Summary of Study ST001950
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001237. The data can be accessed directly via it's Project DOI: 10.21228/M8TB0S This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST001950 |
Study Title | Lipidome Alterations Following Mild Traumatic Brain Injury. |
Study Type | Untargeted Lipidomics |
Study Summary | Traumatic brain injury (TBI) poses a major health challenge, with tens of millions of new cases reported globally every year. Brain damage resulting from TBI can vary significantly due to factors including injury severity, diffusivity, modality, time delay relative to impact, and exposure to repeated injury events. Untargeted lipidomic analysis of Sprague-Dawley rat serum within 24 hours of mild single and repeat controlled cortical impact (CCI) injury events led to the discovery of biomarker candidates of TBI. Lipid biomarkers have a unique potential to serve as objective molecular measures of the body’s response to injury as their alteration in brain tissue can be more freely observed than for larger protein markers. Animal serum was analyzed via ultra-high-performance liquid chromatography-mass spectrometry (UHPLC-MS) in positive and negative ion modes. Known lipid species were identified through matching to in-house tandem MS databases. Machine learning and feature selection approaches were used to construct lipid panels capable of distinguishing serum from injured and uninjured animals across a range of injury severities and timepoints within the first day of injury. The best multivariate lipid panels had over 90% cross-validated sensitivity, selectivity, and accuracy and consisted of species from nine different lipid classes. These mapped onto sphingolipid signaling, autophagy, necroptosis and glycerophospholipid metabolism pathways, with FDR corrected p-values better than 0.05. |
Institute | Georgia Institute of Technology |
Department | Chemistry and Biochemistry |
Laboratory | Facundo Fernández |
Last Name | Gier |
First Name | Eric |
Address | 311 Ferst Drive, Atlanta, GA, 30318, USA |
egier3@gatech.edu | |
Phone | 2246221699 |
Submit Date | 2021-10-24 |
Num Groups | 6 |
Total Subjects | 32 |
Num Males | 14 |
Num Females | 18 |
Study Comments | LC-MS |
Raw Data Available | Yes |
Raw Data File Type(s) | mzML |
Analysis Type Detail | LC-MS |
Release Date | 2022-02-07 |
Release Version | 1 |
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Collection:
Collection ID: | CO002021 |
Collection Summary: | Approximately 200 µL of whole blood was collected from a tail vein punctured by 20-gauge Precision Glide needles and stored on ice. Whole blood samples were allowed to coagulate at room temperature for 45 minutes. Samples were then centrifuged at 4 °C for 15 min at 2500 x g, and serum was collected in 50 μL aliquots and stored at -80 °C. |
Collection Protocol ID: | A100188 |
Collection Protocol Comments: | All procedures involving Sprague-Dawley rat models were performed in accordance with guidelines set forth in the Guide for the Care and Use of Laboratory Animals (U.S. Department of Health and Human Services, Pub no. 85-23, 1985) and were approved by the Georgia Institute of Technology Institutional Animal Care and Use Committee |
Sample Type: | Blood (serum) |
Storage Conditions: | -80℃ |