MassIVE MSV000092241

Partial Public PXD043216

DIA analysis from a large scale patient cohort for Cerebrospinal Fluid Biomarker Discovery in Alzheimer Disease

Description

Diagnosis of Alzheimer disease (AD) primarily relies on cognitive assessments combined with imaging and cerebrospinal fluid (CSF) biomarkers of amyloid and tau proteins. These biomarkers correlate well with levels of neuropathology, but may be inadequate predictors of cognitive trajectory or treatment response to novel therapeutics. Analysis of larger sets of biomarkers together could improve the diagnosis and prognosis of AD, examine the interaction with and differentiate between comorbid pathophysiologies, and measure treatment efficacy. Here, we report data from a Data-independent Acquisition (DIA) analysis used to simultaneously quantify hundreds of proteins in a large-scale patient cohort from a neurology clinic, all of whom had clinical indication for diagnostic lumbar puncture. We aim to define markers that can stratify and diagnose AD in this clinically-complex cohort. Samples from 408 patients were collected from the clinic according to standardized collection and processing protocols. Samples were prepared in 21 different batches of 24 (23 samples plus one common pool) and analyzed by LC-MS/MS on an Orbitrap Fusion using a DIA method with non-overlapping 25m/z windows from 400-1000 m/z, with a resolution of 120K for MS1 and 60K for MS2. Each sample was injected in duplicate with 4 column washes between each sample. All samples from each batch were run sequentially, with multiples days separating each batch. [doi:10.25345/C56Q1SS95] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Alzheimer disease ; Biomarker discovery ; CSF ; Data Independent acquisition ; Large scale patient cohort ; Batch effect removal

Contact

Principal Investigators:
(in alphabetical order)
Becky Carlyle, Massachusetts General Hospital and Harvard Medical School, United States
Steven Arnold, Massachusetts General Hospital, USA
Submitting User: QC_MGH
Number of Files:
Total Size:
Spectra:
Subscribers:
 
Owner Reanalyses
Experimental Design
    Conditions:
    Biological Replicates:
    Technical Replicates:
 
Identification Results
    Proteins (Human, Remapped):
    Proteins (Reported):
    Peptides:
    Variant Peptides:
    PSMs:
 
Quantification Results
    Differential Proteins:
    Quantified Proteins:
 
Browse Dataset Files
 
FTP Download Link (click to copy):

- Dataset Reanalyses


+ Dataset History


Click here to queue conversion of this dataset's submitted spectrum files to open formats (e.g. mzML). This process may take some time.

When complete, the converted files will be available in the "ccms_peak" subdirectory of the dataset's FTP space (accessible via the "FTP Download" link to the right).
Number of distinct conditions across all analyses (original submission and reanalyses) associated with this dataset.

Distinct condition labels are counted across all files submitted in the "Metadata" category having a "Condition" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

Distinct replicate labels are counted across all files submitted in the "Metadata" category having a "BioReplicate" or "Replicate" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct technical replicates across all analyses (original submission and reanalyses) associated with this dataset.

The technical replicate count is defined as the maximum number of times any one distinct combination of condition and biological replicate was analyzed across all files submitted in the "Metadata" category. In the case of fractionated experiments, only the first fraction is considered.

"N/A" means no results of this type were submitted.
Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

"N/A" means no results of this type were submitted.
Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct unmodified peptide sequences reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Total number of peptide-spectrum matches (i.e. spectrum identifications) reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins quantified across all analyses (original submission and reanalyses) associated with this dataset.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

A protein is differentially abundant if its change in abundance across conditions is found to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated with statistical tests for differential abundance.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE. It has been imported to MassIVE for reanalysis purposes, so its spectra data here may consist solely of processed peak lists suitable for reanalysis with most software.