Willette Auriel A, Calhoun Vince D, Egan Josephine M, Kapogiannis Dimitrios
Laboratory of Neurosciences, National Institute on Aging, Biomedical Research Center, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Department of Electrical and Computer Engineering, University of New Mexico, Albuquerque, NM 87131, USA; The Mind Research Network, Albuquerque, NM 87131, USA.
Psychiatry Res. 2014 Nov 30;224(2):81-8. doi: 10.1016/j.pscychresns.2014.08.005. Epub 2014 Aug 17.
Identifying predictors of mild cognitive impairment (MCI) and Alzheimer's disease (AD) can lead to more accurate diagnosis and facilitate clinical trial participation. We identified 320 participants (93 cognitively normal or CN, 162 MCI, 65 AD) with baseline magnetic resonance imaging (MRI) data, cerebrospinal fluid biomarkers, and cognition data in the Alzheimer's Disease Neuroimaging Initiative database. We used independent component analysis (ICA) on structural MR images to derive 30 matter covariance patterns (ICs) across all participants. These ICs were used in iterative and stepwise discriminant classifier analyses to predict diagnostic classification at 24 months for CN vs. MCI, CN vs. AD, MCI vs. AD, and stable MCI (MCI-S) vs. MCI progression to AD (MCI-P). Models were cross-validated with a "leave-10-out" procedure. For CN vs. MCI, 84.7% accuracy was achieved based on cognitive performance measures, ICs, p-tau(181p), and ApoE ε4 status. For CN vs. AD, 94.8% accuracy was achieved based on cognitive performance measures, ICs, and p-tau(181p). For MCI vs. AD and MCI-S vs. MCI-P, models achieved 83.1% and 80.3% accuracy, respectively, based on cognitive performance measures, ICs, and p-tau(181p). ICA-derived MRI biomarkers achieve excellent diagnostic accuracy for MCI conversion, which is little improved by CSF biomarkers and ApoE ε4 status.
识别轻度认知障碍(MCI)和阿尔茨海默病(AD)的预测因素能够实现更准确的诊断,并促进临床试验的参与。我们在阿尔茨海默病神经影像倡议数据库中识别出320名参与者(93名认知正常或CN,162名MCI,65名AD),他们拥有基线磁共振成像(MRI)数据、脑脊液生物标志物和认知数据。我们对结构磁共振图像使用独立成分分析(ICA),以得出所有参与者的30种物质协方差模式(IC)。这些IC被用于迭代和逐步判别分类器分析,以预测24个月时CN与MCI、CN与AD、MCI与AD以及稳定MCI(MCI-S)与进展为AD的MCI(MCI-P)的诊断分类。模型通过“留十法”进行交叉验证。对于CN与MCI,基于认知表现测量、IC、磷酸化tau蛋白(181p)和载脂蛋白Eε4状态,准确率达到了84.7%。对于CN与AD,基于认知表现测量、IC和磷酸化tau蛋白(181p),准确率达到了94.8%。对于MCI与AD以及MCI-S与MCI-P,基于认知表现测量、IC和磷酸化tau蛋白(181p),模型分别达到了83.1%和80.3%的准确率。ICA衍生的MRI生物标志物对MCI转化具有出色的诊断准确性,脑脊液生物标志物和载脂蛋白Eε4状态对此几乎没有改善。