Godrich Dana, Pasteris Jeremy, Martin Eden R, Rundek Tatjana, Schellenberg Gerard, Foroud Tatiana, Vance Jeffery M, Pericak-Vance Margaret A, Cuccaro Michael L, Scott William K, Kukull Walter, Montine Thomas J, Beecham Gary W
Dr. John T Macdonald Foundation Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
Brain Commun. 2024 Nov 22;6(6):fcae369. doi: 10.1093/braincomms/fcae369. eCollection 2024.
Cerebral amyloid angiopathy commonly co-occurs with amyloid β plaques and neurofibrillary degeneration and is proposed to contribute to cognitive impairment. However, the interplay among these pathologic changes of Alzheimer disease is not well understood. Here we replicate and extend findings of a recent study that suggested the association of cerebral amyloid angiopathy and cognitive impairment is mediated by neurofibrillary degeneration. We employed similar approaches but in a larger, clinical-based (as opposed to community-based) set of 4915 autopsied National Alzheimer's Coordinating Center participants (60% with dementia). Neuropathologic lesions were measured ordinally; longitudinal change in cognition was used to measure cognitive impairment. Statistical analyses included ordinal logistic regression, mediation analyses and extension of models to include presence of e4. We show a statistical interaction between cerebral amyloid angiopathy and neuritic plaques that impacts the burden of neurofibrillary tangles. Mediation analyses show that cerebral amyloid angiopathy is associated with cognitive impairment, but only by modifying the impact of neurofibrillary tangles on cognition. We expanded the mediation analysis to include e4 and show similar results. Findings indicate that cerebral amyloid angiopathy plays an important role in the burden and impact of neurofibrillary degeneration contributing to cognitive impairment.
脑淀粉样血管病通常与淀粉样β斑块和神经纤维变性同时出现,并被认为与认知障碍有关。然而,阿尔茨海默病这些病理变化之间的相互作用尚未得到充分理解。在这里,我们重复并扩展了最近一项研究的结果,该研究表明脑淀粉样血管病与认知障碍之间的关联是由神经纤维变性介导的。我们采用了类似的方法,但样本量更大,基于临床(而非社区),共纳入4915名接受尸检的国家阿尔茨海默病协调中心参与者(60%患有痴呆症)。神经病理病变按顺序进行测量;认知的纵向变化用于测量认知障碍。统计分析包括有序逻辑回归、中介分析以及将模型扩展以纳入ε4的存在情况。我们发现脑淀粉样血管病与神经炎性斑块之间存在统计学相互作用,这会影响神经纤维缠结的负担。中介分析表明,脑淀粉样血管病与认知障碍有关,但只是通过改变神经纤维缠结对认知的影响。我们将中介分析扩展到包括ε4,结果相似。研究结果表明,脑淀粉样血管病在神经纤维变性的负担和影响中起重要作用,进而导致认知障碍。