Multiple Brain Markers are Linked to Age-Related Variation in Cognition

被引:114
|
作者
Hedden, Trey [1 ,5 ]
Schultz, Aaron P. [1 ,2 ,3 ]
Rieckmann, Anna [1 ,9 ]
Mormino, Elizabeth C. [2 ]
Johnson, Keith A. [2 ,4 ,5 ,6 ]
Sperling, Reisa A. [1 ,2 ,3 ,6 ]
Buckner, Randy L. [1 ,3 ,5 ,7 ,8 ]
机构
[1] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Dept Radiol, Charlestown, MA USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Neurol, Boston, MA USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Psychiat, Boston, MA USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Nucl Med & Mol Imaging, Boston, MA USA
[5] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Radiol, Boston, MA USA
[6] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Alzheimer Res & Treatment,Dept Neurol, Boston, MA 02115 USA
[7] Harvard Univ, Dept Psychol, 33 Kirkland St, Cambridge, MA 02138 USA
[8] Harvard Univ, Ctr Brain Sci, Cambridge, MA 02138 USA
[9] Umea Univ, Dept Radiat Sci, SE-90187 Umea, Sweden
基金
美国国家卫生研究院;
关键词
aging; amyloid; executive function; memory; white matter; NORMAL OLDER-ADULTS; WHITE-MATTER HYPERINTENSITIES; ALZHEIMERS-DISEASE; AMYLOID DEPOSITION; FUNCTIONAL CONNECTIVITY; EXECUTIVE FUNCTIONS; CEREBRAL-CORTEX; DECLINE; BURDEN; MEMORY;
D O I
10.1093/cercor/bhu238
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Age-related alterations in brain structure and function have been challenging to link to cognition due to potential overlapping influences of multiple neurobiological cascades. We examined multiple brain markers associated with age-related variation in cognition. Clinically normal older humans aged 65-90 from the Harvard Aging Brain Study (N = 186) were characterized on a priori magnetic resonance imaging markers of gray matter thickness and volume, white matter hyperintensities, fractional anisotropy (FA), resting-state functional connectivity, positron emission tomography markers of glucose metabolism and amyloid burden, and cognitive factors of processing speed, executive function, and episodic memory. Partial correlation and mediation analyses estimated age-related variance in cognition shared with individual brain markers and unique to each marker. The largest relationships linked FA and striatum volume to processing speed and executive function, and hippocampal volume to episodic memory. Of the age-related variance in cognition, 70-80% was accounted for by combining all brain markers (but only similar to 20% of total variance). Age had significant indirect effects on cognition via brain markers, with significant markers varying across cognitive domains. These results suggest that most age-related variation in cognition is shared among multiple brain markers, but potential specificity between some brain markers and cognitive domains motivates additional study of age-related markers of neural health.
引用
收藏
页码:1388 / 1400
页数:13
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