MRI and genetic correlates of cognitive function in elders with memory impairment

被引:39
作者
Bartrés-Faz, D
Junqué, C
Clemente, IC
Serra-Grabulosa, JM
Guardia, J
López-Alomar, A
Sánchez-Aldeguer, J
Mercader, JM
Bargalló, N
Olondo, M
Moral, P
机构
[1] Univ Barcelona, Dept Psychiat & Clin Psychobiol, Barcelona 08035, Spain
[2] Univ Barcelona, Anthropol Unit, Barcelona 08035, Spain
[3] Univ Autonoma Barcelona, EU Gimbernat, Barcelona 08035, Spain
[4] Hosp Clin Barcelona, Diagnost Imaging Ctr, Barcelona, Spain
[5] Hosp Clin Barcelona, Dept Radiol & Nucl Med, Barcelona, Spain
关键词
D O I
10.1016/S0197-4580(01)00207-X
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The present study investigated the relationship between genetic variation, MRI measurements and neuropsychological function in a sample of 58 elders exhibiting memory decline. In agreement with previous reports, we found that the epsilon4 allele of the apolipoprotein E (APOE) and the D allele of the angiotensin converting enzyme (ACE) polymorphisms negatively modulated the cognitive performance. Further, we found an association between the A allele of the apolipoprotein C1 (APOC1) polymorphism and poorer memory and frontal lobe function. No clear associations emerged between MRI measures of white matter lesions (WML) or hippocampal sulcal cavities (HSC) and the cognitive performance after controlling for age effects. Further, the degree of WML or HSC lesions was in general not predisposed genetically except for the presence of the A allele of the APOC1 polymorphism that was related to a higher severity of HSC scores. Our results suggest that WML or HSC do not represent important brain correlates of genetic influences on cognitive performance in memory impaired subjects. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:449 / 459
页数:11
相关论文
共 82 条
[1]   WHITE-MATTER HYPERINTENSITY AND NEUROPSYCHOLOGICAL FUNCTIONS IN DEMENTIA AND HEALTHY AGING [J].
ALMKVIST, O ;
WAHLUND, LO ;
ANDERSSONLUNDMAN, G ;
BASUN, H ;
BACKMAN, L .
ARCHIVES OF NEUROLOGY, 1992, 49 (06) :626-632
[2]  
Amar K, 1998, INT J GERIATR PSYCH, V13, P585, DOI 10.1002/(SICI)1099-1166(199809)13:9<585::AID-GPS825>3.0.CO
[3]  
2-0
[4]   The deletion allele of the angiotensin I converting enzyme gene as a genetic susceptibility factor for cognitive impairment [J].
Amouyel, P ;
Richard, F ;
Cottel, D ;
Amant, C ;
Codron, V ;
Helbecque, N .
NEUROSCIENCE LETTERS, 1996, 217 (2-3) :203-205
[5]  
[Anonymous], 2004, Neuropsychological Assessment
[6]   ANGIOTENSIN CONVERTING ENZYME IN ALZHEIMERS-DISEASE - INCREASED ACTIVITY IN CAUDATE-NUCLEUS AND CORTICAL AREAS [J].
ARREGUI, A ;
PERRY, EK ;
ROSSOR, M ;
TOMLINSON, BE .
JOURNAL OF NEUROCHEMISTRY, 1982, 38 (05) :1490-1492
[7]   Apolipoprotein E ε4 allele, temporal lobe atrophy, and white matter lesions in late-life dementias [J].
Barber, R ;
Gholkar, A ;
Scheltens, P ;
Ballard, C ;
McKeith, IG ;
Morris, CM ;
O'Brien, JT .
ARCHIVES OF NEUROLOGY, 1999, 56 (08) :961-965
[8]   Hippocampal sulcal cavities on MRI: Relationship to age and apolipoprotein E genotype [J].
Barboriak, DP ;
Doraiswamy, PM ;
Krishnan, KRR ;
Vidyarthi, S ;
Sylvester, J ;
Charles, HC .
NEUROLOGY, 2000, 54 (11) :2150-2153
[9]   ANGIOTENSIN-II INHIBITS ACETYLCHOLINE-RELEASE FROM HUMAN TEMPORAL CORTEX - IMPLICATIONS FOR COGNITION [J].
BARNES, JM ;
BARNES, NM ;
COSTALL, B ;
HOROVITZ, ZP ;
IRONSIDE, JW ;
NAYLOR, RJ ;
WILLIAMS, TJ .
BRAIN RESEARCH, 1990, 507 (02) :341-343
[10]   ANGIOTENSIN CONVERTING ENZYME DENSITY IS INCREASED IN TEMPORAL CORTEX FROM PATIENTS WITH ALZHEIMERS-DISEASE [J].
BARNES, NM ;
CHENG, CHK ;
COSTALL, B ;
NAYLOR, RJ ;
WILLIAMS, TJ ;
WISCHIK, CM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 200 (2-3) :289-292