Correlations between apolipoprotein E ε4 gene dose and brain-imaging measurements of regional hypometabolism

被引:316
作者
Reiman, EM [1 ]
Chen, KW
Alexander, GE
Caselli, RJ
Bandy, D
Osborne, D
Saunders, AM
Hardy, J
机构
[1] Banner Good Samaritan Med Ctr, Posit Emiss Tomog Ctr, Phoenix, AZ 85006 USA
[2] Univ Arizona, Dept Psychiat, Tucson, AZ 85724 USA
[3] Univ Arizona, Dept Radiol, Tucson, AZ 85724 USA
[4] Arizona State Univ, Dept Math, Tempe, AZ 85287 USA
[5] Arizona State Univ, Dept Psychol, Tempe, AZ 85287 USA
[6] Mayo Clin, Dept Neurol, Scottsdale, AZ 85259 USA
[7] Mayo Clin, Dept Psychol, Scottsdale, AZ 85259 USA
[8] Duke Univ, Joseph & Kathleen Bryan Alzheimers Dis Res Ctr, Dept Med Neurol, Durham, NC 27710 USA
[9] Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA
[10] Translat Genom Res Inst, Phoenix, AZ 85004 USA
[11] Arizona Alzheimers Dis Consortium, Phoenix, AZ USA
关键词
Alzheimer's disease; genetics; positron emission tomography; endophenotype;
D O I
10.1073/pnas.0500579102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Patients with Alzheimer's disease (AD) have abnormally low positron emission tomography (PET) measurements of the cerebral metabolic rate for glucose (CMRgl) in regions of the precuneus and the posterior cingulate, parietotemporal, and frontal cortex. Apolipoprotein E (APOE) epsilon 4 gene dose (i.e., the number of epsilon 4 alleles in a person's APOE genotype) is associated with a higher risk of AD and a younger age at dementia onset. We previously found that cognitively normal late-middle-aged APOE epsilon 4 carriers have abnormally low CMRgI in the same brain regions as patients with probable Alzheimer's dementia. In a PET study of 160 cognitively normal subjects 47-68 years of age, including 36 epsilon 4 homozygotes, 46 heterozygotes, and 78 epsilon 4 noncarriers who were individually matched for their gender, age, and educational level, we now find that epsilon 4 gene dose is correlated with lower CMRgI in each of these brain regions. This study raises the possibility of using PET as a quantitative presymptomatic endophenotype to help evaluate the individual and aggregate effects of putative genetic and nongenetic modifiers of AD risk.
引用
收藏
页码:8299 / 8302
页数:4
相关论文
共 24 条
[1]  
Alexander GE, 1997, AM J PSYCHIAT, V154, P165
[2]   Longitudinal PET evaluation of cerebral metabolic decline in dementia: A potential outcome measure in Alzheimer's disease treatment studies [J].
Alexander, GE ;
Chen, K ;
Pietrini, P ;
Rapoport, SI ;
Reiman, EM .
AMERICAN JOURNAL OF PSYCHIATRY, 2002, 159 (05) :738-745
[3]   Impaired cerebral glucose metabolism and cognitive functioning predict deterioration in mild cognitive impairment [J].
Arnáiz, E ;
Jelic, V ;
Almkvist, O ;
Wahlund, LO ;
Winblad, B ;
Valind, S ;
Nordberg, A .
NEUROREPORT, 2001, 12 (04) :851-855
[4]   Noninvasive quantification of the cerebral metabolic rate for glucose using positron emission tomography, 18F-fluoro-2-deoxyglucose, the Patlak method, and an image-derived input function [J].
Chen, K ;
Bandy, D ;
Reiman, E ;
Huang, SC ;
Lawson, M ;
Feng, D ;
Yun, LS ;
Palant, A .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (07) :716-723
[5]   Mild cognitive impairment -: Can FDG-PET predict who is to rapidly convert to Alzheimer's disease? [J].
Chételat, G ;
Desgranges, B ;
de la Sayette, V ;
Viader, F ;
Eustache, F ;
Baron, JC .
NEUROLOGY, 2003, 60 (08) :1374-1377
[6]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[7]   Cerebral metabolic changes accompanying conversion of mild cognitive impairment into Alzheimer's disease: a PET follow-up study [J].
Drzezga, A ;
Lautenschlager, N ;
Siebner, H ;
Riemenschneider, M ;
Willoch, F ;
Minoshima, S ;
Schwaiger, M ;
Kurz, A .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2003, 30 (08) :1104-1113
[8]   Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease - A meta-analysis [J].
Farrer, LA ;
Cupples, LA ;
Haines, JL ;
Hyman, B ;
Kukull, WA ;
Mayeux, R ;
Myers, RH ;
PericakVance, MA ;
Risch, N ;
vanDuijn, CM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 278 (16) :1349-1356
[9]  
FRACKOWIAK RSJ, 1997, HUMAN BRAIN FUNCTION
[10]   The endophenotype concept in psychiatry: Etymology and strategic intentions [J].
Gottesman, II ;
Gould, TD .
AMERICAN JOURNAL OF PSYCHIATRY, 2003, 160 (04) :636-645