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英文摘要
The Statistical/Data Management Core (SDMC) serves as the analytic “hub” of the EAS, and provides integration of the wide range of data collected by Cores, Projects, and pilot studies. It serves two functions that are essential for the success of the Einstein Aging Study (EAS). First, the SDMC maximizes data quality by implementing database systems that integrate and manage the data collected from the Administrative, Clinical, Neuropathology and Neuroimaging Cores, and from each of the three projects. In addition, it is responsible for secure data transfer across study sites and to/from participant ecological momentary assessment devices. The SDMC assumes responsibility for quality control procedures and for merging data across Projects and Cores. Second, the Statistical Core provides collaborative and consultative support to Project investigators on matters of study design, data analyses and interpretation of results. The Statistical Core is responsible for developing, implementing and interpreting statistical methods appropriate to specific research questions and hypotheses, and it collaborates regularly with Project investigators on scientific manuscripts. Specific Aims of the Statistical/Data Management Core are: Aim 1. To implement and oversee data procedures to facilitate the seamless exchange of data and ideas among Cores and Projects, and to facilitate data transfer for collaborations with investigators outside the EAS. Aim 2. To provide a general analytic framework for hypothesis testing, model building, and integration of results and analyses across measurement constructs (e.g., exposures, mechanisms, outcomes), and to collaborate with investigators regarding the framing and testing of hypotheses and to provide expertise in the design and conduct of analyses. Aim 3. To develop new statistical methodology and to apply existing methodology in innovative ways to help to fulfill the other aims of this Core and the Projects and to further aging research in general, with the emphasis of methods to combine ambulatory and traditional markers to identify early cognitive impairment and disease.
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Correction of Bias in Estimating Risk of AD and Cognitive and Mobile Decline Using Auxiliary Information
Detecting early disease using variability in markers under informative censoring
Detecting early disease using variability in markers under informative censoring
Detecting early disease using variability in markers under informative censoring
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