Myocardial Fibrosis and Prognosis in Heart Transplant Recipients

Andrew Hughes1, Osama Okasha1, Afshin Farzaneh-Far2

  • 1Cardiovascular Division, Department of Medicine, University of Minnesota Medical School, Minneapolis, MN (A.H., O.O., F.K., P.S.N., P.V., C.M.M., C.S.).

Insights

Myocardial fibrosis, detected by cardiac MRI, is present in 18% of heart transplant recipients and independently predicts long-term adverse outcomes, including death and major cardiac events.

Area of Science:

  • Cardiology
  • Transplantation Medicine
  • Medical Imaging

Background:

  • Myocardial fibrosis is a known complication in heart transplant recipients.
  • The independent association between myocardial fibrosis and clinical outcomes remains unclear.

Purpose of the Study:

  • To determine if myocardial fibrosis, visualized via late gadolinium enhancement cardiovascular magnetic resonance imaging (LGE-CMR), is independently linked to long-term all-cause death or major adverse cardiac events (MACE) in heart transplant recipients.

Main Methods:

  • A cohort of heart transplant recipients underwent LGE-CMR.
  • Prevalence and patterns of myocardial fibrosis were assessed.
  • Associations between myocardial fibrosis and a composite endpoint of all-cause death or MACE (retransplantation, myocardial infarction, coronary revascularization, heart failure hospitalization) were analyzed.

Main Results:

  • Myocardial fibrosis was identified in 18% of 152 recipients and associated with cardiac allograft vasculopathy.
  • Over a median follow-up of 2.6 years, myocardial fibrosis independently predicted all-cause death or MACE (HR, 2.88; P<0.001).
  • Each 1% increase in fibrosis correlated with a 6% higher hazard for adverse events (HR, 1.06; P<0.001), with significant incremental prognostic value.

Conclusions:

  • Myocardial fibrosis is present in 18% of heart transplant recipients, detectable by LGE-CMR.
  • Both the presence and extent of myocardial fibrosis are independently associated with increased long-term risk of death or MACE.
Abstract

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