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The clinical value of biomarkers in respiratory complications in hematopoietic SCT

To determine the role of biomarkers in the clinical management of respiratory complications (RC) in hematopoietic stem cell transplantation (HSCT) recipients, we have prospectively evaluated a cohort of 175 patients followed-up for 1 year after HSCT. To avoid misinterpretation, we have excluded both...

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Autores principales: Lucena, C M, Rovira, M, Gabarrús, A, Filella, X, Martínez, C, Domingo, R, Torres, A, Agustí, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094688/
https://www.ncbi.nlm.nih.gov/pubmed/27797370
http://dx.doi.org/10.1038/bmt.2016.280
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author Lucena, C M
Rovira, M
Gabarrús, A
Filella, X
Martínez, C
Domingo, R
Torres, A
Agustí, C
author_facet Lucena, C M
Rovira, M
Gabarrús, A
Filella, X
Martínez, C
Domingo, R
Torres, A
Agustí, C
author_sort Lucena, C M
collection PubMed
description To determine the role of biomarkers in the clinical management of respiratory complications (RC) in hematopoietic stem cell transplantation (HSCT) recipients, we have prospectively evaluated a cohort of 175 patients followed-up for 1 year after HSCT. To avoid misinterpretation, we have excluded both unidentified respiratory infections (RI) and mixed RI. A total of 64 RC were included. Plasma levels of C-reactive protein (CRP), procalcitonin (PCT) and proadrenomedullin (proADM) were measured at diagnosis and on day 3 and 7. Different cytokines were evaluated in serum on the first day. No HSCT recipients without RC were included as a control group. Compared with RI, non-infectious RC showed a significant increase in CRP, proADM and interleukin 6 on day 0 (P=0.005; P=0.03 and P=0.04, respectively). When only RI were considered, we observed that bacterial–fungal PI showed higher levels of CRP (P=0.02), PCT (P=0.04) and proADM (P<0.01). Persistent low levels of proADM biomarkers suggest viral infection (specificity and positive predictive value 100%). Patients dying of RC had PCT and proADM levels higher than survivors (P=0.002 and P=0.03, respectively). In HSCT recipients biomarkers increase in both infectious and non-infectious RC. They may have utility in the assessment of the severity of RC and in suspecting a viral etiology. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/bmt.2016.280) contains supplementary material, which is available to authorized users.
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spelling pubmed-70946882020-03-26 The clinical value of biomarkers in respiratory complications in hematopoietic SCT Lucena, C M Rovira, M Gabarrús, A Filella, X Martínez, C Domingo, R Torres, A Agustí, C Bone Marrow Transplant Article To determine the role of biomarkers in the clinical management of respiratory complications (RC) in hematopoietic stem cell transplantation (HSCT) recipients, we have prospectively evaluated a cohort of 175 patients followed-up for 1 year after HSCT. To avoid misinterpretation, we have excluded both unidentified respiratory infections (RI) and mixed RI. A total of 64 RC were included. Plasma levels of C-reactive protein (CRP), procalcitonin (PCT) and proadrenomedullin (proADM) were measured at diagnosis and on day 3 and 7. Different cytokines were evaluated in serum on the first day. No HSCT recipients without RC were included as a control group. Compared with RI, non-infectious RC showed a significant increase in CRP, proADM and interleukin 6 on day 0 (P=0.005; P=0.03 and P=0.04, respectively). When only RI were considered, we observed that bacterial–fungal PI showed higher levels of CRP (P=0.02), PCT (P=0.04) and proADM (P<0.01). Persistent low levels of proADM biomarkers suggest viral infection (specificity and positive predictive value 100%). Patients dying of RC had PCT and proADM levels higher than survivors (P=0.002 and P=0.03, respectively). In HSCT recipients biomarkers increase in both infectious and non-infectious RC. They may have utility in the assessment of the severity of RC and in suspecting a viral etiology. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/bmt.2016.280) contains supplementary material, which is available to authorized users. Nature Publishing Group UK 2016-10-31 2017 /pmc/articles/PMC7094688/ /pubmed/27797370 http://dx.doi.org/10.1038/bmt.2016.280 Text en © Macmillan Publishers Limited, part of Springer Nature. 2017 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Lucena, C M
Rovira, M
Gabarrús, A
Filella, X
Martínez, C
Domingo, R
Torres, A
Agustí, C
The clinical value of biomarkers in respiratory complications in hematopoietic SCT
title The clinical value of biomarkers in respiratory complications in hematopoietic SCT
title_full The clinical value of biomarkers in respiratory complications in hematopoietic SCT
title_fullStr The clinical value of biomarkers in respiratory complications in hematopoietic SCT
title_full_unstemmed The clinical value of biomarkers in respiratory complications in hematopoietic SCT
title_short The clinical value of biomarkers in respiratory complications in hematopoietic SCT
title_sort clinical value of biomarkers in respiratory complications in hematopoietic sct
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094688/
https://www.ncbi.nlm.nih.gov/pubmed/27797370
http://dx.doi.org/10.1038/bmt.2016.280
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