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Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome

Predicting neurological outcomes in patients with post-cardiac arrest syndrome (PCAS) is crucial for identifying those who will benefit from intensive care. We evaluated the predictive value of 18F-FDG PET. PCAS was induced in Sprague Dawley rats. Baseline and post-3-hour images were acquired. Stand...

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Autores principales: Kim, Daehee, Yoon, Hai-Jeon, Lee, Woon Jeong, Woo, Seon Hee, Kim, Bom Sahn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794298/
https://www.ncbi.nlm.nih.gov/pubmed/31616019
http://dx.doi.org/10.1038/s41598-019-51327-1
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author Kim, Daehee
Yoon, Hai-Jeon
Lee, Woon Jeong
Woo, Seon Hee
Kim, Bom Sahn
author_facet Kim, Daehee
Yoon, Hai-Jeon
Lee, Woon Jeong
Woo, Seon Hee
Kim, Bom Sahn
author_sort Kim, Daehee
collection PubMed
description Predicting neurological outcomes in patients with post-cardiac arrest syndrome (PCAS) is crucial for identifying those who will benefit from intensive care. We evaluated the predictive value of 18F-FDG PET. PCAS was induced in Sprague Dawley rats. Baseline and post-3-hour images were acquired. Standardized uptake value (SUV) changes before and after PCAS induction (SUV(delta)) and SUV ratios (SUVR) of regional SUV normalized to the whole brain SUV were obtained. The Morris water maze (MWM) test was performed after 2 weeks to evaluate neurological outcomes and rats were classified into two groups based on the result. Of 18 PCAS rats, 8 were classified into the good outcome group. The SUV(delta) of forebrain regions were significantly decreased in good outcome group (p < 0.05), while the SUV(delta) of hindbrain regions were not significantly different according to outcomes. The SUVR of forebrain regions were significantly higher and the SUVR of hindbrain regions were significantly lower in good outcome group (p < 0.05). Forebrain-to-hindbrain ratio predicted a good neurological outcome with a sensitivity of 90% and specificity of 100% using an optimal cutoff value of 1.22 (AUC 0.969, p < 0.05). These results suggest the potential utility of 18F-FDG PET in the early prediction of neurological outcomes in PCAS.
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spelling pubmed-67942982019-10-25 Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome Kim, Daehee Yoon, Hai-Jeon Lee, Woon Jeong Woo, Seon Hee Kim, Bom Sahn Sci Rep Article Predicting neurological outcomes in patients with post-cardiac arrest syndrome (PCAS) is crucial for identifying those who will benefit from intensive care. We evaluated the predictive value of 18F-FDG PET. PCAS was induced in Sprague Dawley rats. Baseline and post-3-hour images were acquired. Standardized uptake value (SUV) changes before and after PCAS induction (SUV(delta)) and SUV ratios (SUVR) of regional SUV normalized to the whole brain SUV were obtained. The Morris water maze (MWM) test was performed after 2 weeks to evaluate neurological outcomes and rats were classified into two groups based on the result. Of 18 PCAS rats, 8 were classified into the good outcome group. The SUV(delta) of forebrain regions were significantly decreased in good outcome group (p < 0.05), while the SUV(delta) of hindbrain regions were not significantly different according to outcomes. The SUVR of forebrain regions were significantly higher and the SUVR of hindbrain regions were significantly lower in good outcome group (p < 0.05). Forebrain-to-hindbrain ratio predicted a good neurological outcome with a sensitivity of 90% and specificity of 100% using an optimal cutoff value of 1.22 (AUC 0.969, p < 0.05). These results suggest the potential utility of 18F-FDG PET in the early prediction of neurological outcomes in PCAS. Nature Publishing Group UK 2019-10-15 /pmc/articles/PMC6794298/ /pubmed/31616019 http://dx.doi.org/10.1038/s41598-019-51327-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Daehee
Yoon, Hai-Jeon
Lee, Woon Jeong
Woo, Seon Hee
Kim, Bom Sahn
Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome
title Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome
title_full Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome
title_fullStr Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome
title_full_unstemmed Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome
title_short Prognostic value of (18)F-FDG brain PET as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome
title_sort prognostic value of (18)f-fdg brain pet as an early indicator of neurological outcomes in a rat model of post-cardiac arrest syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794298/
https://www.ncbi.nlm.nih.gov/pubmed/31616019
http://dx.doi.org/10.1038/s41598-019-51327-1
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