Division of Geriatrics, University of Sao Paulo Medical School, Sao Paulo, Brazil.
Department of Medical Surgical Nursing, University of Sao Paulo School of Nursing, Sao Paulo, Brazil.
Brain Pathol. 2019 Nov;29(6):771-781. doi: 10.1111/bpa.12719. Epub 2019 Apr 10.
To compare neuropathological correlates of cognitive impairment between very old and younger individuals from a Brazilian clinicopathological study.
We assessed the frequency of neuropathological lesions and their association with cognitive impairment (Clinical Dementia Rating scale ≥0.5) in the 80 or over age group compared to younger participants, using logistic regression models adjusted for sex, race and education.
Except for infarcts and siderocalcinosis, all neuropathological lesions were more common in the 80 or over age group (n = 412) compared to 50-79 year olds (n = 677). Very old participants had more than twice the likelihood of having ≥2 neuropathological diagnoses than younger participants (OR = 2.66, 95% CI = 2.03-3.50). Neurofibrillary tangles, infarcts and hyaline arteriolosclerosis were associated with cognitive impairment in the two age groups. Siderocalcinosis was associated with cognitive impairment in the younger participants only, while Lewy body disease was associated with cognitive impairment in the very old only. In addition, we found that the association of infarcts and multiple pathologies with cognitive impairment was attenuated in very old adults (Infarcts: P for interaction = 0.04; and multiple pathologies: P = 0.05). However, the predictive value for the aggregate model with all neuropathological lesions showed similar discrimination in both age groups [Area under Receiver Operating Characteristic curve (AUROC) = 0.778 in younger participants and AUROC = 0.765 in the very old].
Despite a higher frequency of neuropathological findings in the very old group, as found in studies with high-income populations, we found attenuation of the effect of infarcts rather than neurofibrillary tangles and plaques as reported previously.
比较巴西临床病理研究中非常老和年轻个体认知障碍的神经病理学相关性。
我们使用逻辑回归模型,根据性别、种族和教育程度对认知障碍(临床痴呆评定量表≥0.5)进行调整,评估 80 岁及以上年龄组与年轻参与者相比,神经病理学病变的频率及其与认知障碍的相关性。
除了梗死和含铁血黄素沉着症外,所有神经病理学病变在 80 岁及以上年龄组(n=412)中比 50-79 岁年龄组(n=677)更为常见。非常老的参与者比年轻的参与者有两倍以上的可能性患有≥2 种神经病理学诊断(OR=2.66,95%CI=2.03-3.50)。神经原纤维缠结、梗死和玻璃样小动脉硬化在两个年龄组中均与认知障碍相关。含铁血黄素沉着症仅与年轻参与者的认知障碍相关,而路易体病仅与非常老的参与者的认知障碍相关。此外,我们发现,梗死和多种病变与认知障碍的相关性在非常老的成年人中减弱(梗死:P 交互=0.04;多种病变:P=0.05)。然而,所有神经病理学病变的综合模型的预测值在两个年龄组中显示出相似的区分度[年轻参与者的Receiver Operating Characteristic 曲线下面积(AUROC)=0.778,非常老的参与者的 AUROC=0.765]。
尽管在高收入人群的研究中发现非常老的组神经病理学发现的频率更高,但我们发现梗死的作用减弱,而不是神经原纤维缠结和斑块,这与之前的报道不同。