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阿尔茨海默病发病年龄与淀粉样β负担的关系。

Relationship of amyloid-β burden with age-at-onset in Alzheimer disease.

机构信息

Department of Neuropsychiatry and Clinical Research Institute, Seoul National University Hospital, Seoul, Korea.

出版信息

Am J Geriatr Psychiatry. 2011 Jul;19(7):627-34. doi: 10.1097/JGP.0b013e318202bf3a.

DOI:10.1097/JGP.0b013e318202bf3a
PMID:21709608
Abstract

OBJECTIVE

To investigate the relationship between in vivo brain amyloid-beta (Aβ) burden, measured by C-labeled Pittsburgh Compound B (C-PiB) retention, and age-at-onset in patients with Alzheimer disease (AD).

DESIGN

Cross-sectional study.

SETTING

University Dementia Clinic.

PARTICIPANTS

Twenty-two AD patients including 11 early-onset AD (EOAD: onset <65 years) and 11 late-onset AD (LOAD: onset ≥65years) cases with matched dementia severity, duration of illness, and apolipoprotein E ε4 allele number.

INTERVENTION

C-PiB positron emission tomography scans.

MEASUREMENTS

Both region of interest and voxel-based analyses were performed to compare C-PiB retention between EOAD and LOAD groups, and to test linear relationship between age-at-onset and C-PiB retention.

RESULTS

Both region of interest (ROI) and voxel-based analyses revealed that EOAD patients had significantly higher C-PIB retentions than LOAD patients in diffuse brain regions including frontal, lateral parietal, lateral temporal, and occipital cortex, and basal ganglia. Subgroup analyses showed that negative correlation between age-at-onset and C-PiB retention was significant in LOAD but not in EOAD.

CONCLUSIONS

Our finding of a heavier Aβ burden in the brain of living EOAD patients than LOAD patients is in agreement with those from postmortem studies. The inverse relationship between age-at-onset and Aβ burden is possibly associated with aging-related decrease of brain or cognitive reserve and with aging-related increase of brain vulnerability.

摘要

目的

研究体内淀粉样蛋白-β(Aβ)负担与阿尔茨海默病(AD)患者发病年龄的关系,该负担通过放射性标记的匹兹堡化合物 B(C-PiB)保留来测量。

设计

横断面研究。

地点

大学痴呆症诊所。

参与者

22 例 AD 患者,包括 11 例早发性 AD(EOAD:发病年龄<65 岁)和 11 例晚发性 AD(LOAD:发病年龄≥65 岁),这些患者的痴呆严重程度、病程和载脂蛋白 E ε4 等位基因数量相匹配。

干预措施

C-PiB 正电子发射断层扫描。

测量

进行了感兴趣区和体素分析,以比较 EOAD 和 LOAD 组之间的 C-PiB 保留情况,并测试发病年龄与 C-PiB 保留之间的线性关系。

结果

ROI 和体素分析均显示,EOAD 患者的大脑弥漫区域(包括额、顶、颞、枕叶皮质和基底节)的 C-PIB 保留显著高于 LOAD 患者。亚组分析显示,LOAD 患者发病年龄与 C-PiB 保留之间存在显著的负相关,而 EOAD 患者则没有。

结论

我们发现,与 LOAD 患者相比,存活的 EOAD 患者大脑中的 Aβ负担更重,这与尸检研究结果一致。发病年龄与 Aβ负担之间的反比关系可能与与年龄相关的大脑或认知储备减少以及与年龄相关的大脑易损性增加有关。

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