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本文引用的文献

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Secular changes in cognitive predictors of dementia and mortality in 70-year-olds.70 岁人群中痴呆症和死亡率的认知预测因素的长期变化。
Neurology. 2010 Aug 31;75(9):779-85. doi: 10.1212/WNL.0b013e3181f0737c.
2
Brain volume and survival from age 78 to 85: the contribution of Alzheimer-type magnetic resonance imaging findings.从 78 岁到 85 岁的脑容量与生存:阿尔茨海默病型磁共振成像发现的作用。
J Am Geriatr Soc. 2010 Apr;58(4):688-95. doi: 10.1111/j.1532-5415.2010.02765.x.
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Diagnostic imaging of patients in a memory clinic: comparison of MR imaging and 64-detector row CT.记忆门诊患者的诊断性成像:磁共振成像与64排CT的比较
Radiology. 2009 Oct;253(1):174-83. doi: 10.1148/radiol.2531082262. Epub 2009 Jul 27.
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Hypothalamic and dietary control of temperature-mediated longevity.下丘脑和饮食对温度介导的寿命的控制。
Ageing Res Rev. 2010 Jan;9(1):41-50. doi: 10.1016/j.arr.2009.07.004. Epub 2009 Jul 23.
5
MRI biomarkers of vascular damage and atrophy predicting mortality in a memory clinic population.记忆门诊人群中预测死亡率的血管损伤和萎缩的MRI生物标志物
Stroke. 2009 Feb;40(2):492-8. doi: 10.1161/STROKEAHA.108.516286. Epub 2008 Dec 24.
6
Depression as a risk factor for the incidence of first-ever stroke in 85-year-olds.抑郁症作为85岁老人首次中风发病的一个风险因素。
Stroke. 2008 Jul;39(7):1960-5. doi: 10.1161/STROKEAHA.107.490797. Epub 2008 May 1.
7
Prevalence of CT-detected cerebral abnormalities in an elderly Swedish population sample.瑞典老年人群样本中CT检测到的脑部异常的患病率。
Acta Neurol Scand. 2008 Oct;118(4):260-7. doi: 10.1111/j.1600-0404.2008.01010.x. Epub 2008 Mar 11.
8
Five-year mortality in relation to dementia and cognitive function in 95-year-olds.95岁老人中与痴呆症和认知功能相关的五年死亡率。
Neurology. 2007 Nov 27;69(22):2069-75. doi: 10.1212/01.wnl.0000280464.59322.af.
9
The significance of medial temporal lobe atrophy: a postmortem MRI study in the very old.内侧颞叶萎缩的意义:一项针对高龄老人的尸检MRI研究
Neurology. 2007 Oct 9;69(15):1521-7. doi: 10.1212/01.wnl.0000277459.83543.99.
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Brain tissue volumes and small vessel disease in relation to the risk of mortality.脑组织体积和小血管疾病与死亡风险的关系。
Neurobiol Aging. 2009 Mar;30(3):450-6. doi: 10.1016/j.neurobiolaging.2007.07.009. Epub 2007 Sep 4.

一项基于人群的研究,探讨了 85 岁以上人群脑萎缩对 20 年生存率的影响。

A population-based study on the influence of brain atrophy on 20-year survival after age 85.

机构信息

Neuropsychiatric Epidemiology Unit, Wallinsgatan 6, 43141 Mölndal, Sweden.

出版信息

Neurology. 2011 Mar 8;76(10):879-86. doi: 10.1212/WNL.0b013e31820f2e26.

DOI:10.1212/WNL.0b013e31820f2e26
PMID:21383324
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3059146/
Abstract

BACKGROUND

Individuals aged 80 years and older is the fastest growing segment of the population worldwide. To understand the biology behind increasing longevity, it is important to examine factors related to survival in this age group. The relationship between brain atrophy and survival after age 85 remains unclear.

METHODS

A population-based sample (n = 239) had head CT scans at age 85 and was then followed until death. Cortical atrophy and ventricular size were assessed. Statistical analyses included Cox proportional hazards models with time to death as the outcome and considering a large number of possible confounders, including baseline cognitive function, incident dementia, and somatic disorders.

RESULTS

Mean survival time (±SD) was 5.0 ± 3.6 years (range 0.10-19.8 years). Decreased survival was associated with temporal, and frontal atrophy, sylvian fissure width and a number of ventricular measures after adjustment for potential confounders. In participants without dementia at baseline (n = 135), decreased survival was associated with temporal lobe atrophy and bifrontal ratio. In those with dementia (n = 104), decreased survival was associated with third ventricle width, cella media ratio, and ventricle-to-brain and ventricle-to-cranial ratio.

CONCLUSIONS

Several indices of brain atrophy were related to decreased survival after age 85, regardless of dementia status. Brain atrophy is rarely mentioned as a significant indicator of survival in the elderly, independent of traditional predictors such as cardiovascular disease or cancer. The biology behind the influence of brain atrophy on survival needs to be further scrutinized.

摘要

背景

80 岁及以上人群是全球人口增长最快的年龄段。为了了解长寿背后的生物学机制,研究与该年龄段人群生存相关的因素非常重要。85 岁以上人群的脑萎缩与生存之间的关系尚不清楚。

方法

一项基于人群的样本(n=239)在 85 岁时进行头部 CT 扫描,然后进行随访直至死亡。评估皮质萎缩和脑室大小。统计分析包括以死亡时间为结局的 Cox 比例风险模型,并考虑了大量可能的混杂因素,包括基线认知功能、新发痴呆和躯体疾病。

结果

平均生存时间(±SD)为 5.0±3.6 年(范围 0.10-19.8 年)。调整潜在混杂因素后,颞叶和额部萎缩、大脑外侧裂宽度以及多个脑室指标与生存时间缩短相关。在基线时无痴呆的参与者(n=135)中,颞叶萎缩和双额比与生存时间缩短相关。在有痴呆的参与者(n=104)中,第三脑室宽度、中隔腔比以及脑室与脑比、脑室与颅比与生存时间缩短相关。

结论

无论痴呆状态如何,脑萎缩的多个指标与 85 岁后生存时间缩短相关。脑萎缩很少被提及为老年人独立于心血管疾病或癌症等传统预测因素的生存的重要指标。脑萎缩对生存影响的生物学机制需要进一步研究。