Wilson R S, Schneider J A, Bienias J L, Arnold S E, Evans D A, Bennett D A
Rush Alzheimer's Disease Center and Rush Institute for Healthy Aging, Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612, USA.
Neurology. 2003 Oct 28;61(8):1102-7. doi: 10.1212/01.wnl.0000092914.04345.97.
Depressive symptoms in old age have been associated with risk of Alzheimer disease (AD), but it is uncertain whether they are an independent risk factor for disease or an early clinical sign of its underlying pathology.
A group of 130 older Catholic nuns, priests, and brothers underwent detailed annual clinical evaluations and brain autopsy at death. The evaluations included administration of a modified 10-item Center for Epidemiologic Studies Depression Scale (CES-D) and 19 cognitive performance tests and clinical classification of dementia and AD. On postmortem examination, neuritic plaques, diffuse plaques, and neurofibrillary tangles in tissue samples from four cortical regions were counted, and a previously established composite measure of cortical plaque and tangle density (range 0 to 2.98) was derived. All analyses were adjusted for age, sex, and education.
Participants reported a mean 1.5 depressive symptoms (SD 1.6) on the CES-D scale averaged across evaluations. In a logistic regression model, the odds of clinically diagnosed AD proximate to death increased by 1.33 (95% CI 1.01 to 1.76) for each depressive symptom and by 8.41 (95% CI 3.49 to 20.26) for each unit on the composite measure of pathology. In subsequent analyses, depressive symptoms were not related to level of pathology and did not modify the relation of pathology to clinical AD. In a series of linear regression models that controlled for pathology, depressive symptoms were related to level of cognitive function proximate to death and did not modify the association of pathology with cognition.
The association of depressive symptoms with clinical AD and cognitive impairment appears to be independent of cortical plaques and tangles.
老年期抑郁症状与阿尔茨海默病(AD)风险相关,但不确定它们是疾病的独立危险因素还是其潜在病理的早期临床征象。
一组130名年长的天主教修女、神父和修士在生前接受了详细的年度临床评估并在死后进行了脑尸检。评估包括使用改良的10项流行病学研究中心抑郁量表(CES-D)、19项认知功能测试以及痴呆和AD的临床分类。尸检时,对四个皮质区域组织样本中的神经炎性斑块、弥漫性斑块和神经原纤维缠结进行计数,并得出先前建立的皮质斑块和缠结密度综合测量值(范围为0至2.98)。所有分析均针对年龄、性别和教育程度进行了调整。
参与者在各次评估中CES-D量表上报告的抑郁症状平均为1.5个(标准差为1.6)。在逻辑回归模型中,临近死亡时临床诊断为AD的几率,每出现一个抑郁症状增加1.33(95%置信区间为1.01至1.76),病理综合测量值每增加一个单位增加8.41(95%置信区间为3.49至20.26)。在后续分析中,抑郁症状与病理水平无关,也未改变病理与临床AD之间的关系。在一系列控制了病理因素的线性回归模型中,抑郁症状与临近死亡时的认知功能水平相关,但未改变病理与认知之间的关联。
抑郁症状与临床AD及认知障碍之间的关联似乎独立于皮质斑块和缠结。