Brickman Adam M, Habeck Christian, Ramos Marco A, Scarmeas Nikolaos, Stern Yaakov
Cognitive Neuroscience Division, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Hum Brain Mapp. 2008 Oct;29(10):1139-46. doi: 10.1002/hbm.20452.
To capture patterns of normal age-associated atrophy, we previously used a multivariate statistical approach applied to voxel based morphometry that identified age-associated gray and white matter covariance networks (Brickman et al. [2007]: Neurobiol Aging 28:284-295). The current study sought to examine the stability of these patterns by forward applying the identified networks to an independent sample of neurologically healthy younger and older adults. Forty-two younger and 35 older adults were imaged with standard high-resolution structural magnetic resonance imaging. Individual images were spatially normalized and segmented into gray and white matter. Covariance patterns that were previously identified with scaled subprofile model analyses were prospectively applied to the current sample to identify to what degree the age-associated patterns were manifested. Older individuals were also assessed with a modified version of the Mini Mental State Examination (mMMSE). Gray matter covariance pattern expression discriminated between younger and older participants with high optimal sensitivity (100%) and specificity (90.5%). While the two groups differed in the degree of white matter pattern expression (t (75) = 5.26, P < 0.001), classification based on white matter expression was relatively low (sensitivity = 80% and specificity = 61.9%). Among older adults, chronological age was significantly associated with increased gray matter pattern expression (r (32) = 0.591, P < 0.001) but not with performance on the mMMSE (r (31) = -0.314, P = 0.085). However, gray matter pattern expression was significantly associated with performance on the mMMSE (r (31) = -0.405, P = 0.024). The findings suggest that the previously derived age-associated covariance pattern for gray matter is reliable and may provide information that is more functionally meaningful than chronological age.
为了捕捉正常年龄相关萎缩的模式,我们之前使用了一种多变量统计方法,应用于基于体素的形态测量学,该方法识别出了年龄相关的灰质和白质协方差网络(Brickman等人,[2007]:《神经生物学衰老》28:284 - 295)。当前的研究试图通过将识别出的网络向前应用于神经健康的年轻和老年成年人的独立样本,来检验这些模式的稳定性。42名年轻人和35名老年人接受了标准的高分辨率结构磁共振成像。个体图像进行空间归一化并分割为灰质和白质。之前通过缩放子轮廓模型分析识别出的协方差模式被前瞻性地应用于当前样本,以确定年龄相关模式在何种程度上得以体现。老年个体还接受了简易精神状态检查表(mMMSE)的修改版评估。灰质协方差模式表达在区分年轻和老年参与者时具有高最佳敏感性(100%)和特异性(90.5%)。虽然两组在白质模式表达程度上存在差异(t(75) = 5.26,P < 0.001),但基于白质表达的分类相对较低(敏感性 = 80%,特异性 = 61.9%)。在老年人中,实际年龄与灰质模式表达增加显著相关(r(32) = 0.591,P < 0.001),但与mMMSE的表现无关(r(31) = -0.314,P = 0.085)。然而,灰质模式表达与mMMSE的表现显著相关(r(31) = -0.405,P = 0.024)。研究结果表明,之前得出的与年龄相关的灰质协方差模式是可靠的,并且可能提供比实际年龄更具功能意义的信息。