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胶质 Tau 病理学与衰老大脑中的 LATE-NC 的关联。

Association of glial tau pathology and LATE-NC in the ageing brain.

机构信息

Dementia Research Centre, Macquarie Medical School, Faculty of Health and Human Sciences, Macquarie University, Sydney, Australia; Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, Ontario, Canada.

Institute of Neurology, Medical University of Vienna, Vienna, Austria.

出版信息

Neurobiol Aging. 2022 Nov;119:77-88. doi: 10.1016/j.neurobiolaging.2022.07.010. Epub 2022 Jul 31.

Abstract

Ageing-related pathologies of the brain include neurofibrillary tangles, argyrophilic grains, ageing-related tau astrogliopathy (ARTAG), limbic-predominant age-related TDP-43 encephalopathy-neuropathological change (LATE-NC), vascular pathology and corpora amylacea. This study used an unbiased approach to evaluate a broad range of pathologies in an unselected European community-dwelling ageing cohort of 101 individuals (77-90 years). Pathological alterations observed included neurofibrillary tangles and corpora amylacea in all cases, ARTAG (79%), Thal amyloid-β phase >1 (60%), cerebral amyloid angiopathy (39%), Lewy bodies (22%), LATE-NC (21%), oligodendroglial tau-positive coiled bodies (33%), and argyrophilic grains (15%). We demonstrate association of LATE-NC with the previously unappreciated age-related tau oligodendrogliopathy (ARTOG) and highlight the association of LATE-NC with various ARTAG types pointing toward common pathogenic aspects. Only neurofibrillary tangles and LATE-NC were associated with cognitive decline. This study broadens the spectrum of age-related brain pathologies and highlights a novel ageing-related tau pathology in oligodendroglia. Results from this study suggest overlapping pathogenic mechanisms between LATE-NC and glial tau pathologies in the medial temporal lobe.

摘要

脑的衰老相关病变包括神经原纤维缠结、嗜银颗粒、衰老相关 tau 星形胶质病(ARTAG)、边缘系统为主的年龄相关性 TDP-43 脑神经病-病理改变(LATE-NC)、血管病变和淀粉样体。本研究采用无偏方法评估了 101 名(77-90 岁)未选择的欧洲社区居住的衰老队列中的广泛病变。观察到的病理改变包括所有病例的神经原纤维缠结和淀粉样体,ARTAG(79%)、Thal 淀粉样-β 相 >1(60%)、脑淀粉样血管病(39%)、路易体(22%)、LATE-NC(21%)、少突胶质细胞 tau 阳性螺旋体(33%)和嗜银颗粒(15%)。我们证明 LATE-NC 与以前未被认识的衰老相关 tau 少突胶质病(ARTOG)有关,并强调 LATE-NC 与各种 ARTAG 类型的关联指向共同的发病方面。只有神经原纤维缠结和 LATE-NC 与认知下降有关。本研究拓宽了与年龄相关的脑病变谱,并强调了少突胶质细胞中与衰老相关的 tau 病理学的新发现。本研究结果表明 LATE-NC 与内侧颞叶的神经胶质 tau 病变之间存在重叠的发病机制。

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