Lewy Bodies
Coomans, E. M., de Koning, L. A., Rikken, R. M., Verfaillie, S. C. J., Visser, D., den Braber, A., Tomassen, J., Beek, M. H. C. T. V., Collij, L. E., Lemstra, A. W., et al. (2023) · Neurology · doi:10.1212/wnl.0000000000207794 · Cited by 27 · see citing works
Cerebral blood flow and cognitive functioning in patients with disorders along the heart–brain axis
Leeuwis, A. E., Hooghiemstra, A. M., Bron, E. E., Kuipers, S., Oudeman, E. A., Kalay, T., Rocca, H. B., Kappelle, L. J., van Oostenbrugge, R. J., Greving, J. P., et al. (2020) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.12034 · Cited by 27 · see citing works
Which Episodic Memory Performance is Associated with Alzheimer’s Disease Biomarkers in Elderly Cognitive Complainers? Evidence from a Longitudinal Observational Study with Four Episodic Memory Tests (Insight-PreAD)
Gagliardi, G. P., for the INSIGHT-preAD study group, Epelbaum, S., Houot, M., Bakardjian, H., Boukadida, L., Revillon, M., Dubois, B., Barba, G. D., & Corte, V. L. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-180966 · Cited by 25 · see citing works
Cognitive decline, sensory impairment, and the use of audio-visual aids by long-term care facility residents
Kwan, R. Y. C., Kwan, C. W., Kor, P. P. K., & Chi, I. (2022) · BMC Geriatrics · doi:10.1186/s12877-022-02895-x · Cited by 25 · see citing works
Application of the Amyloid/Tau/Neurodegeneration Framework in Cognitively Intact Adults: The CABLE Study
Hu, H., Bi, Y., Shen, X., Ma, Y., Ou, Y., Zhang, W., Ma, L., Hu, H., Dong, Q., Tan, L., et al. (2022) · Annals of Neurology · doi:10.1002/ana.26439 · Cited by 25 · see citing works
Classification of negative and positive 18F-florbetapir brain PET studies in subjective cognitive decline patients using a convolutional neural network
de Vries, B. M., Golla, S. S. V., Ebenau, J. L., Verfaillie, S. C. J., Timmers, T., Heeman, F., Cysouw, M. C. F., van Berckel, B. N. M., van der Flier, W. M., Yaqub, M. M., et al. (2020) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-020-05006-3 · Cited by 24 · see citing works
Subjective cognitive decline and self‐reported sleep problems: The SCIENCe project
Exalto, L. G., Hendriksen, H. M. A., Barkhof, F., van den Bosch, K. A., Ebenau, J. L., van Leeuwenstijn‐Koopman, M., Prins, N. D., Teunissen, C. E., Visser, L. N. C., Scheltens, P., et al. (2022) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1002/dad2.12287 · Cited by 24 · see citing works
Effects of a mindfulness-based versus a health self-management intervention on objective cognitive performance in older adults with subjective cognitive decline (SCD): a secondary analysis of the SCD-Well randomized controlled trial
Whitfield, T. J., Demnitz‐King, H., Schlosser, M., Barnhofer, T., Frison, É., Coll‐Padrós, N., Dautricourt, S., Requier, F., Delarue, M., Gonneaud, J., et al. (2022) · Alzheimer s Research & Therapy · doi:10.1186/s13195-022-01057-w · Cited by 25 · see citing works
“The Dichotic Digit Test” as an Index Indicator for Hearing Problem in Dementia: Systematic Review and Meta-Analysis
Utoomprurkporn, N., Hardy, C. J. D., Stott, J. C. H., Costafreda, S. G., Warren, J. D., & Bamiou, D. (2020) · Journal of the American Academy of Audiology · doi:10.1055/s-0040-1718700 · Cited by 24 · see citing works
Long COVID and recovery from Long COVID: quality of life impairments and subjective cognitive decline at a median of 2 years after initial infection
Szewczyk, W., Fitzpatrick, A. L., Fossou, H., Gentile, N. L., Sotoodehnia, N., Vora, S. B., West, T. E., Bertolli, J., Cope, J. R., Lin, J.-M. S., et al. (2024) · BMC Infectious Diseases · doi:10.1186/s12879-024-10158-w · Cited by 27 · see citing works
The clinical heterogeneity of subjective cognitive decline: a data-driven approach on a population-based sample
Ribaldi, F., Rolandi, E., Vaccaro, R., Colombo, M. M., Frisoni, G. B., & Guaita, A. (2022) · Age and Ageing · doi:10.1093/ageing/afac209 · Cited by 24 · see citing works
How does urbanization affect the cognitive function among older adults: A geospatial analysis in China
Tian, W., Cao, K., Kwan, M., Chiu, M. Y.-L., & Chen, H. (2024) · Health & Place · doi:10.1016/j.healthplace.2024.103259 · Cited by 23 · see citing works
How Well Does Subjective Cognitive Decline Correspond to Objectively Measured Cognitive Decline? Assessment of 10–12 Year Change
Gustavson, D. E., Jak, A. J., Elman, J. A., Panizzon, M. S., Franz, C. E., Gifford, K. A., Reynolds, C. A., Toomey, R., Lyons, M. J., & Kremen, W. S. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210123 · Cited by 23 · see citing works
Predicting progression from subjective cognitive decline to mild cognitive impairment or dementia based on brain atrophy patterns
Lerch, O., Ferreira, D., Stomrud, E., van Westen, D., Tideman, P., Palmqvist, S., Mattsson, N., Hort, J., Hansson, O., & Westman, E. (2024) · Alzheimer s Research & Therapy · doi:10.1186/s13195-024-01517-5 · Cited by 22 · see citing works

