Ultrashort Echo Time T1ρ Is Sensitive to Enzymatic Degeneration of Human Menisci.

OBJECTIVE: The aim of the study was to determine whether quantitative ultrashort echo time (UTE) -T1ρ magnetic resonance (MR) measurements are sensitive to proteoglycan degradation in human menisci by trypsin digestion. METHODS: Conventional and quantitative UTE-T1ρ MR sequences were performed on 4 meniscal samples using a 3T scanner. Magnetic resonance imaging was performed before and after 4, 8, and 12 hours of trypsin solution immersion, inducing proteoglycan loss. One sample was used as a control. Digest solutions were analyzed for glycosaminoglycan (GAG) content. The UTE-T1ρ studies were analyzed for quantitative changes. RESULTS: Images showed progressive tissue swelling, fiber disorganization, and increase in signal intensity after GAG depletion. The UTE-T1ρ values tended to increase with time after trypsin treatment (P = 0.06). Cumulative GAG loss into the bath showed a trend of increased values for trypsin-treated samples (P = 0.1). CONCLUSIONS: Ultrashort echo time T1ρ measurements can noninvasively detect and quantify severity of meniscal degeneration, which has been correlated with progression of osteoarthritis.

Ultrashort TE T1ρ magic angle imaging.

An ultrashort TE T(1)ρ sequence was used to measure T(1) ρ of the goat posterior cruciate ligament (n = 1) and human Achilles tendon specimens (n = 6) at a series of angles relative to the B(0) field and spin-lock field strengths to investigate the contribution of dipole-dipole interaction to T(1)ρ relaxation. Preliminary results showed a significant magic angle effect. T(1)ρ of the posterior cruciate ligament increased from 6.9 ± 1.3 ms at 0° to 36 ± 5 ms at 55° and then gradually reduced to 12 ± 3 ms at 90°. Mean T(1)ρ of the Achilles tendon increased from 5.5 ± 2.2 ms at 0° to 40 ± 5 ms at 55°. T(1)ρ dispersion study showed a significant T(1)ρ increase from 2.3 ± 0.9 ms to 11 ± 3 ms at 0° as the spin-lock field strength increased from 150 Hz to 1 kHz, and from 30 ± 3 ms to 42 ± 4 ms at 55° as the spin-lock field strength increased from 100 to 500 Hz. These results suggest that dipolar interaction is the dominant T(1)ρ relaxation mechanism in tendons and ligaments.

Assessment of cortical bone with clinical and ultrashort echo time sequences.

We describe the use of ultrashort echo time (UTE) sequences and fast spin echo sequences to assess cortical bone using a clinical 3T scanner. Regular two- and three-dimensional UTE sequences were used to image both bound and free water in cortical bone. Adiabatic inversion recovery prepared UTE sequences were used to image water bound to the organic matrix. Two-dimensional fast spin echo sequences were used to image free water. Regular UTE sequences were used together with bicomponent analysis to measure T*2s and relative fractions of bound and free water components in cortical bone. Inversion recovery prepared UTE sequences were used to measure the T*2 of bound water. Saturation recovery UTE sequences were used to measure the T1 of bone water. Eight cadaveric human cortical bone samples and a lower leg specimen were studied. Preliminary results show two distinct components in UTE detected signal decay, a single component in inversion recovery prepared UTE detected signal decay, and a single component in saturation recovery UTE detected signal recovery. Regular UTE sequences appear to depict both bound and free water in cortical bone. Inversion recovery prepared UTE sequences appear to depict water bound to the organic matrix. Two-dimensional fast spin echo sequences appear to depict bone structure corresponding to free water in large pores.

Ultrashort echo time spectroscopic imaging (UTESI): an efficient method for quantifying bound and free water.

Biological tissues usually contain distinct water compartments with different transverse relaxation times. In this study, two-dimensional, multi-slice, ultrashort echo time spectroscopic imaging (UTESI) was used with bi-component analysis to detect bound and free water components in musculoskeletal tissues. Feasibility studies were performed using numerical simulation. Imaging was performed on bovine cortical bone, human cadaveric menisci and the Achilles' tendons of volunteers. The simulation study demonstrated that UTESI, together with bi-component analysis, could reliably quantify both T(2)* and fractions of the short and long (2)* components. The in vitro and in vivo studies each took less than 14 min. The bound water components showed a short T(2)* of ~0.3 ms for bovine bone, ~1.8 ms for meniscus and ~0.6 ms for the Achilles' tendon. The free water components showed about an order of magnitude longer T(2)* values, with ~2 ms for bovine bone, ~14 ms for meniscus and ~8 ms for the Achilles' tendon. Bound water fractions of up to ~76% for bovine bone, 50% for meniscus and ~75% for the Achilles' tendon were measured. The corresponding free water components were up to ~24% for bovine bone, 50% for meniscus and ~25% for the Achilles' tendon by volume. These results demonstrate that UTESI, combined with bi-component analysis, can quantify the bound and free water components in musculoskeletal tissues in clinically realistic times.

