Abstract 4365121: Clinical Correlations with Serial Echocardiography and Global Longitudinal Strain in the First and Second Genetically Modified Porcine to Human Cardiac Xenotransplantation

S Sarah Leventhal (University of Maryland, Baltimore, Maryland, United States) M Muhammad Mohiuddin (University of Maryland School of Me, Baltimore, Maryland, United States) A Andrew Tully (Univ of Maryland School of Medicine, Baltimore, Maryland, United States) J Javier Galindo (University of Maryland, Baltimore, Baltomire, Maryland, United States) T Timm Dickfeld (Univ of Maryland School of Medicine, Baltimore, Maryland, United States) A Alison Grazioli (University of Maryland, Baltimore, Maryland, United States) A Allison Lankford (University of Maryland, Baltimore, Maryland, United States) A Albert Hicks (Univ of Maryland School of Medicine, Baltimore, Maryland, United States) B Brian Barr (Univ of Maryland School of Medicine, Baltimore, Maryland, United States) A Anuj Gupta E Erika Feller (Medstar, Baltimore, Maryland, United States) D David Ayares B Bartley Griffith (Univ of Maryland School of Medicine, Baltimore, Maryland, United States) S Susie Hong-Zohlman (Univ of Maryland School of Medicine, Baltimore, Maryland, United States)

Abstract

Background: Our institution performed the first two genetically modified porcine cardiac xenotransplantation in humans, conducting serial longitudinal transthoracic echocardiograms (TTE) with global longitudinal strain (GLS). Both recipients exhibited marked right ventricular (RV) hypertrophy and worsening GLS at the time of graft failure. Methods: Serial TTE measurements were made in both xenotransplanted patients, including RV wall thickness (RVWT), end diastolic diameter (EDD), and GLS. Measurement ratios were compared to endomyocardial biopsies (EMBx), clinically correlating to terminal graft failure. Results: From post-operative day (POD) 1 of xenotransplant to end-of-life, RVWT increased 80.9% (CI 95.6-118.5%) while EDD decreased 40.2% (CI 20.3-64.1%). For the first recipient, RVWT/EDD increased from 0.22 (POD 1) to 0.53 (POD 58), when the graft terminally failed from restrictive myopathy (LVEF 55%, GLS -7.7), confirmed by EMBx. For the second recipient, RVWT/EDD increased from 0.18 (POD 1) to 0.68 (POD 40) (Figure 1), when the graft terminally failed due to combined systolic and diastolic dysfunction (LVEF 25%, GLS -7.6), confirmed by EMBx. For both xenografts, GLS worsened by an average of 42.3% (CI 42.2-42.4%) when the RVWT/EDD ratio reached 0.50 - 0.55, demonstrating a linear correlation (r= 0.8). Conclusion: Increased RVWT/EDD ratio is associated with worsening GLS, xenotransplant graft failure, and recipient mortality. TTE provided real-time noninvasive histological correlation in the first two cardiac xenotransplants. In future cardiac xenotransplantation, serial noninvasive measurements identifying early graft failure will be essential for monitoring and management.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (14)

S

Sarah Leventhal

University of Maryland, Baltimore, Maryland, United States

M

Muhammad Mohiuddin

University of Maryland School of Me, Baltimore, Maryland, United States

A

Andrew Tully

Univ of Maryland School of Medicine, Baltimore, Maryland, United States

J

Javier Galindo

University of Maryland, Baltimore, Baltomire, Maryland, United States

T

Timm Dickfeld

Univ of Maryland School of Medicine, Baltimore, Maryland, United States

A

Alison Grazioli

University of Maryland, Baltimore, Maryland, United States

A

Allison Lankford

University of Maryland, Baltimore, Maryland, United States

A

Albert Hicks

Univ of Maryland School of Medicine, Baltimore, Maryland, United States

B

Brian Barr

Univ of Maryland School of Medicine, Baltimore, Maryland, United States

A

Anuj Gupta

E

Erika Feller

Medstar, Baltimore, Maryland, United States

D

David Ayares

B

Bartley Griffith

Univ of Maryland School of Medicine, Baltimore, Maryland, United States

S

Susie Hong-Zohlman

Univ of Maryland School of Medicine, Baltimore, Maryland, United States