Apolipoprotein E Genotype Is Related to Progression of White Matter Lesion Load

被引:49
作者
Godin, Ophelia [1 ,2 ]
Tzourio, Christophe [2 ]
Maillard, Pauline [3 ,4 ]
Alperovitch, Annick [2 ]
Mazoyer, Bernard [3 ,4 ,5 ,6 ]
Dufouil, Carole [2 ]
机构
[1] Hosp Salpetriere, INSERM, Unit Neuroepidemiol 708, F-75651 Paris 13, France
[2] Univ Paris 06, Paris, France
[3] Ctr Imaging Neurosci & Applicat Pathol, CNRS, CEA, UMR6232, Caen, France
[4] Univ Caen Basse Normande, Caen, France
[5] Inst Univ France, Paris, France
[6] Ctr Hosp & Univ Caen, Caen, France
关键词
ApoE; cerebrovascular; elderly; epidemiology; MRI; CEREBRAL AMYLOID ANGIOPATHY; ALZHEIMERS-DISEASE; EPSILON-4; ALLELE; APOE GENOTYPE; HYPERINTENSITIES; DEMENTIA; 3-CITY; RISK; BETA; MRI;
D O I
10.1161/STROKEAHA.109.555839
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-The relationship between white matter lesions (WMLs) and the apolipoprotein E genotype has been controversial from cross-sectional studies and no longitudinal finding has been reported. We investigated whether the apolipoprotein E genotype influences baseline and evolution over 4-year follow-up of WML volumes in a population-based sample of 1779 nondemented subjects aged 65 to 80 years old at enrollment. Methods-The sample consisted of 3C-Dijon study participants who had 2 cerebral MRIs, at entry and at 4-year follow-up. WML volumes were estimated using a fully automatic procedure. We performed analysis of covariance to evaluate the relationship between apolipoprotein E genotype and WML load and progression. Results-Multivariable analyses showed that epsilon 4 epsilon 4 individuals had both significantly higher WML volume at baseline and higher WML increase over 4-year follow-up than noncarriers and heterozygous of the epsilon 4 allele for apolipoprotein E genotype. Conclusion-These findings suggest it might be important to take into account WML severity when assessing the relationship between apolipoprotein E and dementia. (Stroke. 2009;40:3186-3190.)
引用
收藏
页码:3186 / 3190
页数:5
相关论文
共 21 条
[1]   Vascular factors and risk of dementia: Design of the three-city study and baseline characteristics of the study population [J].
Alperovitch, A .
NEUROEPIDEMIOLOGY, 2003, 22 (06) :316-325
[2]   White matter lesions in Alzheimer patients are influenced by apolipoprotein E genotype [J].
Bronge, L ;
Fernaeus, SE ;
Blomberg, M ;
Ingelson, M ;
Lannfelt, L ;
Isberg, B ;
Wahlund, LO .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 1999, 10 (02) :89-96
[3]   Neuroimaging and APOE genotype:: A systematic qualitative review [J].
Cherbuin, Nicolas ;
Leach, Liana S. ;
Christensen, Helen ;
Anstey, Kaarin J. .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2007, 24 (05) :348-362
[4]   Periventricular cerebral white matter lesions predict rate of cognitive decline [J].
de Groot, JC ;
de Leeuw, FE ;
Oudkerk, M ;
van Gijn, J ;
Hofman, A ;
Jolles, J ;
Breteler, MMB .
ANNALS OF NEUROLOGY, 2002, 52 (03) :335-341
[5]   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
[6]   APOE genotype, cholesterol level, lipid-lowering treatment, and dementia -: The Three-City Study [J].
Dufouil, C ;
Richard, F ;
Fiévet, N ;
Dartigues, JF ;
Ritchie, K ;
Tzourio, C ;
Amouyel, P ;
Alpérovitch, A .
NEUROLOGY, 2005, 64 (09) :1531-1538
[7]   Cerebral amyloid angiopathy and apolipoprotein E: Bad news for the good allele? [J].
Greenberg, SM ;
Hyman, BT .
ANNALS OF NEUROLOGY, 1997, 41 (06) :701-702
[8]   Plasma β-amyloid and white matter lesions in AD, MCI, and cerebral amyloid angiopathy [J].
Gurol, ME ;
Irizarry, MC ;
Smith, EE ;
Raju, S ;
Diaz-Arrastia, R ;
Bottiglieri, T ;
Rosand, J ;
Growdon, JH ;
Greenberg, SM .
NEUROLOGY, 2006, 66 (01) :23-29
[9]   Effect of the apolipoprotein E ε4 allele on white matter hyperintensities in dementia [J].
Hirono, N ;
Yasuda, M ;
Tanimukai, S ;
Kitagaki, H ;
Mori, E .
STROKE, 2000, 31 (06) :1263-1268
[10]   The role of apolipoprotein E in Alzheimer's disease, acute brain injury and cerebrovascular disease: evidence of common mechanisms and utility of animal models [J].
Horsburgh, K ;
McCarron, MO ;
White, F ;
Nicoll, JAR .
NEUROBIOLOGY OF AGING, 2000, 21 (02) :245-255