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Serum lipidome associates with neuroimaging features in patients with traumatic brain injury
Dalarna University, School of Information and Engineering, Microdata Analysis. Örebro University, Örebro.
Division of Anaesthesia, Department of Medicine, University of Cambridge, Cambridge, UK, GB.
Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland, FI; Department of Chemistry, University of Turku, Turku, Finland, FI.
Division of Anaesthesia, Department of Medicine, University of Cambridge, Cambridge, UK, GB.
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2024 (English)In: iScience, E-ISSN 2589-0042, Vol. 27, no 9, article id 110654Article in journal (Refereed) Published
Abstract [en]

Acute traumatic brain injury (TBI) is associated with substantial abnormalities in lipid biology, including changes in the structural lipids that are present in the myelin in the brain. We investigated the relationship between traumatic microstructural changes in white matter from magnetic resonance imaging (MRI) and quantitative lipidomic changes from blood serum. The study cohort included 103 patients from the Collaborative European NeuroTrauma Effectiveness Research in TBI (CENTER-TBI) study. Diffusion tensor fitting generated fractional anisotropy (FA) and mean diffusivity (MD) maps for the MRI scans while ultra-high-performance liquid chromatography quadrupole time-of-flight mass spectrometry was applied to analyze the lipidome. Increasing severity of TBI was associated with higher MD and lower FA values, which scaled with different lipidomic signatures. There appears to be consistent patterns of lipid changes associating with the specific microstructure changes in the CNS white matter, but also regional specificity, suggesting that blood-based lipidomics may provide an insight into the underlying pathophysiology of TBI.

Place, publisher, year, edition, pages
2024. Vol. 27, no 9, article id 110654
Keywords [en]
Lipidomics, Neuroscience, Systems biology
National Category
Neurology
Identifiers
URN: urn:nbn:se:du-49363DOI: 10.1016/j.isci.2024.110654ISI: 001301339800001PubMedID: 39252979Scopus ID: 2-s2.0-85201440012OAI: oai:DiVA.org:du-49363DiVA, id: diva2:1898857
Available from: 2024-09-18 Created: 2024-09-18 Last updated: 2024-09-30Bibliographically approved

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