Nuclear Osteopontin Is a Marker of Advanced Heart Failure and Cardiac Allograft Vasculopathy: Evidence From Transplant and Retransplant Hearts

• Published in: Frontiers in physiology Vol. 11; p. 928
• Main Authors: Irion, Camila Iansen, Dunkley, Julian C, John-Williams, Krista, Condor Capcha, José Manuel, Shehadeh, Serene A, Pinto, Andre, Loebe, Matthias, Webster, Keith A, Brozzi, Nicolas A, Shehadeh, Lina A
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 13.08.2020
• Subjects: cardiac allograft vasculopathy; dilated cardiomyopathy; endomyocardial biopsy; heart retransplantation; heart transplant; osteopontin; Physiology; endomyocardial biopsy; cardiac allograft vasculopathy; heart transplant; heart retransplantation; osteopontin; dilated cardiomyopathy
• ISSN: 1664-042X; 1664-042X
• DOI: 10.3389/fphys.2020.00928

Heart transplant is the gold standard therapy for patients with advanced heart failure. Over 5,500 heart transplants are performed every year worldwide. Cardiac allograft vasculopathy (CAV) is a common complication post-heart transplant which reduces survival and often necessitates heart retransplantation. Post-transplant follow-up requires serial coronary angiography and endomyocardial biopsy (EMB) for CAV and allograft rejection screening, respectively; both of which are invasive procedures. This study aims to determine whether osteopontin (OPN) protein, a fibrosis marker often present in chronic heart disease, represents a novel biomarker for CAV. Expression of OPN was analyzed in cardiac tissue obtained from patients undergoing heart retransplantation using immunofluorescence imaging ( = 20). Tissues from native explanted hearts and three serial follow-up EMB samples of transplanted hearts were also analyzed in five of these patients. Fifteen out of 20 patients undergoing retransplantation had CAV. 13/15 patients with CAV expressed nuclear OPN. 5/5 patients with multiple tissue samples expressed nuclear OPN in both 1 and 2 explanted hearts, while 0/5 expressed nuclear OPN in any of the follow-up EMBs. 4/5 of these patients had an initial diagnosis of dilated cardiomyopathy (DCM). Nuclear localization of OPN in cardiomyocytes of patients with CAV was evident at the time of cardiac retransplant as well as in patients with DCM at the time of the 1 transplant. The results implicate nuclear OPN as a novel biomarker for severe CAV and DCM.