DeCarli C, Mungas D, Harvey D, Reed B, Weiner M, Chui H, Jagust W
Department of Neurology, University of California at San Francisco, USA.
Neurology. 2004 Jul 27;63(2):220-7. doi: 10.1212/01.wnl.0000130531.90205.ef.
Mild cognitive impairment (MCI) is widely viewed as the transition phase between normal aging and Alzheimer disease (AD). Given that MCI can also result from cerebrovascular disease (CVD), the authors used clinical, MRI, and cognitive measures of AD and CVD to test the hypothesis that CVD increases the likelihood of progression from MCI to dementia within 3 years.
To examine the impact of CVD on progression of MCI to dementia.
Fifty-two consecutive patients with MCI (71% men) including many with symptomatic CVD were longitudinally evaluated for 3.1 +/- 1.3 years. MCI was defined as a Clinical Dementia Rating Scale (CDR) score of 0.5. Dementia was defined as progression to a CDR score of > or =1.0.
Forty-four percent of the MCI patients had MRI infarcts, 50% of which were symptomatic. Thirty-three percent of patients progressed to dementia, and 37.8% of these had MRI infarcts. Clinically probable or possible AD was diagnosed in approximately 82% of converters. Of the clinical and MRI measures, only hippocampal volume was associated with increased risk to progression (hazard ratio [HR] = 0.31 [95% CI 0.1 to 0.92], p = 0.03). When neuropsychological measures were included in the analysis, memory (HR = 0.90 [95% CI 0.84 to 0.96], p = 0.002) and executive function (HR = 0.96 [95% CI 0.92 to 1.0], p = 0.045) were associated with increased risk of dementia progression, whereas APOE genotype, cerebrovascular risk factors, clinical stroke, presence or absence of lacunes, and extent of white matter hyperintensities did not predict progression.
Within a heterogenous group of MCI patients, including many with clinically significant CVD, baseline memory and executive performance significantly predicted likelihood to develop dementia.
轻度认知障碍(MCI)被广泛视为正常衰老与阿尔茨海默病(AD)之间的过渡阶段。鉴于MCI也可能由脑血管疾病(CVD)引起,作者使用AD和CVD的临床、MRI及认知测量方法来检验CVD会增加3年内MCI进展为痴呆症可能性的假设。
研究CVD对MCI进展为痴呆症的影响。
对52例连续的MCI患者(71%为男性,其中许多患有有症状的CVD)进行了3.1±1.3年的纵向评估。MCI定义为临床痴呆评定量表(CDR)评分为0.5。痴呆症定义为进展至CDR评分≥1.0。
44%的MCI患者有MRI梗死灶,其中50%有症状。33%的患者进展为痴呆症,其中37.8%有MRI梗死灶。在大约82%的病情转化者中诊断为临床可能或确诊的AD。在临床和MRI测量指标中,只有海马体积与进展风险增加相关(风险比[HR]=0.31[95%CI 0.1至0.92],p=0.03)。当分析中纳入神经心理学测量指标时,记忆(HR=0.90[95%CI 0.84至0.96],p=0.002)和执行功能(HR=0.96[95%CI 0.92至1.0],p=0.045)与痴呆症进展风险增加相关,而APOE基因型、脑血管危险因素、临床中风、腔隙的有无以及白质高信号的程度均不能预测进展情况。
在一组异质性的MCI患者中,包括许多患有具有临床意义的CVD的患者,基线记忆和执行功能显著预测了发生痴呆症的可能性。