Aya Kino

Myocardial perfusion MRI with sliding-window conjugate-gradient HYPR

First‐pass perfusion MRI is a promising technique for detecting ischemic heart disease. However, the diagnostic value of the method is limited by the low spatial coverage, resolution, signal‐to‐noise ratio (SNR), and cardiac motion‐related image artifacts. In this study we investigated the feasibility of using a method that combines sliding window and CG‐HYPR methods (SW‐CG‐HYPR) to reduce the acquisition window for each slice while maintaining the temporal resolution of one frame per heartbeat in myocardial perfusion MRI. This method allows an increased number of slices, reduced motion artifacts, and preserves the relatively high SNR and spatial resolution of the “composite images.” Results from eight volunteers demonstrate the feasibility of SW‐CG‐HYPR for accelerated myocardial perfusion imaging with accurate signal intensity changes of left ventricle blood pool and myocardium. Using this method the acquisition time per cardiac cycle was reduced by a factor of 4 and the number of slices was increased from 3 to 8 as compared to the conventional technique. The SNR of the myocardium at peak enhancement with SW‐CG‐HYPR (13.83 ± 2.60) was significantly higher (P < 0.05) than the conventional turbo‐FLASH protocol (8.40 ± 1.62). Also, the spatial resolution of the myocardial perfection images was significantly improved. SW‐CG‐HYPR is a promising technique for myocardial perfusion MRI. Magn Reson Med, 2009.

Three-Dimensional Phase-Sensitive Inversion-Recovery Turbo FLASH Sequence for the Evaluation of Left Ventricular Myocardial Scar

OBJECTIVE The purpose of this study was to evaluate a new free-breathing 3D phase-sensitive inversion-recovery (PSIR) turbo FLASH pulse sequence for the detection of left ventricular myocardial scar. SUBJECTS AND METHODS Patients with suspected myocardial scar were examined on a 1.5-T MR scanner for myocardial late enhancement after the administration of gadopentetate dimeglumine using a segmented 2D PSIR turbo FLASH sequence followed by a navigator-gated 3D PSIR turbo FLASH sequence. Image quality was scored by two independent readers using a 4-point Likert scale (0 = poor, nondiagnostic; 1 = fair, diagnostics may be impaired; 2 = good, some artifacts but not interfering in diagnostics; 3 = excellent, no artifacts). Scars were compared quantitatively in volume and graded qualitatively on the basis of size (area) and location. RESULTS Thirty-three patients were scanned using both techniques. In 25 patients, the quality of the 3D PSIR images was acceptable. Scars were detected in 12 patients. Hyperenhanced scar volumes (p = 0.43), qualitative analysis of scar area (p = 0.78), and scar location (p = 0.68) were similar for both techniques. More small hyperenhanced scars, corresponding mostly to nonischemic distribution patterns, were detected using 3D PSIR than 2D PSIR. Although 2D and 3D results were found to be highly correlated for scar volume, Bland-Altman analysis indicated a systematic smaller infarct volume on the 2D PSIR scans (R(2) = 0.84). CONCLUSION Free-breathing 3D PSIR turbo FLASH imaging is a promising technique for the assessment of left ventricular scar particularly for scar quantification and the detection of small nonischemic scars in the myocardium.

Mitotically inactivated embryonic stem cells can be used as an in vivo feeder layer to nurse damaged myocardium after acute myocardial infarction: a preclinical study.

