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September 21, 2010; 75 (12) Articles

Neurodegenerative basis of age-related cognitive decline

R.S. Wilson, S.E. Leurgans, P.A. Boyle, J.A. Schneider, D.A. Bennett
First published September 15, 2010, DOI: https://doi.org/10.1212/WNL.0b013e3181f39adc
R.S. Wilson
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S.E. Leurgans
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P.A. Boyle
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J.A. Schneider
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D.A. Bennett
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Citation
Neurodegenerative basis of age-related cognitive decline
R.S. Wilson, S.E. Leurgans, P.A. Boyle, J.A. Schneider, D.A. Bennett
Neurology Sep 2010, 75 (12) 1070-1078; DOI: 10.1212/WNL.0b013e3181f39adc

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Abstract

Objective: To assess the contribution of dementia-related neuropathologic lesions to age-related and disease-related change in cognitive function.

Methods: A total of 354 Catholic nuns, priests, and brothers had annual clinical evaluations for up to 13 years, died, and underwent brain autopsy. The clinical evaluations included detailed testing of cognitive function from which previously established composite measures of global cognition and specific cognitive functions were derived. As part of a uniform neuropathologic evaluation, the density of neurofibrillary tangles was summarized in a composite measure and the presence of Lewy bodies and gross and microscopic cerebral infarction was noted.

Results: During follow-up, rate of global cognitive decline was gradual at first and then more than quadrupled in the last 4 to 5 years of life consistent with the onset of progressive dementia. Neurofibrillary tangles, cerebral infarction, and neocortical Lewy bodies all contributed to gradual age-related cognitive decline and little age-related decline was evident in the absence of these lesions. Neurofibrillary tangles and neocortical Lewy bodies contributed to precipitous disease-related cognitive decline, but substantial disease-related decline was evident even in the absence of these lesions.

Conclusion: Mild age-related decline in cognitive function is mainly due to the neuropathologic lesions traditionally associated with dementia.

Footnotes

  • Supplemental data at www.neurology.org

    e-Pub ahead of print on September 15, 2010, at www.neurology.org.

    Study funding: Supported by the NIH/NIA (R01AG015819, P30AG010161, and R01AG034374). The sponsors had no role in the design and conduct of the study; in the collection, management, analysis, or interpretation of the data; or in the preparation, review, or approval of the manuscript.

    Disclosure: Author disclosures are provided at the end of the article.

    Received February 11, 2010. Accepted in final form May 17, 2010.

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