Cognitive Profile of Amyloid Burden and White Matter Hyperintensities in Cognitively Normal Older Adults

被引:152
作者
Hedden, Trey [1 ,5 ]
Mormino, Elizabeth C. [2 ]
Amariglio, Rebecca E. [2 ,6 ]
Younger, Alayna P. [1 ,3 ]
Schultz, Aaron P. [1 ,2 ,3 ]
Becker, J. Alex [4 ]
Buckner, Randy L. [1 ,3 ,5 ,7 ,8 ,9 ]
Johnson, Keith A. [2 ,4 ,5 ,6 ]
Sperling, Reisa A. [1 ,2 ,6 ]
Rentz, Dorene M. [2 ,6 ]
机构
[1] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Dept Radiol, Charlestown, MA 02129 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Neurol, Boston, MA 02114 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Psychiat, Boston, MA 02114 USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Nucl Med & Mol Imaging, Boston, MA 02114 USA
[5] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Radiol, Boston, MA 02114 USA
[6] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Alzheimer Res & Treatment,Dept Neurol, Boston, MA 02115 USA
[7] Harvard Univ, Dept Psychol, Cambridge, MA 02138 USA
[8] Harvard Univ, Ctr Brain Sci, Cambridge, MA 02138 USA
[9] Harvard Univ, Howard Hughes Med Inst, Cambridge, MA 02115 USA
基金
美国国家卫生研究院;
关键词
ALZHEIMERS-DISEASE; FRONTAL-LOBE; IN-VIVO; EXECUTIVE FUNCTIONS; DEMENTIA; MEMORY; AGE; DEPOSITION; DECLINE; RESERVE;
D O I
10.1523/JNEUROSCI.2462-12.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Amyloid burden and white matter hyperintensities (WMH) are two common markers of neurodegeneration present in advanced aging. Each represents a potential early indicator of an age-related neurological disorder that impacts cognition. The presence of amyloid is observed in a substantial subset of cognitively normal older adults, but the literature remains equivocal regarding whether amyloid in nondemented populations is deleterious to cognition. Similarly, WMH are detected in many nondemented older adults and there is a body of evidence indicating that WMH are associated with decreased executive function and other cognitive domains. The current study investigated amyloid burden and WMH in clinically normal older adult humans aged 65-86 (N = 168) and examined each biomarker's relation with cognitive domains of episodic memory, executive function, and speed of processing. Factors for each domain were derived from a neuropsychological battery on a theoretical basis without reference to the relation between cognition and the biomarkers. Amyloid burden and WMH were not correlated with one another. Age was associated with lower performance in all cognitive domains, while higher estimated verbal intelligence was associated with higher performance in all domains. Hypothesis-driven tests revealed that amyloid burden and WMH had distinct cognitive profiles, with amyloid burden having a specific influence on episodic memory and WMH primarily associated with executive function but having broad (but lesser) effects on the other domains. These findings suggest that even before clinical impairment, amyloid burden and WMH likely represent neuropathological cascades with distinct etiologies and dissociable influences on cognition.
引用
收藏
页码:16233 / 16242
页数:10
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