Pillai Jagan A, Butler Robert S, Bonner-Jackson Aaron, Leverenz James B
Lou Ruvo Center for Brain Health, Cleveland Clinic, Cleveland, Ohio, USA.
Dement Geriatr Cogn Disord. 2016;42(1-2):106-16. doi: 10.1159/000448243. Epub 2016 Sep 14.
We examined the effect of vascular or Lewy body co-pathologies in subjects with autopsy-confirmed Alzheimer's disease (AD) on the rate of cognitive and functional decline and transition to dementia.
In an autopsy sample of prospectively characterized subjects from the National Alzheimer's Coordinating Center database, neuropathology diagnosis was used to define the groups of pure AD (pAD, n = 84), mixed vascular and AD (ADV, n = 54), and mixed Lewy body disease and AD (ADLBD, n = 31). Subjects had an initial Clinical Dementia Rating-Global (CDR-G) score <1, Mini-Mental State Examination ≥15, a final visit CDR-G >1, ≥3 evaluations, and Braak tangle stage ≥III. We compared the rate of cognitive and functional decline between the groups.
The rate of functional and cognitive decline was lower for ADV, and ADV patients had less severe deficits on CDR-G and the CDR-Sum of Boxes scores at the last visit than pAD and ADLBD patients. No significant differences were noted between ADLBD and pAD patients. After controlling for age at death, the odds of reaching CDR ≥1 at the last visit were lower in the ADV subjects compared to the pAD subjects.
The mean rate of functional and cognitive decline among ADV subjects was slower than among either pAD or ADLBD patients. Vascular pathology did not increase the odds of attaining CDR ≥1 when occurring with AD in this national cohort.
我们研究了经尸检确诊为阿尔茨海默病(AD)的受试者中,血管或路易体共病对认知和功能衰退率以及向痴呆转变的影响。
在来自国家阿尔茨海默病协调中心数据库的前瞻性特征明确的受试者尸检样本中,神经病理学诊断用于定义纯AD组(pAD,n = 84)、血管性与AD混合组(ADV,n = 54)以及路易体病与AD混合组(ADLBD,n = 31)。受试者初始临床痴呆评定量表 - 总体(CDR - G)评分<1,简易精神状态检查表≥15,最后一次访视时CDR - G>1,进行≥3次评估,且Braak神经缠结分期≥III。我们比较了各组之间的认知和功能衰退率。
ADV组的功能和认知衰退率较低,且ADV组患者在最后一次访视时CDR - G和CDR - 方框总和评分的 deficits 比pAD组和ADLBD组患者轻。ADLBD组和pAD组患者之间未观察到显著差异。在控制死亡年龄后,与pAD组受试者相比,ADV组受试者在最后一次访视时达到CDR≥1的几率较低。
ADV组受试者的功能和认知衰退平均速率比pAD组或ADLBD组患者慢。在这个全国性队列中,血管病理学与AD同时出现时,并未增加达到CDR≥1的几率。