Longitudinal structural, functional, and cellular myocardial alterations with chronic centrifugal continuous-flow left ventricular assist device support

Kavitha Muthiah; David T Humphreys; Desiree Robson; Kumud Dhital; Phillip Spratt; Paul Jansz; Peter S Macdonald; Christopher S Hayward

doi:10.1016/j.healun.2016.05.017

Longitudinal structural, functional, and cellular myocardial alterations with chronic centrifugal continuous-flow left ventricular assist device support

J Heart Lung Transplant. 2017 Jul;36(7):722-731. doi: 10.1016/j.healun.2016.05.017. Epub 2016 May 20.

Authors

Kavitha Muthiah¹, David T Humphreys², Desiree Robson³, Kumud Dhital¹, Phillip Spratt³, Paul Jansz⁴, Peter S Macdonald¹, Christopher S Hayward⁵

Affiliations

¹ Heart Failure and Transplant Unit, St. Vincent's Hospital, Sydney, New South Wales, Australia; Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia; Victor Chang Cardiac Research Institute, Sydney, New South Wales, Australia.
² Victor Chang Cardiac Research Institute, Sydney, New South Wales, Australia.
³ Heart Failure and Transplant Unit, St. Vincent's Hospital, Sydney, New South Wales, Australia.
⁴ Heart Failure and Transplant Unit, St. Vincent's Hospital, Sydney, New South Wales, Australia; Victor Chang Cardiac Research Institute, Sydney, New South Wales, Australia.
⁵ Heart Failure and Transplant Unit, St. Vincent's Hospital, Sydney, New South Wales, Australia; Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia; Victor Chang Cardiac Research Institute, Sydney, New South Wales, Australia. Electronic address: cshayward@stvincents.com.au.

PMID: 27373819
DOI: 10.1016/j.healun.2016.05.017

Abstract

Background: Left ventricular assist device (LVAD) support triggers adaptations within failing hearts. The HeartWare (HeartWare International, Inc., Framingham, MA) LVAD exhibits different flow profiles and afterload dependence compared with previous-generation devices, which may alter remodelling patterns. We sought to characterize myocardial adaptation to third-generation centrifugal-flow LVADs at a functional, hemodynamic, and structural level in addition to profiling transcriptomal changes using next-generation sequencing platforms.

Methods: We studied 37 patients supported with the HeartWare device with paired measurements of invasive hemodynamics, serial longitudinal left ventricular (LV) and right ventricular (RV) 3-dimensional echocardiography, and N-terminal of the prohormone brain natriuretic peptide (NT-proBNP) measurements. Paired samples for comparison of histologic myocardial cellular size and transcriptomal profiling were performed on specimens taken at pump implant and transplantation.

Results: The mean support duration was 280 ± 163 days. Mechanical unloading after HeartWare support resulted in reduced filling pressures (mean pulmonary capillary wedge pressure 27.1 ± 6.6 to 14.8 ± 5.1 mm Hg, p < 0.0001). Mean LV cardiomyocyte cell size decreased from 2,789.7 ± 671.8 to 2,290.8 ± 494.2 μm² (p = 0.02). LV and RV ejection fractions improved significantly (24% ± 8% to 35% ± 9% [p < 0.001] and 35% ± 11% to 40% ± 8% [p < 0.02], respectively). NT-proBNP levels fell 4.8-fold by Day 90 after support, consistent with a decrease in LV wall stress. Despite these concordant beneficial findings, the microRNA transcriptome did not change significantly across the group.

Conclusions: Reverse remodelling is evident at multiple levels with chronic HeartWare support in the absence of changes in the microRNA transcriptome. Successful myocardial unloading is associated with a decrease in wall stress, regression of cardiomyocyte hypertrophy, and an improvement in LV and RV ejection fractions.

Keywords: 3D echocardiography; N-terminal pro-BNP; left ventricular assist device; microRNA transcriptome; myocardial adaptation; remodeling pattern.

MeSH terms

Adult
Female
Follow-Up Studies
Heart Failure / pathology
Heart Failure / physiopathology*
Heart Failure / therapy*
Heart-Assist Devices*
Humans
Male
Middle Aged
Myocardium / pathology*
Natriuretic Peptide, Brain
Peptide Fragments
Time Factors
Ventricular Remodeling / physiology*

Substances

Peptide Fragments
pro-brain natriuretic peptide (1-76)
Natriuretic Peptide, Brain