Direct imaging and quantification of carotid plaque calcification.

Carotid plaque calcification normally appears as a signal void with clinical MR sequences. Here, we describe the use of an adiabatic inversion recovery prepared two-dimensional ultrashort echo time sequence to image and characterize carotid plaque calcification using a clinical 3-T scanner. T(1), T 2*, and free water content were measured for seven carotid samples, and the results were compared with micro-CT imaging. Conventional gradient echo and fast spin echo images were also acquired for comparison. Correlations between T(1), T 2*, free water concentration, and mineral density were performed. There was a close correspondence between inversion recovery prepared two-dimensional ultrashort echo time morphologic and micro-CT appearances. Carotid plaque calcification varied significantly from sample to sample, with T(1) s ranging from 94 ± 19 to 328 ± 21 msec, T 2*s ranging from 0.31 ± 0.12 to 2.15 ± 0.25 msec, and free water concentration ranging from 5.7 ± 2.3% to 16.8 ± 3.4%. There was a significant positive correlation between T(1)(R = 0.709; P < 0.074), T 2* (R = 0.816; P < 0.025), and free water concentration, a negative correlation between T(1) (R = 0.773; P < 0.042), T 2* (R = 0.948; P < 0.001) and CT measured mineral density, and a negative correlation between free water concentration (R = 0.936; P < 0.002) and mineral density.

Optimizing MR signal contrast of the temporomandibular joint disk.

PURPOSE: To use a tissue specific algorithm to numerically optimize UTE sequence parameters to maximize contrast within temporomandibular joint (TMJ) donor tissue. MATERIALS AND METHODS: A TMJ specimen tissue block was sectioned in a true sagittal plane and imaged at 3 Tesla (T) using UTE pulse sequences with dual echo subtraction. The MR tissue properties (PD, T(2) , T(2) *, and T(1) ) were measured and subsequently used to calculate the optimum sequences parameters (repetition time [TR], echo time [TE], and θ). RESULTS: It was found that the main contrast available in the TMJ could be obtained from T(2) (or T(2) *) contrast. With the first echo time fixed at 8 µs and using TR = 200 ms, the optimum parameters were found to be: θ ≈ 60°, and TE2 ≈ 15 ms, when the second echo is acquired using a gradient echo and θ ≈ 120°, and TE2 ≈ 15 ms, when the second echo is acquired using a spin echo. CONCLUSION: Our results show that MR signal contrast can be optimized between tissues in a systematic manner. The MR contrast within the TMJ was successfully optimized with facile delineation between disc and soft tissues.

Magnetic resonance imaging of the temporomandibular joint disc: feasibility of novel quantitative magnetic resonance evaluation using histologic and biomechanical reference standards.

AIMS: To use the ultrashort time-to-echo magnetic resonance imaging (UTE MRI) technique to quantify short T2* properties (obtained through gradient echo) of a disc from the human temporomandibular joint (TMJ) and to corroborate regional T2* values with biomechanical properties and histologic appearance of the discal tissues. METHODS: A cadaveric human TMJ was sliced sagittally and imaged by conventional and UTE MRI techniques. The slices were then subjected to either biomechanical indentation testing or histologic evaluation, and linear regression was used for comparison to T2* maps obtained from UTE MRI data. Feasibility of in vivo UTE MRI was assessed in two human volunteers. RESULTS: The UTE MRI technique of the specimens provided images of the TMJ disc with greater signal-to-noise ratio (~3 fold) and contrast against surrounding tissues than conventional techniques. Higher T2* values correlated with lower indentation stiffness (softer) and less collagen organization as indicated by polarized light microscopy. T2* values were also obtained from the volunteers. CONCLUSION: UTE MRI facilitates quantitative characterization of TMJ discs, which may reflect structural and functional properties related to TMJ dysfunction.

Ultrashort echo time MR imaging of osteochondral junction of the knee at 3 T: identification of anatomic structures contributing to signal intensity.

