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Anticoagulant protein S in COVID-19: low activity, and associated with outcome
Laura Elena Stoichitoiu1, Larisa Pinte1,2, Marius Ioan Balea3
1Colentina University Hospital Bucharest, Department of Internal Medicine.
Insights
COVID-19 patients often have decreased protein S activity, a key factor in blood clotting. Lower protein S levels are linked to increased mortality and disease severity in COVID-19 patients.
Area of Science:
- Hematology
- Infectious Diseases
- Critical Care Medicine
Background:
- COVID-19 is associated with thrombo-embolic events and microvascular thrombi.
- Antiphospholipid antibodies have been observed in some COVID-19 patients.
- The prothrombotic state in COVID-19 requires further investigation into contributing factors.
Purpose of the Study:
- To assess protein S activity in COVID-19 patients.
- To determine if protein S deficiency contributes to the prothrombotic state in COVID-19.
- To evaluate the association between protein S activity and COVID-19 patient outcomes.
Main Methods:
- Prospective cohort study of 91 COVID-19 patients admitted to a university hospital.
- Exclusion of patients on vitamin K antagonists or with liver disease.
- Measurement of protein S activity at admission, with survival, clinical severity, and lung damage as outcomes.
Main Results:
- Protein S activity was reduced in 65% of COVID-19 patients.
- Lower protein S activity was significantly associated with increased mortality (p < 0.001).
- A dose-response relationship was observed between decreased protein S activity and increased disease severity and lung damage.
Conclusions:
- Protein S activity is frequently decreased in COVID-19 patients.
- Reduced protein S activity is linked to poorer survival and greater disease severity.
- Protein S deficiency may play a role in the thrombotic complications of COVID-19.
Abstract:
Introduction. COVID-19 disease was associated with both thrombo-embolic events and in-situ thrombi formation in small vessels. Antiphospholipidic antibodies were found in some studies.Aim. Assessment of protein S activity in patients with COVID-19 as a cause of this prothrombotic state, and of the association of protein S activity with worse outcome.Methods. All patients admitted for COVID-19 disease in a university hospital between 15th of May and 15th of July 2020 were prospectively enrolled into this cohort study. Patients treated with antivitamin K anticoagulants and with liver disease were excluded. All patients had protein S activity determined at admission. The main outcome was survival, while secondary outcomes were clinical severity and lung damage.Results. 91 patients were included, of which 21 (23.3%) died. Protein S activity was decreased in 65% of the patients. Death was associated with lower activity of protein S (median 42% vs. 58%, p < 0.001), and the association remained after adjustment for age, inflammation markers and ALAT. There was a dose-response relationship between protein S activity and clinical severity (Kendall_tau coefficient = -0.320, p < 0.001; Jonckheere-Terpstra for trend: p < 0.001) or pulmonary damage on CT scan (Kendall_tau coefficient = -0.290, p < 0.001; Jonckheere-Terpstra for trend: p < 0.001). High neutrophil count was also independently associated with death (p = 0.002).Conclusion. Protein S activity was lower in COVID-19 patients, and its level was associated with survival and disease severity, suggesting that it may have a role in the thrombotic manifestations of the disease.
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