Division of Biostatistics, Department of Public Health Sciences, University of California, Davis, Davis, CA 95616, USA.
Neurobiol Aging. 2010 Aug;31(8):1419-28. doi: 10.1016/j.neurobiolaging.2010.04.025. Epub 2010 Jun 9.
Cerebrospinal fluid (CSF) and structural magnetic resonance imaging (MRI) show patterns of change in Alzheimer's disease (AD) that precede dementia. The Alzheimer's Disease Neuroimaging Initiative (ADNI) studied normal controls (NC), subjects with mild cognitive impairment (MCI), and subjects with AD to identify patterns of biomarkers to aid in early diagnosis and effective treatment of AD. Two hundred twenty-two NC underwent baseline MRI and clinical examination at baseline and at least one follow-up. One hundred twelve also provided CSF at baseline. Unsupervised clustering based on initial CSF and MRI measures was used to identify clusters of participants with similar profiles. Repeated measures regression modeling assessed the relationship of individual measures, and of cluster membership, to cognitive change over 3 years. Most individuals showed little cognitive change. Individual biomarkers had limited predictive value for cognitive decline, but membership in the cluster with the most extreme profile was associated with more rapid decline in ADAS-cog. Subtypes among NC based on multiple biomarkers may represent the earliest stages of subclinical cognitive decline and AD.
脑脊液 (CSF) 和结构磁共振成像 (MRI) 显示了阿尔茨海默病 (AD) 发生变化的模式,这些变化先于痴呆。阿尔茨海默病神经影像学倡议 (ADNI) 研究了正常对照组 (NC)、轻度认知障碍 (MCI) 患者和 AD 患者,以确定生物标志物模式,以帮助早期诊断和有效治疗 AD。222 名 NC 在基线时接受了 MRI 和临床检查,并在至少一次随访时进行了检查。其中 112 名还在基线时提供了 CSF。基于初始 CSF 和 MRI 测量值的无监督聚类用于识别具有相似特征的参与者聚类。重复测量回归模型评估了个体测量值和聚类成员关系与 3 年内认知变化的关系。大多数人认知变化很小。单个生物标志物对认知下降的预测价值有限,但具有最极端特征聚类的成员与 ADAS-cog 下降更快有关。基于多种生物标志物的 NC 亚型可能代表亚临床认知下降和 AD 的最早阶段。