Left Ventricular Longitudinal Dyssynchrony by CMR Feature Tracking Is Related to Adverse Prognosis in Advanced

Yanyan Song1, Lu Li2, Xiuyu Chen1

  • 1Department of Magnetic Resonance Imaging, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Insights

Left ventricular longitudinal dyssynchrony (LVLD) measured by cardiovascular magnetic resonance-feature tracking (CMR-FT) predicts adverse outcomes in arrhythmogenic cardiomyopathy (ACM) patients with right ventricular dysfunction. Elevated LVLD is an independent risk factor for cardiovascular and arrhythmic events, aiding prognosis.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Biomedical Engineering

Background:

  • Arrhythmogenic cardiomyopathy (ACM) is characterized by right ventricular (RV) dysfunction, but left ventricular (LV) involvement significantly impacts prognosis.
  • Accurate assessment of LV mechanics is crucial for risk stratification in ACM patients, especially those with coexisting RV dysfunction.

Purpose of the Study:

  • To evaluate left ventricular (LV) mechanics using cardiovascular magnetic resonance-feature tracking (CMR-FT) in arrhythmogenic cardiomyopathy (ACM) patients with right ventricular (RV) dysfunction.
  • To determine the prognostic value of LV mechanical parameters, specifically LV longitudinal dyssynchrony (LVLD), for cardiovascular and arrhythmic events.

Main Methods:

  • Retrospective analysis of 89 ACM patients diagnosed by revised Task Force Criteria (rTFC).
  • Cardiovascular magnetic resonance (CMR) examinations including LV and RV strain and dyssynchrony analysis via feature tracking (FT).
  • Follow-up assessment for composite cardiovascular events (arrhythmic events and heart transplantation) and secondary outcome of arrhythmic events.

Main Results:

  • Patients experiencing cardiovascular events showed impaired LV global longitudinal strain, impaired LV global circumferential strain, and greater LV longitudinal dyssynchrony (LVLD).
  • LVLD emerged as a significant predictor, with LVLD ≥89.15 ms being an independent risk factor for both cardiovascular events (HR: 4.50) and arrhythmic events (HR: 4.79) after multivariable adjustment.
  • The study identified specific thresholds for impaired LV strain and elevated LVLD associated with adverse outcomes in this cohort.

Conclusions:

  • Left ventricular longitudinal dyssynchrony (LVLD), assessed by CMR-FT, is an independent predictor of adverse cardiovascular and arrhythmic events in advanced ACM.
  • CMR-FT derived LVLD provides valuable prognostic information for stratifying risk in ACM patients with coexisting RV dysfunction.
  • This quantitative imaging biomarker can aid clinicians in identifying high-risk ACM patients requiring closer monitoring and potentially earlier intervention.

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