Donor-Derived Cell-Free DNA Versus Left Ventricular Longitudinal Strain and Strain-Derived
Myocardial Work Indices for Identification of Heart Transplant Injury
Nemzeti Kardiovaszkuláris Laboratórium(RRF-2.3.1-21-2022-00003) Támogató: NKFIH
János Bolyai Research Scholarship of the Hungarian Academy of Sciences
Background/Objectives: Donor-derived cell-free DNA (dd-cfDNA) is a marker of graft
injury that increases in acute rejection and has excellent negative predictive value.
Left ventricular global longitudinal strain (LVGLS) and strain-derived myocardial
work indices are novel echocardiographic parameters with growing applications. Still,
they have been poorly investigated in heart transplant (HTx) recipients so far. We
sought to examine the diagnostic impact of left ventricular longitudinal strain-derived
indices in diagnosing myocardial injury as assessed by dd-cfDNA after HTx. Methods:
Since October 2022, HTx recipients have been shifted from our endomyocardial biopsy
(EMB)-based rejection surveillance protocol to a monthly dd-cfDNA-led rejection assessment.
We analysed the percentage of donor-derived to total cell-free DNA. For echocardiographic
analysis, patient selection was restricted to those transplanted ≥ 6 months. We used
2D speckle-tracking echocardiography to assess LVGLS and strain-derived myocardial
work parameters. Results: We analysed four hundred and forty-nine dd-cfDNA samples
from seventy-one patients until November 2024. The mean dd-cfDNA fraction remained
very low (0.13 ± 0.06%). Eighty-eight percent of surveillance EMBs that would have
otherwise been performed were avoided. The mean LVGLS was lower than the literature
reference values. We found no correlation between dd-cfDNA and LVGLS. Transplanted
hearts had different myocardial work indices than the reference values reported in
the literature. Conclusions: dd-cfDNA effectively rules out clinically significant
acute rejection and decreases the need for invasive surveillance EMBs. LVGLS seems
less sensitive than dd-cfDNA for the identification of myocardial injury in the early
stages of HTx rejection in patients at low risk for rejection.