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The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis

Previous studies on the association between cytomegalovirus (CMV) infection and cardiac allograft vasculopathy (CAV) were conducted on patients transplanted in the prevalganciclovir prophylaxis era. The aim of our study is to evaluate this relation in heart transplantation (HTx) recipients treated a...

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Autores principales: Klimczak-Tomaniak, Dominika, Roest, Stefan, Brugts, Jasper J., Caliskan, Kadir, Kardys, Isabella, Zijlstra, Felix, Constantinescu, Alina A., Voermans, Jolanda J.C., van Kampen, Jeroen J.A., Manintveld, Olivier C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306257/
https://www.ncbi.nlm.nih.gov/pubmed/31644496
http://dx.doi.org/10.1097/TP.0000000000003015
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author Klimczak-Tomaniak, Dominika
Roest, Stefan
Brugts, Jasper J.
Caliskan, Kadir
Kardys, Isabella
Zijlstra, Felix
Constantinescu, Alina A.
Voermans, Jolanda J.C.
van Kampen, Jeroen J.A.
Manintveld, Olivier C.
author_facet Klimczak-Tomaniak, Dominika
Roest, Stefan
Brugts, Jasper J.
Caliskan, Kadir
Kardys, Isabella
Zijlstra, Felix
Constantinescu, Alina A.
Voermans, Jolanda J.C.
van Kampen, Jeroen J.A.
Manintveld, Olivier C.
author_sort Klimczak-Tomaniak, Dominika
collection PubMed
description Previous studies on the association between cytomegalovirus (CMV) infection and cardiac allograft vasculopathy (CAV) were conducted on patients transplanted in the prevalganciclovir prophylaxis era. The aim of our study is to evaluate this relation in heart transplantation (HTx) recipients treated according to current prophylactic and immunosuppressive regimens. METHODS. This single-center retrospective study included all consecutive adult patients that underwent HTx between January 1, 2000, and May 31, 2018. Clinically relevant CMV infection was defined as either plasma CMV DNAemia ≥ 1000 IU/mL with/without clinical symptoms or <1000 IU/mL with symptoms. The primary endpoint was first manifestation of CAV diagnosed by coronary angiography. For statistical analysis, the cause-specific hazard regression model was applied, with clinically relevant CMV infection and any CMV infection as time-dependent variables. RESULTS. In total, 260 patients were included in the analysis. The median (interquartile range) follow-up was 7.88 (4.21–12.04) years. During the follow-up, clinically relevant CMV infection was diagnosed in 96 (37%) patients and CAV in 149 (57%) patients. In the multivariate regression analysis, independent predictors of CAV were: number of rejection episodes (cause-specific hazard ratio [95% confidence interval]: 1.18 [1.04-1.34], P = 0.01), hypertension (1.61 [1.11-2.34], P = 0.01), treatment with mycophenolate mofetil (0.68 [0.47-0.97], P = 0.03). No significant association was observed between CMV infection and CAV, except for patients who experienced a breakthrough CMV infection (n = 24) during prophylaxis (1.94 [1.11-3.40], P = 0.02). CONCLUSIONS. In the era of contemporary immunosuppression and valganciclovir prophylaxis, a significant effect of CMV infection on the risk of CAV was seen only among HTx recipients with CMV breakthrough infection.
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spelling pubmed-73062572020-07-09 The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis Klimczak-Tomaniak, Dominika Roest, Stefan Brugts, Jasper J. Caliskan, Kadir Kardys, Isabella Zijlstra, Felix Constantinescu, Alina A. Voermans, Jolanda J.C. van Kampen, Jeroen J.A. Manintveld, Olivier C. Transplantation Original Clinical Science—General Previous studies on the association between cytomegalovirus (CMV) infection and cardiac allograft vasculopathy (CAV) were conducted on patients transplanted in the prevalganciclovir prophylaxis era. The aim of our study is to evaluate this relation in heart transplantation (HTx) recipients treated according to current prophylactic and immunosuppressive regimens. METHODS. This single-center retrospective study included all consecutive adult patients that underwent HTx between January 1, 2000, and May 31, 2018. Clinically relevant CMV infection was defined as either plasma CMV DNAemia ≥ 1000 IU/mL with/without clinical symptoms or <1000 IU/mL with symptoms. The primary endpoint was first manifestation of CAV diagnosed by coronary angiography. For statistical analysis, the cause-specific hazard regression model was applied, with clinically relevant CMV infection and any CMV infection as time-dependent variables. RESULTS. In total, 260 patients were included in the analysis. The median (interquartile range) follow-up was 7.88 (4.21–12.04) years. During the follow-up, clinically relevant CMV infection was diagnosed in 96 (37%) patients and CAV in 149 (57%) patients. In the multivariate regression analysis, independent predictors of CAV were: number of rejection episodes (cause-specific hazard ratio [95% confidence interval]: 1.18 [1.04-1.34], P = 0.01), hypertension (1.61 [1.11-2.34], P = 0.01), treatment with mycophenolate mofetil (0.68 [0.47-0.97], P = 0.03). No significant association was observed between CMV infection and CAV, except for patients who experienced a breakthrough CMV infection (n = 24) during prophylaxis (1.94 [1.11-3.40], P = 0.02). CONCLUSIONS. In the era of contemporary immunosuppression and valganciclovir prophylaxis, a significant effect of CMV infection on the risk of CAV was seen only among HTx recipients with CMV breakthrough infection. Lippincott Williams & Wilkins 2019-10-21 2020-07 /pmc/articles/PMC7306257/ /pubmed/31644496 http://dx.doi.org/10.1097/TP.0000000000003015 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Clinical Science—General
Klimczak-Tomaniak, Dominika
Roest, Stefan
Brugts, Jasper J.
Caliskan, Kadir
Kardys, Isabella
Zijlstra, Felix
Constantinescu, Alina A.
Voermans, Jolanda J.C.
van Kampen, Jeroen J.A.
Manintveld, Olivier C.
The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis
title The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis
title_full The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis
title_fullStr The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis
title_full_unstemmed The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis
title_short The Association Between Cytomegalovirus Infection and Cardiac Allograft Vasculopathy in the Era of Antiviral Valganciclovir Prophylaxis
title_sort association between cytomegalovirus infection and cardiac allograft vasculopathy in the era of antiviral valganciclovir prophylaxis
topic Original Clinical Science—General
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306257/
https://www.ncbi.nlm.nih.gov/pubmed/31644496
http://dx.doi.org/10.1097/TP.0000000000003015
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