Utility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.

<h4>Objective</h4>To investigate whether changes in the plasma level of soluble urokinase plasminogen activator receptor (suPAR) can be used to monitor tuberculosis (TB) treatment efficacy.<h4>Design</h4>This prospective cohort study included 278 patients diagnosed with activ...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Paulo Rabna, Andreas Andersen, Christian Wejse, Ines Oliveira, Victor Francisco Gomes, Maya Bonde Haaland, Peter Aaby, Jesper Eugen-Olsen
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2012
Materias:
R
Q
Acceso en línea:https://doaj.org/article/1b94c15df9c04928978ae2d95e2390e8
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:1b94c15df9c04928978ae2d95e2390e8
record_format dspace
spelling oai:doaj.org-article:1b94c15df9c04928978ae2d95e2390e82021-11-18T07:07:26ZUtility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.1932-620310.1371/journal.pone.0043933https://doaj.org/article/1b94c15df9c04928978ae2d95e2390e82012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22937128/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Objective</h4>To investigate whether changes in the plasma level of soluble urokinase plasminogen activator receptor (suPAR) can be used to monitor tuberculosis (TB) treatment efficacy.<h4>Design</h4>This prospective cohort study included 278 patients diagnosed with active pulmonary TB and followed throughout the 8-month treatment period.<h4>Results</h4>Mortality during treatment was higher in the highest inclusion quartile of suPAR (23%) compared to the lowest three quartiles (7%), the risk ratio being 3.1 (95% CI 1.65-6.07). No association between early smear conversion and subsequent mortality or inclusion suPAR was observed. After 1 and 2 months of treatment, an increase in suPAR compared to at diagnosis was associated with a Mortality Rate Ratio (MRR) of 4.5 (95%CI: 1.45-14.1) and 2.1 (95%CI 0.62-6.82), respectively, for the remaining treatment period.<h4>Conclusions</h4>The present study confirmed that elevated suPAR level at time of initiation of TB treatment is associated with increased risk of mortality. Furthermore, increased suPAR levels after one month of treatment was associated with increased risk of mortality during the remaining 7-month treatment period.Paulo RabnaAndreas AndersenChristian WejseInes OliveiraVictor Francisco GomesMaya Bonde HaalandPeter AabyJesper Eugen-OlsenPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 8, p e43933 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Paulo Rabna
Andreas Andersen
Christian Wejse
Ines Oliveira
Victor Francisco Gomes
Maya Bonde Haaland
Peter Aaby
Jesper Eugen-Olsen
Utility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.
description <h4>Objective</h4>To investigate whether changes in the plasma level of soluble urokinase plasminogen activator receptor (suPAR) can be used to monitor tuberculosis (TB) treatment efficacy.<h4>Design</h4>This prospective cohort study included 278 patients diagnosed with active pulmonary TB and followed throughout the 8-month treatment period.<h4>Results</h4>Mortality during treatment was higher in the highest inclusion quartile of suPAR (23%) compared to the lowest three quartiles (7%), the risk ratio being 3.1 (95% CI 1.65-6.07). No association between early smear conversion and subsequent mortality or inclusion suPAR was observed. After 1 and 2 months of treatment, an increase in suPAR compared to at diagnosis was associated with a Mortality Rate Ratio (MRR) of 4.5 (95%CI: 1.45-14.1) and 2.1 (95%CI 0.62-6.82), respectively, for the remaining treatment period.<h4>Conclusions</h4>The present study confirmed that elevated suPAR level at time of initiation of TB treatment is associated with increased risk of mortality. Furthermore, increased suPAR levels after one month of treatment was associated with increased risk of mortality during the remaining 7-month treatment period.
format article
author Paulo Rabna
Andreas Andersen
Christian Wejse
Ines Oliveira
Victor Francisco Gomes
Maya Bonde Haaland
Peter Aaby
Jesper Eugen-Olsen
author_facet Paulo Rabna
Andreas Andersen
Christian Wejse
Ines Oliveira
Victor Francisco Gomes
Maya Bonde Haaland
Peter Aaby
Jesper Eugen-Olsen
author_sort Paulo Rabna
title Utility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.
title_short Utility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.
title_full Utility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.
title_fullStr Utility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.
title_full_unstemmed Utility of the plasma level of suPAR in monitoring risk of mortality during TB treatment.
title_sort utility of the plasma level of supar in monitoring risk of mortality during tb treatment.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/1b94c15df9c04928978ae2d95e2390e8
work_keys_str_mv AT paulorabna utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
AT andreasandersen utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
AT christianwejse utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
AT inesoliveira utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
AT victorfranciscogomes utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
AT mayabondehaaland utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
AT peteraaby utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
AT jespereugenolsen utilityoftheplasmalevelofsuparinmonitoringriskofmortalityduringtbtreatment
_version_ 1718423902136303616