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大脑外阿尔茨海默病病理学与痴呆症的高发病几率相关。

Alzheimer's Disease Pathology Outside of the Cerebrum Is Related to a Higher Odds of Dementia.

机构信息

Rush Alzheimer's Disease Research Center, Rush University Medical Center, Chicago, IL, USA.

Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.

出版信息

J Alzheimers Dis. 2023;96(2):563-578. doi: 10.3233/JAD-230223.

Abstract

BACKGROUND

Assessments of Alzheimer's disease pathology do not routinely include lower brainstem, olfactory bulb, and spinal cord.

OBJECTIVE

Test if amyloid-β (Aβ) and paired helical filament (PHF) tau-tangles outside the cerebrum are associated with the odds of dementia.

METHODS

Autopsies were obtained in decedents with cognitive testing (n = 300). Aβ plaques and PHF tau-tangles were assessed in 24 sites: cerebrum (n = 14), brainstem (n = 5), olfactory bulb, and four spinal cord levels. Since spinal Aβ were absent in the first 165 cases, it was not assessed in the remaining cases.

RESULTS

Age at death was 91 years old. About 90% had Aβ in cerebrum and of these, half had Aβ in the brainstem. Of the latter, 85% showed Aβ in the olfactory bulb. All but one participant had tau-tangles in the cerebrum and 86% had brainstem tau-tangles. Of the latter, 80% had tau-tangles in olfactory bulb and 36% tau-tangles in one or more spinal cord levels. About 90% of adults with tau-tangles also had Aβ in one or more regions. In a logistic model controlling for demographics, Aβ and tau-tangles within the cerebrum, the presence of Aβ in olfactory bulb [OR, 1.74(1.00, 3.05)]; tau-tangles in brainstem [OR, 4.00(1.1.57,10.21)]; and spinal cord [OR, 1.87 (1.21,3.11)] were independently associated with higher odds of dementia.

CONCLUSION

Regional differences in Aβ and tau-tangle accumulation extend beyond cerebrum to spinal cord and their presence outside the cerebrum are associated with a higher odds of dementia. Further studies are needed to clarify the extent, burden, and consequences of AD pathology outside of cerebrum.

摘要

背景

对阿尔茨海默病病理的评估通常不包括脑桥下部、嗅球和脊髓。

目的

检验大脑外的淀粉样蛋白-β(Aβ)和双螺旋细丝(PHF)tau 缠结与痴呆的可能性是否相关。

方法

对接受认知测试的死者进行尸检(n=300)。评估了 24 个部位的 Aβ 斑块和 PHF tau 缠结:大脑(n=14)、脑桥下部(n=5)、嗅球和四个脊髓水平。由于前 165 例脊髓 Aβ 缺失,因此在后 135 例中未评估。

结果

死亡时的年龄为 91 岁。约 90%的大脑中有 Aβ,其中一半的大脑中有 Aβ在脑桥下部。在后一组中,85%的嗅球中存在 Aβ。除了一名参与者之外,所有参与者的大脑中都有 tau 缠结,而 86%的脑桥下部有 tau 缠结。在后一组中,80%的嗅球中有 tau 缠结,36%的脊髓一个或多个水平中有 tau 缠结。约 90%的 tau 缠结患者在一个或多个区域也有 Aβ。在控制人口统计学的逻辑模型中,大脑内的 Aβ和 tau 缠结、嗅球中 Aβ的存在[比值比(OR),1.74(1.00,3.05)];脑桥下部的 tau 缠结[OR,4.00(1.10,15.70)];和脊髓[OR,1.87(1.21,3.11)]与痴呆的可能性较高独立相关。

结论

Aβ 和 tau 缠结的区域性差异不仅存在于大脑,还延伸至脊髓,而大脑外的存在与痴呆的可能性较高有关。需要进一步研究以阐明大脑外 AD 病理学的程度、负担和后果。

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