Non-invasive quantification of acute macrophagic lung inflammation with [

Acute respiratory distress syndrome Inflammation Positron emission tomography Tissue compartment kinetic model Ventilator-induced lung injury [11C](R)-PK11195

Journal

European journal of nuclear medicine and molecular imaging
ISSN: 1619-7089
Titre abrégé: Eur J Nucl Med Mol Imaging
Pays: Germany
ID NLM: 101140988

Informations de publication

Date de publication:
06 2022
Historique:
received: 23 09 2021
accepted: 30 01 2022
pubmed: 8 2 2022
medline: 26 5 2022
entrez: 7 2 2022
Statut: ppublish

Résumé

Imaging of acute lung inflammation is pivotal to evaluate innovative ventilation strategies. We aimed to develop and validate a three-tissue compartment kinetic model (3TCM) of [ We analyzed the data of 38 positron emission tomography (PET) studies performed in 21 swine with or without experimental ARDS, receiving general anesthesia and mechanical ventilation. Model input function was a plasma, metabolite-corrected, image-derived input function measured in the main pulmonary artery. Regional lung analysis consisted in applying both the 3TCM and the two-tissue compartment model (2TCM); in each region, the best model was selected using a selection algorithm with a goodness-of-fit criterion. Regional best model binding potentials (BP The 3TCM was preferred in 142 lung regions (62%, 95% confidence interval: 56 to 69%). BP To assess the intensity and spatial distribution of acute macrophagic lung inflammation in the context of experimental ARDS with mechanical ventilation, PET quantification of [

Identifiants

pubmed: 35129652
doi: 10.1007/s00259-022-05713-z
pii: 10.1007/s00259-022-05713-z
doi:

Substances chimiques

Isoquinolines 0
PK 11195 YNF83VN1RL

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2122-2136

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Laurent Bitker (L)

Service de Médecine Intensive - Réanimation, Hôpital de La Croix Rousse, Hospices Civils de Lyon, 103 Grande Rue de la Croix Rousse, 69004, Lyon, France. laurent.bitker@chu-lyon.fr.
Univ Lyon, INSA-Lyon, Université Claude Bernard Lyon 1, UJM-Saint Etienne, CNRS, Inserm, CREATIS UMR 5220, U1294, F-69621, Villeurbanne, France. laurent.bitker@chu-lyon.fr.
Université Lyon 1 Claude Bernard, Lyon, France. laurent.bitker@chu-lyon.fr.

François Dhelft (F)

Service de Médecine Intensive - Réanimation, Hôpital de La Croix Rousse, Hospices Civils de Lyon, 103 Grande Rue de la Croix Rousse, 69004, Lyon, France.

Sophie Lancelot (S)

Université Lyon 1 Claude Bernard, Lyon, France.
CERMEP - Imagerie du Vivant, Lyon, France.
Hospices Civils de Lyon, Lyon, France.

Didier Le Bars (D)

Université Lyon 1 Claude Bernard, Lyon, France.
CERMEP - Imagerie du Vivant, Lyon, France.
Hospices Civils de Lyon, Lyon, France.

Nicolas Costes (N)

Université Lyon 1 Claude Bernard, Lyon, France.
CERMEP - Imagerie du Vivant, Lyon, France.

Nazim Benzerdjeb (N)

Centre d'Anatomie Et Cytologie Pathologique, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Lyon, France.

Maciej Orkisz (M)

Univ Lyon, INSA-Lyon, Université Claude Bernard Lyon 1, UJM-Saint Etienne, CNRS, Inserm, CREATIS UMR 5220, U1294, F-69621, Villeurbanne, France.

Jean-Christophe Richard (JC)

Service de Médecine Intensive - Réanimation, Hôpital de La Croix Rousse, Hospices Civils de Lyon, 103 Grande Rue de la Croix Rousse, 69004, Lyon, France.
Univ Lyon, INSA-Lyon, Université Claude Bernard Lyon 1, UJM-Saint Etienne, CNRS, Inserm, CREATIS UMR 5220, U1294, F-69621, Villeurbanne, France.
Université Lyon 1 Claude Bernard, Lyon, France.

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