Williams Monique M, Xiong Chengjie, Morris John C, Galvin James E
Department of Medicine, Alzheimer Disease Research Center, Washington University School of Medicine, 4488 Forest Park, Suite 130, St. Louis, MO 63108, USA.
Neurology. 2006 Dec 12;67(11):1935-41. doi: 10.1212/01.wnl.0000247041.63081.98.
To determine whether dementia with Lewy bodies (DLB) progresses more rapidly than Alzheimer disease (AD).
We compared 315 participants (63 with DLB and 252 with AD) enrolled in a prospective longitudinal study of memory and aging with annual clinical and cognitive assessments and followed until death. The main outcome measure was dementia progression to institutionalization and death. Neuropathologic examinations were performed on all participants in this study. Subject classification (DLB vs AD) was based on neuropathology.
Patients with DLB had an increased risk of mortality vs patients with AD (hazard ratio [HR] 1.88, 95% CI: 1.4 to 2.5). The median survival time for DLB was 78.0 years and for AD was 84.6 years (chi(2) = 19.9, p < 0.001) with significant modification effects due to gender (HR 1.51, 95% CI: 1.0 to 2.3) and the presence of at least 1 APOE epsilon4 allele (HR 1.50, 95% CI: 1.0 to 2.2). Survival after dementia onset was also different between DLB and AD (7.3 vs 8.5 years; chi(2) = 5.4, p < 0.02). DLB cases had similar risks of institutionalization and survival in long-term care facilities to AD cases. Self-reports of depression and the presence of extrapyramidal signs were important covariates. The rate of cognitive decline as measured by psychometric performance and clinical staging methods did not differ between DLB and AD.
Dementia with Lewy bodies (DLB) increases the risk of mortality compared with Alzheimer disease (AD), but the two groups did not differ in rate of cognitive decline. The greater risk for noncognitive disease progression for DLB compared with AD suggests clinically meaningful differences for the two disorders.
确定路易体痴呆(DLB)是否比阿尔茨海默病(AD)进展更快。
我们比较了315名参与者(63名DLB患者和252名AD患者),他们参与了一项关于记忆与衰老的前瞻性纵向研究,接受年度临床和认知评估,并随访至死亡。主要结局指标是痴呆进展至入住机构照料及死亡。本研究的所有参与者均接受了神经病理学检查。受试者分类(DLB与AD)基于神经病理学。
与AD患者相比,DLB患者的死亡风险增加(风险比[HR] 1.88,95%置信区间:1.4至2.5)。DLB的中位生存时间为78.0岁,AD为84.6岁(χ² = 19.9,p < 0.001),存在因性别(HR 1.51,95%置信区间:1.0至2.3)和至少存在1个APOE ε4等位基因(HR 1.50,95%置信区间:1.0至2.2)导致的显著修正效应。痴呆发病后的生存情况在DLB和AD之间也有所不同(7.3年对8.5年;χ² = 5.4,p < 0.02)。DLB病例与AD病例在长期护理机构中的入住机构照料风险及生存情况相似。抑郁的自我报告及锥体外系体征的存在是重要的协变量。通过心理测量表现和临床分期方法测得的认知衰退率在DLB和AD之间没有差异。
与阿尔茨海默病(AD)相比,路易体痴呆(DLB)增加了死亡风险,但两组在认知衰退率方面没有差异。与AD相比,DLB在非认知疾病进展方面的更大风险表明这两种疾病在临床上存在有意义的差异。