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本文引用的文献

1
Cerebral amyloid angiopathy and its co-occurrence with Alzheimer's disease and other cerebrovascular neuropathologic changes.脑淀粉样血管病及其与阿尔茨海默病和其他脑血管神经病理变化的共存。
Neurobiol Aging. 2015 Oct;36(10):2702-8. doi: 10.1016/j.neurobiolaging.2015.06.028. Epub 2015 Jul 8.
2
Age, Sex, and APOE ε4 Effects on Memory, Brain Structure, and β-Amyloid Across the Adult Life Span.年龄、性别和APOE ε4对成年期记忆、脑结构及β淀粉样蛋白的影响。
JAMA Neurol. 2015 May;72(5):511-9. doi: 10.1001/jamaneurol.2014.4821.
3
Neuropathologically mixed Alzheimer's and Lewy body disease: burden of pathological protein aggregates differs between clinical phenotypes.神经病理学混合性阿尔茨海默病和路易体病:临床表型之间病理蛋白聚集物的负担不同。
Acta Neuropathol. 2015 May;129(5):729-48. doi: 10.1007/s00401-015-1406-3. Epub 2015 Mar 11.
4
Vascular and amyloid pathologies are independent predictors of cognitive decline in normal elderly.血管病变和淀粉样病变是正常老年人认知功能衰退的独立预测因素。
Brain. 2015 Mar;138(Pt 3):761-71. doi: 10.1093/brain/awu393. Epub 2015 Jan 15.
5
A systematic review of cognitive decline in dementia with Lewy bodies versus Alzheimer's disease.路易体痴呆与阿尔茨海默病认知功能衰退的系统评价
Alzheimers Res Ther. 2014 Sep 16;6(5-8):53. doi: 10.1186/s13195-014-0053-6. eCollection 2014.
6
Prevalence of mixed pathologies in the aging brain.衰老大脑中混合病理状态的患病率。
Alzheimers Res Ther. 2014 Nov 21;6(9):82. doi: 10.1186/s13195-014-0082-1. eCollection 2014.
7
Vascular risk and Aβ interact to reduce cortical thickness in AD vulnerable brain regions.血管风险与β淀粉样蛋白相互作用,导致阿尔茨海默病易损脑区的皮质厚度降低。
Neurology. 2014 Jul 1;83(1):40-7. doi: 10.1212/WNL.0000000000000550. Epub 2014 Jun 6.
8
Higher working memory predicts slower functional decline in autopsy-confirmed Alzheimer's disease.更高的工作记忆预示着经尸检确诊的阿尔茨海默病患者功能衰退速度较慢。
Dement Geriatr Cogn Disord. 2014;38(3-4):224-33. doi: 10.1159/000362715. Epub 2014 Jun 4.
9
Relation of neuropathology with cognitive decline among older persons without dementia.老年人认知衰退与神经病理学的关系。
Front Aging Neurosci. 2013 Sep 9;5:50. doi: 10.3389/fnagi.2013.00050. eCollection 2013.
10
Non-Alzheimer neurodegenerative pathologies and their combinations are more frequent than commonly believed in the elderly brain: a community-based autopsy series.在老年人的大脑中,非阿尔茨海默病的神经退行性病变及其组合比人们通常认为的更为常见:一项基于社区的尸检系列研究。
Acta Neuropathol. 2013 Sep;126(3):365-84. doi: 10.1007/s00401-013-1157-y. Epub 2013 Jul 31.

阿尔茨海默病、路易体病和血管共病对一个国家尸检队列中临床转变为痴呆症的影响。

Impact of Alzheimer's Disease, Lewy Body and Vascular Co-Pathologies on Clinical Transition to Dementia in a National Autopsy Cohort.

作者信息

Pillai Jagan A, Butler Robert S, Bonner-Jackson Aaron, Leverenz James B

机构信息

Lou Ruvo Center for Brain Health, Cleveland Clinic, Cleveland, Ohio, USA.

出版信息

Dement Geriatr Cogn Disord. 2016;42(1-2):106-16. doi: 10.1159/000448243. Epub 2016 Sep 14.

DOI:10.1159/000448243
PMID:27623397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5451902/
Abstract

AIMS

We examined the effect of vascular or Lewy body co-pathologies in subjects with autopsy-confirmed Alzheimer's disease (AD) on the rate of cognitive and functional decline and transition to dementia.

METHODS

In an autopsy sample of prospectively characterized subjects from the National Alzheimer's Coordinating Center database, neuropathology diagnosis was used to define the groups of pure AD (pAD, n = 84), mixed vascular and AD (ADV, n = 54), and mixed Lewy body disease and AD (ADLBD, n = 31). Subjects had an initial Clinical Dementia Rating-Global (CDR-G) score <1, Mini-Mental State Examination ≥15, a final visit CDR-G >1, ≥3 evaluations, and Braak tangle stage ≥III. We compared the rate of cognitive and functional decline between the groups.

RESULTS

The rate of functional and cognitive decline was lower for ADV, and ADV patients had less severe deficits on CDR-G and the CDR-Sum of Boxes scores at the last visit than pAD and ADLBD patients. No significant differences were noted between ADLBD and pAD patients. After controlling for age at death, the odds of reaching CDR ≥1 at the last visit were lower in the ADV subjects compared to the pAD subjects.

CONCLUSIONS

The mean rate of functional and cognitive decline among ADV subjects was slower than among either pAD or ADLBD patients. Vascular pathology did not increase the odds of attaining CDR ≥1 when occurring with AD in this national cohort.

摘要

目的

我们研究了经尸检确诊为阿尔茨海默病(AD)的受试者中,血管或路易体共病对认知和功能衰退率以及向痴呆转变的影响。

方法

在来自国家阿尔茨海默病协调中心数据库的前瞻性特征明确的受试者尸检样本中,神经病理学诊断用于定义纯AD组(pAD,n = 84)、血管性与AD混合组(ADV,n = 54)以及路易体病与AD混合组(ADLBD,n = 31)。受试者初始临床痴呆评定量表 - 总体(CDR - G)评分<1,简易精神状态检查表≥15,最后一次访视时CDR - G>1,进行≥3次评估,且Braak神经缠结分期≥III。我们比较了各组之间的认知和功能衰退率。

结果

ADV组的功能和认知衰退率较低,且ADV组患者在最后一次访视时CDR - G和CDR - 方框总和评分的 deficits 比pAD组和ADLBD组患者轻。ADLBD组和pAD组患者之间未观察到显著差异。在控制死亡年龄后,与pAD组受试者相比,ADV组受试者在最后一次访视时达到CDR≥1的几率较低。

结论

ADV组受试者的功能和认知衰退平均速率比pAD组或ADLBD组患者慢。在这个全国性队列中,血管病理学与AD同时出现时,并未增加达到CDR≥1的几率。