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Participation in Cognitively Stimulating Activities and Risk of Incident Alzheimer Disease
Abstract
CONTEXT: Frequent participation in cognitively stimulating activities has been hypothesized to reduce risk of Alzheimer disease (AD), but prospective data regarding an association are lacking. OBJECTIVE: To test the hypothesis that frequent participation in cognitive activities is associated with a reduced risk of AD. DESIGN: Longitudinal cohort study with baseline evaluations performed between January 1994 and July 2001 and mean follow-up of 4.5 years. PARTICIPANTS AND SETTING: A total of 801 older Catholic nuns, priests, and brothers without dementia at enrollment, recruited from 40 groups across the United States. At baseline, they rated frequency of participation in common cognitive activities (eg, reading a newspaper), from which a previously validated composite measure of cognitive activity frequency was derived. MAIN OUTCOME MEASURES: Clinical diagnosis of AD by a board-certified neurologist using National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer's Disease and Related Disorders Association criteria and change in global and specific measures of cognitive function, compared by cognitive activity score at baseline. RESULTS: Baseline scores on the composite measure of cognitive activity ranged from 1.57 to 4.71 (mean, 3.57; SD, 0.55), with higher scores indicating more frequent activity. During an average of 4.5 years of follow-up, 111 persons developed AD. In a proportional hazards model that controlled for age, sex, and education, a 1-point increase in cognitive activity score was associated with a 33% reduction in risk of AD (hazard ratio, 0.67; 95% confidence interval, 0.49-0.92). Results were comparable when persons with memory impairment at baseline were excluded and when terms for the apolipoprotein E epsilon4 allele and other medical conditions were added. In random-effects models that controlled for age, sex, education, and baseline level of cognitive function, a 1-point increase in cognitive activity was associated with reduced decline in global cognition (by 47%), working memory (by 60%), and perceptual speed (by 30%). CONCLUSION: These results suggest that frequent participation in cognitively stimulating activities is associated with reduced risk of AD.
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Tenchov, R., Sasso, J. M., & Zhou, Q. A. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00339 · Cited by 170
Cognitive Impairment in the Age-Related Eye Disease Study: AREDS Report No. 16
(2006) · Archives of Ophthalmology · doi:10.1001/archopht.124.4.537 · Cited by 163
The apolipoprotein E varepsilon2 allele and decline in episodic memory
Wilson, R. S. (2002) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.73.6.672 · Cited by 161
Self-citationSpace and location of cerebral microbleeds, cognitive decline, and dementia in the community
Ding, J., Sigurðsson, S., Jónsson, P. V., Eiriksdottir, G., Meirelles, O., Kjartansson, O., Lopez, O. L., van Buchem, M. A., Gudnason, V., & Launer, L. J. (2017) · Neurology · doi:10.1212/wnl.0000000000003983 · Cited by 159
Change in risk of Alzheimer disease over time
Hebert, L. E., Bienias, J. L., Aggarwal, N. T., Wilson, R. S., Bennett, D. A., Shah, R. C., & Evans, D. A. (2010) · Neurology · doi:10.1212/wnl.0b013e3181f0754f · Cited by 158
Self-citationThomas, A. G., Dennis, A., Rawlings, N. B., Stagg, C. J., Matthews, L., Morris, M., Kolind, S. H., Foxley, S., Jenkinson, M., Nichols, T. E., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.090 · Cited by 152
“This result is particularly relevant given the growing recognition of the importance of lifestyle during middle age for lifelong cognitive health (Wilson et al., 2002; Karp et al., 2006; Young et al., 2015).”
BackgroundStern, Y., Zarahn, E., Habeck, C., Holtzer, R., Rakitin, B. C., Kumar, A., Flynn, J., Steffener, J., & Brown, T. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm134 · Cited by 143
Physical Activity, Cognitive Activity, and Cognitive Decline in a Biracial Community Population
Sturman, M. T., Morris, M. C., Mendes de Leon, C. F., Bienias, J. L., Wilson, R. S., & Evans, D. A. (2005) · Archives of Neurology · doi:10.1001/archneur.62.11.1750 · Cited by 142
Self-citationSoetanto, A., Wilson, R. S., Talbot, K., Un, A., Schneider, J. A., Sobiesk, M., Kelly, J., Leurgans, S., Bennett, D. A., & Arnold, S. E. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.48 · Cited by 148
Self-citationWomen Who Maintain Optimal Cognitive Function into Old Age
Barnes, D. E., Cauley, J. A., Lui, L., Fink, H. A., McCulloch, C., Stone, K. L., & Yaffe, K. (2007) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2007.01040.x · Cited by 145
Saczynski, J. S., Jonsdottir, M. K., Garcia, M. E., Jonsson, P. V., Peila, R., Eiriksdottir, G., Olafsdottir, E., Harris, T. B., Gudnason, V., & Launer, L. J. (2008) · American Journal of Epidemiology · doi:10.1093/aje/kwn228 · Cited by 142
SUMOWSKI, J. F., CHIARAVALLOTI, N., WYLIE, G., & DELUCA, J. (2009) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617709090912 · Cited by 132
Tranter, L. J., & Koutstaal, W. (2008) · Aging Neuropsychology and Cognition · doi:10.1080/13825580701322163 · Cited by 130
Cognitive Activities During Adulthood Are More Important than Education in Building Reserve
Reed, B. R., Dowling, M., Tomaszewski Farias, S., Sonnen, J., Strauss, M., Schneider, J. A., Bennett, D. A., & Mungas, D. (2011) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617711000014 · Cited by 121
Lee, A. T. C., Richards, M., Chan, W. C., Chiu, H. F. K., Lee, R. S. Y., & Lam, L. C. W. (2018) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2018.0657 · Cited by 124
Cellular, synaptic, and biochemical features of resilient cognition in Alzheimer’s disease
Arnold, S. E., Louneva, N., Cao, K., Wang, L.-S., Han, L.-Y., Wolk, D. A., Negash, S., Leurgans, S. E., Schneider, J. A., Buchman, A. S., et al. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.03.004 · Cited by 123
Self-citation
Metadata
- Authors
- Wilson, R. S.
- Venue
- JAMA
- Publisher
- American Medical Association (AMA)
- Published
- 2002-02-13
- Volume
- 287
- Issue
- 6
- Pages
- 742
- ISSN
- 0002-9955 (ISSN-L)
- 0098-7484
- OpenAlex
- W2134717514
- Cited by
- 1,326
- References
- 13
- FWCI
- 32.12
- Type
- journal article
- Language
- en
- Open access
- closed
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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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.