Yu Lei, Boyle Patricia A, Leurgans Sue, Schneider Julie A, Kryscio Richard J, Wilson Robert S, Bennett David A
Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL, USA; Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.
Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL, USA; Department of Behavioral Sciences, Rush University Medical Center, Chicago, IL, USA.
Neurobiol Aging. 2015 Jul;36(7):2225-2231. doi: 10.1016/j.neurobiolaging.2015.04.006. Epub 2015 Apr 22.
Brain pathologies of Alzheimer's (AD), cerebrovascular, and Lewy body diseases are common in old age, but the relationship of these pathologies with progression from normal cognitive function to the various stages of cognitive impairment is unknown. In this study, we fit latent Markov models from longitudinal cognitive data to empirically derive 3 latent stages corresponding to no impairment, mild impairment, and moderate impairment; then, we examined the associations of common neuropathologies with the rates of transition among these stages. Cognitive and neuropathological data were available from 653 autopsied participants in 2 ongoing cohort studies of aging who were cognitively healthy at baseline (mean baseline age 79.1 years) and had longitudinal cognitive data. On average, participants in these analyses developed mild impairment 5 years after enrollment, progressed to moderate impairment after an additional 3.4 years, and stayed impaired for 2.8 years until death. AD and chronic macroscopic infarcts were associated with a higher risk of progression to mild impairment and subsequently to moderate impairment. By contrast, Lewy bodies were associated only with progression from mild to moderate impairment. The 5-year probability of progression to mild or moderate impairment was 20% for persons without any of these 3 pathologies, 38% for AD only, 51% for AD and macroscopic infarcts, and 56% for AD, infarcts, and Lewy bodies. Thus, the presence of AD pathology alone nearly doubles the risk of developing cognitive impairment in late life, and the presence of multiple pathologies further increases this risk over multiple years before death.
阿尔茨海默病(AD)、脑血管疾病和路易体病的脑部病变在老年人群中很常见,但这些病变与认知功能从正常到认知障碍各个阶段进展之间的关系尚不清楚。在本研究中,我们根据纵向认知数据拟合潜在马尔可夫模型,以实证得出对应无损害、轻度损害和中度损害的3个潜在阶段;然后,我们研究了常见神经病理学与这些阶段之间转换率的关联。认知和神经病理学数据来自两项正在进行的衰老队列研究中的653名尸检参与者,他们在基线时认知健康(平均基线年龄79.1岁)且有纵向认知数据。平均而言,这些分析中的参与者在入组5年后出现轻度损害,再过3.4年后进展为中度损害,并在损害状态下持续2.8年直至死亡。AD和慢性宏观梗死与进展为轻度损害及随后进展为中度损害的较高风险相关。相比之下,路易体仅与从轻度到中度损害的进展相关。对于没有这三种病变中任何一种的人,进展为轻度或中度损害的5年概率为20%,仅患有AD的人为38%,患有AD和宏观梗死的人为51%,患有AD、梗死和路易体的人为56%。因此,仅AD病理学的存在使晚年发生认知障碍的风险几乎增加一倍,而多种病变的存在在死亡前的多年里进一步增加了这种风险。