Mungas D, Reed B R, Jagust W J, DeCarli C, Mack W J, Kramer J H, Weiner M W, Schuff N, Chui H C
Department of Neurology, School of Medicine, University of California, Davis, USA.
Neurology. 2002 Sep 24;59(6):867-73. doi: 10.1212/wnl.59.6.867.
To examine volumetric MRI correlates of longitudinal cognitive decline in normal aging, AD, and subcortical cerebrovascular brain injury (SCVBI).
Previous cross-sectional studies examining the relationship between cognitive impairment and dementia have shown that hippocampal and cortical gray matter atrophy are the most important predictors of cognitive impairment, even in cases with SCVBI. The authors hypothesized that hippocampal and cortical gray matter volume also would best predict rate of cognitive decline in cases with and without SCVBI.
Subjects were recruited for a multicenter study of contributions to dementia of AD and SCVBI. The sample (n = 120) included cognitively normal, cognitively impaired, and demented cases with and without lacunes identified by MRI. Cases with cortical strokes were excluded. Average length of follow-up was 3.0 years. Measures of hippocampal volume, volume of cortical gray matter, presence of subcortical lacunes, and volume of white matter hyperintensity were derived from MRI. Random effects modeling of longitudinal data was used to assess effects of baseline MRI variables on longitudinal change in a measure of global cognitive ability.
Cortical gray matter atrophy predicted cognitive decline regardless of whether lacunes were present. Hippocampal atrophy predicted decline only in those without lacunes. Neither lacunes nor white matter hyperintensity independently predicted decline.
Results suggest that cortical atrophy is an index of disease severity in both AD and subcortical cerebrovascular brain injury and consequently predicts faster progression. Hippocampal volume may index disease severity and predict progression in AD. The absence of this effect in cases with lacunes suggests that this group is etiologically heterogeneous and is not composed simply of cases of AD with incidental stroke.
研究正常衰老、阿尔茨海默病(AD)和皮质下脑血管性脑损伤(SCVBI)患者纵向认知衰退的容积性磁共振成像(MRI)相关性。
既往关于认知障碍与痴呆关系的横断面研究表明,海马体和皮质灰质萎缩是认知障碍最重要的预测因素,即使在患有SCVBI的病例中也是如此。作者推测,海马体和皮质灰质体积也将最能预测有无SCVBI病例的认知衰退速度。
招募受试者参与一项关于AD和SCVBI对痴呆影响的多中心研究。样本(n = 120)包括经MRI鉴定有无腔隙的认知正常、认知受损和痴呆病例。排除有皮质中风的病例。平均随访时间为3.0年。海马体体积、皮质灰质体积、皮质下腔隙的存在情况以及白质高信号体积的测量值均来自MRI。纵向数据的随机效应模型用于评估基线MRI变量对整体认知能力测量值纵向变化的影响。
无论有无腔隙,皮质灰质萎缩均能预测认知衰退。海马体萎缩仅能预测无腔隙者的认知衰退。腔隙和白质高信号均不能独立预测认知衰退。
结果表明,皮质萎缩是AD和皮质下脑血管性脑损伤疾病严重程度的指标,因此可预测更快的进展。海马体体积可能是AD疾病严重程度的指标并可预测其进展。有腔隙的病例中不存在这种效应,这表明该组病因学上具有异质性,并非简单地由伴有偶发性中风的AD病例组成。