Rationale: Various types of viable stem cells have been reported to result in modest improvement in cardiac function after acute myocardial infarction. The mechanisms for improvement from different stem cell populations remain unknown. Objective: To determine whether irradiated (nonviable) embryonic stem cells (iESCs) improve postischemic cardiac function without adverse consequences. Methods and Results: After coronary artery ligation-induced cardiac infarction, either conditioned media or male murine or male human iESCs were injected into the penumbra of ischemic myocardial tissue of female mice or female rhesus macaque monkeys, respectively. Murine and human iESCs, despite irradiation doses that prevented proliferation and induced cell death, significantly improved cardiac function and decreased infarct size compared with untreated or media-treated controls. Fluorescent in situ hybridization of the Y chromosome revealed disappearance of iESCs within the myocardium, whereas 5-bromo-2′-deoxyuridine assays revealed de novo in vivo cardiomyocyte DNA synthesis. Microarray gene expression profiling demonstrated an early increase in metabolism, DNA proliferation, and chromatin remodeling pathways, and a decrease in fibrosis and inflammatory gene expression compared with media-treated controls. Conclusions: As a result of irradiation before injection, ex vivo and in vivo iESC existence is transient, yet iESCs provide a significant improvement in cardiac function after acute myocardial infarction. The mechanism(s) of action of iESCs seems to be related to cell-cell exchange, paracrine factors, and a scaffolding effect between iESCs and neighboring host cardiomyocytes.

Accelerated Two- and Three-dimensional Cine MR Imaging of the Heart by Using a 32-Channel Coil

PURPOSE To compare accelerated real-time two-dimensional (2D) and segmented three-dimensional (3D) cine steady-state free precession magnetic resonance (MR) imaging techniques by using a 32-channel coil with a conventional 2D cine imaging approach for imaging the heart and to evaluate any difference caused by free breathing and breath holding for real-time imaging. MATERIALS AND METHODS In this institutional review board-approved HIPAA-compliant study, 10 healthy volunteers and 22 consecutive patients who were suspected of having or were known to have heart disease underwent cardiac MR imaging by using a 32-channel coil. A conventional multisection 2D real-time cine sequence was used as the reference standard, and three additional accelerated cine sequences were implemented. Volumetric parameters, including ejection fraction (EF), end-diastolic volume (EDV), end-systolic volume (ESV), stroke volume(SV), and myocardial mass, were derived. Wall motion and image quality were assessed by two radiologists. In addition, image time was registered. An additional set of images was acquired by using real-time sequences with free breathing, and quantitative measurements were compared with measurements on images obtained with breath holding. For quantitative analysis, repeated-measures analysis of variance, paired t test, and Bland-Altman analysis were used; for qualitative analysis, nonparametric Wilcoxon signed-rank test was used. RESULTS All volumetric measurements were significantly correlated with those of the standard sequence (r > 0.80, P < .01). No significant difference among protocols was observed in terms of mean levels for EF or ESV (P > .05). However, a significant difference was indicated for EDV and SV (P < .01).The accelerated protocols had significantly shorter image times (P < .001). Wall motion scores were concordant with the standard sequence in 43-44 (93%-96%) segments for the accelerated protocols, with a strong interreader agreement (intraclass correlation coefficient, > or =0.93). No significant difference was identified between real-time protocols with free breathing and those with breath holding for measurement of volumetric parameters. CONCLUSION Accelerated real-time 2D and segmented 3D cine techniques are comparable to the standard clinical protocol in assessment of left ventricular global and regional parameters in substantially shorter image times.

Free‐breathing myocardial perfusion MRI using SW‐CG‐HYPR and motion correction

First‐pass perfusion MRI is a promising technique to detect ischemic heart disease. Sliding window (SW) conjugate‐gradient (CG) highly constrained back‐projection reconstruction (HYPR) (SW‐CG‐HYPR) has been proposed to increase spatial coverage, spatial resolution, and SNR. However, this method is sensitive to respiratory motion and thus requires breath‐hold. This work presents a non‐model‐based motion correction method combined with SW‐CG‐HYPR to perform free‐breathing myocardial MR imaging. Simulation studies were first performed to show the effectiveness of the proposed motion correction method and its independence from the pattern of the respiratory motion. After that, in vivo studies were performed in six healthy volunteers. From all of the volunteer studies, the image quality score of free breathing perfusion images with motion correction (3.11 ± 0.34) is improved compared with that of images without motion correction (2.27 ± 0.32), and is comparable with that of successful breath‐hold images (3.12 ± 0.38). This result was further validated by a quantitative sharpness analysis. The left ventricle and myocardium signal changes in motion corrected free‐breathing perfusion images were closely correlated to those observed in breath‐hold images. The correlation coefficient is 0.9764 for myocardial signals. Bland–Altman analysis confirmed the agreement between the free‐breathing SW‐CG‐HYPR method with motion correction and the breath‐hold SW‐CG‐HYPR. This technique may allow myocardial perfusion MRI during free breathing. Magn Reson Med, 2010.

