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(18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques

BACKGROUND: There is currently no consensus on the methodology for quantification of (18)F-FDG uptake in inflammation in atherosclerosis. In this study, we explore different methods for quantification of (18)F-FDG uptake in carotid atherosclerotic plaques and correlate the uptake values to histologi...

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Autores principales: Johnsrud, Kjersti, Skagen, Karolina, Seierstad, Therese, Skjelland, Mona, Russell, David, Revheim, Mona-Elisabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517604/
https://www.ncbi.nlm.nih.gov/pubmed/29209949
http://dx.doi.org/10.1007/s12350-017-1121-7
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author Johnsrud, Kjersti
Skagen, Karolina
Seierstad, Therese
Skjelland, Mona
Russell, David
Revheim, Mona-Elisabeth
author_facet Johnsrud, Kjersti
Skagen, Karolina
Seierstad, Therese
Skjelland, Mona
Russell, David
Revheim, Mona-Elisabeth
author_sort Johnsrud, Kjersti
collection PubMed
description BACKGROUND: There is currently no consensus on the methodology for quantification of (18)F-FDG uptake in inflammation in atherosclerosis. In this study, we explore different methods for quantification of (18)F-FDG uptake in carotid atherosclerotic plaques and correlate the uptake values to histological assessments of inflammation. METHODS AND RESULTS: Forty-four patients with atherosclerotic stenosis ≥70% of the internal carotid artery underwent (18)F-FDG PET/CT. Maximum standardized uptake values (SUV(max)) from all plaque-containing slices were collected. SUV(max) for the single highest and the mean of multiple slices with and without blood background correction (by subtraction (cSUV) or by division (target-to-background ratio (TBR)) were calculated. Following endarterectomy 30 plaques were assessed histologically. The length of the plaques at CT was 6-32 mm. The (18)F-FDG uptake in the plaques was 1.15-2.66 for uncorrected SUVs, 1.16-3.19 for TBRs, and 0.20-1.79 for cSUVs. There were significant correlations between the different uptake values (r = 0.57-0.99, P < 0.001). Methods with and without blood background correction showed similar, moderate correlations to the amount of inflammation assessed at histology (r = 0.44-0.59, P < 0.02). CONCLUSIONS: In large stenotic carotid plaques, (18)F-FDG uptake reflects the inflammatory status as assessed at histology. Increasing number of PET slices or background correction did not change the correlation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12350-017-1121-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-65176042019-06-05 (18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques Johnsrud, Kjersti Skagen, Karolina Seierstad, Therese Skjelland, Mona Russell, David Revheim, Mona-Elisabeth J Nucl Cardiol Original Article BACKGROUND: There is currently no consensus on the methodology for quantification of (18)F-FDG uptake in inflammation in atherosclerosis. In this study, we explore different methods for quantification of (18)F-FDG uptake in carotid atherosclerotic plaques and correlate the uptake values to histological assessments of inflammation. METHODS AND RESULTS: Forty-four patients with atherosclerotic stenosis ≥70% of the internal carotid artery underwent (18)F-FDG PET/CT. Maximum standardized uptake values (SUV(max)) from all plaque-containing slices were collected. SUV(max) for the single highest and the mean of multiple slices with and without blood background correction (by subtraction (cSUV) or by division (target-to-background ratio (TBR)) were calculated. Following endarterectomy 30 plaques were assessed histologically. The length of the plaques at CT was 6-32 mm. The (18)F-FDG uptake in the plaques was 1.15-2.66 for uncorrected SUVs, 1.16-3.19 for TBRs, and 0.20-1.79 for cSUVs. There were significant correlations between the different uptake values (r = 0.57-0.99, P < 0.001). Methods with and without blood background correction showed similar, moderate correlations to the amount of inflammation assessed at histology (r = 0.44-0.59, P < 0.02). CONCLUSIONS: In large stenotic carotid plaques, (18)F-FDG uptake reflects the inflammatory status as assessed at histology. Increasing number of PET slices or background correction did not change the correlation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12350-017-1121-7) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-12-05 2019 /pmc/articles/PMC6517604/ /pubmed/29209949 http://dx.doi.org/10.1007/s12350-017-1121-7 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
Johnsrud, Kjersti
Skagen, Karolina
Seierstad, Therese
Skjelland, Mona
Russell, David
Revheim, Mona-Elisabeth
(18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques
title (18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques
title_full (18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques
title_fullStr (18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques
title_full_unstemmed (18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques
title_short (18)F-FDG PET/CT for the quantification of inflammation in large carotid artery plaques
title_sort (18)f-fdg pet/ct for the quantification of inflammation in large carotid artery plaques
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517604/
https://www.ncbi.nlm.nih.gov/pubmed/29209949
http://dx.doi.org/10.1007/s12350-017-1121-7
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