HEARTBiT: A Transcriptomic Signature for Excluding Acute Cellular Rejection in Adult Heart Allograft Patients.


Journal

The Canadian journal of cardiology
ISSN: 1916-7075
Titre abrégé: Can J Cardiol
Pays: England
ID NLM: 8510280

Informations de publication

Date de publication:
08 2020
Historique:
received: 05 07 2019
revised: 30 10 2019
accepted: 07 11 2019
pubmed: 20 6 2020
medline: 19 5 2021
entrez: 20 6 2020
Statut: ppublish

Résumé

Nine mRNA transcripts associated with acute cellular rejection (ACR) in previous microarray studies were ported to the clinically amenable NanoString nCounter platform. Here we report the diagnostic performance of the resulting blood test to exclude ACR in heart allograft recipients: HEARTBiT. Blood samples for transcriptomic profiling were collected during routine post-transplantation monitoring in 8 Canadian transplant centres participating in the Biomarkers in Transplantation initiative, a large (n = 1622) prospective observational study conducted between 2009 and 2014. All adult cardiac transplant patients were invited to participate (median age = 56 [17 to 71]). The reference standard for rejection status was histopathology grading of tissue from endomyocardial biopsy (EMB). All locally graded ISHLT ≥ 2R rejection samples were selected for analysis (n = 36). ISHLT 1R (n = 38) and 0R (n = 86) samples were randomly selected to create a cohort approximately matched for site, age, sex, and days post-transplantation, with a focus on early time points (median days post-transplant = 42 [7 to 506]). ISHLT ≥ 2R rejection was confirmed by EMB in 18 and excluded in 92 samples in the test set. HEARTBiT achieved 47% specificity (95% confidence interval [CI], 36%-57%) given ≥ 90% sensitivity, with a corresponding area under the receiver operating characteristic curve of 0.69 (95% CI, 0.56-0.81). HEARTBiT's diagnostic performance compares favourably to the only currently approved minimally invasive diagnostic test to rule out ACR, AlloMap (CareDx, Brisbane, CA) and may be used to inform care decisions in the first 2 months post-transplantation, when AlloMap is not approved, and most ACR episodes occur.

Sections du résumé

BACKGROUND
Nine mRNA transcripts associated with acute cellular rejection (ACR) in previous microarray studies were ported to the clinically amenable NanoString nCounter platform. Here we report the diagnostic performance of the resulting blood test to exclude ACR in heart allograft recipients: HEARTBiT.
METHODS
Blood samples for transcriptomic profiling were collected during routine post-transplantation monitoring in 8 Canadian transplant centres participating in the Biomarkers in Transplantation initiative, a large (n = 1622) prospective observational study conducted between 2009 and 2014. All adult cardiac transplant patients were invited to participate (median age = 56 [17 to 71]). The reference standard for rejection status was histopathology grading of tissue from endomyocardial biopsy (EMB). All locally graded ISHLT ≥ 2R rejection samples were selected for analysis (n = 36). ISHLT 1R (n = 38) and 0R (n = 86) samples were randomly selected to create a cohort approximately matched for site, age, sex, and days post-transplantation, with a focus on early time points (median days post-transplant = 42 [7 to 506]).
RESULTS
ISHLT ≥ 2R rejection was confirmed by EMB in 18 and excluded in 92 samples in the test set. HEARTBiT achieved 47% specificity (95% confidence interval [CI], 36%-57%) given ≥ 90% sensitivity, with a corresponding area under the receiver operating characteristic curve of 0.69 (95% CI, 0.56-0.81).
CONCLUSIONS
HEARTBiT's diagnostic performance compares favourably to the only currently approved minimally invasive diagnostic test to rule out ACR, AlloMap (CareDx, Brisbane, CA) and may be used to inform care decisions in the first 2 months post-transplantation, when AlloMap is not approved, and most ACR episodes occur.

Identifiants

pubmed: 32553820
pii: S0828-282X(19)31442-4
doi: 10.1016/j.cjca.2019.11.017
pii:
doi:

Substances chimiques

RNA, Messenger 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1217-1227

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.

Auteurs

Casey P Shannon (CP)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada. Electronic address: casey.shannon@hli.ubc.ca.

Zsuzsanna Hollander (Z)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.

Darlene L Y Dai (DLY)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.

Virginia Chen (V)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.

Sara Assadian (S)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.

Karen K Lam (KK)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada; Department of Pathology, University of British Columbia, Vancouver, British Columbia, Canada.

Janet E McManus (JE)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.

Marek Zarzycki (M)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada; Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

YoungWoong Kim (Y)

Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Ji-Young V Kim (JV)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada; Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

Robert Balshaw (R)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada; Department of Statistics, University of British Columbia, Vancouver, British Columbia, Canada.

Olof Gidlöf (O)

Department of Cardiology, Skåne University Hospital, Lund University, Lund, Sweden.

Jenny Öhman (J)

Department of Cardiology, Skåne University Hospital, Lund University, Lund, Sweden.

J Gustav Smith (JG)

Department of Cardiology, Skåne University Hospital, Lund University, Lund, Sweden.

Mustafa Toma (M)

Department of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Andrew Ignaszewski (A)

Department of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Ross A Davies (RA)

Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Diego Delgado (D)

University Health Network/Mount Sinai Hospital, Toronto, Ontario, Canada.

Haissam Haddad (H)

Department of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

Debra Isaac (D)

Department of Medicine, University of Alberta, Calgary, Aberta, Canada.

Daniel Kim (D)

Department of Medicine, University of Alberta, Calgary, Aberta, Canada.

Alice Mui (A)

Department of Surgery, University of British Columbia, Vancouver, British Columbia, Canada.

Miroslaw Rajda (M)

Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.

Lori West (L)

Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.

Michel White (M)

Institut de Cardiologie de Montréal, Montréal, Québec, Canada.

Shelley Zieroth (S)

Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Scott J Tebbutt (SJ)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada; Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Paul A Keown (PA)

Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

W Robert McMaster (WR)

Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

Raymond T Ng (RT)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada; Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada; Department of Computer Science, University of British Columbia, Vancouver, British Columbia, Canada.

Bruce M McManus (BM)

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada; Department of Pathology, University of British Columbia, Vancouver, British Columbia, Canada. Electronic address: bruce.mcmanus@hli.ubc.ca.

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