Proton density fat fraction and T2* mapping have been used to characterize fat tissue in the human supraclavicular fossa with the aim of detecting brown adipose tissue and its response to activation by changes of the two. However, chemical shift encoding-based water-fat separation in that region has been primarily performed in free-breathing mode. The present work reports on breathing-induced B0 fluctuations in the human supraclavicular fossa, and the severe bias introduced on both PDFF and T2* quantification, as shown with simulated B0 fluctuation effects. The effect of respiratory triggering on artefact reduction is investigated in a cohort of 13 volunteers.
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