PURPOSE: To image cartilage-bone interfaces in naturally occurring and experimentally prepared human cartilage-bone specimens at 3 T by using ultrashort echo time (TE) (UTE) and conventional pulse sequences to (a) determine the appearance of the signal intensity patterns and (b) identify the structures contributing to signal intensity on the UTE MR images. MATERIALS AND METHODS: This study was exempted by the institutional review board, and informed consent was not required. Five cadaveric (mean age, 86 years +/- 4) patellae were imaged by using proton density-weighted fat-suppressed (repetition time msec/TE msec, 2300/34), T1-weighted (700/10), and UTE (300/0.008, 6.6, with or without dual-inversion preparations at inversion time 1 = 135 msec and inversion time 2 = 95 msec) sequences. The UTE images were compared with proton density-weighted fat-suppressed and T1-weighted images and were evaluated by two radiologists. To identify the sources of signal on the UTE images, samples including specific combinations of tissues (uncalcified cartilage [UCC] only, calcified cartilage [CC] and subchondral bone [bone] [CC/bone], bone only; and UCC, CC, and bone [UCC/CC/bone]) were prepared and imaged by using the UTE sequence. RESULTS: On the UTE MR images, all patellar sections exhibited a high-intensity linear signal near the osteochondral junction, which was not visible on protein density-weighted fat-suppressed or T1-weighted images. In some sections, focal regions of thickened or diminished signal intensity were also found. In the prepared samples, UCC only, CC/bone, and UCC/CC/bone samples exhibited high signal intensity on the UTE images, whereas bone-only samples did not. CONCLUSION: These results show that the high signal intensity on UTE images of human articular joints originates from the CC and the deepest layer of the UCC, without a definite contribution from subchondral bone. UTE sequences may provide a way of evaluating abnormalities at or near the osteochondral junction. (c) RSNA, 2010.

Orientational analysis of the Achilles tendon and enthesis using an ultrashort echo time spectroscopic imaging sequence.

Tendons and entheses are magnetic resonance (MR) "invisible" when imaged with conventional clinical pulse sequences. When the highly ordered, collagen-rich fibers in tendons and entheses are placed at the magic angle, dipolar interactions are decreased and their T2s are often considerably increased. The bulk magnetic susceptibility of tendons and entheses also varies with orientation to B(0), leading to a direction-dependent resonance frequency shift. Ultrashort echo time (UTE) sequences with a minimum TE of 8 mus provide high signal from both tendons and entheses. The combination of a UTE sequence with an interleaved undersampled variable TE acquisition scheme provides a new approach for fast spectroscopic imaging of short T2 tissues. This UTE spectroscopic imaging (UTESI) technique provides quantitative information including T2, chemical shift and resonance frequency shift due to bulk susceptibility effect. In this article, the orientational effects on tendons and entheses were investigated using a UTESI sequence on a clinical 3-T scanner. T2 was found to increase fivefold for tendons and twofold for entheses due to the magic angle effect. A resonance frequency shift up to 1.2 ppm was observed for both tendons and entheses due to the bulk susceptibility effect when their orientation was changed from 0 degree to 90 degrees relative to B(0).

Magic angle effect in magnetic resonance imaging of the Achilles tendon and enthesis.

Collagen fibers in tendons and entheses are highly ordered. The protons within the bound water are subject to dipolar interactions whose strength depends on the orientation of the fibers to the static magnetic field B(0). Clinical pulse sequences have been employed to investigate this magic angle effect of the Achilles tendon, but only limited to imaging appearance with a signal void at many angular orientations due to its short T2. Here we investigated the magic angle effect of the Achilles tendons and entheses on a clinical 3-T scanner using clinical sequences as well as an ultrashort TE sequence with a minimal TE of 8 micros. Qualitative and quantitative investigation of the angular-dependent imaging appearance, T1 and T2* values were performed on five ankle specimens. There was a significant increase in signal intensity for all pulse sequences near the magic angle. Mean T2* for tendon increased from 1.94+/-0.28 ms at 0 degrees relative to the B(0) field to 15.25+/-2.13 ms at 55 degrees, and mean T1 increased from 598+/-37 ms at 0 degrees to 621+/-44 ms at 55 degrees. There was less magic angle effect for enthesis whose mean T2* increased from 4.12+/-0.37 ms at 0 degrees to 12.46+/-1.78 ms at 55 degrees, and mean T1 increased from 685+/-41 ms at 0 degrees to 718+/-56 ms at 55 degrees.