Cited by 239Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsNeurological Disease Mechanisms and Treatments

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Higher brain BDNF gene expression is associated with slower cognitive decline in older adults

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Abstract

OBJECTIVES: We tested whether brain-derived neurotrophic factor (BDNF) gene expression levels are associated with cognitive decline in older adults. METHODS: Five hundred thirty-five older participants underwent annual cognitive assessments and brain autopsy at death. BDNF gene expression was measured in the dorsolateral prefrontal cortex. Linear mixed models were used to examine whether BDNF expression was associated with cognitive decline adjusting for age, sex, and education. An interaction term was added to determine whether this association varied with clinical diagnosis proximate to death (no cognitive impairment, mild cognitive impairment, or dementia). Finally, we examined the extent to which the association of Alzheimer disease (AD) pathology with cognitive decline varied by BDNF expression. RESULTS: Higher brain BDNF expression was associated with slower cognitive decline (p < 0.001); cognitive decline was about 50% slower with the 90th percentile BDNF expression vs 10th. This association was strongest in individuals with dementia. The level of BDNF expression was lower in individuals with pathologic AD (p = 0.006), but was not associated with macroscopic infarcts, Lewy body disease, or hippocampal sclerosis. BDNF expression remained associated with cognitive decline in a model adjusting for age, sex, education, and neuropathologies (p < 0.001). Furthermore, the effect of AD pathology on cognitive decline varied by BDNF expression such that the effect was strongest for high levels of AD pathology (p = 0.015); thus, in individuals with high AD pathology (90th percentile), cognitive decline was about 40% slower with the 90th percentile BDNF expression vs 10th. CONCLUSIONS: Higher brain BDNF expression is associated with slower cognitive decline and may also reduce the deleterious effects of AD pathology on cognitive decline.

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References 23 · Cited by 239

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  1. SAS/STAT® User's Guide, version 9.3 [computer Program]. Cary, NC: SAS Institute Inc.; 2011.

Metadata

Authors
Buchman, A. S., Yu, L., Boyle, P. A., Schneider, J. A., De Jager, P. L., & Bennett, D. A.
Affiliations
  • Broad Institute (US)
  • From the Rush Alzheimer's Disease Center (A.S.B., L.Y., P.A.B., J.A.S., D.A.B.), Neurological Science (A.S.B., L.Y., J.A.S., D.A.B.), Behavioral Sciences (P.A.B.), Pathology (Neuropathology) (J.A.S.), Rush University Medical Center, Chicago, IL; Program in Translational NeuroPsychiatric Genomics (P.L.D.), Institute for the Neurosciences, Departments of Neurology and Psychiatry, Brigham and Women's Hospital, Boston; Harvard Medical School (P.L.D.), Boston; and Program in Medical and Population...
Venue
Neurology
Published
2016-02-23
Volume
86
Issue
8
Pages
735-741
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2287080163
Cited by
239
References
23
Citations by year
2026: 17 · 2025: 23 · 2024: 30 · 2023: 27 · 2022: 20 · 2021: 25 · 2020: 20 · 2019: 21 · 2018: 22 · 2017: 20 · 2016: 13
FWCI
22.22
Type
journal article
Language
en
Open access
Locations
  • Neurology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institute on Aging (R01AG043379, R01AG017917, U02AG46152, R01AG042210, R02AG36836, R01AG015819, P30AG010161, RF1AG015819, R01AG034374)
  • National Institute of Neurological Disorders and Stroke (R01NS078009)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
Keywords
brain-derived neurotrophic factor, BDNF expression, cognitive decline, older adults, Alzheimer disease pathology, dementia, mild cognitive impairment, dorsolateral prefrontal cortex, neuropathology, Lewy body disease, hippocampal sclerosis, cerebral infarction
MeSH terms
Aged, Aged, 80 and over, Aging, Brain, Cognition Disorders, Follow-Up Studies, Gene Expression Regulation, Humans, Longitudinal Studies, Male, Brain-Derived Neurotrophic Factor

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