Laboratory markers associated with COVID-19 progression in patients with or without comorbidity: A retrospective

Zaishu Chen1, Furong Zhang2, Weihua Hu3

  • 1Jiayu People's Hospital, Jiayu, China.

Insights

Lactate dehydrogenase (LDH) is a key marker for COVID-19 severity and mortality, especially in patients with comorbidities. Different medical conditions show unique laboratory risk factors for COVID-19 mortality.

Area of Science:

  • Infectious Diseases
  • Clinical Laboratory Science
  • Epidemiology

Background:

  • COVID-19 progression and mortality are influenced by patient comorbidities.
  • Identifying reliable laboratory markers is crucial for managing COVID-19 severity.
  • Understanding disease mechanisms requires analyzing laboratory data in diverse patient groups.

Purpose of the Study:

  • To identify laboratory markers predicting COVID-19 severity and mortality.
  • To investigate how comorbidities affect the association between laboratory markers and COVID-19 outcomes.
  • To explore differences in mortality risk factors among patients with various comorbidities.

Main Methods:

  • Multicenter retrospective study of 836 COVID-19 cases.
  • Principal Component Analysis (PCA) and Partial Least Squares Discriminant Analysis (PLS-DA) for laboratory data overview.
  • Multivariable logistic and Cox regression analyses for risk factor identification; survival analysis for comorbidity groups.

Main Results:

  • Lactate dehydrogenase (LDH) and prealbumin correlated with COVID-19 severity, with or without comorbidities.
  • In patients with comorbidities, mortality risk was linked to age, LDH, C-reactive protein (CRP), D-dimer, and lymphopenia.
  • CRP predicted short-term mortality in hypertension but not liver disease; D-dimer predicted mortality in liver disease.

Conclusions:

  • Lactate dehydrogenase (LDH) is a consistent predictor of COVID-19 severity and mortality across different patient conditions.
  • Laboratory biomarkers for mortality risk vary among patients with comorbidities, indicating diverse pathophysiological pathways in COVID-19.
Abstract

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