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阿尔茨海默病的发病率在第十个十年达到峰值,之后会降低。

Alzheimer's disease frequency peaks in the tenth decade and is lower afterwards.

机构信息

Rush Alzheimer's Disease Center, Rush University Medical Center, 1750 W. Harrison, Suite 1000, Chicago, IL, 60612, USA.

Department of Pathology, Rush University Medical Center, Chicago, IL, USA.

出版信息

Acta Neuropathol Commun. 2019 Jul 3;7(1):104. doi: 10.1186/s40478-019-0752-0.

DOI:10.1186/s40478-019-0752-0
PMID:31269985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6609405/
Abstract

Age is the most robust risk factor for Alzheimer's dementia, however there is little data on the relation of age to Alzheimer's disease (AD) and other common neuropathologies that contribute to Alzheimer's dementia. We use data from two community-based, clinical-pathologic cohorts to examine the association of age with AD and other common pathologies. Participants were 1420 autopsied individuals from the Religious Orders Study or Rush Memory and Aging Project who underwent annual clinical evaluations for diagnosis of Alzheimer's dementia, mild cognitive impairment (MCI), and level of cognition. The neuropathologic traits of interest were pathologic AD according to modified NIA-Reagan criteria, three quantitative measures of AD pathology (global AD pathology score, β-amyloid load and PHFtau tangle density), macro- and micro-scopic infarcts, neocortical Lewy bodies, TDP-43 and hippocampal sclerosis. Semiparametric generalized additive models examined the nonlinear relationship between age and the clinical and pathological outcomes. The probability of Alzheimer's dementia at death increased with age such that for every additional year of age, the log odds of Alzheimer's dementia was 0.067 higher, corresponding to an odds ratio of 1.070 (p < 0.001). Results were similar for cognitive impairment and level of cognition. By contrast, a nonlinear relationship of age with multiple indices of AD pathology was observed (all ps < 0.05), such that pathologic AD reached a peak around 95 years of age and leveled off afterwards; the quantitative measures of AD pathology were significantly lower at ages above 95. The association of age with other neuropathologies was quite distinct from that of AD in that most increased with advancing age. AD pathology appears to peak around 95 years of age while other common pathologies continue to increase with age.

摘要

年龄是阿尔茨海默病痴呆的最强风险因素,但关于年龄与阿尔茨海默病(AD)和导致阿尔茨海默病痴呆的其他常见神经病理学之间的关系的数据很少。我们使用来自两个基于社区的临床病理队列的数据来研究年龄与 AD 和其他常见病理之间的关系。参与者是来自宗教秩序研究或拉什记忆和衰老项目的 1420 名接受尸检的个体,他们接受了年度临床评估以诊断阿尔茨海默病痴呆、轻度认知障碍(MCI)和认知水平。感兴趣的神经病理学特征是根据改良的 NIA-Reagan 标准的病理性 AD、AD 病理学的三种定量测量(总体 AD 病理学评分、β-淀粉样蛋白负荷和 PHFtau 缠结密度)、宏观和微观梗死、新皮质路易体、TDP-43 和海马硬化。半参数广义加性模型检查了年龄与临床和病理结果之间的非线性关系。死亡时阿尔茨海默病的概率随年龄增加而增加,即每增加一年,阿尔茨海默病的对数几率增加 0.067,对应的优势比为 1.070(p<0.001)。认知障碍和认知水平的结果相似。相比之下,观察到年龄与 AD 病理学多个指标的非线性关系(所有 p<0.05),即病理性 AD 在 95 岁左右达到峰值,随后趋于平稳;AD 病理学的定量测量在 95 岁以上的年龄显著降低。年龄与其他神经病理学的关系与 AD 的关系截然不同,因为大多数随着年龄的增长而增加。AD 病理学似乎在 95 岁左右达到峰值,而其他常见病理则随着年龄的增长而继续增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ba/6609405/7c5f6235b314/40478_2019_752_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ba/6609405/fef88aebda88/40478_2019_752_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ba/6609405/ae5f3371b76f/40478_2019_752_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ba/6609405/7c5f6235b314/40478_2019_752_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ba/6609405/fef88aebda88/40478_2019_752_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ba/6609405/ae5f3371b76f/40478_2019_752_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ba/6609405/7c5f6235b314/40478_2019_752_Fig3_HTML.jpg

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J Alzheimers Dis. 2018;64(s1):S161-S189. doi: 10.3233/JAD-179939.
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Limbic-predominant age-related TDP-43 encephalopathy (LATE-NC): Co-pathologies and genetic risk factors provide clues about pathogenesis.以边缘系统为主的与年龄相关的 TDP-43 脑病(LATE-NC):共病和遗传风险因素为发病机制提供线索。
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