Peripheral granular lymphocytopenia and dysmorphic leukocytosis as simple prognostic markers in COVID-19

Yuki Horiuchi1, Fumiaki Hayashi2, Yosuke Iwasaki2

  • 1Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.

Insights

Peripheral blood examination can predict coronavirus disease (COVID-19) prognosis. Severe COVID-19 cases show distinct blood cell count and morphology changes, indicating bone marrow stress and immune system disruption.

Area of Science:

  • Hematology
  • Infectious Diseases
  • Prognostic Biomarkers

Background:

  • Prognostic markers aid clinical decision-making.
  • Peripheral blood (PB) examination is a universally accessible diagnostic tool.
  • Investigating PB markers for COVID-19 prognosis is crucial.

Purpose of the Study:

  • To determine if PB examination can predict prognosis in coronavirus disease (COVID-19).
  • To identify specific hematological changes associated with COVID-19 severity.

Main Methods:

  • Complete blood count (CBC) and PB cell morphology analyzed in 40 COVID-19 patients (26 mild, 14 severe) and 38 healthy controls.
  • Automated hematology analyzers (Sysmex XN-3000) and image-recognition systems (Sysmex DI-60) were utilized.
  • Convolutional neural network-based automatic image-recognition system employed for cell analysis.

Main Results:

  • Severe COVID-19 cases exhibited significantly higher anemia, lymphopenia, and leukocytosis compared to mild cases.
  • Granular lymphocyte counts decreased in severe/fatal cases, with temporary increases correlating with survival.
  • Elevated red cell distribution width, neutrophil dysplasia, giant neutrophils, and toxic granulation/Döhle bodies were observed in severe COVID-19.

Conclusions:

  • Basic peripheral blood examination effectively predicts COVID-19 prognosis.
  • SARS-CoV-2 infection induces multi-lineage blood cell count and morphological changes.
  • These hematological alterations correlate with disease severity and may reflect bone marrow stress and immune disruption.
Abstract

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