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Updated: Jul 1, 2025

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Lipidomics and Transcriptomics in Neurological Diseases
Published on: March 18, 2022
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Plasma Lipidomic Profiling Using Mass Spectrometry for Multiple Sclerosis Diagnosis and Disease Activity
Seyed Siyawasch Justus Lattau1, Lisa-Marie Borsch1, Kristina Auf dem Brinke1
1Department of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
International Journal of Molecular Sciences
|March 13, 2024
Summary
Plasma lipidomic signatures can help diagnose Multiple Sclerosis (MS) and track disease activity. Specific lipid profiles correlate with distinct clinical features, enabling personalized MS therapy and deeper understanding of the pathology.
Area of Science:
- Neuroimmunology
- Metabolomics
- Biochemistry
Background:
- Multiple Sclerosis (MS) diagnosis and monitoring present challenges.
- Plasma lipid profiles are increasingly recognized for their potential as biomarkers.
Purpose of the Study:
- To investigate plasma lipidomic signatures for MS diagnosis.
- To correlate lipid profiles with clinical course and disease activity in MS patients.
Main Methods:
- Quantitative shotgun lipidomics on plasma samples from 60 MS patients and 60 controls.
- Multivariate statistical analyses including PCA, oPLS-DA, and Random Forest.
- Class Composition Visualization (CCV) to assess lipid class alterations.
Main Results:
- Identified 670 lipids across 16 classes; significant differences observed in MS patients.
- Increased diacylglycerols (DAG), particularly DAG 16:0;0_18:1;0, showed high predictive ability for MS.
- Distinct alterations in phosphatidylethanolamines (PE) and ether-bound PEs (PE O-) were associated with relapsing-remitting MS (RRMS) and chronic progressive MS (CPMS), respectively.
- Reduced cholesteryl esters (CE) in CPMS and triglycerides (TAG) in RRMS were noted.
Conclusions:
- Distinct plasma lipidomic signatures are associated with MS diagnosis and clinical phenotypes.
- Lipid profiles offer insights into MS pathology and disease activity.
- These findings support the potential for personalized MS therapy based on lipidomic data.
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