Abstract

The potentially detrimental effects of the worldwide deficiency of Omega-3 fatty acids on the COVID-19 pandemic have been underestimated. The Omega-3 Index (O3I), clinical variables, biometric indices, and nutritional information were directly determined for 74 patients with severe COVID-19 and 10 healthy quality-control subjects. The relationships between the OI3 and mechanical ventilation (MV) and death were analyzed. Results: Patients with COVID-19 exhibited low O3I (mean: 4.15%; range: 3.06–6.14%)—consistent with insufficient fish and Omega-3 supplement consumption, and markedly lower than the healthy control subjects (mean: 7.84%; range: 4.65–10.71%). Inverse associations were observed between O3I and MV (OR = 0.459; C.I.: 0.211–0.997) and death (OR = 0.28; C.I.: 0.08–0.985) in severe COVID-19, even after adjusting for sex, age, and well-known risk factors. Conclusion: We present preliminary evidence to support the hypothesis that the risk of severe COVID-19 can be stratified by the O3I quartile. Further investigations are needed to assess the value of the O3I as a blood marker for COVID-19.

Highlights

  • Resolution of acute inflammation has been progressively recognized as an active biochemical process that is necessary for timely recovery of tissue homeostasis after injury [7,8,9]; the factors that determine unresolved inflammation in COVID-19 have been poorly investigated

  • The unresolved inflammation in COVID-19 could largely be determined by deficiency in the long-chain Omega-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) [10]; this scenario represents one of the most extended micronutrient deficiencies worldwide and is severe in Western countries [11,12]

  • EPA and DHA are the main precursors of a novel superfamily of autacoids, termed specialized proresolving mediators (SPMs), that are critically involved in the homeostasis of inflammation resolution and airway mucosal immunity [10,13,14,15]

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Summary

Introduction

The more severe spectrum of Coronavirus disease 2019 (COVID-19) represents an unprecedented challenge to modern public health and critical care medicine worldwide. The unresolved inflammation in COVID-19 could largely be determined by deficiency in the long-chain Omega-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) [10]; this scenario represents one of the most extended micronutrient deficiencies worldwide and is severe in Western countries [11,12]. EPA and DHA are the main precursors of a novel superfamily of autacoids, termed specialized proresolving mediators (SPMs), that are critically involved in the homeostasis of inflammation resolution and airway mucosal immunity [10,13,14,15].

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