Long-term episodic memory decline is associated with olfactory deficits only in carriers of ApoE-ε4

被引:37
|
作者
Olofsson, Jonas K. [1 ,2 ]
Josefsson, Maria [3 ]
Ekstrom, Ingrid [1 ]
Wilson, Donald [4 ]
Nyberg, Lars [5 ]
Nordin, Steven [6 ]
Adolfsson, Annelie Nordin [7 ]
Adolfsson, Rolf [7 ]
Nilsson, Lars-Goran [1 ]
Larsson, Maria [1 ]
机构
[1] Stockholm Univ, Dept Psychol, Gosta Ekman Lab, S-10691 Stockholm, Sweden
[2] Swedish Coll Adv Study, Uppsala, Sweden
[3] Umea Univ, Ctr Demog & Ageing Res, Umea, Sweden
[4] NYU, Langone Med Ctr, New York, NY USA
[5] Umea Univ, Dept Radiat Sci, Umea, Sweden
[6] Umea Univ, Dept Psychol, S-90187 Umea, Sweden
[7] Umea Univ, Dept Clin Sci, Umea, Sweden
基金
瑞典研究理事会;
关键词
Dementia; Alzheimer disease; Olfactory perception; Memory; Aging; Mild cognitive impairment; MILD COGNITIVE IMPAIRMENT; APOLIPOPROTEIN-E EPSILON-4; ODOR IDENTIFICATION DEFICIT; ALZHEIMERS-DISEASE; HIPPOCAMPAL VOLUME; BRAIN ATROPHY; DEMENTIA; CONVERSION; POPULATION; PATHOLOGY;
D O I
10.1016/j.neuropsychologia.2016.03.004
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
The epsilon 4 allele of the Apolipoprotein E gene is a genetic risk factor for late-onset dementia of the Alzheimers' type (DAT), which is characterized by loss of both episodic memory and olfactory functions. Little is known about the possible role of epsilon 4 in the association between ongoing episodic memory decline and olfactory deficits in the general population, but such information is relevant in determining the relevance of olfaction as a marker of DAT risk. The present study was based on a large, population-based sample (n=1087, aged 45-90 years, of which 324 were epsilon 4-carriers). Episodic memory change rates were established using data collected every 5 years for a 10-20 year interval leading up to an olfactory assessment using the Scandinavian Odor Identification Test at the last wave of data collection. Participants were classified according to whether or not their episodic memory ability declined more rapidly than the age-typical norm (by > 1SD). Our main result is that only in epsilon 4-carriers was episodic memory decline associated with odor identification impairment. In individuals without epsilon 4, odor identification was unrelated to episodic memory decline status. Follow-up analyses indicated that this moderation by epsilon 4 was due to the olfactory nature of the identification test, and that the effect was not caused by 63 individuals with dementia. Our results suggest that the epsilon 4 determines the functional association between ongoing episodic memory decline and olfaction. These findings are consistent with the notion that epsilon 4-carriers with DAT, compared to non-carriers, display a cortical atrophy pattern that is more focused on mediotemporal lobe regions supporting olfactory and episodic memory functions. Olfactory and memory assessments might provide complementary information on mediotemporal atrophy prior to clinical dementia onset, but the epsilon 4 should be considered when using olfactory assessment as an early-stage indicator. (C) 2016 Published by Elsevier Ltd.
引用
收藏
页码:1 / 9
页数:9
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