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Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction

Pulmonary arterial hypertension (PAH) is a life-threatening condition, characterized by an imbalance of vasoactive substances and remodeling of pulmonary vasculature. Nitric oxide, formed from l-arginine, is essential for homeostasis and smooth muscle cell relaxation in PAH. Our aim was to compare p...

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Autores principales: Sandqvist, Anna, Schneede, Jörn, Kylhammar, David, Henrohn, Dan, Lundgren, Jakob, Hedeland, Mikael, Bondesson, Ulf, Rådegran, Göran, Wikström, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847178/
https://www.ncbi.nlm.nih.gov/pubmed/28975394
http://dx.doi.org/10.1007/s00380-017-1055-7
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author Sandqvist, Anna
Schneede, Jörn
Kylhammar, David
Henrohn, Dan
Lundgren, Jakob
Hedeland, Mikael
Bondesson, Ulf
Rådegran, Göran
Wikström, Gerhard
author_facet Sandqvist, Anna
Schneede, Jörn
Kylhammar, David
Henrohn, Dan
Lundgren, Jakob
Hedeland, Mikael
Bondesson, Ulf
Rådegran, Göran
Wikström, Gerhard
author_sort Sandqvist, Anna
collection PubMed
description Pulmonary arterial hypertension (PAH) is a life-threatening condition, characterized by an imbalance of vasoactive substances and remodeling of pulmonary vasculature. Nitric oxide, formed from l-arginine, is essential for homeostasis and smooth muscle cell relaxation in PAH. Our aim was to compare plasma concentrations of l-arginine, asymmetric dimethylarginine (ADMA), and symmetric dimethylarginine (SDMA) in PAH compared to left ventricular systolic dysfunction (LVSD) and healthy subjects. This was an observational, multicenter study comparing 21 patients with PAH to 14 patients with LVSD and 27 healthy subjects. Physical examinations were obtained and blood samples were collected. Plasma levels of ADMA, SDMA, l-arginine, l-ornithine, and l-citrulline were analyzed using liquid chromatography–tandem mass spectrometry (LC–MS/MS). Plasma levels of ADMA and SDMA were higher, whereas l-arginine and l-arginine/ADMA ratio were lower in PAH patients compared to healthy subjects (p < 0.001). Patients with PAH also had lower levels of l-arginine than patients with LVSD (p < 0.05). l-Arginine correlated to 6 min walking distance (6MWD) (r (s) = 0.58, p = 0.006) and l-arginine/ADMA correlated to WHO functional class (r (s) = −0.46, p = 0.043) in PAH. In conclusion, l-arginine levels were significantly lower in treatment naïve PAH patients compared to patients with LVSD. Furthermore, l-arginine correlated with 6MWD in PAH. l-arginine may provide useful information in differentiating PAH from LVSD.
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spelling pubmed-58471782018-03-20 Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction Sandqvist, Anna Schneede, Jörn Kylhammar, David Henrohn, Dan Lundgren, Jakob Hedeland, Mikael Bondesson, Ulf Rådegran, Göran Wikström, Gerhard Heart Vessels Original Article Pulmonary arterial hypertension (PAH) is a life-threatening condition, characterized by an imbalance of vasoactive substances and remodeling of pulmonary vasculature. Nitric oxide, formed from l-arginine, is essential for homeostasis and smooth muscle cell relaxation in PAH. Our aim was to compare plasma concentrations of l-arginine, asymmetric dimethylarginine (ADMA), and symmetric dimethylarginine (SDMA) in PAH compared to left ventricular systolic dysfunction (LVSD) and healthy subjects. This was an observational, multicenter study comparing 21 patients with PAH to 14 patients with LVSD and 27 healthy subjects. Physical examinations were obtained and blood samples were collected. Plasma levels of ADMA, SDMA, l-arginine, l-ornithine, and l-citrulline were analyzed using liquid chromatography–tandem mass spectrometry (LC–MS/MS). Plasma levels of ADMA and SDMA were higher, whereas l-arginine and l-arginine/ADMA ratio were lower in PAH patients compared to healthy subjects (p < 0.001). Patients with PAH also had lower levels of l-arginine than patients with LVSD (p < 0.05). l-Arginine correlated to 6 min walking distance (6MWD) (r (s) = 0.58, p = 0.006) and l-arginine/ADMA correlated to WHO functional class (r (s) = −0.46, p = 0.043) in PAH. In conclusion, l-arginine levels were significantly lower in treatment naïve PAH patients compared to patients with LVSD. Furthermore, l-arginine correlated with 6MWD in PAH. l-arginine may provide useful information in differentiating PAH from LVSD. Springer Japan 2017-10-03 2018 /pmc/articles/PMC5847178/ /pubmed/28975394 http://dx.doi.org/10.1007/s00380-017-1055-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Sandqvist, Anna
Schneede, Jörn
Kylhammar, David
Henrohn, Dan
Lundgren, Jakob
Hedeland, Mikael
Bondesson, Ulf
Rådegran, Göran
Wikström, Gerhard
Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction
title Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction
title_full Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction
title_fullStr Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction
title_full_unstemmed Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction
title_short Plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction
title_sort plasma l-arginine levels distinguish pulmonary arterial hypertension from left ventricular systolic dysfunction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847178/
https://www.ncbi.nlm.nih.gov/pubmed/28975394
http://dx.doi.org/10.1007/s00380-017-1055-7
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