Comparison of Static and Dynamic <sup>18</sup>F-FDG PET/CT for Quantification of Pulmonary Inflammation in Acute Lung Injury.
Where this comes from
- Record sourced from PubMed, PMID 31053684.
- Also identified by DOI 10.2967/jnumed.119.226597.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
PET imaging with <sup>18</sup>F-FDG followed by mathematic modeling of the pulmonary uptake rate (K<sub>i</sub>) is the gold standard for assessment of pulmonary inflammation in experimental studies of acute respiratory distress syndrome (ARDS). However, dynamic PET requires long imaging and allows the assessment of only 1 cranio-caudal field of view (∼15 cm). We investigated whether static <sup>18</sup>F-FDG PET/CT and analysis of SUV or standardized uptake ratios (SUR<sub>stat</sub>, uptake time-corrected ratio of <sup>18</sup>F-FDG concentration in lung tissue and blood plasma) might be an alternative to dynamic <sup>18</sup>F-FDG PET/CT and Patlak analysis for quantification of pulmonary inflammation in experimental ARDS. <b>Methods:</b> ARDS was induced by saline lung lavage followed by injurious mechanical ventilation in 14 anesthetized pigs (29.5-40.0 kg). PET/CT imaging sequences were acquired before and after 24 h of mechanical ventilation. K<sub>i</sub> and the apparent volume of distribution were calculated from dynamic <sup>18</sup>F-FDG PET/CT scans using the Patlak analysis. Static <sup>18</sup>F-FDG PET/CT scans were obtained immediately after dynamic PET/CT and used for calculations of SUV and SUR<sub>stat</sub> Mean K<sub>i</sub> values of the whole imaged field of view and of 5 ventro-dorsal lung regions were compared with corresponding SUV and SUR<sub>stat</sub> values, respectively, by means of linear regression and concordance analysis. The variability of the <sup>18</sup>F-FDG concentration in blood plasma (arterial input function) was analyzed. <b>Results:</b> Both for the whole imaged field of view and ventro-dorsal subregions, K<sub>i</sub> was linearly correlated with SUR<sub>stat</sub> (<i>r</i><sup>2</sup> ≥ 0.84), whereas K<sub>i</sub>-SUV correlations were worse (<i>r</i><sup>2</sup> ≤ 0.75). The arterial input function exhibited an essentially invariant shape across all animals and time points and can be described by an inverse power law. Compared with K<sub>i</sub>, SUR<sub>stat</sub> and SUV tracked the same direction of change in regional lung inflammation in 98.6% and 84.3% of measurements, respectively. <b>Conclusion:</b> The K<sub>i</sub>-SUR<sub>stat</sub> correlations were considerably stronger than the K<sub>i</sub>-SUV correlations. The good K<sub>i</sub>-SUR<sub>stat</sub> correlations suggest that static <sup>18</sup>F-FDG PET/CT and SUR<sub>stat</sub> analysis provides an alternative to dynamic <sup>18</sup>F-FDG PET/CT and Patlak analysis, allowing the assessment of inflammation of whole lungs, repeated measurements within the period of <sup>18</sup>F-FDG decay, and faster data acquisition.
Medical subject headings
- Acute Lung Injury
- Fluorodeoxyglucose F18
- Pneumonia
- Positron Emission Tomography Computed Tomography