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首页> 外文期刊>Journal of Alzheimer's disease: JAD >Neuropathologic Correlates of Psychiatric Symptoms in Alzheimer's Disease
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Neuropathologic Correlates of Psychiatric Symptoms in Alzheimer's Disease

机译:阿尔茨海默病中精神病症状的神经病理学相关性

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摘要

Clarifying the relationships between neuropsychiatric symptoms and Alzheimer's disease (AD)-related pathology may open avenues for effective treatments. Here, we investigate the odds of developing neuropsychiatric symptoms across increasing burdens of neurofibrillary tangle and amyloid-beta pathology. Participants who passed away between 2004 and 2014 underwent comprehensive neuropathologic evaluation at the Biobank for Aging Studies from the Faculty of Medicine at the University of Sao Paulo. Postmortem interviews with reliable informants were used to collect information regarding neuropsychiatric and cognitive status. Of 1,092 cases collected, those with any non-Alzheimer pathology were excluded, bringing the cohort to 455 cases. Braak staging was used to evaluate neurofibrillary tangle burden, and the CERAD neuropathology score was used to evaluate amyloid-beta burden. The 12-item neuropsychiatric inventory was used to evaluate neuropsychiatric symptoms and CDR-SOB score was used to evaluate dementia status. In Braak I/II, significantly increased odds were detected for agitation, anxiety, appetite changes, depression, and sleep disturbances, compared to controls. Increased odds of agitation continue into Braak III/IV. Braak V/VI is associated with higher odds for delusions. No increased odds for neuropsychiatric symptoms were found to correlate with amyloid-beta pathology. Increased odds of neuropsychiatric symptoms are associated with early neurofibrillary tangle pathology, suggesting that subcortical neurofibrillary tangle accumulation with minimal cortical pathology is sufficient to impact quality of life and that neuropsychiatric symptoms are a manifestation of AD biological processes.
机译:澄清神经精神症状与阿尔茨海默病(AD)的关系(AD)的病理可能打开有效治疗的途径。在这里,我们探讨了在增加神经纤维缠结和淀粉样蛋白β病理学中增加神经精神症状的几率。在2004年至2014年之间消除的参与者在Biobank中接受了综合神经病理学评估,以便在圣保罗大学医学院的老化研究。与可靠的线人的后期面试用于收集有关神经精神和认知状态的信息。收集了1,092例,其中排除了任何非阿尔茨海默病病的病例,将队列带到455例。 Braak分期用于评估神经原纤维缠结负担,并且使用Cerad神经病理学评分来评估淀粉样蛋白β负担。 12项神经精神计量库存用于评估神经精神症状,CDR-SOB评分用于评估痴呆状态。与对照相比,在Braak I / II中,检测到搅拌,焦虑,食欲改变,抑郁和睡眠障碍的显着增加。搅拌的几率越来越多地进入Brak III / IV。 Braak v / vi与妄想的赔率较高有关。发现神经精神症状没有增加的几率与淀粉样蛋白β病理学相关。神经精神症状的差异增加与早期神经纤维缠结病理有关,表明皮质神经原纤维缠结积聚具有最小的皮质病理学,足以影响生活质量,并且神经精神症状是AD生物过程的表现。

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