Biomedical subjects

Andreas Greiser

Publications and source records attributed to Andreas Greiser.

3 recordsLinked to original sources

PubMed2005

Improved cardiac sodium MR imaging by density-weighted phase-encoding.

PURPOSE: To show that density-weighted (DW) k-space sampling improves the quality of human cardiac sodium imaging, a novel method was implemented that combines the high signal-to-noise efficiency of three-dimensional phase-encoding with the advantageous localization performance of nonuniform sampling. A simulation demonstrates substantially reduced blood contamination in the myocardium. MATERIALS AND METHODS: At 2.0 T, DW cardiac "fast" sodium images with a voxel size of 844 microL in seven minutes and "high-resolution" scans in 30 minutes with a voxel size of 570 microL were acquired. For comparison, conventional gradient-echo imaging was also performed. RESULTS: In the DW images, a myocardial signal-to-noise ratio (SNR) of 16.0 in the left ventricle and 8.5 in the septum (N = 4) was measured. With longer experimental duration (about 30 minutes; N = 3), the image quality and the SNR could be further improved (voxel size: 570 microL; SNR: blood 16.1, septum 10.6). Compared to the gradient-echo images, the image quality was substantially improved. CONCLUSION: This new method for human cardiac sodium imaging provides high image quality combined with optimal sensitivity and thus may improve the clinical applicability of 23Na cardiac MRI.

Computer Simulation↗

PubMed2003

Chronic coronary artery stenosis induces impaired function of remote myocardium: MRI and spectroscopy study in rat.

Our purpose was to study morphological, functional, and metabolic changes induced by chronic ischemia in myocardium supplied by the stenotic vessel and in the remote area by MR techniques. A new technique of image fusion is proposed for analysis of coronary artery stenosis involving coronary MR angiography and spectroscopic imaging. Cine-MRI was performed 2 wk after induction of coronary stenosis. Global heart function and regional wall thickening were determined in 11 Wistar rats with stenosis and compared with 7 control rats. Two weeks after stenosis was induced, spin-labeling MRI for measurement of perfusion was performed in 14 isolated hearts. In eight isolated hearts with coronary stenosis, MR spectroscopy was performed, followed by angiography. 31P metabolite maps were fused with three-dimensional coronary angiograms. Induction of stenosis led to reduced segmental wall thickening (control: 75 +/- 9%, ischemic region: 9 +/- 3%, P < 0.05 vs. control) but also to impaired function of the remote region and lower cardiac output. Perfusion was reduced by 74.9 +/- 4.0% within ischemic segments compared with a septal control region. The phosphocreatine (PCr)/ATP ratio as a marker of ischemia was reduced in the region associated with stenosis (1.09 +/- 0.09) compared with remote (1.27 +/- 0.08) and control hearts (1.43 +/- 0.08; P < 0.05). The histological fraction of fibrosis within the ischemic region (12.8 +/- 1.4%) correlated to ATP signal reduction from remote to the ischemic region (r = 0.71, P < 0.05), but not to reduced wall thickening. Coronary narrowing caused declining function accompanied by diminished PCr/ATP, indicating impaired energy metabolism. Neither decline of function nor PCr signal decline correlated to fraction of fibrosis in histology. In contrast, reduction of ATP correlated to fibrosis and therefore to loss of viability. Impaired function within the ischemic region is associated with decreased PCr. Function of the remote region was affected as well. The fusion of PCr metabolite maps and the coronary angiogram may help to assess coronary morphology and resulting metabolic changes simultaneously.

Animals↗

PubMed2003

Efficient k-space sampling by density-weighted phase-encoding.

Acquisition-weighting improves the localization of MRI experiments. An approach to acquisition-weighting in a purely phase-encoded experiment is presented that is based on a variation of the sampling density in k-space. In contrast to conventional imaging or to accumulation-weighting, where k-space is sampled with uniform increments, density-weighting varies the distance between neighboring sampling points Deltak to approximate a given radial weighting function. A fast, noniterative algorithm has been developed to calculate the sampling matrix in one, two, and three dimensions from a radial weighting function w(k), the desired number of scans NA(tot) and the nominal spatial resolution Deltax(nom). Density-weighted phase-encoding combines the improved shape of the spatial response function and the high SNR of acquisition-weighting with an extended field of view. The artifact energy that results from aliasing due to a small field of view is substantially reduced. The properties of density-weighting are compared to uniform and to accumulation-weighted phase-encoding in simulations and experiments. Density-weighted (31)P 3D chemical shift imaging of the human heart is shown which demonstrates the superior performance of density-weighted metabolic imaging.

Heart↗