Cargando…

(18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study

The past decade has seen increased application of 18-flurodeoxyglucose positron emission tomography ((18)FDG-PET) imaging to help diagnose and monitor disease, particularly in oncology, vasculitis and atherosclerosis. Disordered glycolytic metabolism and infiltration of plexiform lesions by inflamma...

Descripción completa

Detalles Bibliográficos
Autores principales: Hagan, Guy, Southwood, Mark, Treacy, Carmen, Ross, Robert MacKenzie, Soon, Elaine, Coulson, James, Sheares, Karen, Screaton, Nicholas, Pepke-Zaba, Joanna, Morrell, Nicholas W., Rudd, James H.F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329074/
https://www.ncbi.nlm.nih.gov/pubmed/22530099
http://dx.doi.org/10.4103/2045-8932.93543
_version_ 1782229816810930176
author Hagan, Guy
Southwood, Mark
Treacy, Carmen
Ross, Robert MacKenzie
Soon, Elaine
Coulson, James
Sheares, Karen
Screaton, Nicholas
Pepke-Zaba, Joanna
Morrell, Nicholas W.
Rudd, James H.F.
author_facet Hagan, Guy
Southwood, Mark
Treacy, Carmen
Ross, Robert MacKenzie
Soon, Elaine
Coulson, James
Sheares, Karen
Screaton, Nicholas
Pepke-Zaba, Joanna
Morrell, Nicholas W.
Rudd, James H.F.
author_sort Hagan, Guy
collection PubMed
description The past decade has seen increased application of 18-flurodeoxyglucose positron emission tomography ((18)FDG-PET) imaging to help diagnose and monitor disease, particularly in oncology, vasculitis and atherosclerosis. Disordered glycolytic metabolism and infiltration of plexiform lesions by inflammatory cells has been described in idiopathic pulmonary arterial hypertension (IPAH). We hypothesized that increased (18)FDG uptake may be present in the lungs, large pulmonary arteries and right ventricle of patients with pulmonary hypertension, and that this uptake would be related to markers of immune activation. We imaged the thorax of 14 patients with pulmonary hypertension (idiopathic and chronic thromboembolic) and six controls by (18)FDG-PET/computed tomography (CT) and measured uptake in the lung parenchyma, large pulmonary arteries and right ventricle. (18)FDG uptake in the lungs and pulmonary arteries was normalized for venous blood activity to give a target-to-background ratio (TBR). Blood was contemporaneously drawn for high-sensitivity CRP - C-reactive protein (CRP) (hsCRP), N-Terminal Probrain natriuteric peptide (NT-ProBNP) and other inflammatory cytokines. IPAH patients had significantly higher lung parenchymal TBR (P=0.034) and right ventricle FDG uptake (P=0.007) than controls. Uptake in the main pulmonary arteries was similar in chronic thromboembolic pulmonary hypertension, IPAH and controls. There were no correlations between (18)FDG uptake and hsCRP or inflammatory cytokine levels. NT-ProBNP correlated with RV uptake in those with pulmonary hypertension (r=0.55, P=0.04). In this pilot study, we found increased (18)FDG uptake in the lung parenchyma and right ventricle of subjects with IPAH. The lung uptake might be useful as a surrogate marker of increased cellular metabolism and immune activation as underlying mechanisms in this disease. Further evaluation of the impact of targeted therapies in treatment-naïve patients and the significance of right ventricular uptake is suggested.
format Online
Article
Text
id pubmed-3329074
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-33290742012-04-23 (18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study Hagan, Guy Southwood, Mark Treacy, Carmen Ross, Robert MacKenzie Soon, Elaine Coulson, James Sheares, Karen Screaton, Nicholas Pepke-Zaba, Joanna Morrell, Nicholas W. Rudd, James H.F. Pulm Circ Research Article The past decade has seen increased application of 18-flurodeoxyglucose positron emission tomography ((18)FDG-PET) imaging to help diagnose and monitor disease, particularly in oncology, vasculitis and atherosclerosis. Disordered glycolytic metabolism and infiltration of plexiform lesions by inflammatory cells has been described in idiopathic pulmonary arterial hypertension (IPAH). We hypothesized that increased (18)FDG uptake may be present in the lungs, large pulmonary arteries and right ventricle of patients with pulmonary hypertension, and that this uptake would be related to markers of immune activation. We imaged the thorax of 14 patients with pulmonary hypertension (idiopathic and chronic thromboembolic) and six controls by (18)FDG-PET/computed tomography (CT) and measured uptake in the lung parenchyma, large pulmonary arteries and right ventricle. (18)FDG uptake in the lungs and pulmonary arteries was normalized for venous blood activity to give a target-to-background ratio (TBR). Blood was contemporaneously drawn for high-sensitivity CRP - C-reactive protein (CRP) (hsCRP), N-Terminal Probrain natriuteric peptide (NT-ProBNP) and other inflammatory cytokines. IPAH patients had significantly higher lung parenchymal TBR (P=0.034) and right ventricle FDG uptake (P=0.007) than controls. Uptake in the main pulmonary arteries was similar in chronic thromboembolic pulmonary hypertension, IPAH and controls. There were no correlations between (18)FDG uptake and hsCRP or inflammatory cytokine levels. NT-ProBNP correlated with RV uptake in those with pulmonary hypertension (r=0.55, P=0.04). In this pilot study, we found increased (18)FDG uptake in the lung parenchyma and right ventricle of subjects with IPAH. The lung uptake might be useful as a surrogate marker of increased cellular metabolism and immune activation as underlying mechanisms in this disease. Further evaluation of the impact of targeted therapies in treatment-naïve patients and the significance of right ventricular uptake is suggested. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3329074/ /pubmed/22530099 http://dx.doi.org/10.4103/2045-8932.93543 Text en Copyright: © Pulmonary Circulation http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hagan, Guy
Southwood, Mark
Treacy, Carmen
Ross, Robert MacKenzie
Soon, Elaine
Coulson, James
Sheares, Karen
Screaton, Nicholas
Pepke-Zaba, Joanna
Morrell, Nicholas W.
Rudd, James H.F.
(18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study
title (18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study
title_full (18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study
title_fullStr (18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study
title_full_unstemmed (18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study
title_short (18)FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study
title_sort (18)fdg pet imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: a proof-of-principle study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329074/
https://www.ncbi.nlm.nih.gov/pubmed/22530099
http://dx.doi.org/10.4103/2045-8932.93543
work_keys_str_mv AT haganguy 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT southwoodmark 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT treacycarmen 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT rossrobertmackenzie 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT soonelaine 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT coulsonjames 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT sheareskaren 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT screatonnicholas 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT pepkezabajoanna 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT morrellnicholasw 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy
AT ruddjameshf 18fdgpetimagingcanquantifyincreasedcellularmetabolisminpulmonaryarterialhypertensionaproofofprinciplestudy