Assessment of Ventricular Repolarization in Sickle Cell Anemia Patients: The Role of QTc Interval, Tp-e Interval and

Adeola Olubunmi Ajibare1, Olatunde Peter Olabode2, Emmanuel Yemi Fagbemiro3

  • 1Department of Medicine, Lagos State University College of Medicine Ikeja, Lagos, Nigeria.

Insights

Sickle cell anemia (SCA) patients show altered ventricular repolarization, with prolonged QTc intervals. Male SCA patients have increased risk of arrhythmias, while BMI and PAI-1 may indicate repolarization issues.

Area of Science:

  • Cardiology
  • Hematology
  • Electrophysiology

Background:

  • Sickle cell anemia (SCA) is associated with electrocardiographic abnormalities and increased risk of ventricular arrhythmias.
  • Ventricular repolarization abnormalities, assessed by corrected QT (QTc) interval, Tp-e interval, and Tp-e/QTc ratio, are crucial indicators of arrhythmogenesis risk in SCA.

Purpose of the Study:

  • To evaluate ventricular repolarization abnormalities in SCA patients using QTc, Tp-e, and Tp-e/QTc.
  • To investigate gender differences in these repolarization parameters.
  • To identify determinants of ventricular repolarization abnormalities in SCA.

Main Methods:

  • Sixty SCA patients and 60 healthy controls underwent ECG, physical examination, and hematological/biochemical evaluation.
  • QT and Tp-e intervals were measured from ECGs; QTc was calculated using Bazett's formula.
  • Derived Tp-e/QT and Tp-e/QTc ratios for comprehensive repolarization assessment.

Main Results:

  • SCA subjects exhibited prolonged QT and QTc intervals.
  • Male SCA subjects showed prolonged Tp-e interval and Tp-e/QTc ratio, while females showed paradoxical shortening.
  • Plasminogen activator inhibitor-1 (PAI-1) and body mass index (BMI) were identified as independent determinants of repolarization parameters.

Conclusions:

  • Male SCA subjects demonstrate an elevated risk for ventricular arrhythmogenesis.
  • Increased BMI and PAI-1 levels may serve as potential markers for ventricular repolarization abnormalities in SCA patients.
Abstract

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