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Taylor, Y.

Publications and source records attributed to Taylor, Y..

2 recordsLinked to original sources

Sensitivity analysis of models of gas exchange for lung hyperpolarised 129-Xe MRS and MRI.

PurposeSensitivity analysis enables the identification of influential parameters and the optimisation of model composition. Such methods have not previously been applied systematically to models describing hyperpolarised 129Xe gas exchange in the lung. Here, we evaluate current 129Xe gas exchange models to assess their precision for identifying alterations in pulmonary-vascular function and lung microstructure. MethodsWe assess sensitivity using established univariate methods and scatter plots for parameter interactions. We apply them to the model described by Patz and MOXE et al., examining their ability to measure: i) importance (rank), ii) temporal dependence, and iii) interaction effects of each parameter across healthy and diseased ranges. ResultsThe univariate methods and scatter plot analyses demonstrate consistently similar results for the importance of parameters common to both models evaluated. Alveolar surface area to volume ratio is identified as the parameter to which model signals are most sensitive. The alveolar-capillary barrier thickness is identified as a low-sensitivity parameter for the MOXE model. An acquisition window of at least 200 ms effectively demonstrates model sensitivity to most parameters. Scatter plots reveal interaction effects in both models, impacting output variability and sensitivity. ConclusionOur sensitivity analysis ranks the parameters within the model described by Patz et al and within the MOXE model. The MOXE model shows low sensitivity to alveolar-capillary barrier thickness, highlighting the need for designing acquisition protocols optimised for the measurement of this parameter. The presence of parameter interaction effects highlights the requirement for care in interpreting model outputs.

bioengineering↗

Dynamic oxygen-enhanced MRI of the lung at 3 T: feasibility, repeatability and reproducibility

PurposeDynamic T1-weighted lung oxygen enhanced MRI (OE-MRI) is challenging at 3 T due to decreased longitudinal relaxivity of oxygen and increased magnetic susceptibility difference between air and tissue interfaces relative to 1.5 T, leading to poor signal quality. In this work, we evaluate the robustness of an alternative T2*-sensitised lung dynamic OE-MRI protocol in humans at 3 T. MethodsSimulations were performed to predict OE contrast behaviour and optimise the MRI protocol. Sixteen healthy subjects underwent dynamic free-breathing OE-MRI acquisitions using a dual echo RF-spoiled gradient echo acquisition at 3 T on two MRI scanners at different institutions. Non-linear registration and tissue density variation correction were applied. Percent signal enhancement (PSE) maps and {Delta}R2* were derived. Intra-class correlation coefficient (ICC) and Bland-Altman analyses were used to evaluate reproducibility of the OE indices across two sites and vendors as well as scan-rescan repeatability. ResultsSimulations and experimental data show negative contrast on oxygen inhalation due to substantial dominance of {Delta}R2* at TE longer than 0.2 ms when using our chosen flip angle and TR. Mean PSE values were TE dependent and mean {Delta}R2* was 0.14 ms-1 {+/-} 0.03 ms-1, ICC values for intra-scanner (ICCintra) and inter-scanner (ICCinter) variability for OE indices were high (ICCintra > 0.74; ICCinter = 0.70) and 95% limits of agreement showed strong agreement of repeated measures. ConclusionOur results demonstrate excellent scan-rescan repeatability for the PSE indices and good reproducibility for {Delta}R2* across two sites and vendors, suggesting potential utility in multi-centre clinical studies.

biophysics↗