P4‐153: Subjective Cognitive Decline and Progression to Dementia Due to AD and Non‐AD in Memory Clinic and Community‐Based Cohorts
Slot, R. E. R., Sikkes, S. A. M., Verfaillie, S. C. J., Wolfsgruber, S., Brodaty, H., Buckley, R. F., Hampel, H. J., Kochan, N. A., Luck, T., Maruff, P. T., et al. (2016) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2016.06.2245 · Cited by 1 · see citing works
P3‐211: Differential risk of incident Alzheimer's disease dementia in stable versus unstable patterns of subjective cognitive decline
Wagner, M., Wolfsgruber, S., Kleineidam, L., Koppara, A., Riedel-Heller, S. G., Maier, W., Scherer, M., & Jessen, F. (2015) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2015.06.1583 · Cited by 2 · see citing works
Subjective Cognitive Decline Plus and Longitudinal Assessment and Risk for Cognitive Impairment
Kang, M.-I., Li, C., Mahajan, A., Spat‐Lemus, J., Durape, S., Chen, J., Gurnani, A. S., Devine, S., Auerbach, S. H., Ang, T. F. A., et al. (2024) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2024.1678 · Cited by 54 · see citing works
Subjective cognitive decline, APOE genotype, and incident Alzheimer’s disease: The AGES‐Reykjavik Study
Geerlings, M. I., Gerritsen, L., Vonk, J. M. J., Gudnason, V. G., & Launer, L. J. (2020) · Alzheimer s & Dementia · doi:10.1002/alz.041875
Dyadic patterns of subjective cognitive reports as predictors of incident dementia
Numbers, K. T., Lam, B. C. P., Crawford, J. D., Kochan, N. A., Sachdev, P. S., & Brodaty, H. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.061351

