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Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model
Schistosomiasis represents one of the most devastating worm parasitosis in the world. Current diagnostic methods are insufficient to determine the infection grade and the disease related organ damage. We herein investigated whether discrimination of infection grade and its correlation to liver damag...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566647/ https://www.ncbi.nlm.nih.gov/pubmed/33060721 http://dx.doi.org/10.1038/s41598-020-74226-2 |
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author | Lindner, Tobias Stenzel, Jan Koslowski, Nicole Hohn, Alexander Glass, Änne Schwarzenböck, Sarah M. Krause, Bernd J. Vollmar, Brigitte Reisinger, Emil C. Sombetzki, Martina |
author_facet | Lindner, Tobias Stenzel, Jan Koslowski, Nicole Hohn, Alexander Glass, Änne Schwarzenböck, Sarah M. Krause, Bernd J. Vollmar, Brigitte Reisinger, Emil C. Sombetzki, Martina |
author_sort | Lindner, Tobias |
collection | PubMed |
description | Schistosomiasis represents one of the most devastating worm parasitosis in the world. Current diagnostic methods are insufficient to determine the infection grade and the disease related organ damage. We herein investigated whether discrimination of infection grade and its correlation to liver damage could be accurately performed by multimodal imaging in a mouse model of Schistosoma mansoni infection. Therefore, groups of uninfected and infected mice underwent MRI and [(18)F]FDG PET/CT imaging. Anatomical MRI images were used for liver volumetry and for quantification of hepatic granulomas. For PET/CT images a volume of interest based analyses were employed to calculate the [(18)F]FDG uptake in liver, portal vein, spleen and abdomen. Herein, we demonstrate that the combined use of [(18)F]FDG-PET/CT and MRI represents an appropriate diagnostic tool for Schistosoma mansoni infection, but fails to discriminate the infection grade and the linked organ damage. Only the splenic [(18)F]FDG uptake in the 25 cercariae group (5.68 ± 0.90%ID/cc) and 50 cercariae group (4.98 ± 1.43%ID/cc) was significantly higher compared to the control group (2.13 ± 0.69%ID/cc). Nevertheless, future multimodal imaging studies with new radiopharmaceuticals could build a highly sensitive and specific basis for the diagnosis and evaluation of organ damage of schistosomiasis. |
format | Online Article Text |
id | pubmed-7566647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75666472020-10-19 Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model Lindner, Tobias Stenzel, Jan Koslowski, Nicole Hohn, Alexander Glass, Änne Schwarzenböck, Sarah M. Krause, Bernd J. Vollmar, Brigitte Reisinger, Emil C. Sombetzki, Martina Sci Rep Article Schistosomiasis represents one of the most devastating worm parasitosis in the world. Current diagnostic methods are insufficient to determine the infection grade and the disease related organ damage. We herein investigated whether discrimination of infection grade and its correlation to liver damage could be accurately performed by multimodal imaging in a mouse model of Schistosoma mansoni infection. Therefore, groups of uninfected and infected mice underwent MRI and [(18)F]FDG PET/CT imaging. Anatomical MRI images were used for liver volumetry and for quantification of hepatic granulomas. For PET/CT images a volume of interest based analyses were employed to calculate the [(18)F]FDG uptake in liver, portal vein, spleen and abdomen. Herein, we demonstrate that the combined use of [(18)F]FDG-PET/CT and MRI represents an appropriate diagnostic tool for Schistosoma mansoni infection, but fails to discriminate the infection grade and the linked organ damage. Only the splenic [(18)F]FDG uptake in the 25 cercariae group (5.68 ± 0.90%ID/cc) and 50 cercariae group (4.98 ± 1.43%ID/cc) was significantly higher compared to the control group (2.13 ± 0.69%ID/cc). Nevertheless, future multimodal imaging studies with new radiopharmaceuticals could build a highly sensitive and specific basis for the diagnosis and evaluation of organ damage of schistosomiasis. Nature Publishing Group UK 2020-10-15 /pmc/articles/PMC7566647/ /pubmed/33060721 http://dx.doi.org/10.1038/s41598-020-74226-2 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lindner, Tobias Stenzel, Jan Koslowski, Nicole Hohn, Alexander Glass, Änne Schwarzenböck, Sarah M. Krause, Bernd J. Vollmar, Brigitte Reisinger, Emil C. Sombetzki, Martina Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model |
title | Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model |
title_full | Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model |
title_fullStr | Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model |
title_full_unstemmed | Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model |
title_short | Anatomical MRI and [(18)F]FDG PET/CT imaging of Schistosoma mansoni in a NMRI mouse model |
title_sort | anatomical mri and [(18)f]fdg pet/ct imaging of schistosoma mansoni in a nmri mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566647/ https://www.ncbi.nlm.nih.gov/pubmed/33060721 http://dx.doi.org/10.1038/s41598-020-74226-2 |
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