TTP-like syndrome and its relationship with complement activation in critically ill patients with COVID-19: A

Mohammadreza Ardalan1, Mohammadreza Moslemi1, Azin Pakmehr2

  • 1Kidney Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Heliyon
|June 23, 2023
PubMed

Insights

Thrombotic thrombocytopenic purpura-like syndrome (TTPS) affects 9.1% of critically ill COVID-19 patients. Lower C3 complement levels in these patients suggest complement activation plays a role in TTPS development during COVID-19.

Area of Science:

  • Critical Care Medicine
  • Hematology
  • Immunology

Background:

  • COVID-19 pandemic has seen an increase in thromboembolic events, including thrombotic thrombocytopenic purpura (TTP).
  • Complement system activation is increasingly implicated in TTP and TTP-like syndromes.
  • The prevalence and role of complement in COVID-19-associated TTP-like syndrome require further investigation.

Purpose of the Study:

  • To determine the prevalence of TTP-like syndrome in critically ill COVID-19 patients.
  • To investigate the association between TTP-like syndrome and complement activity (C3, C4, CH50) in this patient group.

Main Methods:

  • Study included 77 critically ill COVID-19 patients admitted to ICU.
  • TTP-like syndrome diagnosed based on thrombocytopenia, microangiopathic hemolysis, and end-organ injury.
  • Complement levels (C3, C4, CH50) were measured; ADAMTS13 activity was not assessed due to logistical constraints.

Main Results:

  • Seven patients (9.1%) were diagnosed with TTP-like syndrome.
  • Patients with TTP-like syndrome exhibited significantly lower C3 levels compared to those without (p=0.014).
  • No significant differences in C4 or CH50 levels were observed between groups.

Conclusions:

  • TTP-like syndrome is a notable complication in critically ill COVID-19 patients.
  • Reduced C3 levels suggest complement activation is a potential contributing factor to TTPS in COVID-19.
  • Further research is needed to elucidate the precise mechanisms and develop targeted therapies.
Abstract

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