Breathhold time-resolved three-directional MR velocity mapping of aortic flow in patients after aortic valve-sparing surgery

To evaluate the utility of breathhold time‐resolved three‐directional MR velocity mapping for quantifying the restoration of normal flow patterns in patients after aortic valve‐sparing surgery.

Analysis of the thoracic aorta using a semi-automated post processing tool

OBJECTIVE To evaluates a semi-automated method for Thoracic Aortic Aneurysm (TAA) measurement using ECG-gated Dual Source CT Angiogram (DSCTA). METHODS This retrospective HIPAA compliant study was approved by our IRB. Transaxial maximum diameters of outer wall to outer wall were studied in fifty patients at seven anatomic locations of the thoracic aorta: annulus, sinus, sinotubular junction (STJ), mid ascending aorta (MAA) at the level of right pulmonary artery, proximal aortic arch (PROX) immediately proximal to innominate artery, distal aortic arch (DIST) immediately distal to left subclavian artery, and descending aorta (DESC) at the level of diaphragm. Measurements were performed using a manual method and semi-automated software. All readers repeated their measurements. Inter-method, intra-observer and inter-observer agreements were evaluated according to intraclass correlation coefficient (ICC) and Bland-Altman plot. The number of cases with manual contouring or center line adjustment for the semi-automated method and also the post-processing time for each method were recorded. RESULTS The mean difference between semi-automated and manual methods was less than 1.3mm at all seven points. Strong inter-method, inter-observer and intra-observer agreement was recorded at all levels (ICC ≥ 0.9). The maximum rate of manual adjustment of center line and contour was at the level of annulus. The average time for manual post-processing of the aorta was 19 ± 0.3 min, while it took 8.26 ± 2.1 min to do the measurements with the semi-automated tool (Vitrea version 6.0.0.1 software). The center line was edited manually at all levels, with most corrections at the level of annulus (60%), while the contour was adjusted at all levels with highest and lowest number of corrections at the levels of annulus and DESC (75% and 0.07% of the cases), respectively. CONCLUSION Compared to the commonly used manual method, semi-automated measurement of vessel dimensions is feasible in the thoracic aorta with the advantage of reduced post-processing time.

T2 Mapping of the myocardium, a quantitative tool for assessment of myocarditis

Background To quantify myocardial T2 value in patients with myocarditis and correlate the distribution of abnormal T2 values with the extent of macroscopic late gadolinium enhancement (LGE). Methods 25 patients with myocarditis were retrospectively evaluated for the utility of T2 mapping in diagnosing myocarditis. Patients with elevated troponins, negative coronary angiogram, and atypical LGE were diagnosed as acute myocarditis. Patients with normal troponins and macroscopic LGE at the time of cardiac MRI were diagnosed as remote myocarditis. As per our institutional protocol, T2 mapping sequences were performed in all cases with suspected myocarditis in addition to standard LGE images on 1.5 T scanner (Magnetom Aera and Avanto, Siemens medical solutions). T2 mapping was performed on three short axis images (base, mid chamber, and apex), yielding 16 myocardial segments for analysis (AHA segments). Single 4 chamber view image was obtained in addition. Minimum, peak and mean segmental T2 values were calculated by the first reader. Average segmental T2 values were documented along with documentation of the number of segments with elevated T2 values. The presence or absence of LGE was documented by a second reader blinded to the T2 results. Average segmental T2 values were then correlated with troponin levels at the time of the MRI examination. Results In patients with acute myocarditis, mean T2 values were elevated in segments showing LGE (average T2 value of 70 msec). The T2 values were also elevated in myocardial segments with no macroscopic LGE (avg 60 msec). On an average, there were 6 additional segments that showed elevated T2 values and no macroscopic LGE. In patients with remote myocarditis, the T2 values were normal in areas of LGE.

