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10.1002/rmv.2141

http://scihub22266oqcxt.onion/10.1002/rmv.2141
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32845568!7460877!32845568
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suck abstract from ncbi


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pmid32845568      Rev+Med+Virol 2020 ; 30 (6): 1-9
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  • Interleukin-6 in Covid-19: A systematic review and meta-analysis #MMPMID32845568
  • Coomes EA; Haghbayan H
  • Rev Med Virol 2020[Nov]; 30 (6): 1-9 PMID32845568show ga
  • Coronaviruses may activate dysregulated host immune responses. As exploratory studies have suggested that interleukin-6 (IL-6) levels are elevated in cases of complicated Covid-19, we undertook a systematic review and meta-analysis to assess the evidence in this field. We systematically searched MEDLINE and EMBASE for studies investigating the immunological response in Covid-19; additional grey literature searches were undertaken. Study selection and data abstraction was undertaken independently by two authors. Meta-analysis was undertaken using random effects models to compute ratios of means with 95% confidence intervals (95%CIs). Eight published studies and two preprints (n = 1798) were eligible for inclusion. Meta-analysis of mean IL-6 concentrations demonstrated 2.9-fold higher levels in patients with complicated Covid-19 compared with patients with noncomplicated disease (six studies; n = 1302; 95%CI, 1.17-7.19; I(2) = 100%). Consistent results were found in sensitivity analyses exclusively restricted to studies comparing patients requiring ICU admission vs no ICU admission (two studies; n = 540; ratio of means = 3.24; 95%CI, 2.54-4.14; P < .001; I(2) = 87%). Nine of ten studies were assessed to have at least moderate risk of bias. In patients with Covid-19, IL-6 levels are significantly elevated and associated with adverse clinical outcomes. Inhibition of IL-6 may be a novel target for therapeutics for the management of dysregulated host responses in patients with Covid-19 and high-quality studies of intervention in this field are urgently required.
  • |*Host-Pathogen Interactions[MESH]
  • |Biomarkers[MESH]
  • |COVID-19/complications/*metabolism/therapy/*virology[MESH]
  • |Cytokine Release Syndrome/etiology[MESH]
  • |Cytokines/metabolism[MESH]
  • |Humans[MESH]
  • |Interleukin-6/*metabolism[MESH]
  • |Prognosis[MESH]
  • |Publication Bias[MESH]


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