Snitz Beth E, Weissfeld Lisa A, Cohen Ann D, Lopez Oscar L, Nebes Robert D, Aizenstein Howard J, McDade Eric, Price Julie C, Mathis Chester A, Klunk William E
Department of Neurology, University of Pittsburgh, Pittsburgh, PA.
Statistics Collaborative, Inc., Washington, D.C.
Am J Geriatr Psychiatry. 2015 Sep;23(9):985-93. doi: 10.1016/j.jagp.2015.01.008. Epub 2015 Feb 11.
Subjective cognitive complaints in otherwise normal aging are common but may be associated with preclinical Alzheimer disease in some individuals. Little is known about who is mostly likely to show associations between cognitive complaints and preclinical Alzheimer pathology. We sought to demonstrate associations between subjective complaints and brain amyloid-β in cognitively normal older adults; and to explore personality factors as potential moderators of this association.
Cross-sectional observational study.
Clinical neuroimaging research center.
Community volunteer sample of 92 healthy older adults, screened for normal cognition with comprehensive neuropsychological evaluation.
Subjective cognitive self-report measures included the Memory Functioning Questionnaire (MFQ), Cognitive Failures Questionnaire, and the Subjective Cognitive Complaint Scale. Personality was measured with the NEO Five Factor Inventory. Brain amyloid-β deposition was assessed with Pittsburgh compound B (PiB)-PET imaging.
One of three cognitive complaint measures, the MFQ, was associated with global PiB retention (standardized beta = -0.230, p = 0.046, adjusting for age, sex and depressive symptoms). Neuroticism moderated this association such that only high neuroticism individuals showed the predicted pattern of high complaint-high amyloid-β association.
Evidence for association between subjective cognition and brain amyloid-β deposition in healthy older adults is demonstrable but measure-specific. Neuroticism may moderate the MFQ-amyloid-β association such that it is observed in the context of higher trait neuroticism. Subjective cognitive complaints and neuroticism may reflect a common susceptibility toward psychological distress and negative affect, which are in turn risk factors for cognitive decline in aging and incident Alzheimer disease.
在其他方面正常衰老的个体中,主观认知抱怨很常见,但在某些个体中可能与临床前阿尔茨海默病有关。对于谁最有可能表现出认知抱怨与临床前阿尔茨海默病病理学之间的关联,人们知之甚少。我们试图证明认知正常的老年人主观抱怨与脑淀粉样蛋白-β之间的关联;并探索人格因素作为这种关联的潜在调节因素。
横断面观察性研究。
临床神经影像研究中心。
92名健康老年人的社区志愿者样本,通过全面神经心理学评估筛选出认知正常者。
主观认知自我报告测量包括记忆功能问卷(MFQ)、认知失误问卷和主观认知抱怨量表。使用NEO五因素问卷测量人格。用匹兹堡化合物B(PiB)-PET成像评估脑淀粉样蛋白-β沉积。
三项认知抱怨测量中的一项,即MFQ,与整体PiB滞留有关(标准化β=-0.230,p=0.046,校正年龄、性别和抑郁症状)。神经质调节了这种关联,使得只有高神经质个体表现出高抱怨-高淀粉样蛋白-β关联的预测模式。
健康老年人主观认知与脑淀粉样蛋白-β沉积之间存在关联的证据是可证明的,但具有测量特异性。神经质可能调节MFQ-淀粉样蛋白-β关联,使其在较高特质神经质的背景下被观察到。主观认知抱怨和神经质可能反映了对心理困扰和负面影响的共同易感性,而心理困扰和负面影响又是衰老和偶发性阿尔茨海默病认知衰退的危险因素。