Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.

BACKGROUND: Although inflammation is an important feature of pulmonary arterial hypertension (PAH), the usefulness of local inflammatory markers as biomarkers for PAH is unknown. In this study, we tested whether plasma concentrations of human pentraxin 3 (PTX3), a local inflammatory marker, would be...

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Main Authors: Yuichi Tamura, Tomohiko Ono, Masataka Kuwana, Kenji Inoue, Makoto Takei, Tsunehisa Yamamoto, Takashi Kawakami, Jun Fujita, Masaharu Kataoka, Kensuke Kimura, Motoaki Sano, Hiroyuki Daida, Toru Satoh, Keiichi Fukuda
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3448700?pdf=render
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author Yuichi Tamura
Tomohiko Ono
Masataka Kuwana
Kenji Inoue
Makoto Takei
Tsunehisa Yamamoto
Takashi Kawakami
Jun Fujita
Masaharu Kataoka
Kensuke Kimura
Motoaki Sano
Hiroyuki Daida
Toru Satoh
Keiichi Fukuda
author_facet Yuichi Tamura
Tomohiko Ono
Masataka Kuwana
Kenji Inoue
Makoto Takei
Tsunehisa Yamamoto
Takashi Kawakami
Jun Fujita
Masaharu Kataoka
Kensuke Kimura
Motoaki Sano
Hiroyuki Daida
Toru Satoh
Keiichi Fukuda
author_sort Yuichi Tamura
collection DOAJ
description BACKGROUND: Although inflammation is an important feature of pulmonary arterial hypertension (PAH), the usefulness of local inflammatory markers as biomarkers for PAH is unknown. In this study, we tested whether plasma concentrations of human pentraxin 3 (PTX3), a local inflammatory marker, would be a useful biomarker for detecting PAH. METHODS: Plasma PTX3 concentrations were evaluated in 50 PAH patients (27 with idiopathic PAH, 17 with PAH associated with connective tissue disease (CTD-PAH), and six with congenital heart disease), 100 age and sex-matched healthy controls, and 34 disease-matched CTD patients without PAH. Plasma concentrations of B-type natriuretic peptide (BNP) and C-reactive protein (CRP) were also determined. RESULTS: Mean PTX3 levels were significantly higher in all PAH patients than in the healthy controls (4.40±0.37 vs. 1.94±0.09 ng/mL, respectively; P<0.001). Using a threshold level of 2.84 ng/mL, PTX3 yielded a sensitivity of 74.0% and a specificity of 84.0% for the detection of PAH. In CTD-PAH patients, mean PTX3 concentrations were significantly higher than in CTD patients without PAH (5.02±0.69 vs. 2.40±0.14 ng/mL, respectively; P<0.001). There was no significant correlation between plasma levels of PTX3 and BNP or CRP. Receiver operating characteristic (ROC) curves for screening PAH in patients with CTD revealed that PTX3 (area under the ROC curve 0.866) is superior to BNP. Using a PTX3 threshold of 2.85 ng/mL maximized true-positive and false-negative results (sensitivity 94.1%, specificity 73.5%). CONCLUSION: Plasma concentrations of PTX3 may be a better biomarker of PAH than BNP, especially in patients with CTD.
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spelling doaj.art-208b687a2afa4ecfb8aa141916f675972022-12-21T19:50:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4583410.1371/journal.pone.0045834Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.Yuichi TamuraTomohiko OnoMasataka KuwanaKenji InoueMakoto TakeiTsunehisa YamamotoTakashi KawakamiJun FujitaMasaharu KataokaKensuke KimuraMotoaki SanoHiroyuki DaidaToru SatohKeiichi FukudaBACKGROUND: Although inflammation is an important feature of pulmonary arterial hypertension (PAH), the usefulness of local inflammatory markers as biomarkers for PAH is unknown. In this study, we tested whether plasma concentrations of human pentraxin 3 (PTX3), a local inflammatory marker, would be a useful biomarker for detecting PAH. METHODS: Plasma PTX3 concentrations were evaluated in 50 PAH patients (27 with idiopathic PAH, 17 with PAH associated with connective tissue disease (CTD-PAH), and six with congenital heart disease), 100 age and sex-matched healthy controls, and 34 disease-matched CTD patients without PAH. Plasma concentrations of B-type natriuretic peptide (BNP) and C-reactive protein (CRP) were also determined. RESULTS: Mean PTX3 levels were significantly higher in all PAH patients than in the healthy controls (4.40±0.37 vs. 1.94±0.09 ng/mL, respectively; P<0.001). Using a threshold level of 2.84 ng/mL, PTX3 yielded a sensitivity of 74.0% and a specificity of 84.0% for the detection of PAH. In CTD-PAH patients, mean PTX3 concentrations were significantly higher than in CTD patients without PAH (5.02±0.69 vs. 2.40±0.14 ng/mL, respectively; P<0.001). There was no significant correlation between plasma levels of PTX3 and BNP or CRP. Receiver operating characteristic (ROC) curves for screening PAH in patients with CTD revealed that PTX3 (area under the ROC curve 0.866) is superior to BNP. Using a PTX3 threshold of 2.85 ng/mL maximized true-positive and false-negative results (sensitivity 94.1%, specificity 73.5%). CONCLUSION: Plasma concentrations of PTX3 may be a better biomarker of PAH than BNP, especially in patients with CTD.http://europepmc.org/articles/PMC3448700?pdf=render
spellingShingle Yuichi Tamura
Tomohiko Ono
Masataka Kuwana
Kenji Inoue
Makoto Takei
Tsunehisa Yamamoto
Takashi Kawakami
Jun Fujita
Masaharu Kataoka
Kensuke Kimura
Motoaki Sano
Hiroyuki Daida
Toru Satoh
Keiichi Fukuda
Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.
PLoS ONE
title Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.
title_full Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.
title_fullStr Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.
title_full_unstemmed Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.
title_short Human pentraxin 3 (PTX3) as a novel biomarker for the diagnosis of pulmonary arterial hypertension.
title_sort human pentraxin 3 ptx3 as a novel biomarker for the diagnosis of pulmonary arterial hypertension
url http://europepmc.org/articles/PMC3448700?pdf=render
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