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Integrative Modeling of Quantitative Plasma Lipoprotein, Metabolic, and Amino Acid Data Reveals a Multiorgan Pathological Signature of SARS-CoV-2 Infection
- Source :
- Journal of Proteome Research
- Publication Year :
- 2020
- Publisher :
- American Chemical Society (ACS), 2020.
-
Abstract
- The metabolic effects of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection on human blood plasma were characterized using multi-platform metabolic phenotyping with Nuclear Magnetic Resonance (NMR) spectroscopy and liquid chromatography-mass spectrometry (LC-MS). Quantitative measurements of lipoprotein sub-fractions, alpha-1-acid glycoprotein, glucose and biogenic amines were made on samples from symptomatic coronavirus disease 19 (COVID-19) patients who had tested positive for the SARS-CoV-2 virus (n = 17) and from age and gender-matched controls (n = 25). Data were analyzed using an orthogonal-projections to latent structures (O-PLS) method and used to construct an exceptionally strong (AUROC=1) hybrid NMR-MS model that enabled detailed metabolic discrimination between the groups and their biochemical relationships. Key discriminant metabolites included markers of inflammation including elevated alpha-1 acid glycoprotein and an increased kynurenine/tryptophan ratio. There was also an abnormal lipoprotein, glucose and amino acid signature consistent with diabetes and coronary artery disease (low total and HDL Apolipoprotein A1, low HDL triglycerides, high LDL and VLDL triglycerides). Plus, multiple highly significant amino acid markers of liver dysfunction (including the elevated glutamine/glutamate and Fischer’s ratios) that present themselves as part of a distinct SARS-CoV-2 infection pattern. A multivariate training-test set model was validated using independent samples from additional SARS-CoV-2 positive patients and controls. The predictive model showed a sensitivity of 100% for SARS-CoV-2 positivity. The breadth of the disturbed pathways indicates a systemic signature of SARS-CoV-2 positivity that includes elements of liver dysfunction, dyslipidaemia, diabetes, and coronary heart disease risk that are consistent with recent reports that COVID-19 is a systemic disease affecting multiple organs and systems. Metabolights study reference: MTBLS2014.
- Subjects :
- Blood Glucose
Male
0301 basic medicine
Very low-density lipoprotein
Magnetic Resonance Spectroscopy
medicine.disease_cause
Biochemistry
mosaic disease
chemistry.chemical_compound
Medicine
mass spectrometry
Coronavirus
biology
multiorgan damage
Middle Aged
systems model
Metabolome
Female
Apolipoprotein A1
Coronavirus Infections
03 Chemical Sciences
Biochemistry & Molecular Biology
medicine.medical_specialty
metabolic phenotyping
Multiple Organ Failure
Pneumonia, Viral
Models, Biological
Article
Betacoronavirus
03 medical and health sciences
NMR spectroscopy
Diabetes mellitus
Internal medicine
Humans
Pandemics
Aged
amino acids
030102 biochemistry & molecular biology
SARS-CoV-2
business.industry
COVID-19
biomarkers
General Chemistry
06 Biological Sciences
medicine.disease
lipoproteins
Glutamine
030104 developmental biology
Endocrinology
chemistry
biology.protein
business
Kynurenine
Dyslipidemia
Lipoprotein
Subjects
Details
- ISSN :
- 15353907 and 15353893
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Journal of Proteome Research
- Accession number :
- edsair.doi.dedup.....8422129ca9ad0362d5e7975b25e1b74f