Clinical predictors of progression and clearance of low-level CMV DNAemia in solid organ transplant recipients.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 17 04 2019
revised: 10 06 2019
accepted: 04 10 2019
pubmed: 5 11 2019
medline: 3 10 2020
entrez: 3 11 2019
Statut: ppublish

Résumé

Low-level CMV DNAemia is common and in the absence of treatment may either progress to higher viral loads that require therapy, or may spontaneously resolve. The clinical predictors of progression and spontaneous viral clearance are not well defined. We performed a retrospective cohort study of organ transplant recipients who had untreated low-level CMV DNAemia (<1000 IU/mL). Outcomes were evaluated for 8 weeks after initial viral detection, and progression to CMV high viral load was defined as CMV viral load ≥1000 IU/mL. CMV DNAemia doubling time was calculated for a subset of patients with sufficient viral load timepoints. Of the 297 patients analyzed, 118/297 (39.7%) patients progressed to a high viral load and the remaining cleared DNAemia spontaneously (46.8%) or remained at low level (13.4%). In multivariate analysis, progression was significantly more likely in lung transplant recipients (odds ratio 3.09) and less likely in those with an episode of previously treated CMV infection (odds ratio 0.081). In a subset of 27 patients with progression, the doubling time for CMV DNAemia was a median of 6.1 days (range 2.4-21.8). We found that previous CMV infection significantly decreased the likelihood of low-level DNAemia progression suggesting that CMV immunity plays a role in progression vs spontaneous clearance.

Sections du résumé

BACKGROUND BACKGROUND
Low-level CMV DNAemia is common and in the absence of treatment may either progress to higher viral loads that require therapy, or may spontaneously resolve. The clinical predictors of progression and spontaneous viral clearance are not well defined.
METHODS METHODS
We performed a retrospective cohort study of organ transplant recipients who had untreated low-level CMV DNAemia (<1000 IU/mL). Outcomes were evaluated for 8 weeks after initial viral detection, and progression to CMV high viral load was defined as CMV viral load ≥1000 IU/mL. CMV DNAemia doubling time was calculated for a subset of patients with sufficient viral load timepoints.
RESULTS RESULTS
Of the 297 patients analyzed, 118/297 (39.7%) patients progressed to a high viral load and the remaining cleared DNAemia spontaneously (46.8%) or remained at low level (13.4%). In multivariate analysis, progression was significantly more likely in lung transplant recipients (odds ratio 3.09) and less likely in those with an episode of previously treated CMV infection (odds ratio 0.081). In a subset of 27 patients with progression, the doubling time for CMV DNAemia was a median of 6.1 days (range 2.4-21.8).
CONCLUSION CONCLUSIONS
We found that previous CMV infection significantly decreased the likelihood of low-level DNAemia progression suggesting that CMV immunity plays a role in progression vs spontaneous clearance.

Identifiants

pubmed: 31677321
doi: 10.1111/tid.13207
doi:

Substances chimiques

DNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13207

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

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Auteurs

Yoichiro Natori (Y)

Division of Infectious Diseases, Miami Transplant Institute, Jackson Health System, University of Miami, Miami, FL, USA.

Ali Alghamdi (A)

Division of Infectious Diseases, Miami Transplant Institute, Jackson Health System, University of Miami, Miami, FL, USA.
Division of Infectious Diseases, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Shahid Husain (S)

Multi Organ Transplant Program, University Health Network, Toronto, ON, Canada.

Coleman Rotstein (C)

Multi Organ Transplant Program, University Health Network, Toronto, ON, Canada.

Nazia Selzner (N)

Multi Organ Transplant Program, University Health Network, Toronto, ON, Canada.

Jussi Tikkanen (J)

Multi Organ Transplant Program, University Health Network, Toronto, ON, Canada.

Jeffrey Schiff (J)

Multi Organ Transplant Program, University Health Network, Toronto, ON, Canada.

Atul Humar (A)

Multi Organ Transplant Program, University Health Network, Toronto, ON, Canada.

Deepali Kumar (D)

Multi Organ Transplant Program, University Health Network, Toronto, ON, Canada.

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