Authors: Slot, R. E. R., Sikkes, S. A. M., Berkhof, J., Brodaty, H., Buckley, R., Cavedo, E., Dardiotis, E., Guillo‐Benarous, F., Hampel, H., Kochan, N. A., Lista, S., Luck, T., Maruff, P., Molinuevo, J. L., Kornhuber, J., Reisberg, B., Riedel‐Heller, S. G., Risacher, S. L., Roehr, S., Sachdev, P. S., Scarmeas, N., Scheltens, P., Shulman, M. B., Saykin, A. J., Verfaillie, S. C. J., Visser, P. J., Vos, S. J. B., Wagner, M., Wolfsgruber, S., Jessen, F., Initiative, T. A. D. N., the DESCRIPA working group, the INSIGHT‐preAD study group, SCD‐I working group, & van der Flier, W. M.
Affiliations: Amsterdam Neuroscience (NL)
Amsterdam University Medical Centers (NL)
UNSW Sydney (AU)
Harvard University (US)
Centre National de la Recherche Scientifique (FR)
University of Thessaly (GR)
NYU Langone Health (US)
Nordhausen University of Applied Sciences (DE)
Florey Institute of Neuroscience and Mental Health (AU)
Neurology Department Hospital Clínic i Universitari‐IDIBAPS and BarcelonaBeta Brain Research Center Pasqual Maragall Foundation Barcelona Spain
Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
Institute of Social Medicine Occupational Health and Public Health (ISAP) Faculty of Medicine University of Leipzig Leipzig Germany
Indiana University Indianapolis (US)
National and Kapodistrian University of Athens (GR)
Maastricht University (NL)
University of Bonn (DE)
University of Cologne (DE)
Alzheimer Center Amsterdam Department of Neurology Amsterdam Neuroscience Vrije Universiteit Amsterdam Amsterdam UMC Amsterdam the Netherlands
Corresponding author: the Alzheimer's Disease Neuroimaging Initiative
ORCID: Slot, Rosalinde E.R.
Sikkes, Sietske A.M.
Berkhof, Johannes
Brodaty, Henry
Buckley, Rachel
Cavedo, Enrica
Dardiotis, Efthimios
Hampel, Harald
Kochan, Nicole A.
Lista, Simone
Luck, Tobias
Maruff, Paul
Kornhuber, Johannes
Reisberg, Barry
Risacher, Shannon L.
Sachdev, Perminder S.
Scarmeas, Nikolaos
Scheltens, Philip
Shulman, Melanie B.
Saykin, Andrew J.
Verfaillie, Sander C.J.
Visser, Pieter Jelle
Vos, Stephanie J.B.
Wagner, Michael
Wolfsgruber, Steffen
Jessen, Frank
Venue: Alzheimer's & Dementia
Publisher: Wiley
Published: 2018-12-13
Volume: 15
Issue: 3
Pages: 465-476
ISSN: 1552-5260 (ISSN-L)
1552-5279
DOI: 10.1016/j.jalz.2018.10.003
PMC: PMC6465066
OpenAlex: W2904079367
Cited by: 428
References: 61
Citations by year: 2026: 39 · 2025: 55 · 2024: 68 · 2023: 65 · 2022: 65 · 2021: 54 · 2020: 62 · 2019: 17 · 2018: 3
FWCI: 26.57
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-nd
creativecommons.org/licenses/by-nc-nd/4.0/ (am)
creativecommons.org/licenses/by-nc-nd/4.0/ (vor)
Locations: Alzheimer s & Dementia (publishedVersion, cc-by-nc-nd)
PubMed (publishedVersion)
Pure Amsterdam UMC (publishedVersion, cc-by)
VU Research Portal (publishedVersion, other-oa)
Europe PMC (PubMed Central) (acceptedVersion, cc-by-nc-nd)
PubMed Central (acceptedVersion, cc-by-nc-nd)
Minerva Access (University of Melbourne) (submittedVersion, cc-by-nc-nd)
HAL (submittedVersion, cc-by-nc-nd)
Research Publications (Maastricht University) (submittedVersion, cc-by-nc-nd)
University of Thessaly Institutional Repository (University of Thessaly) (submittedVersion)
CINECA IRIS Institutial Research Information System (University of Genoa) (submittedVersion, other-oa)
Massey Research Online (Massey University) (submittedVersion)
Amsterdam UMC (VU Amsterdam) - Institutional Repository (submittedVersion, other-oa)
IUScholarWorks (Indiana University) (submittedVersion)
Purdue University Indianapolis (Indiana University) (submittedVersion)
Research Publications (Maastricht University) (submittedVersion, other-oa)
Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
Funders: ZonMw
Alzheimer's Association (IIRG-09-133014)
Centre Hospitalier Universitaire de Bordeaux (CIC EC7)
AXA Research Fund
U.S. Department of Health and Human Services (AG08051, AG03051)
National Institute on Aging (P30 AG010133, R01 AG019771, K01 AG049050)
U.S. Department of Defense (W81XWH-12-2-0012)
National Institute of Biomedical Imaging and Bioengineering
Topics: Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cancer-related cognitive impairment studies
Keywords: subjective cognitive decline, Alzheimer's disease
MeSH terms: Aged, Aged, 80 and over, Dementia, Female, Humans, Male, Middle Aged, Risk Factors, Self Concept, Cohort Studies, Incidence, Disease Progression, Diagnostic Self Evaluation, Cognitive Dysfunction

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 ›

Are you an author, or do you see a problem with this page? Request a review

Subjective cognitive decline and rates of incident Alzheimer's disease and non-Alzheimer's disease dementia

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Self-check

Cites

Cited by

Related

Record

About these checks