Computed Tomography Imaging Features in Acute Uncomplicated Stanford Type-B Aortic Dissection Predict Late Adverse EventsCLINICAL PERSPECTIVE

Background— Medical treatment of initially uncomplicated acute Stanford type-B aortic dissection is associated with a high rate of late adverse events. Identification of individuals who potentially benefit from preventive endografting is highly desirable. Methods and Results— The association of computed tomography imaging features with late adverse events was retrospectively assessed in 83 patients with acute uncomplicated Stanford type-B aortic dissection, followed over a median of 850 (interquartile range 247–1824) days. Adverse events were defined as fatal or nonfatal aortic rupture, rapid aortic growth (>10 mm/y), aneurysm formation (≥6 cm), organ or limb ischemia, or new uncontrollable hypertension or pain. Five significant predictors were identified using multivariable Cox regression analysis: connective tissue disease (hazard ratio [HR] 2.94, 95% confidence interval [CI]: 1.29–6.72; P=0.01), circumferential extent of false lumen in angular degrees (HR 1.03 per degree, 95% CI: 1.01–1.04, P=0.003), maximum aortic diameter (HR 1.10 per mm, 95% CI: 1.02–1.18, P=0.015), false lumen outflow (HR 0.999 per mL/min, 95% CI: 0.998–1.000; P=0.055), and number of intercostal arteries (HR 0.89 per n, 95% CI: 0.80–0.98; P=0.024). A prediction model was constructed to calculate patient specific risk at 1, 2, and 5 years and to stratify patients into high-, intermediate-, and low-risk groups. The model was internally validated by bootstrapping and showed good discriminatory ability with an optimism-corrected C statistic of 70.1%. Conclusions— Computed tomography imaging-based morphological features combined into a prediction model may be able to identify patients at high risk for late adverse events after an initially uncomplicated type-B aortic dissection.

Measurement of extracellular volume fraction by cardiac magnetic resonance imaging detects diffuse myocardial fibrosis in systemic sclerosis

Summary We measured extracellular volume fraction (Ve) from pre- and post-contrast T1 maps of the left ventricle in 13 patients with systemic sclerosis (SSc) and 13 agematched controls. SSc patients and controls were similar with regard to LV and RV mass, volumes, and function. However, Ve was significantly higher in SSc patients than in controls, even when patients with visible late gadolinium enhancement were excluded. Ve correlated with SSc severity as measured by the modified Rodnan Skin Score. Ve may be valuable for detection of myocardial involvement in SSc, even when conventional CMR appears normal. Background Primary cardiac involvement is common in systemic sclerosis (SSc) and responsible for 25% of deaths. Myocardial extracellular volume fraction (Ve), derived from cardiac magnetic resonance (CMR) T1 mapping of the myocardium, has been shown to quantify diffuse myocardial fibrosis (DMF) - but its utility in SSc has not been studied. We hypothesized that subjects with SSc have a higher Ve compared to controls and that patients with worse SSc severity have higher Ve. Methods CMR was performed in 13 SSc patients (5 diffuse and 8 limited cutaneous) and 13 age-matched controls. Cine, pre- and post- contrast T1 mapping, and late gadolinium enhanced (LGE) imaging was performed. LV mass index (LVMi), LV end-diastolic volume index (LVEDVi), LV ejection fraction (EF), RV mass index (RVMi), RV