The Difference in Serum Metabolomic Profiles between the Good and Poor Outcome Groups at 3 Months in the Early and Late Phases of Aneurysmal Subarachnoid Hemorrhage

Author:

Orban Brigitta1,Tengölics Roland234ORCID,Zavori Laszlo5ORCID,Simon Diana6,Erdo-Bonyar Szabina6ORCID,Molnar Tihamer7ORCID,Schwarcz Attila1,Csecsei Peter1ORCID

Affiliation:

1. Department of Neurosurgery, Medical School, University of Pecs, 7632 Pecs, Hungary

2. Metabolomics Lab, Biological Research Centre, Hungarian Research Network, 6726 Szeged, Hungary

3. Core Facilities, Biological Research Centre, Hungarian Research Network, 6726 Szeged, Hungary

4. Hungarian Centre of Excellence for Molecular Medicine—Biological Research Centre Metabolic Systems Biology Lab, 6726 Szeged, Hungary

5. Emergency Department, Saudi German Hospital, Dubai 391093, United Arab Emirates

6. Department of Immunology and Biotechnology, Medical School, University of Pecs, 7632 Pecs, Hungary

7. Department of Anaesthesiology and Intensive Care, Medical School, University of Pecs, 7632 Pecs, Hungary

Abstract

We aimed to investigate the characteristics of serum metabolomics in aneurysmal subarachnoid hemorrhage patients (aSAH) with different 3-month outcomes (good = modified Rankin score: 0–3 vs. poor = mRS 4–6). We collected serum samples from 46 aSAH patients at 24 (D1) and 168 (D7) hours after injury for analysis by liquid chromatography-mass spectrometry. Ninety-six different metabolites were identified. Groups were compared using multivariate (orthogonal partial least squares discriminant analysis), univariate, and receiving operator characteristic (ROC) methods. We observed a marked decrease in serum homocysteine levels at the late phase (D7) compared to the early phase (D1). At both D1 and D7, mannose and sorbose levels were notably higher, alongside elevated levels of kynurenine (D1) and increased 2-hydroxybutyrate, methyl-galactoside, creatine, xanthosine, p-hydroxyphenylacetate, N-acetylalanine, and N-acetylmethionine (all D7) in the poor outcome group. Conversely, levels of guanidinoacetate (D7) and several amino acids (both D1 and D7) were significantly lower in patients with poor outcomes. Our results indicate significant changes in energy metabolism, shifting towards ketosis and alternative energy sources, both in the early and late phases, even with adequate enteral nutrition, particularly in patients with poor outcomes. The early activation of the kynurenine pathway may also play a role in this process.

Funder

University of Pecs, KA

Hungarian NRDI Fund

Publisher

MDPI AG

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