4.5 Article

Left ventricular geometry transition in hypertensive patients with heart failure with preserved ejection fraction

Journal

ESC HEART FAILURE
Volume 8, Issue 4, Pages 2784-2790

Publisher

WILEY PERIODICALS, INC
DOI: 10.1002/ehf2.13349

Keywords

Hypertension; Left ventricular hypertrophy; Heart failure; Transition

Funding

  1. National Natural Science Foundation of China [82070381, 81670293]
  2. Shanghai Ninth People's Hospital [JYLJ201803, 201911, YBKA201910]
  3. Shanghai Science and Technology Commission [20ZR1431100, 19ZR1446000]

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This study found that a quarter of patients with hypertensive left ventricular hypertrophy and HFpEF progress to systolic dysfunction during a 5-year follow-up, with poor clinical outcomes. Beta-blocker therapy may play a protective role in preserving LVEF, and the transition of LV geometry is uncommon.
Aims Heart failure with preserved ejection fraction (HFpEF) develops in response to hypertensive left ventricular (LV) hypertrophy and is associated with increased cardiovascular events. Although the progression to systolic heart failure is a known consequence of LV hypertrophy and HFpEF, few data are available on the LV geometry change and frequency of deterioration to systolic dysfunction in this population. Methods and results We evaluated the baseline and follow-up characteristics in 680 patients with LV hypertrophy and HFpEF in this prospective cohort study. The primary endpoint was 5 year all-cause mortality. The changes of LV geometry and heart failure transition were analysed. Systolic dysfunction [left ventricular ejection fraction (LVEF) < 50%] occurred in 182 patients (26.8%) during a 5 year follow-up. Patients with LVEF deterioration were associated with a lower survival rate. Beta-blocker prescription was a protective factor for preserved LVEF. And concentric LV geometry shifted to eccentric hypertrophy was uncommon (10.6%) during a 5 year follow-up. Conclusions A quarter of patients with hypertensive LV hypertrophy and HFpEF progresses to systolic dysfunction during a 5 year follow-up, which was accompanied by poor clinical outcomes. And beta-blocker therapy might play a protective role for preserved LVEF in this population.

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