biostudies-literature00530Johnson CPNIBIB NIH HHSNCRR NIH HHSNHLBI NIH HHS348-57https://www.ebi.ac.uk/biostudies/studies/S-EPMC3514637biostudies-literatureUnknown70(2)Time-resolved three-dimensional contrast-enhanced MR angiography often relies on view sharing of peripheral k-space data to enable acquisition of angiograms with both high spatial resolution and a rapid frame rate. It is typically assumed that k-space will be fully sampled during passage of the contrast bolus arterial phase. However, this is not the case when view sharing is incomplete, for example, at the leading edge of an enhancing vessel or if acquisition time is limited as in fluoroscopic tracking for multistation bolus chase MR angiography. Incomplete view sharing will degrade image quality, for example, by reducing vessel signal and sharpness and increasing undersampling artifacts. In this work, the evolution of angiogram quality with view sharing is quantitatively assessed in phantom experiments and in vivo contrast-enhanced MR angiography calf studies. It is demonstrated that there are multiple sets of sequence parameters that can yield a target image update time, but the choice of parameters can profoundly affect how image quality evolves with view sharing. A fundamental tradeoff between vessel signal and sharpness and its relationship to the sequence temporal footprint is investigated and discussed.Magnetic resonance in medicineBuildup of image quality in view-shared time-resolved 3D CE-MRA.PMC3514637RR018898R01 HL070620C06 RR018898R01 EB000212HL070620R56 HL070620EB000212Riederer SJYoung PMPolley TWJohnson CPGlockner JF53falseBuildup of image quality in view-shared time-resolved 3D CE-MRA.Time-resolved three-dimensional contrast-enhanced MR angiography often relies on view sharing of peripheral k-space data to enable acquisition of angiograms with both high spatial resolution and a rapid frame rate. It is typically assumed that k-space will be fully sampled during passage of the contrast bolus arterial phase. However, this is not the case when view sharing is incomplete, for example, at the leading edge of an enhancing vessel or if acquisition time is limited as in fluoroscopic tracking for multistation bolus chase MR angiography. Incomplete view sharing will degrade image quality, for example, by reducing vessel signal and sharpness and increasing undersampling artifacts. In this work, the evolution of angiogram quality with view sharing is quantitatively assessed in phantom experiments and in vivo contrast-enhanced MR angiography calf studies. It is demonstrated that there are multiple sets of sequence parameters that can yield a target image update time, but the choice of parameters can profoundly affect how image quality evolves with view sharing. A fundamental tradeoff between vessel signal and sharpness and its relationship to the sequence temporal footprint is investigated and discussed.2013-01-01T00:00:00Z2013 Aug2024-12-03T23:45:18.659Z2019-03-27T01:01:27ZS-EPMC35146372293657410.1002/mrm.24466