APOE genotype predicts depression in women with Alzheimer's disease: A retrospective study

被引:43
作者
Delano-Wood, Lisa [2 ]
Houston, Wes S. [3 ]
Emond, Jennifer A. [4 ]
Marchant, Natalie L.
Salmons, David P. [5 ]
Jeste, Dilip V. [2 ,5 ]
Thal, Leon J. [5 ]
Bondi, Mark W. [1 ,2 ]
机构
[1] VA San Diego Healthcare Syst, Psychol Serv 116B, San Diego, CA 92161 USA
[2] Univ Calif San Diego, Sch Med, Dept Psychiat, La Jolla, CA 92093 USA
[3] Univ Iowa, Div Cognit Neurosci, Dept Neurol, Iowa City, IA 52242 USA
[4] Univ Calif San Diego, Sch Med, Dept Biostat, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Sch Med, Dept Neurosci, La Jolla, CA 92093 USA
关键词
Alzheimer's disease; depression; APOE; APOE genotype; APOE epsilon 4 allele;
D O I
10.1002/gps.1953
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
Objective The association between the APOE epsilon 4 allele and depression was investigated in a retrospective study of 323 AD patients. Methods Patients were divided into demographically comparable groups based on the presence or absence of depression. Results Results showed that the frequency of APOE epsilon 4 allele was significantly higher in the depressed vs non-depressed AD patients (72% and 58%, respectively), and an interaction revealed that women possessing the APOE epsilon 4 allele were almost four times more likely to be depressed than those without the epsilon 4 allele. Conclusion Results are consistent with recent suggestions that the APOE epsilon 4 genotype may be over-represented among depressed women with AD and highlight the need for additional research investigating the links between APOE genotype, mood, and gender. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:632 / 636
页数:5
相关论文
共 29 条
[1]   The apolipoprotein E ε4 allele and incident Alzheimer's disease in persons with mild cognitive impairment [J].
Aggarwal, NT ;
Wilson, RS ;
Beck, TL ;
Bienias, JL ;
Berry-Kravis, E ;
Bennett, DA .
NEUROCASE, 2005, 11 (01) :3-7
[2]  
ALEXOPOULOS GS, 1997, J NEUROSCI, V17, P516
[3]   Acute myocardial infarction in young adults: Prognostic role of angiotensin-converting enzyme, angiotensin II type I receptor, apolipoprotein E, endothelial constitutive nitric oxide synthase, and glycoprotein IIIa genetic polymorphisms at medium-term follow-up [J].
Brscic, E ;
Bergerone, S ;
Gagnor, A ;
Colajanni, E ;
Matullo, G ;
Scaglione, L ;
Cassader, M ;
Gaschino, G ;
Di Leo, M ;
Brusca, A ;
Pagano, GF ;
Piazza, A ;
Trevi, GP .
AMERICAN HEART JOURNAL, 2000, 139 (06) :979-984
[4]   Association analysis of apolipoprotein E genotype and risk of depressive symptoms in Alzheimer's disease [J].
Craig, D ;
Hart, DJ ;
Mcllroy, SP ;
Passmore, AP .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2005, 19 (2-3) :154-157
[5]   Apolipoprotein E and atherosclerosis: insight from animal and human studies [J].
Davignon, J ;
Cohn, JS ;
Mabile, L ;
Bernier, L .
CLINICA CHIMICA ACTA, 1999, 286 (1-2) :115-143
[6]   Interaction between hypertension, apoE, and cerebral white matter lesions [J].
de Leeuw, FE ;
Richard, F ;
de Groot, JC ;
van Duijn, CM ;
Hofman, A ;
van Gijn, J ;
Breteler, MMB .
STROKE, 2004, 35 (05) :1057-1060
[7]  
FOLSTEIN MF, 1975, J PSYCHIATR RES, V12, P198
[8]   Depression and dementia in relation to apolipoprotein E polymorphism in a population sample age 75+ [J].
Forsell, Y ;
Corder, EH ;
Basun, H ;
Lannfelt, L ;
Viitanen, M ;
Winblad, B .
BIOLOGICAL PSYCHIATRY, 1997, 42 (10) :898-903
[9]   Behavioural pathology in Alzheimer's disease with special reference to apolipoprotein E genotype [J].
Gabryelewicz, T ;
Religa, D ;
Styczynska, M ;
Peplonska, B ;
Pfeffer, A ;
Wasiak, B ;
Luczywek, E ;
Golebiowski, M ;
Androsiuk, W ;
Czyzewski, K ;
Przekop, I ;
Barcikowska, M .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2002, 14 (04) :208-212
[10]   CEREBRAL BLOOD-FLOW IN DEMENTIA [J].
HACHINSKI, VC ;
ILIFF, LD ;
ZILHKA, E ;
DUBOULAY, GH ;
MCALLISTER, VL ;
MARSHALL, J ;
RUSSELL, RWR ;
SYMON, L .
ARCHIVES OF NEUROLOGY, 1975, 32 (09) :632-637