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. 2020 Sep 24;48(4):1070–1080. doi: 10.1007/s00259-020-05034-z

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© 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/.

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Fig. 3 — Quantitative analysis of [¹⁸F]Galacto-RGD uptake. Box-and-whisker plots of [¹⁸F]Galacto-RGD uptake in infarct areas of all patients, depicted as lesion/remote-ratio (A), lesion/blood-ratio (B), and lesion/liver ratio (C). In 5 patients there was clear tracer uptake visible with a lesion/blood ratio of 1 or more. In the other patients, there was only little tracer uptake, which in 3 patients was even lower than in normal myocardium. Note that lesion/liver ratios were relatively low due to physiologically pronounced liver uptake of [¹⁸F]Galacto-RGD. There was no correlation between [¹⁸F]Galacto-RGD lesion/remote-ration and infarct-to-scan time (D)