Metabolomics in MS

Metabolomic signatures associated with disease severity in multiple sclerosis.Villoslada P, Alonso C, Agirrezabal I, Kotelnikova E, Zubizarreta I, Pulido-Valdeolivas I, Saiz A, Comabella M, Montalban X, Villar L, Alvarez-Cermeño JC, Fernández O, Alvarez-Lafuente R, Arroyo R, Castro A. Neurol Neuroimmunol Neuroinflamm. 2017 Jan 27;4(2):e321.

OBJECTIVE:To identify differences in the metabolomic profile in the serum of patients with multiple sclerosis (MS) compared to controls and to identify biomarkers of disease severity.
METHODS:We studied 2 cohorts of patients with MS: a retrospective longitudinal cohort of 238 patients and 74 controls and a prospective cohort of 61 patients and 41 controls with serial serum samples. Patients were stratified into active or stable disease based on 2 years of prospective assessment accounting for presence of clinical relapses or changes in disability measured with the Expanded Disability Status Scale (EDSS). Metabolomic profiling (lipids and amino acids) was performed by ultra-high-performance liquid chromatography coupled to mass spectrometry in serum samples. Data analysis was performed using parametric methods, principal component analysis, and partial least square discriminant analysis for assessing the differences between cases and controls and for subgroups based on disease severity.
RESULTS:We identified metabolomics signatures with high accuracy for classifying patients vs controls as well as for classifying patients with medium to high disability (EDSS >3.0). Among them, sphingomyelin and lysophosphatidylethanolamine were the metabolites that showed a more robust pattern in the time series analysis for discriminating between patients and controls. Moreover, levels of hydrocortisone, glutamic acid, tryptophan, eicosapentaenoic acid, 13S-hydroxyoctadecadienoic acid, lysophosphatidylcholines, and lysophosphatidylethanolamines were associated with more severe disease (non-relapse-free or increase in EDSS).
CONCLUSIONS:We identified metabolomic signatures composed of hormones, lipids, and amino acids associated with MS and with a more severe course.

Last week we had metabolomics telling us what type of MS you were getting so it is interesting that a look-see study reported a week later did not get excited about the trypophan metabolomics but they did report that tryptophan is associated with EDSS not sure if it increased or decreased like the study from Australia

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  • It's strange because they came to the conclusion that metabolites hormone, amino acid and lipid are associated with a more severe course of MS, but EDSS didn't increase.
    Is it possible to have a more aggressive MS and the EDSS score does not increase? Confused…

    • i'm neither a doc nor a scientist, but in my view, yes. people who have ridiculously common relapses/lesion creation with temp edss increase which then returns to normal as relapse sbusides.

      of course, in those cases, edss is just a matter of time, isn't it?

      aggressive ms = aggressive for 4 years, before any real permanent reflection in edss is maintained over the long terms.

      seems it's all just a matter of time?

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