Biomedical subjects

Steven M Conolly

Publications and source records attributed to Steven M Conolly.

6 recordsLinked to original sources

PubMed2005

Echo time optimization for linear combination myelin imaging.

A 3-echo linear combination myelin imaging method is presented. The echo times and weights are chosen such that the signal-to-noise ratio (SNR) of myelin-water is maximized, and signals from other white matter components are sufficiently suppressed. Interfering tissue water and cerebrospinal fluid (CSF) signals are much stronger than myelin due to their longer T2 and abundance. By carefully optimizing the echo times a 50-fold tissue water suppression is achieved along with a 10-fold CSF suppression. For comparison 4, 5, and 32 echo filters are also designed using the same method. The SNR efficiency of these filters is very similar. The 3-echo filter design was validated by phantom scans. In addition, multislice in vivo myelin images were acquired from both a healthy volunteer and a multiple sclerosis patient. Total scan time was 5 min. A uniform T2 filter is also designed to pass all white matter species with uniform gain. The myelin-water fraction of the in vivo 3-echo data set is then measured by dividing the myelin image by the uniformly filtered image. Obtained myelin-water fractions compare well with previous work.

Algorithms↗

PubMed2005

Positive contrast magnetic resonance imaging of cells labeled with magnetic nanoparticles.

Contrast agents incorporating superparamagnetic iron-oxide nanoparticles have shown promise as a means to visualize labeled cells using MRI. Labeled cells cause significant signal dephasing due to the magnetic field inhomogeneity induced in water molecules near the cell. With the resulting signal void as the means for detection, the particles behave as a negative contrast agent, which can suffer from partial-volume effects. In this paper, a new method is described for imaging labeled cells with positive contrast. Spectrally selective RF pulses are used to excite and refocus the off-resonance water surrounding the labeled cells so that only the fluid and tissue immediately adjacent to the labeled cells are visible in the image. Phantom, in vitro, and in vivo experiments show the feasibility of the new method. A significant linear correlation (r = 0.87, P < 0.005) between the estimated number of cells and the signal was observed.

Animals↗

PubMed2004

Time-optimal multidimensional gradient waveform design for rapid imaging.

Magnetic resonance imaging (MRI) is limited in many cases by long scan times and low spatial resolution. Recent advances in gradient systems hardware allow very rapid imaging sequences, such as steady-state free precession (SSFP), which has repetition times (TRs) of 2-5 ms. The design of these rapid sequences demands time-optimal preparatory gradient waveforms to provide maximum readout duty-cycle, and preserve spatial resolution and SNR while keeping TRs low. Time-optimal gradient waveforms can be synthesized analytically for certain simple cases. However, certain problems, such as time-optimal 2D and 3D gradient design with moment constraints, either may not have a solution or must be solved numerically. We show that time-optimal gradient design is a convex-optimization problem, for which very efficient solution methods exist. These methods can be applied to solve gradient design problems for oblique gradient design, spiral imaging, and flow-encoding using either a constant slew rate or the more exact voltage-limited gradient models. Ultimately, these methods provide a time-optimal solution to many 2D and 3D gradient design problems in a sufficiently short time for interactive imaging.

Magnetic Resonance Imaging↗

PubMed2004

Variable-rate selective excitation for rapid MRI sequences.

Balanced steady-state free precession (SSFP) imaging sequences require short repetition times (TRs) to avoid off-resonance artifacts. The use of slab-selective excitations is common, as this can improve imaging speed by limiting the field of view (FOV). However, the necessarily short-duration excitations have poor slab profiles. This results in unusable slices at the slab edge due to significant flip-angle variations or aliasing in the slab direction. Variable-rate selective excitation (VERSE) is a technique by which a time-varying gradient waveform is combined with a modified RF waveform to provide the same excitation profile with different RF power and duration characteristics. With the use of VERSE, it is possible to design short-duration pulses with dramatically improved slab profiles. These pulses achieve high flip angles with only minor off-resonance sensitivity, while meeting SAR limits at 1.5 T. The improved slab profiles will enable more rapid 3D imaging of limited volumes, with more consistent image contrast across the excited slab.

Computer Simulation↗

PubMed2004

Shim design using a linear programming algorithm.

The advent of open magnetic resonance imaging (MRI) scanners and dedicated MRI scanners tailored to specific body parts has led to an increasing number of noncylindrical MRI scanner geometries, for which noncylindrical gradients and shims are needed. These new scanner geometries are driving the need for fast, flexible shim design methods that can design shim coils for any geometry. A linear programming (LP) algorithm was developed to design minimum-power resistive shim coils on an arbitrary surface. These coils can be designed to produce any order shim field over an arbitrarily shaped target region, which can be placed anywhere within the coil. The resulting designs are relatively sparse and can be readily constructed. This algorithm was used to design and construct a seven-coil cylindrical shim set for a knee imaging magnet with a cylindrical homogeneous region. The algorithm was then used to design shim coils for a biradial head imager with an asymmetrically located spherical target region for brain imaging.

Algorithms↗

PubMed2002

Oscillating dual-equilibrium steady-state angiography.

A novel technique of generating noncontrast angiograms is presented. This method, called oscillating dual-equilibrium steady-state angiography (ODESSA), utilizes a modified steady-state free precession (SSFP) pulse sequence. The SSFP sequence is modified such that flowing material reaches a steady state which oscillates between two equilibrium values, while stationary material attains a single, nonoscillatory steady state. Subtraction of adjacent echoes results in large, uniform signal from all flowing spins and zero signal from stationary spins. Venous signal can be suppressed based on its reduced T2. ODESSA arterial signal is more than three times larger than that of traditional phase-contrast angiography (PCA) in the same scan time, and also compares favorably with other techniques of MR angiography (MRA). Pulse sequences are implemented in 2D, 3D, and volumetric-projection modes. Angiograms of the lower leg, generated in as few as 5 s, show high arterial signal-to-noise ratio (SNR) and full suppression of other tissues.

Artifacts↗