Intrinsic changes of left ventricular function in patients with Behçet disease and comparison according to systemic

Byung Joo Sun1, Jae-Hyeong Park1, Su-Jin Yoo2

  • 1Division of Cardiology, Department of Internal Medicine, School of Medicine, Chungnam National University, Chungnam National University Hospital, Daejeon, Korea.

Insights

Behçet disease (BD) patients show reduced heart function (GLS) even without routine echocardiogram abnormalities. This cardiac dysfunction in BD is present regardless of systemic disease activity.

Area of Science:

  • Cardiology
  • Rheumatology
  • Internal Medicine

Background:

  • Behçet disease (BD) is a multisystem inflammatory disorder.
  • Cardiac involvement in BD is known but often diagnosed late.
  • Early detection of cardiac manifestations is crucial for patient management.

Purpose of the Study:

  • To identify early cardiac manifestations in Behçet disease patients.
  • To classify systemic BD activity and correlate it with cardiac findings.
  • To investigate subclinical cardiac dysfunction in BD.

Main Methods:

  • Prospective study of 85 BD patients without prior heart disease.
  • Speckle tracking echocardiography used for assessment.
  • Analysis of left ventricular global longitudinal strain (GLS) and ejection fraction (LVEF).
  • Comparison with 145 age- and gender-matched controls.
  • BD patients categorized by systemic activity: minimal, controlled, active.

Main Results:

  • 81 BD patients analyzed; mean LVEF was normal (64±5%).
  • BD patients showed significantly reduced GLS compared to controls (-17.1±2.9% vs -20.8±2.2%).
  • Reduced GLS was observed across all systemic BD activity groups (minimal, controlled, active).
  • No significant difference in cardiac manifestations based on systemic BD activity level.

Conclusions:

  • Behçet disease patients exhibit intrinsic left ventricular dysfunction.
  • This dysfunction is detectable via GLS even with normal LVEF on routine echocardiography.
  • Cardiac manifestations in BD are not directly proportional to systemic disease activity.
Abstract

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