Objective Although COVID-19 is a respiratory disease, all organs can be affected including the brain. To date, specific investigations of brain injury markers (BIM) and endothelial injury markers (EIM) have been limited. Additionally, a male bias in disease severity and mortality after COVID-19 is evident globally. Sex differences in the immune response to COVID-19 may mediate this disparity. We investigated BIM, EIM and inflammatory cytokine/chemokine (CC) levels after COVID-19 and in across sexes. Methods Plasma samples from 57 subjects at < 48 h of COVID-19 hospitalization, and 20 matched controls were interrogated for the levels of six BIMs—including GFAP, S100B, Syndecan-1, UCHLI, MAP2 and NSE, two EIMs—including sICAM1 and sVCAM1. Additionally, several cytokines/chemokines were analyzed by multiplex. Statistical and bioinformatics methods were used to measure differences in the marker profiles across (a) COVID-19 vs. controls and (b) men vs. women. Results Three BIMs: MAP2, NSE and S100B, two EIMs: sICAM1 and sVCAM1 and seven CCs: GRO IL10, sCD40L, IP10, IL1Ra, MCP1 and TNFα were significantly ( p < 0.05) elevated in the COVID-19 cohort compared to controls. Bioinformatics analysis reveal a stronger positive association between BIM/CC/EIMs in the COVID-19 cohort. Analysis across sex revealed that several BIMs and CCs including NSE, IL10, IL15 and IL8 were significantly ( p < 0.05) higher in men compared to women. Men also expressed a more robust BIM/ EIM/CC association profile compared to women. Conclusion The acute elevation of BIMs, CCs, and EIMs and the robust associations among them at COVID-19 hospitalization are suggestive of brain and endothelial injury. Higher BIM and inflammatory markers in men additionally suggest that men are more susceptible to the risk compared to women. Supplementary Information The online version contains supplementary material available at 10.1186/s12974-021-02323-8.
【저자키워드】 COVID-19, SARS-CoV-2, Inflammation, sex differences, brain injury, endothelial injury, 【초록키워드】 immune response, Cytokines, Mortality, disease severity, bioinformatics, inflammatory markers, Sex, risk, chemokines, chemokine, Brain, Respiratory disease, male, Control, COVID-19 hospitalization, Inflammatory marker, endothelial injury, syndecan, women, Syndecan-1, respiratory, multiplex, Bioinformatics analysis, Inflammatory cytokine, GFAp, association, marker, IP10, S100B, Analysis, Inflammatory, Injury, IL1RA, matched controls, supplementary material, profile, subject, TNFα, positive, IL10, organ, IL15, COVID-19 cohort, MAP2, MCP1, men, objective, susceptible, controls, robust, Seven, Result, analyzed, affected, significantly, investigated, elevated, IL8, were used, expressed, EIM, 【제목키워드】 Inflammatory marker, Injury, alteration, Express, elevated,