Nicastrin gene polymorphisms, cognitive ability level and cognitive ageing

被引:18
作者
Deary, IJ
Hamilton, G
Hayward, C
Whalley, LJ
Powell, J
Starr, JM
Lovestone, S
机构
[1] Univ Edinburgh, Dept Psychol, Edinburgh EH8 9JZ, Midlothian, Scotland
[2] Inst Psychiat, London, England
[3] MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland
[4] Univ Aberdeen, Inst Appl Hlth Sci, Aberdeen, Scotland
[5] Univ Edinburgh, Dept Geriatr Med, Edinburgh, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
nicastrin; IQ polymorphism; intelligence; cognition ageing; Scottish mental survey; dementia;
D O I
10.1016/j.neulet.2004.09.073
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The hypothesis that polymorphisms in the gene for nicastrin (NCSTN) are associated with differences in cognitive level and ageing was tested in 462 relatively healthy surviving participants of the Scottish Mental Survey 1932. None had a history of dementia. They were tested on the Moray House Test of verbal reasoning at age 11 in 1932 and at age 79 between 1999 and 2001. At age 79 they also took tests of non-verbal reasoning, short- and long-term verbal declarative memory, Verbal Fluency, and a short screening test for dementia. Subjects who possessed at least one copy of the NCSTN B haplotype (Hap B) had higher scores on the Moray House Test (a test principally of verbal reasoning) at age 11 (p = 0.036) and age 79 (p = 0.027). The effect of Hap B on cognition at age 79 was non-significant after adjusting for the effect at age 11. Therefore, the effect of Hap B in this sample is on the life-long stable trait of cognitive ability, and not on age-related cognitive change. The possibility that this result might be a selection effect was not supported by the samples being in Hardy-Weinberg equilibrium with respect to the distribution of NCSTN genotypes. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:110 / 114
页数:5
相关论文
共 28 条
[1]  
[Anonymous], 1977, MANUAL RAVENS PROGRE
[2]  
[Anonymous], 2004, Neuropsychological Assessment
[3]   Results of a high-resolution genome screen of 437 Alzheimer's Disease families [J].
Blacker, D ;
Bertram, L ;
Saunders, AJ ;
Moscarillo, TJ ;
Albert, MS ;
Wiener, H ;
Perry, RT ;
Collins, JS ;
Harrell, LE ;
Go, RCP ;
Mahoney, A ;
Beaty, T ;
Fallin, MD ;
Avramopoulos, D ;
Chase, GA ;
Folstein, MF ;
McInnis, MG ;
Bassett, SS ;
Doheny, KJ ;
Pugh, EW ;
Tanzi, RE .
HUMAN MOLECULAR GENETICS, 2003, 12 (01) :23-32
[4]   Genetic and environmental influences on human psychological differences [J].
Bouchard, TJ ;
McGue, M .
JOURNAL OF NEUROBIOLOGY, 2003, 54 (01) :4-45
[5]   Mild cognitive impairment in older people [J].
Burns, A ;
Zaudig, M .
LANCET, 2002, 360 (9349) :1963-1965
[6]   No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease [J].
Cousin, E ;
Hannequin, D ;
Macé, S ;
Dubois, B ;
Ricard, S ;
Génin, E ;
Brun, C ;
Chansac, C ;
Pradier, L ;
Frebourg, T ;
Brice, A ;
Campion, D ;
Deleuze, JF .
NEUROSCIENCE LETTERS, 2003, 353 (02) :153-155
[7]   Aph-1, Pen-2, and nicastrin with presenilin generate an active γ-secretase complex [J].
De Strooper, B .
NEURON, 2003, 38 (01) :9-12
[8]   Apolipoprotein E gene variability and cognitive functions at age 79: A follow-up of the Scottish Mental Survey of 1932 [J].
Deary, IJ ;
Whiteman, MC ;
Pattie, A ;
Starr, JM ;
Hayward, C ;
Wright, AF ;
Visscher, PM ;
Tynan, MC ;
Whalley, LJ .
PSYCHOLOGY AND AGING, 2004, 19 (02) :367-371
[9]   Searching for genetic influences on normal cognitive ageing [J].
Deary, IJ ;
Wright, AF ;
Harris, SE ;
Whalley, LJ ;
Starr, JM .
TRENDS IN COGNITIVE SCIENCES, 2004, 8 (04) :178-184
[10]   The impact of childhood intelligence on later life: Following up the Scottish Mental Surveys of 1932 and 1947 [J].
Deary, IJ ;
Whiteman, MC ;
Starr, JM ;
Whalley, LJ ;
Fox, HC .
JOURNAL OF PERSONALITY AND SOCIAL PSYCHOLOGY, 2004, 86 (01) :130-147