Association Between ApoE Phenotypes and Telomere Erosion in Alzheimer's Disease

被引:40
|
作者
Takata, Yusuke
Kikukawa, Masayuki [1 ]
Hanyu, Haruo
Koyama, Shunichi
Shimizu, Soichiro
Umahara, Takahiko
Sakurai, Hirofumi
Iwamoto, Toshihiko
Ohyashiki, Kazuma [2 ]
Ohyashiki, Junko H. [3 ]
机构
[1] Tokyo Med Univ, Dept Geriatr Med, Shinjuku Ku, Tokyo 1600023, Japan
[2] Tokyo Med Univ, Dept Internal Med 1, Tokyo 1600023, Japan
[3] Tokyo Med Univ, Inst Med Sci, Tokyo 1600023, Japan
关键词
Telomere length; Alzheimer's disease; ApoE phenotype; Quantitative real-time PCR; PERIPHERAL-BLOOD CELLS; APOLIPOPROTEIN-E; OXIDATIVE STRESS; LIPID-PEROXIDATION; LENGTH; ALLELE; DEMENTIA; GENOTYPE; BRAIN; RISK;
D O I
10.1093/gerona/glr185
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
Although several reports suggest that Alzheimer's disease (AD) is associated with shortened telomere length, the clinical relevance of this has not yet been fully elucidated. This study was conducted to clarify the correlation of telomere length with clinical characteristics and ApoE phenotypes in 74 AD patients. Telomere length was determined from genomic DNA extracted from whole blood by quantitative real-time polymerase chain reaction. We found no significant difference in telomere length between the AD and non-dementia elderly control (n = 35) groups. Furthermore, no significant correlation was found among telomere length and the severity of cognitive decline and disease duration, age, or gender difference. However, telomere length was significantly shorter in AD patients with the ApoE4 homozygote than in those with the ApoE4 heterozygote (p < .001) and noncarriers (p < .001). These findings suggest that shortened telomere length may be associated with the ApoE4 homozygote in AD patients.
引用
收藏
页码:330 / 335
页数:6
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