Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.
Department of Integrative Biology, University of California, Berkeley, Berkeley, CA, USA.
J Alzheimers Dis. 2018;66(1):115-126. doi: 10.3233/JAD-180688.
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-β 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 São 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-β 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-β 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.
阐明神经精神症状与阿尔茨海默病(AD)相关病理之间的关系,可能为有效治疗方法开辟新途径。在此,我们研究了神经原纤维缠结和淀粉样蛋白-β病理负担增加与神经精神症状发展之间的关联。2004 年至 2014 年间去世的参与者在圣保罗大学医学院老龄化研究生物库接受了全面的神经病理学评估。通过可靠的知情者进行的死后访谈收集了有关神经精神和认知状况的信息。在所收集的 1092 例病例中,排除了任何非阿尔茨海默病的病理,使队列减少到 455 例。使用 Braak 分期评估神经原纤维缠结负担,使用 CERAD 神经病理学评分评估淀粉样蛋白-β负担。使用 12 项神经精神病学量表评估神经精神症状,使用 CDR-SOB 评分评估痴呆状态。与对照组相比,在 Braak I/II 期,激越、焦虑、食欲改变、抑郁和睡眠障碍的发生几率显著增加。激越的发生几率增加持续到 Braak III/IV 期。Braak V/VI 期与妄想发生几率增加相关。与淀粉样蛋白-β病理无相关性的神经精神症状发生几率增加。神经精神症状发生几率增加与早期神经原纤维缠结病理相关,表明皮质下神经原纤维缠结积累伴最小皮质病理足以影响生活质量,且神经精神症状是 AD 生物学过程的表现。