Evaluation of PET imaging as a tool for detecting neonatal hypoxic-ischemic encephalopathy in a preclinical animal model
| dc.contributor.author | Saha Emma | |
| dc.contributor.author | Shimochi Saeka | |
| dc.contributor.author | Keller Thomas | |
| dc.contributor.author | Eskola Olli | |
| dc.contributor.author | López-Picón Francisco | |
| dc.contributor.author | Rajander Johan | |
| dc.contributor.author | Löyttyniemi Eliisa | |
| dc.contributor.author | Forsback Sarita | |
| dc.contributor.author | Solin Olof | |
| dc.contributor.author | Grönroos Tove | |
| dc.contributor.author | Parikka Vilhelmiina | |
| dc.contributor.organization | fi=InFLAMES Lippulaiva|en=InFLAMES Flagship| | |
| dc.contributor.organization | fi=MediCity|en=MediCity| | |
| dc.contributor.organization | fi=PET-keskus|en=Turku PET Centre| | |
| dc.contributor.organization | fi=biostatistiikka|en=Biostatistics| | |
| dc.contributor.organization | fi=kemian laitos|en=Department of Chemistry| | |
| dc.contributor.organization | fi=lastentautioppi|en=Paediatrics and Adolescent Medicine| | |
| dc.contributor.organization | fi=tyks, vsshp|en=tyks, varha| | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.14646305228 | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.27622076134 | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.40612039509 | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.68445910604 | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.83772236069 | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.89365200099 | |
| dc.converis.publication-id | 182443927 | |
| dc.converis.url | https://research.utu.fi/converis/portal/Publication/182443927 | |
| dc.date.accessioned | 2025-08-28T02:37:36Z | |
| dc.date.available | 2025-08-28T02:37:36Z | |
| dc.description.abstract | <p>Hypoxic-ischemic encephalopathy due to insufficient oxygen delivery to brain tissue is a leading cause of death or severe morbidity in neonates. The early recognition of the most severely affected individuals remains a clinical challenge. We hypothesized that hypoxic-ischemic injury can be detected using PET radiotracers for hypoxia ([<sup>18</sup>F]EF5), glucose metabolism ([<sup>18</sup>F]FDG), and inflammation ([<sup>18</sup>F]F-DPA).<br></p><p>Methods</p><p>A preclinical model of neonatal hypoxic-ischemic brain injury was made in 9-d-old rat pups by permanent ligation of the left common carotid artery followed by hypoxia (8% oxygen and 92% nitrogen) for 120 min. <i>In vivo</i> PET imaging was performed immediately after injury induction or at different timepoints up to 21 d later. After imaging, <i>ex vivo</i> brain autoradiography was performed. Brain sections were stained with cresyl violet to evaluate the extent of the brain injury and to correlate it with [<sup>18</sup>F]FDG uptake.<br></p><p>Results</p><p>PET imaging revealed that all three of the radiotracers tested had significant uptake in the injured brain hemisphere. <i>Ex vivo</i> autoradiography revealed high [<sup>18</sup>F]EF5 uptake in the hypoxic hemisphere immediately after the injury (<i>P</i> < 0.0001), decreasing to baseline even 1 d postinjury. [<sup>18</sup>F]FDG uptake was highest in the injured hemisphere on the day of injury (<i>P</i> < 0.0001), whereas [<sup>18</sup>F]F-DPA uptake was evident after 4 d (<i>P</i> = 0.029), peaking 7 d postinjury (<i>P</i> < 0.0001), and remained significant 21 d after the injury. Targeted evaluation demonstrated that [<sup>18</sup>F]FDG uptake measured by <i>in vivo</i> imaging 1 d postinjury correlated positively with the brain volume loss detected 21 d later (<i>r</i> = 0.72, <i>P</i> = 0.028).<br></p><p>Conclusion</p><p>Neonatal hypoxic-ischemic brain injury can be detected using PET imaging. Different types of radiotracers illustrate distinct phases of hypoxic brain damage. PET may be a new useful technique, worthy of being explored for clinical use, to predict and evaluate the course of the injury.</p> | |
| dc.identifier.eissn | 1090-2430 | |
| dc.identifier.jour-issn | 0014-4886 | |
| dc.identifier.olddbid | 209422 | |
| dc.identifier.oldhandle | 10024/192449 | |
| dc.identifier.uri | https://www.utupub.fi/handle/11111/45460 | |
| dc.identifier.url | https://doi.org/10.1016/j.expneurol.2023.114673 | |
| dc.identifier.urn | URN:NBN:fi-fe2025082792362 | |
| dc.language.iso | en | |
| dc.okm.affiliatedauthor | Saha, Emma | |
| dc.okm.affiliatedauthor | Shimochi, Saeka | |
| dc.okm.affiliatedauthor | Keller, Tomas | |
| dc.okm.affiliatedauthor | Eskola, Olli | |
| dc.okm.affiliatedauthor | Lopez Picon, Francisco | |
| dc.okm.affiliatedauthor | Löyttyniemi, Eliisa | |
| dc.okm.affiliatedauthor | Forsback, Sarita | |
| dc.okm.affiliatedauthor | Solin, Olof | |
| dc.okm.affiliatedauthor | Grönroos, Tove | |
| dc.okm.affiliatedauthor | Parikka, Vilhelmiina | |
| dc.okm.affiliatedauthor | Dataimport, tyks, vsshp | |
| dc.okm.discipline | 3126 Surgery, anesthesiology, intensive care, radiology | en_GB |
| dc.okm.discipline | 3126 Kirurgia, anestesiologia, tehohoito, radiologia | fi_FI |
| dc.okm.internationalcopublication | not an international co-publication | |
| dc.okm.internationality | International publication | |
| dc.okm.type | A1 ScientificArticle | |
| dc.publisher | Elsevier | |
| dc.publisher.country | United States | en_GB |
| dc.publisher.country | Yhdysvallat (USA) | fi_FI |
| dc.publisher.country-code | US | |
| dc.relation.articlenumber | 114673 | |
| dc.relation.doi | 10.1016/j.expneurol.2023.114673 | |
| dc.relation.ispartofjournal | Experimental Neurology | |
| dc.relation.volume | 373 | |
| dc.source.identifier | https://www.utupub.fi/handle/10024/192449 | |
| dc.title | Evaluation of PET imaging as a tool for detecting neonatal hypoxic-ischemic encephalopathy in a preclinical animal model | |
| dc.year.issued | 2024 |
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