Schneider Julie A, Arvanitakis Zoe, Bang Woojeong, Bennett David A
Rush Alzheimer's Disease Center, Rush University Medical Center, Armour Academic Center, 600 S. Paulina Street, Suite 1022F, Chicago, IL 60612, USA.
Neurology. 2007 Dec 11;69(24):2197-204. doi: 10.1212/01.wnl.0000271090.28148.24. Epub 2007 Jun 13.
To examine the spectrum of neuropathology in persons from the Rush Memory and Aging Project, a longitudinal community-based clinical-pathologic cohort study.
The study includes older persons who agreed to annual clinical evaluation and brain donation. We examined the neuropathologic diagnoses, including Alzheimer disease (AD) (NIA-Reagan Criteria), cerebral infarctions, and Parkinson disease/Lewy body disease (PD/LBD), in the first 141 autopsies. We calculated the frequency of each diagnosis alone and mixed diagnoses. We used logistic regression to compare one to multiple diagnoses on the odds of dementia.
Twenty persons (14.2%) had no acute or chronic brain abnormalities. The most common chronic neuropathologic diagnoses were AD (n = 80), cerebral infarctions (n = 52), and PD/LBD (n = 24). In persons with dementia (n = 50), 38.0% (n = 19) had AD and infarcts, 30.0% (n = 15) had pure AD, and 12% each had vascular dementia (n = 6) and AD with PD/LBD (n = 6). In those without dementia (n = 91), 28.6% (n = 26) had no chronic diagnostic abnormalities, 24.2% (n = 22) had pure AD, and 17.6% (n = 16) had infarctions. In persons with dementia, over 50% had multiple diagnoses (AD, PD/LBD, or infarcts), whereas, in persons without dementia, over 80% had one or no diagnosis. After accounting for age, persons with multiple diagnoses were almost three times (OR = 2.8; 95% CI = 1.2, 6.7) more likely to exhibit dementia compared to those with one pathologic diagnosis.
The majority of community-dwelling older persons have brain pathology. Those with dementia most often have multiple brain pathologies, which greatly increases the odds of dementia.
在拉什记忆与衰老项目(一项基于社区的纵向临床病理队列研究)中,研究神经病理学谱。
该研究纳入了同意接受年度临床评估和脑捐赠的老年人。我们检查了前141例尸检的神经病理学诊断结果,包括阿尔茨海默病(AD)(NIA-里根标准)、脑梗死以及帕金森病/路易体病(PD/LBD)。我们计算了每种单独诊断以及混合诊断的频率。我们使用逻辑回归来比较单一诊断与多种诊断对痴呆几率的影响。
20人(14.2%)没有急性或慢性脑异常。最常见的慢性神经病理学诊断是AD(n = 80)、脑梗死(n = 52)和PD/LBD(n = 24)。在患有痴呆的人群(n = 50)中,38.0%(n = 19)患有AD和梗死,30.0%(n = 15)患有单纯AD,各有12%患有血管性痴呆(n = 6)以及AD合并PD/LBD(n = 6)。在未患痴呆的人群(n = 91)中,28.6%(n = 26)没有慢性诊断异常,24.2%(n = 22)患有单纯AD,17.6%(n = 16)患有梗死。在患有痴呆的人群中,超过50%有多种诊断(AD、PD/LBD或梗死),而在未患痴呆的人群中,超过80%有一项诊断或无诊断。在考虑年龄因素后,与有一项病理诊断的人相比,有多种诊断的人出现痴呆的可能性几乎是其三倍(OR = 2.8;95% CI = 1.2, 6.7)。
大多数居住在社区的老年人存在脑病理学改变。患有痴呆的人最常出现多种脑病理学改变,这大大增加了患痴呆的几率。