[HTML][HTML] Thromboinflammatory biomarkers in COVID-19: systematic review and meta-analysis of 17,052 patients

R Chaudhary, J Garg, DE Houghton, MH Murad… - … : Innovations, Quality & …, 2021 - Elsevier
R Chaudhary, J Garg, DE Houghton, MH Murad, A Kondur, R Chaudhary, WE Wysokinski…
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, 2021Elsevier
Objective To evaluate differences in thromboinflammatory biomarkers between patients with
severe coronavirus disease 2019 (COVID-19) infection/death and mild infection. Patients
and Methods MEDLINE, Cochrane Central Register of Controlled Trials, EMBASE, EBSCO,
Web of Science, and CINAHL databases were searched for studies comparing
thromboinflammatory biomarkers in COVID-19 among patients with severe COVID-19
disease or death (severe/nonsurvivors) and those with nonsevere disease or survivors …
Objective
To evaluate differences in thromboinflammatory biomarkers between patients with severe coronavirus disease 2019 (COVID-19) infection/death and mild infection.
Patients and Methods
MEDLINE, Cochrane Central Register of Controlled Trials, EMBASE, EBSCO, Web of Science, and CINAHL databases were searched for studies comparing thromboinflammatory biomarkers in COVID-19 among patients with severe COVID-19 disease or death (severe/nonsurvivors) and those with nonsevere disease or survivors (nonsevere/survivors) from January 1, 2020, through July 11, 2020. Inclusion criteria were (1) hospitalized patients 18 years or older comparing severe/nonsurvivors vs nonsevere/survivors and (2) biomarkers of inflammation and/or thrombosis. A random-effects model was used to estimate the weighted mean difference (WMD) between the 2 groups of COVID-19 severity.
Results
We included 75 studies with 17,052 patients. The severe/nonsurvivor group was older, had a greater proportion of men, and had a higher prevalence of hypertension, diabetes, cardiac or cerebrovascular disease, chronic kidney disease, malignancy, and chronic obstructive pulmonary disease. Thromboinflammatory biomarkers were significantly higher in patients with severe disease, including D-dimer (WMD, 0.60; 95% CI, 0.49 to 0.71; I2=83.85%), fibrinogen (WMD, 0.42; 95% CI, 0.18 to 0.67; I2=61.88%; P<.001), C-reactive protein (CRP) (WMD, 35.74; 95% CI, 30.16 to 41.31; I2=85.27%), high-sensitivity CRP (WMD, 62.68; 95% CI, 45.27 to 80.09; I2=0%), interleukin 6 (WMD, 22.81; 95% CI, 17.90 to 27.72; I2=90.42%), and ferritin (WMD, 506.15; 95% CI, 356.24 to 656.06; I2=52.02%). Moderate to significant heterogeneity was observed for all parameters (I2 > 25%). Subanalysis based on disease severity, mortality, and geographic region of the studies revealed similar inferences.
Conclusion
Thromboinflammatory biomarkers (D-dimer, fibrinogen, CRP, high-sensitivity CRP, ferritin, and interleukin 6) and marker of end-organ damage (high-sensitivity troponin I) are associated with increased severity and mortality in COVID-19 infection.
Elsevier
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