Conversion to Sirolimus as Primary Immunosuppression Attenuates the Progression of Allograft Vasculopathy After Cardiac Transplantation

  • Eugenia Raichlin
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Jang-Ho Bae
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Zain Khalpey
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Brooks S. Edwards
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Walter K. Kremers
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Alfredo L. Clavell
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Richard J. Rodeheffer
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Robert P. Frantz
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Charanjit Rihal
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Amir Lerman
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.
  • Sudhir S. Kushwaha
    From the William J. von Liebig Transplant Center and the Division of Cardiovascular Diseases, Center for Coronary Physiology and Imaging, Mayo Clinic, Rochester, Minn.

説明

<jats:p> <jats:bold> <jats:italic>Background—</jats:italic> </jats:bold> We investigated the potential of conversion to sirolimus (SRL) as a primary immunosuppressant in attenuating cardiac allograft vasculopathy progression. </jats:p> <jats:p> <jats:bold> <jats:italic>Methods and Results—</jats:italic> </jats:bold> Twenty-nine cardiac transplant recipients were converted to SRL 3.8±3.4 years after transplantation with complete calcineurin inhibitor (CNI) withdrawal. Secondary immunosuppressants (azathioprine or mycophenolate) and steroids remained unchanged. Forty patients (controls) 4.8±4.0 years from transplantation were maintained on CNIs. Three-dimensional intravascular ultrasound studies were performed at baseline and 12.1±2.6 months later. Mean plaque (media and intima) volume (PV) and plaque index (PI) (PV/vessel volume percent) increased significantly in the CNI group (1.28±2.86 mm <jats:sup>3</jats:sup> /mm, <jats:italic>P</jats:italic> =0.004; and 6±8%, <jats:italic>P</jats:italic> =0.0001) but not in the SRL group (0.1±1.13 mm <jats:sup>3</jats:sup> /mm, <jats:italic>P</jats:italic> =0.63; and 0.1±8%, <jats:italic>P</jats:italic> =0.94). In patients enrolled within 2 years after transplantation, the increases in PV (0.06±1.06 versus 1.77±1.65 mm <jats:sup>3</jats:sup> /mm; <jats:italic>P</jats:italic> =0.0081) and PI (0±9% versus 10±8%; <jats:italic>P</jats:italic> =0.0145) were smaller in the SRL group (n=11) than in the CNI (n=12) group. In patients enrolled ≥2 years after transplantation, the increase in PI was less in the SRL group compared with the CNI group (0.1±6.5% versus 5±8%; <jats:italic>P</jats:italic> =0.033), but changes in PV did not differ significantly. Treatment with azathioprine or mycophenolate did not affect PV or PI in either the SRL group (PV: 0.22±0.66 versus 0.05±1.45 mm <jats:sup>3</jats:sup> /mm, <jats:italic>P</jats:italic> =0.46; PI: 1.5±6% versus −1.6±8.5%, <jats:italic>P</jats:italic> =0.29) or the CNI group (PV: 1.42±1.39 versus 1.06±2.28 mm <jats:sup>3</jats:sup> /mm, <jats:italic>P</jats:italic> =0.49; PI: 7.8±8.7% versus 4.8±7.3%, <jats:italic>P</jats:italic> =0.23). </jats:p> <jats:p> <jats:bold> <jats:italic>Conclusions—</jats:italic> </jats:bold> Substituting CNI with SRL as primary immunosuppression attenuates cardiac allograft vasculopathy progression. </jats:p>

収録刊行物

  • Circulation

    Circulation 116 (23), 2726-2733, 2007-12-04

    Ovid Technologies (Wolters Kluwer Health)

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