Apolipoprotein E4 Frequencies in a Japanese Population with Alzheimer's Disease and Dementia with Lewy Bodies

被引:30
作者
Kobayashi, Seiju [1 ]
Tateno, Masaru [1 ]
Park, Tae Woo [1 ]
Utsumi, Kumiko [2 ]
Sohma, Hitoshi [3 ,5 ]
Ito, Yoichi M. [4 ]
Kokai, Yasuo [5 ]
Saito, Toshikazu [1 ]
机构
[1] Sapporo Med Univ, Dept Neuropsychiat, Sch Med, Sapporo, Hokkaido, Japan
[2] Sunagawa City Med Ctr, Dept Psychiat, Sunagawa, Japan
[3] Sapporo Med Univ, Dept Educ Dev, Ctr Med Educ, Sapporo, Hokkaido, Japan
[4] Hokkaido Univ, Grad Sch Med, Hokkaido Org Translat Res, Sapporo, Hokkaido, Japan
[5] Sapporo Med Univ, Dept Biomed Engn, Sch Med, Sapporo, Hokkaido, Japan
基金
日本学术振兴会;
关键词
BRAIN PERFUSION SPECT; SCORE IMAGING-SYSTEM; E ALLELE EPSILON-4; BODY DISEASE; VASCULAR DEMENTIA; E GENOTYPE; E GENE; ONSET; DIAGNOSIS; AGE;
D O I
10.1371/journal.pone.0018569
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
Background: The apolipoprotein E (APOE) epsilon 4 allele has been reported to be a risk factor for Alzheimer's disease (AD) and dementia with Lewy bodies (DLB). Previous neuropathological studies have demonstrated similar frequencies of the APOE epsilon 4 allele in AD and DLB. However, the few ante-mortem studies on APOE allele frequencies in DLB have shown lower frequencies than post-mortem studies. One reason for this may be inaccuracy of diagnosis. We examined APOE genotypes in subjects with AD, DLB, and a control group using the latest diagnostic criteria and MRI, SPECT, and MIBG myocardial scintigraphy. Methods: The subjects of this study consisted of 145 patients with probable AD, 50 subjects with probable DLB, and a control group. AD subjects were divided into two groups based on age of onset: early onset AD (EOAD) and late onset AD (LOAD). All subjects had characteristic features on MRI, SPECT, and/or myocardial scintigraphy. Results: The rate of APOE4 carrier status was 18.3% and the frequency of the epsilon 4 allele was 9.7% in controls. The rate of APOE4 carrier status and the frequency of the epsilon 4 allele were 47% and 27% for LOAD, 50% and 31% for EOAD, and 42% and 31% for DLB, respectively. Conclusion: The APOE4 genotypes in this study are consistent with previous neuropathological studies suggesting accurate diagnosis of AD and DLB. APOE4 genotypes were similar in AD and DLB, giving further evidence that the epsilon 4 allele is a risk factor for both disorders.
引用
收藏
页数:5
相关论文
共 41 条
[1]  
AKATSUHIROYASU K, 2004, PSYCHOGERIATRICS, V4, P8
[2]   APOLIPOPROTEIN-E GENE IN DIFFUSE LEWY BODY DISEASE WITH OR WITHOUT COEXISTING ALZHEIMERS-DISEASE [J].
ARAI, H ;
HIGUCHI, S ;
MURAMATSU, T ;
IWATSUBO, T ;
SASAKI, H ;
TROJANOWSKI, JQ .
LANCET, 1994, 344 (8932) :1307-1307
[3]   Neuron-specific apolipoprotein E4 proteolysis is associated with increased tau phosphorylation in brains of transgenic mice [J].
Brecht, WJ ;
Harris, FM ;
Chang, SJ ;
Tesseur, I ;
Yu, GQ ;
Xu, Q ;
Fish, JD ;
Wyss-Coray, T ;
Buttini, M ;
Mucke, L ;
Mahley, RW ;
Huang, YD .
JOURNAL OF NEUROSCIENCE, 2004, 24 (10) :2527-2534
[4]  
Garcia FC, 2008, NEUROLOGIA, V23, P152
[5]   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
[6]   Cognitive and behavioral heterogeneity in Alzheimer's disease: seeking the neurobiological basis [J].
Cummings, JL .
NEUROBIOLOGY OF AGING, 2000, 21 (06) :845-861
[7]   ASSOCIATION OF APOLIPOPROTEIN E4 WITH SPORADIC ALZHEIMERS-DISEASE IS MORE PRONOUNCED IN EARLY-ONSET TYPE [J].
DAI, XY ;
NANKO, S ;
HATTORI, M ;
FUKUDA, R ;
NAGATA, K ;
ISSE, K ;
UEKI, A ;
KAZAMATSURI, H .
NEUROSCIENCE LETTERS, 1994, 175 (1-2) :74-76
[8]   Cholesterol metabolism in the central nervous system during early development and in the mature animal [J].
Dietschy, JM ;
Turley, SD .
JOURNAL OF LIPID RESEARCH, 2004, 45 (08) :1375-1397
[9]   Prospective Belgian study of neurodegenerative and vascular dementia:: APOE genotype effects [J].
Engelborghs, S ;
Dermaut, B ;
Goeman, J ;
Saerens, J ;
Mariën, P ;
Pickut, BA ;
Van den Broeck, M ;
Serneels, S ;
Cruts, M ;
Van Broeckhoven, C ;
De Deyn, PP .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2003, 74 (08) :1148-1151
[10]  
Farrer LA, 1997, JAMA-J AM MED ASSOC, V278, P1349, DOI 10.1001/jama.1997.03550160069041