Olfactory Impairment in Presymptomatic Alzheimer's Disease

被引:174
作者
Wilson, Robert S. [1 ,2 ,3 ]
Arnold, Steven E. [5 ,6 ]
Schneider, Julie A. [1 ,2 ,4 ]
Boyle, Patricia A. [1 ,3 ]
Buchman, Aron S. [1 ,2 ]
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, Dept Neurol Sci, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Behav Sci, Chicago, IL 60612 USA
[4] Rush Univ, Med Ctr, Dept Pathol, Chicago, IL 60612 USA
[5] Univ Penn, Ctr Neurobiol & Behav, Cellular & Mol Neuropathol Program, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
来源
INTERNATIONAL SYMPOSIUM ON OLFACTION AND TASTE | 2009年 / 1170卷
关键词
olfaction; Alzheimer's disease; mild cognitive impairment; MILD COGNITIVE IMPAIRMENT; E EPSILON-4 ALLELE; ODOR IDENTIFICATION; DEFICITS; PATHOLOGY; DECLINE; MARKERS; DEMENTIA; SYSTEMS; MEMORY;
D O I
10.1111/j.1749-6632.2009.04013.x
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Alzheimer's disease (AD) impairs olfaction, but it is uncertain how early this occurs in the disease process and whether the effect can be accounted for by other behavioral or genetic markers of the disease. We administered the Brief Smell Identification Test (BSIT) to 471 older people without dementia or cognitive impairment who then completed annual clinical evaluations and brain autopsy at death. BSIT score was associated with more rapid decline in episodic memory and with increased risk of developing incident mild cognitive impairment (MCI), even after controlling for baseline level of episodic memory and possession of an apolipoprotein E epsilon 4 allele. In 34 people who died without evidence of cognitive impairment, lower BSIT score was associated with higher level of AD pathology, even after controlling for epsilon 4 and for level of episodic memory function when olfaction was assessed. These analyses suggest that among older people without clinical manifestations of AD or MCI, olfactory dysfunction is related to both the level of AD pathology in the brain and the risk of subsequently developing prodromal symptoms of the disease, and that these associations persist after accounting for the effects of other recognized behavioral and genetic markers of the disease.
引用
收藏
页码:730 / 735
页数:6
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