4.6 Article

Metabolomic Profiles of Men and Women Ischemic Stroke Patients

Journal

DIAGNOSTICS
Volume 11, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/diagnostics11101786

Keywords

ischemic stroke; metabolomics; male patients; female patients

Funding

  1. NIH R25 Grant [1 R25 GM123935-01A1]

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Using metabolomics analysis, this study identified multiple metabolic pathways and metabolites associated with male and female AIS patients. Female AIS patients had 14 distinct altered metabolic pathways and 49 corresponding metabolites, while male patients had 39 metabolites and 5 metabolic pathways. Further research is needed to understand how these metabolites are linked to the pathophysiology in male and female AIS patients.
Background: Stroke is known to affect both men and women; however, incidence and outcomes differ between them. Therefore, the discovery of novel, sex-specific, blood-based biomarkers for acute ischemic stroke (AIS) patients has the potential to enhance the understanding of the etiology of this deadly disease in the content of sex. The objective of this study was to identify serum metabolites associated with male and female AIS patients. Methods: Metabolites were measured with the use of untargeted, reverse-phase ultra-performance liquid chromatography-tandem mass spectrometry quantification from blood specimens collected from AIS patients. Samples were collected from 36 patients comprising each of 18 men and women with matched controls. Metabolic pathway analysis and principal component analysis (PCA) was used to differentiate metabolite profiles for male and female AIS patients from the control, while logistic regression was used to determine differences in metabolites between male and female AIS patients. Results: In female AIS patients, 14 distinct altered metabolic pathways and 49 corresponding metabolites were identified, while 39 metabolites and 5 metabolic pathways were identified in male patients. Metabolites that are predictive of ischemic stroke in female patients were 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) (AUC = 0.914, 0.765-1.000), 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) (AUC = 0.840, 0.656-1.000), and 5,6-dihydrouracil (P-16:0/20:2) (AUC = 0.815, 0.601-1.000). Significant metabolites that were predictive of stroke in male patients were 5alpha-androstan-3alpha,17beta-diol disulfate (AUC = 0.951, 0.857-1.000), alpha-hydroxyisocaproate (AUC = 0.938, 0.832-1.000), threonate (AUC = 0.877, 0.716-1.000), and bilirubin (AUC = 0.817, 0.746-1.000). Conclusions: In the current study, the untargeted serum metabolomics platform identified multiple pathways and metabolites associated with male and female AIS patients. Further research is necessary to characterize how these metabolites are associated with the pathophysiology in male and female AIS patients.

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