Relative Change in Donor-Derived Cell-free DNA is Superior to Absolute Values for Diagnosis of Acute Lung Allograft Dysfunction.


Journal

Transplantation direct
ISSN: 2373-8731
Titre abrégé: Transplant Direct
Pays: United States
ID NLM: 101651609

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 31 03 2023
accepted: 04 04 2023
medline: 30 5 2023
pubmed: 30 5 2023
entrez: 30 5 2023
Statut: epublish

Résumé

Donor-derived cell-free DNA (dd-cfDNA%) is a biomarker of early acute lung allograft dysfunction (ALAD), with a value of ≥1.0% indicating injury. Whether dd-cfDNA% is a useful biomarker in patients >2 y posttransplant is unknown. Our group previously demonstrated that median dd-cfDNA% in lung recipients ≥2 y posttransplant without ALAD was 0.45%. In that cohort, biologic variability of dd-cfDNA% was estimated by a reference change value (RCV) of 73%, suggesting that change exceeding 73% may be pathologic. In this study, we aimed to determine whether dd-cfDNA% variability or absolute thresholds are optimal for detecting ALAD. We prospectively measured plasma dd-cfDNA% every 3 to 4 mo in patients ≥2 y post-lung transplant. ALAD was defined as infection, acute cellular rejection, possible antibody-mediated rejection, or change in forced expiratory volume in 1 s >10%, and was adjudicated retrospectively. We analyzed area under the curve for RCV and absolute dd-cfDNA% and reported performance of RCV ≥73% versus absolute value >1% for discriminating ALAD. Seventy-one patients had ≥2 baseline measurements of dd-cfDNA%; 30 developed ALAD. RCV of dd-cfDNA% at ALAD had a greater area under the receiver operator characteristic curve than absolute dd-cfDNA% values (0.87 versus 0.69, Relative change in dd-cfDNA% has improved test characteristics for diagnosing ALAD compared with absolute values.

Identifiants

pubmed: 37250487
doi: 10.1097/TXD.0000000000001487
pmc: PMC10212612
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e1487

Informations de copyright

Copyright © 2023 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

A.J.T. is a scientific advisor for CareDx, Inc. A.J.T. and C.M.S. have received grant funding from CareDx, Inc. The other authors declare no conflicts of interest.

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Auteurs

Anil J Trindade (AJ)

Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Vanderbilt Transplant Center, Nashville, TN.

Kaitlyn C Chapin (KC)

Vanderbilt Transplant Center, Nashville, TN.

Jennifer N Gray (JN)

CareDx, Inc. Brisbane, CA.

Yuka Furuya (Y)

CareDx, Inc. Brisbane, CA.

Amy Mullican (A)

Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.

Haley Hoy (H)

Vanderbilt Transplant Center, Nashville, TN.

Caitlin T Demarest (CT)

Vanderbilt Transplant Center, Nashville, TN.
Department of Thoracic Surgery, Vanderbilt University Medical Center, Nashville, TN.

Ivan M Robbins (IM)

Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Vanderbilt Transplant Center, Nashville, TN.

Matthew Bacchetta (M)

Department of Thoracic Surgery, Vanderbilt University Medical Center, Nashville, TN.
Department of Cardiac Surgery, Vanderbilt University Medical Center, Nashville, TN.
Department of Biomedical Engineering, Vanderbilt University Medical Center, Nashville, TN.

David B Erasmus (DB)

Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Vanderbilt Transplant Center, Nashville, TN.

Ciara M Shaver (CM)

Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Vanderbilt Transplant Center, Nashville, TN.

Classifications MeSH