Delineating sex-specific circulating host response signatures associated with COVID-19 severity and mortality.

Publication date: Nov 15, 2024

Male SARS-CoV-2-infected patients have higher hospitalization rates, ICU admissions, and mortality compared to females, yet with unclear underlying mechanisms. We investigated the influence of biological sex on COVID-19 severity and patient outcomes. We profiled 41 circulating host response markers and identified differentially regulated proteins based on disease severity using covariates, such as sex, age, BMI, diabetes, and corticosteroid administration. IL-8, D-dimer, S100B, IL-6, Angpt-2, MMP-8, TNF-R1, u-PAR, u-PA, osteopontin, IL-13, TNF-α, pentraxin-3, P-selectin, fractalkine, and SP-D levels were elevated in critically ill COVID-19 males compared to severe cases. In contrast, IL-8, D-dimer, IL-6, Angpt-2, Tie-2, uPAR, and SP-D were higher in females with critical-COVID-19 than in severe cases. Notably, D-dimer, IL-6, pentraxin-3, and S100B were associated with male mortality, yet none of the measured plasma proteins associated with female mortality. Our study delineated distinct sex-specific plasma protein signatures linked to the severity and mortality of COVID-19 patients.

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Concepts Keywords
Covid Microbiology
Diabetes Molecular biology
Hospitalization Virology
Males
Pentraxin

Semantics

Type Source Name
disease IDO host
disease MESH COVID-19
disease MESH critically ill
disease MESH acute respiratory distress syndrome
disease MESH infection
disease IDO susceptibility
disease MESH long COVID
disease MESH syndrome
disease MESH inflammation
drug DRUGBANK Fibrinogen Human
pathway REACTOME Apoptosis
disease MESH Infectious Diseases
disease MESH complications
disease MESH pulmonary embolism
disease MESH stroke
disease MESH acute kidney injury
disease MESH co infection
drug DRUGBANK Pidolic Acid
disease IDO blood
drug DRUGBANK Leptin
drug DRUGBANK Coenzyme M
disease MESH liver dysfunction
disease MESH Comorbidity
disease MESH Pulmonary disease
disease MESH cardiac disease
disease MESH Chronic kidney disease
disease MESH Hypertension

Original Article

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