Abstract

The Corona Virus Disease 2019 (COVID-19) pandemic represents an ongoing worldwide challenge. The present large study sought to understand independent and overlapping metabolic features of samples from acutely ill patients (n = 831) that tested positive (n = 543) or negative (n = 288) for COVID-19. High-throughput metabolomics analyses were complemented with antigen and enzymatic activity assays on plasma from acutely ill patients collected while in the emergency department, at admission, or during hospitalization. Lipidomics analyses were also performed on COVID-19-positive or -negative subjects with the lowest and highest body mass index (n = 60/group). Significant changes in amino acid and fatty acid/acylcarnitine metabolism emerged as highly relevant markers of disease severity, progression, and prognosis as a function of biological and clinical variables in these patients. Further, machine learning models were trained by entering all metabolomics and clinical data from half of the COVID-19 patient cohort and then tested on the other half, yielding ~78% prediction accuracy. Finally, the extensive amount of information accumulated in this large, prospective, observational study provides a foundation for mechanistic follow-up studies and data sharing opportunities, which will advance our understanding of the characteristics of the plasma metabolism in COVID-19 and other acute critical illnesses.

Highlights

  • On 28 April 2020, we began performing one of the earliest investigations on the impact of SARS-CoV-2 infection on the circulating metabolome [1]

  • Metabolomics analyses performed for 543 samples from hospitalized acutely ill COVID-19-positive patients were compared with those performed for 288 samples from acutely ill COVID-19-negative patients (Figure 1A)

  • Previous metabolomics studies on COVID-19 were not powered to characterize the effects of other variables critical for disease severity and prognosis

Read more

Summary

Introduction

On 28 April 2020, we began performing one of the earliest investigations on the impact of SARS-CoV-2 infection on the circulating metabolome [1]. Despite public health interventions and the advent of multiple vaccination strategies, SARS-CoV-2 remains a serious global threat. This may be explained by multiple factors, including (i) vaccination rates lagging behind the percentage required to reach herd immunity; (ii) reopening too early, while discontinuing public health mandates; (iii) the emergence of variants with more efficient transmission [9,10], which may escape acquired immunity and/or vaccination [11,12]; and waning immunity from vaccination or previous infection [13,14]. Efforts aimed at identifying strategies to treat SARS-CoV-2, including metabolic interventions or repurposing drugs with potential metabolic targets [15], remain important

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call