Nonspectroscopic magnetic resonance (MR) imaging often shows that a slice is composed of several compartments, each of which can be assumed to have a spatially homogeneous magnetic resonance spectrum, e.g., a limb composed of fat, muscle, bone marrow, and tumor. We show how to use structural information from such a nonspectroscopic image in order to increase the efficiency of subsequent localized spectroscopic measurements. Specifically, knowledge of the boundaries of N compartments makes it possible to reconstruct compartmental spectra from spectroscopic signals from an entire cross section with N or more different degrees of phase encoding. Experimental studies of a two-compartment phantom show that this method (SLIM) can be used to derive regional hydrogen spectra of a single slice from signals with as few as 2 phase-encoding steps, although Fourier transform chemical-shift imaging requires 64 steps to achieve a result of comparable accuracy. SLIM required only 16 phase-encoding steps to obtain accurate regional single slice spectra in a human limb with three compartments. Spectra of similar quality, obtained by Fourier transform chemical-shift imaging, required 256 to 1024 steps.
Brain and cerebrospinal fluid (CSF) movements are influenced by the anatomy and mechanical properties of intracranial tissues, as well as by the waveforms of driving vascular pulsations. The authors analyze these movements so that the purely hemodynamic factors are removed and the underlying mechanical couplings between brain, CSF, and the vasculature are characterized in global fashion. These measurements were used to calculate a set of impulse response functions or modulation transfer functions, characterizing global aspects of the vasculature's mechanical coupling to the intracranial tissues, the cervical CSF, and the cervical spinal cord. These functions showed that a sudden influx of blood into the head was rapidly accommodated by some type of intracranial reserve or capacity. After this initial response, an equal volume of CSF was driven through the foramen magnum over the next 200-300 ms as the intracranial reserve relaxed to its base-line state.
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