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Similar Clinical Course and Significance of Circulating Innate and Adaptive Immune Cell Counts in STEMI and COVID-19. | LitMetric

AI Article Synopsis

  • The study examined the changes in neutrophil and lymphocyte counts, along with their ratio (NLR), in patients with ST-segment elevation myocardial infarction (STEMI) and COVID-19 to understand their links to clinical outcomes and organ damage.
  • Both STEMI and COVID-19 showed similar dynamics in immune cell counts, with higher neutrophils and lower lymphocytes linked to worse clinical outcomes and structural damage.
  • The findings highlight a disrupted immune response in these conditions, suggesting that elevated neutrophils and reduced lymphocytes are associated with increased health risks, pointing towards the need for new treatment approaches.

Article Abstract

This study aimed to assess the time course of circulating neutrophil and lymphocyte counts and their ratio (NLR) in ST-segment elevation myocardial infarction (STEMI) and coronavirus disease (COVID)-19 and explore their associations with clinical events and structural damage. Circulating neutrophil, lymphocyte and NLR were sequentially measured in 659 patients admitted for STEMI and in 103 COVID-19 patients. The dynamics detected in STEMI (within a few hours) were replicated in COVID-19 (within a few days). In both entities patients with events and with severe structural damage displayed higher neutrophil and lower lymphocyte counts. In both scenarios, higher maximum neutrophil and lower minimum lymphocyte counts were associated with more events and more severe organ damage. NLR was higher in STEMI and COVID-19 patients with the worst clinical and structural outcomes. A canonical deregulation of the immune response occurs in STEMI and COVID-19 patients. Boosted circulating innate (neutrophilia) and depressed circulating adaptive immunity (lymphopenia) is associated with more events and severe organ damage. A greater understanding of these critical illnesses is pivotal to explore novel alternative therapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692467PMC
http://dx.doi.org/10.3390/jcm9113484DOI Listing

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