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

被引:184
作者
Buchman, Aron S. [1 ,2 ]
Yu, Lei [1 ,2 ]
Boyle, Patricia A. [1 ,3 ]
Schneider, Julie A. [1 ,2 ,4 ]
De Jager, Philip L. [5 ,6 ,7 ,8 ]
Bennett, David A. [1 ,2 ]
机构
[1] Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Neurol Sci, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Behav Sci, Chicago, IL 60612 USA
[4] Rush Univ, Med Ctr, Pathol Neuropathol, Chicago, IL 60612 USA
[5] Brigham & Womens Hosp, Program Translat NeuroPsychiat Genom, Inst Neurosci, Dept Neurol, 75 Francis St, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Dept Psychiat, 75 Francis St, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Boston, MA USA
[8] Broad Inst, Program Med & Populat Genet, Cambridge, MA USA
关键词
ALZHEIMERS-DISEASE PATIENTS; NEUROTROPHIC FACTOR; SUSCEPTIBILITY; IMPAIRMENT; MEMORY;
D O I
10.1212/WNL.0000000000002387
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:735 / 741
页数:7
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