Smith Eric E, Egorova Svetlana, Blacker Deborah, Killiany Ronald J, Muzikansky Alona, Dickerson Bradford C, Tanzi Rudolph E, Albert Marilyn S, Greenberg Steven M, Guttmann Charles R G
Neurology Clinical Trials Unit, Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Arch Neurol. 2008 Jan;65(1):94-100. doi: 10.1001/archneurol.2007.23.
To determine whether magnetic resonance imaging (MRI) white matter hyperintensities (WMH), whole-brain atrophy, and cardiovascular risk factors predict the development of cognitive decline and dementia.
Subjects were recruited into this prospective cohort study and followed for incident cognitive decline for mean (SD) 6.0 (4.1) years. Magnetic resonance imaging dual-echo sequences, obtained at baseline, were used to determine the volume of WMH and the brain parenchymal fraction (BPF), the proportion of the intracranial cavity occupied by brain. White matter hyperintensity volume was analyzed as the percentage of intracranial volume (WMHr); "high WMH" was defined as a WMHr more than 1 SD above the mean.
General community.
Volunteer sample consisting of 67 subjects with normal cognition and 156 subjects with mild cognitive impairment (MCI).
Time to diagnosis of MCI (among those with normal cognition at baseline) or time to diagnosis of dementia, either all-cause or probable Alzheimer disease (AD) (among those with MCI at baseline). Cox proportional hazards models were used for multivariable analysis.
High WMH was a predictor of progression from normal to MCI (adjusted hazard ratio [HR], 3.30; 95% confidence interval [CI], 1.33-8.17; P= .01) but not conversion from MCI to all-cause dementia. Conversely, BPF did not predict progression from normal to MCI but did predict conversion to dementia (adjusted HR, 1.10 for each 1% decrease in BPF; 95% CI, 1.02-1.19; P= .02). When conversion to AD dementia was considered as the outcome, BPF was likewise a predictor (adjusted HR, 1.16 for each 1% decrease in BPF; 95% CI, 1.08-1.24; P< .001), but high WMH was not. Past tobacco smoking was associated with both progression from normal to MCI (adjusted HR, 2.71; 95% CI, 1.12-6.55; P= .03) and conversion to all-cause dementia (adjusted HR, 2.08; 95% CI, 1.13-3.82; P= .02), but not AD dementia.
These findings suggest that WMH are associated with the risk of progressing from normal to MCI. In persons whose cognitive abilities are already impaired, BPF predicts the conversion to dementia.
确定磁共振成像(MRI)白质高信号(WMH)、全脑萎缩和心血管危险因素是否可预测认知功能下降和痴呆的发生。
将受试者纳入这项前瞻性队列研究,并对其进行平均(标准差)6.0(4.1)年的随访,以观察认知功能下降事件。在基线时获得的磁共振成像双回波序列用于确定WMH的体积和脑实质分数(BPF),即脑在颅腔内所占的比例。白质高信号体积以颅内体积的百分比(WMHr)进行分析;“高WMH”定义为WMHr高于平均值1个标准差以上。
普通社区。
由67名认知正常的受试者和156名轻度认知障碍(MCI)受试者组成的志愿者样本。
从正常状态诊断为MCI(基线时认知正常者)的时间,或从MCI诊断为全因性痴呆或可能的阿尔茨海默病(AD)痴呆(基线时为MCI者)的时间。采用Cox比例风险模型进行多变量分析。
高WMH是从正常进展为MCI的预测因素(调整后风险比[HR],3.30;95%置信区间[CI],1.33 - 8.17;P = 0.01),但不是从MCI转变为全因性痴呆的预测因素。相反,BPF不能预测从正常进展为MCI,但可预测转变为痴呆(BPF每降低1%,调整后HR为1.10;95% CI,1.02 - 1.19;P = 0.02)。当将转变为AD痴呆作为观察结果时,BPF同样是一个预测因素(BPF每降低1%,调整后HR为1.16;95% CI,1.08 - 1.24;P < 0.001),但高WMH不是。既往吸烟与从正常进展为MCI(调整后HR,2.71;95% CI,1.12 - 6.55;P = 0.03)以及转变为全因性痴呆(调整后HR,2.08;95% CI,1.13 - 3.82;P = 0.02)均相关,但与AD痴呆无关。
这些发现表明,WMH与从正常进展为MCI的风险相关。在认知能力已经受损的人群中,BPF可预测转变为痴呆。