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The mineral content of bone can be determined by measuring the absorption by bone of a monochromatic, low-energy photon beam which originates in a radioactive source (iodine-125 at 27.3 kev or americium 241 at 59.6 kev). The intensity of the beam transmitted by the bone is measured by counting with a scintillation detector. Since the photon source and detector are well collimated, errors resulting from scattered radiation are reduced. From measurements of the intensity of the transmitted beam, made at intervals across the bone, the total mineral content of the bone can be determined. The results are accurate and reproducible to within about 3 percent.

Off-resonance spin locking is investigated as a low power method for achieving low field spin-lattice relaxation contrast using high field clinical MR imaging systems (e.g., 1.5 tesla). Spin-lattice relaxation times and equilibrium magnetizations in the off-resonance rotating frame (T1 rho(off), beta) were measured for tissue-mimicking phantom materials as a function of the ratio of the amplitude to the resonance offset of the spin-locking pulse (f1/delta). The phantom materials consisted of vegetable oil to simulate fat and two different gels containing 2% and 4% agar to simulate nonfatty tissues with different macromolecular compositions. These measurements were used to verify a signal strength equation for a multislice off-resonance spin-locking technique implemented on a clinical MR imaging system operating at 1.5 tesla. Although the oil showed little change in image contrast with increasing f1/delta, the two gels demonstrated a strong variation which provided improved discrimination compared to T1-weighted imaging. Off-resonance spin locking is suggested as a method for improving delineation of breast lesions and a preliminary clinical example from a patient volunteer is presented.

When constructing MR images from acquired spatial frequency data, it can be beneficial to apply a low-pass filter to remove high frequency noise from the resulting images. This amounts to attenuating high spatial frequency fluctuations that can affect detected MR signal. A study is presented of spatially filtering MR data and possible ramifications on detecting regionally specific activation signal. It is shown that absolute activation levels are strongly dependent on the parameters of the filter used in image construction and that significance of an activation signal can be enhanced through appropriate filter selection. A comparison is made between spatially filtering MR image data and applying a Gaussian convolution kernel to statistical parametric maps.

Application of two-dimensional (2D) J-resolved MR spectroscopy, fully localized in three dimensions to monitor the metabolites in human brain tumors in vivo on a whole body MR scanner is presented. A modified PRESS sequence with [90 degrees - 180 degrees - t1/2 - 180 degrees - t1/ 2-acquisition] was used for voxel localization (2D J point-resolved spectroscopy [PRESS]); chemical shift selective (CHESS) sequence was used for suppression of water. The incremental delay (t1/2) added to the intervals before and after the last slice-selective 180 degrees RF pulse allowed the monitoring of the J-evolution in a localized 2D NMR spectrum. The addition of the second frequency dimension in 2D J-resolved spectroscopy to encode the indirect spin-spin coupling allowed the visualization of lactate peaks not observed in the 1D MR spectrum because of severe overlap with lipid peaks. 2D spectra of a two-layer phantom with 100 mM alanine and corn oil and also from three patients with tumors are presented here. The 2D spectra show that the J-coupled lactate peaks could be separated even when the lipids peaks severely overlap.

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