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Cited by 217

The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.

Combined neuropathological pathways account for age‐related risk of dementia

Open access
Power, Melinda C., Mormino, Elizabeth, Soldan, Anja, James, Bryan D., Yu, Lei, Armstrong, Nicole M., Bangen, Katherine J., Delano‐Wood, Lisa, Lamar, Melissa, Lim, Yen Ying, Nudelman, Kelly, Zahodne, Laura, Gross, Alden L., Mungas, Dan, Widaman, Keith F., Schneider, Julie·2018·Annals of Neurology

Abstract

Objective: Our objectives were to characterize the inter‐relation of known dementia‐related neuropathologies in one comprehensive model and quantify the extent to which accumulation of neuropathologies accounts for the association between age and dementia. Methods: We used data from 1,362 autopsied participants of three community‐based clinicopathological cohorts: the Religious Orders Study, the Rush Memory and Aging Project, and the Minority Aging Research Study. We estimated a series of structural equation models summarizing a priori hypothesized neuropathological pathways between age and dementia risk individually and collectively. Results: At time of death (mean age, 89 years), 44% of our sample had a clinical dementia diagnosis. When considered individually, our vascular, amyloid/tau, neocortical Lewy body, and TAR DNA‐binding protein 43 (TDP‐43)/hippocampal sclerosis pathology pathways each accounted for a substantial proportion of the association between age and dementia. When considered collectively, the four pathways fully accounted for all variance in dementia risk previously attributable to age. Pathways involving amyloid/tau, neocortical Lewy bodies, and TDP‐43/hippocampal sclerosis were interdependent, attributable to the importance of amyloid beta plaques in all three. The importance of the pathways varied, with the vascular pathway accounting for 32% of the association between age and dementia, wheraes the remaining three inter‐related degenerative pathways together accounted for 68% (amyloid/tau, 24%; the Lewy body, 1%; and TDP‐43/hippocampal sclerosis, 43%). Interpretation: Age‐related increases in dementia risk can be attributed to accumulation of multiple pathologies, each of which contributes to dementia risk. Multipronged approaches may be necessary if we are to develop effective therapies. Ann Neurol 2018;84:10–22

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Metadata

Authors
Power, M. C., Mormino, E., Soldan, A., James, B. D., Yu, L., Armstrong, N. M., Bangen, K. J., Delano‐Wood, L., Lamar, M., Lim, Y. Y., Nudelman, K., Zahodne, L., Gross, A. L., Mungas, D., Widaman, K. F., & Schneider, J.
Venue
Annals of Neurology
Publisher
Wiley
Published
2018-06-26
Volume
84
Issue
1
Pages
10-22
ISSN
  • 0364-5134 (ISSN-L)
  • 1531-8249
OpenAlex
W2810507529
Cited by
217
References
15
FWCI
16.65
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Combined neuropathological pathways account for age‐related risk of dementia. https://app.cochat.ai/papers/10.1002/ana.25246
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Power, M. C., Mormino, E., Soldan, A., James, B. D., Yu, L., Armstrong, N. M., Bangen, K. J., Delano‐Wood, L., Lamar, M., Lim, Y. Y., Nudelman, K., Zahodne, L., Gross, A. L., Mungas, D., Widaman, K. F., & Schneider, J. (2018). Combined neuropathological pathways account for age‐related risk of dementia. Annals of Neurology. https://doi.org/10.1002/ana.25246

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