Impact of age and cardiac disease on regional left and right ventricular myocardial motion in healthy controls and patients with repaired tetralogy of fallot

• DOI: 10.1007/s10554-019-01544-6
• Publication Date: 2019-02-04T06:31:18Z
• Authors: Alexander Ruh; Roberto Sarnari; Haben Berhane; Kenny Sidoryk; Kai Lin; Ryan Dolan; Arleen Li; Michael J. Rose; Joshua D. Robinson; James C. Carr; Cynthia K. Rigsby; Michael Markl
• Keywords: Adult; Male; Time Factors; Adolescent; Age Factors; Infant; Pilot Projects; Middle Aged; Magnetic Resonance Imaging; Biomechanical Phenomena; 3. Good health; 03 medical and health sciences; Treatment Outcome; 0302 clinical medicine; Case-Control Studies; Child, Preschool; Tetralogy of Fallot; Feasibility Studies; Humans; Female; Cardiac Surgical Procedures; Child; Aged

The assessment of both left (LV) and right ventricular (RV) motion is important to understand the impact of heart disease on cardiac function. The MRI technique of tissue phase mapping (TPM) allows for the quantification of regional biventricular three-directional myocardial velocities. The goal of this study was to establish normal LV and RV velocity parameters across a wide range of pediatric to adult ages and to investigate the feasibility of TPM for detecting impaired regional biventricular function in patients with repaired tetralogy of Fallot (TOF). Thirty-six healthy controls (age = 1-75 years) and 12 TOF patients (age = 5-23 years) underwent cardiac MRI including TPM in short-axis locations (base, mid, apex). For ten adults, a second TPM scan was used to assess test-retest reproducibility. Data analysis included the calculation of biventricular radial, circumferential, and long-axis velocity components, quantification of systolic and diastolic peak velocities in an extended 16 + 10 LV + RV segment model, and assessment of inter-ventricular dyssynchrony. Biventricular velocities showed good test-retest reproducibility (mean bias ≤ 0.23 cm/s). Diastolic radial and long-axis peak velocities for LV and RV were significantly reduced in adults compared to children (19-61%, p < 0.001-0.02). In TOF patients, TPM identified significantly reduced systolic and diastolic LV and RV long-axis peak velocities (20-50%, p < 0.001-0.05) compared to age-matched controls. In conclusion, tissue phase mapping enables comprehensive analysis of global and regional biventricular myocardial motion. Changes in myocardial velocities associated with age underline the importance of age-matched controls. This pilot study in TOF patients shows the feasibility to detect regionally abnormal LV and RV motion.