The 18.3 Data Release includes updates from longitudinal studies, MODEL-AD data, and a web application.
Human
Drug Repurposing in Alzheimer’s Disease (DRIAD)
This is a web application that evaluates gene sets for their ability to predict the progression of Alzheimer’s disease (AD). It utilizes expression data from post-mortem samples of AD patients collected by the AMP-AD consortium, using data from the ROSMAP and MSBB studies. See Rodriguez and Hug et.al.The ROSMAP_CognitiveResilience Study
This study provides proteomics data and bulk brain RNAseq data from Brodmann Areas 6 and 37 from two longitudinal studies of aging – the Religious Orders Study and the Memory and Aging Project (ROSMAP). Included are ROSMAP individuals who came to autopsy without dementia, but with high levels of Alzheimer’s disease pathology. A future release will include proteomics from synaptic fractions and 3D dendritic spine morphometry on these individuals.- This release adds:
- Quantitative proteomics data (TMT) for 128 individuals from BA6 and BA37
- This release adds:
The DiCAD Study
This study provides longitudinal clinical and imaging data, as well as proteomics, metabolomics, GWAS, and plasma biomarker data on a cohort of 200 community dwelling late middle-aged Hispanic individuals without dementia.- This release adds:
- Updated clinical assessments, laboratory data, MRI and PET imaging data, and data description documentation
- GWAS data
- Plasma AD biomarkers from single-molecule array (SiMoA) immunoassay
- LC-MSMS metabolomics data
- Proximity extension assay proteomics data
- Reformatted and updated individual, biospecimen, and assay metadata files for all specimens and assays
- Previous APOE genotype data was moved to the individual metadata file
- This release adds:
Models
The UCI_5XFAD Study
This study provides deep phenotyping data from the 5XFAD mouse model- This release updates the Abeta40 and Abeta42 measurements in plasma from mice at 4, 8, 12, and 18 months (assay=electrochemiluminescence). The previous file had an incorrect set of mice.
The Jax.IU.Pitt_PrimaryScreen Study
This study provides an initial molecular and behavioral characterization of mouse models of Late-Onset Alzheimer’s Disease as part of the MODEL-AD Program. Provided is gene expression as measured by a NanoString nCounter® Mouse AD pane, and frailty assessment-
- This release updates the following:
- The biospecimen file by correcting the tissue used for the gene expression from ‘whole brain’ to ‘right cerebral hemisphere’.
- The removal of 8 NanoString nCounter® output files with measurements from samples that are not part of the study.
- This release updates the following:
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