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Redefining the molecular rejection states in 3230 heart transplant biopsies: Relationships to parenchymal injury and graft survival

PF. Halloran, K. Madill-Thomsen, AZ. Aliabadi-Zuckermann, M. Cadeiras, MG. Crespo-Leiro, EC. Depasquale, M. Deng, J. Gökler, S. Hall, A. Jamil, DH. Kim, J. Kobashigawa, P. Macdonald, V. Melenovsky, J. Patel, L. Potena, K. Shah, J. Stehlik, A. Zuckermann

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc24019606

The first-generation Molecular Microscope (MMDx) system for heart transplant endomyocardial biopsies used expression of rejection-associated transcripts (RATs) to diagnose not only T cell-mediated rejection (TCMR) and antibody-mediated rejection (ABMR) but also acute injury. However, the ideal system should detect rejection without being influenced by injury, to permit analysis of the relationship between rejection and parenchymal injury. To achieve this, we developed a new rejection classification in an expanded cohort of 3230 biopsies: 1641 from INTERHEART (ClinicalTrials.gov NCT02670408), plus 1589 service biopsies added to improve the power of the machine learning algorithms. The new system used 6 rejection classifiers instead of RATs and generated 7 rejection archetypes: No rejection, 48%; Minor, 24%; TCMR1, 2.3%; TCMR2, 2.7%; TCMR/mixed, 2.7%; early-stage ABMR, 3.9%; and fully developed ABMR, 16%. Using rejection classifiers eliminated cross-reactions with acute injury, permitting separate assessment of rejection and injury. TCMR was associated with severe-recent injury and late atrophy-fibrosis and rarely had normal parenchyma. ABMR was better tolerated, seldom producing severe injury, but in later biopsies was often associated with atrophy-fibrosis, indicating long-term risk. Graft survival and left ventricular ejection fraction were reduced not only in hearts with TCMR but also in hearts with severe-recent injury and atrophy-fibrosis, even without rejection.

Citace poskytuje Crossref.org

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$a Madill-Thomsen, Katelynn $u Department of Medicine, University of Alberta, Edmonton, Alberta, Canada
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$a Aliabadi-Zuckermann, Arezu Z $u Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria
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$a Cadeiras, Martin $u Ronald Reagan UCLA Medical Center, Los Angeles, California, USA
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$a Crespo-Leiro, Marisa G $u Advanced Heart Failure and Heart Transplant Unit, Complexo Hospitalario Universitario A Coruña, A Coruña, Spain
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$a Depasquale, Eugene C $u Ronald Reagan UCLA Medical Center, Los Angeles, California, USA
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$a Gökler, Johannes $u Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria
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$a Hall, Shelley $u Baylor Scott & White Health, Dallas, Texas, USA
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$a Kim, Daniel H $u Department of Medicine, University of Alberta, Edmonton, Alberta, Canada
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$a Macdonald, Peter $u The Victor Chang Cardiac Research Institute, Sydney, Australia
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$a Shah, Keyur $u Department of Cardiology, Virginia Commonwealth University, Richmond, Virginia, USA
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