Evaluation of left ventricular diastolic function by 2-d speckle tracking echocardiography in patients with connective tissue disease-associated pulmonary artery hypertension

The purpose of this study was to evaluate the role of 2-D speckle tracking imaging in assessing left ventricular diastolic function in patients with connective tissue disease (CTD). A total of 98 CTD patients and 32 healthy controls were prospectively recruited. Early (E) and late (A) diastolic velocities of the transmitral flow were measured by pulsed Doppler echocardiography. Peak early diastolic myocardial velocity (E?) was calculated on tissue Doppler echocardiography. The longitudinal strain rate (SR) was calculated as the average of three apical views, while circumferential and radial SRs were measured in three short-axis views. Pulmonary arterial hypertension (PAH) was defined as systolic pulmonary arterial pressure (sPAP) >36 mm Hg. Compared with the control group, CTD patients exhibited significant impairment of left ventricular diastolic function, manifested as lower global SR during early diastole (SRe) in the longitudinal deformation and higher E/SRe in both longitudinal and radial deformation. CTD-PAH patients had significantly lower SRe and higher E/SRe values in both the longitudinal and radial deformation compared with the patients with CTD without PAH. Pearson?s correlation analysis revealed that sPAP levels correlated positively with E/E0, longitudinal E/SRe, circumferential E/ SRe and radial SRe, and it correlated negatively with septal E0 and radial E/SRe. Receiver operating characteristic curve analysis suggested that E/E0, longitudinal E/SRe and radial SRe could be used to predict PAH. The present study indicates that 2-D speckle tracking imaging is a useful method for evaluation of left ventricular diastolic function, and these derived parameters can serve as good predictors of PAH, but it may not be superior to the commonly used E/E0 in CTD patients. (E-mail addresses: zhoulei@njmu.edu.cn wuhongping0808@163. com) ? 2021 Published by Elsevier Inc. on behalf of World Federation for Ultrasound in Medicine & Biology.