Simultaneous MR quantification of hepatic fat content, fatty acid composition, transverse relaxation time and magnetic susceptibility for the diagnosis of non-alcoholic steatohepatitis.

Non-alcoholic steatohepatitis (NASH) is characterized at histology by steatosis, hepatocyte ballooning and inflammatory infiltrates, with or without fibrosis. Although diamagnetic material in fibrosis and inflammation can be detected with quantitative susceptibility imaging, fatty acid composition changes in NASH relative to simple steatosis have also been reported. Therefore, our aim was to develop a single magnetic resonance (MR) acquisition and post-processing scheme for the diagnosis of steatohepatitis by the simultaneous quantification of hepatic fat content, fatty acid composition, T2 * transverse relaxation time and magnetic susceptibility in patients with non-alcoholic fatty liver disease. MR acquisition was performed at 3.0 T using a three-dimensional, multi-echo, spoiled gradient echo sequence. Phase images were unwrapped to compute the B0 field inhomogeneity (ΔB0 ) map. The ΔB0 -demodulated real part images were used for fat-water separation, T2 * and fatty acid composition quantification. The external and internal fields were separated with the projection onto dipole field method. Susceptibility maps were obtained after dipole inversion from the internal field map with single-orientation Bayesian regularization including spatial priors. Method validation was performed in 32 patients with biopsy-proven, non-alcoholic fatty liver disease from which 12 had simple steatosis and 20 NASH. Liver fat fraction and T2 * did not change significantly between patients with simple steatosis and NASH. In contrast, the saturated fatty acid fraction increased in patients with NASH relative to patients with simple steatosis (48 ± 2% versus 44 ± 4%; p < 0.05) and the magnetic susceptibility decreased (-0.30 ± 0.27 ppm versus 0.10 ± 0.14 ppm; p < 0.001). The area under the receiver operating characteristic curve for magnetic susceptibility as NASH marker was 0.91 (95% CI: 0.79-1.0). Simultaneous MR quantification of fat content, fatty acid composition, T2 * and magnetic susceptibility is feasible in the liver. Our preliminary results suggest that quantitative susceptibility imaging has a high diagnostic performance for the diagnosis of NASH.

Can we justify not doing liver perfusion imaging in 2013?

Liver perfusion imaging is a quantitative functional investigation. Liver perfusion imaging is complicated because of the liver's dual vascular supply, artefacts due to respiratory movements and the fenestrated sinusoidal capillaries which allow the contrast medium to diffuse out. Liver perfusion can be examined by ultrasound, CT or MRI: each technique has its limitations and specific features. The major indications in hepatology are oncology (detection, characterization and tumor response) and non-invasive investigation of patients with chronic liver disease. Work is needed to standardize acquisition and modeling methods to allow wider use of results and more widespread use of the technique.

[Diffusion-weighted MR imaging of the liver]. / Imagerie de diffusion hépatique.

Diffusion-weighted imaging studies the motion of water molecules within a given tissue. Initially used for neuroradiological applications, it is now routinely used for abdominal imaging, especially liver imaging. The diffusion pulse sequence is a T2 echo-planar sequence where diffusion gradients are applied. In this article, we will review the sequence itself and the parameters used to optimize the sequence, quantitative and qualitative image evaluation, and the main applications for liver imaging: characterization of focal lesions, detection of focal lesions, evaluation of response to therapy and quantification of liver fibrosis.

[Magnetic resonance imaging for quantifying hepatis steatosis and hepatic fibrosis]. / L'imagerie par résonance magnétique quantitative de la stéatose et de la fibrose hépatique.

The reference method for detecting and quantifying hepatic steatosis and fibrosis is the histopathological analysis of liver biopsies. Studies performed in animals and humans have shown that magnetic resonance imaging (MRI) is useful for the accurate and non-invasive quantification of these lesions. For fibrosis quantification, functional MRI methods have to be used, including perfusion MRI, diffusion MRI, and more particularly MR elastography. Modifications of the visco-elastic parameters of the liver can also be observed with MR elastography in hepatic diseases without fibrosis, such as the early stages ofnon-alcoholi steatohepatitis. Finally, accurate quantification of liver steatosis can be performed by observing the difference of resonance frequencies between the protons of fat and water at spectroscopy or chemical shift MRI. In conclusion, combined quantification of liver steatosis and fibrosis can be performed with MRI.

MR elastography.

Magnetic resonance (MR) elastography is an emerging method for measuring the viscoelastic properties of tissues. Hepatic fibrosis, which increases the elasticity or stiffness of the liver, can be detected and staged by MR elastography. The technique has several advantages compared with transient ultrasound elastography (FibroScan): it can evaluate much larger liver volumes; it can be performed in obese patients and in those with ascites; and it can assess the full three-dimensional displacement vector, allowing a more precise analysis of viscoelastic parameters. These technical advantages mean that MR elastography is more accurate forstaging liver fibrosis than is transient ultrasound elastography. Moreover, it has been shown in animal studies using MR elastography that parameters other than fibrosis can also increase liver elasticity, including inflammation and myofibroblast activation before extracellular matrix deposition. Because of its greater accuracy-but also its higher cost-MR elastography will probably have a complementary role alongside ultrasound elastography. Nevertheless, this role should be further studied, especially in terms of response to treatment and the early detection of chronic liver diseases such as steatohepatitis.

Diagnosis of cholangiocarcinoma.

Cholangiocarcinoma is suspected based on signs of biliary obstruction, abnormal liver function tests, elevated tumor markers (carbohydrate antigen 19-9 and carcinoembryonic antigen), and ultrasonography showing a bile stricture or a mass, especially in intrahepatic cholangiocarcinoma. Magnetic resonance imaging (MRI) or computed tomography (CT) is performed for the diagnosis and staging of cholangiocarcinomas. However, differentiation of an intraductal cholangiocarcinoma from a hypovascular metastasis is limited at imaging. Therefore, reasonable exclusion of an extrahepatic primary tumor should be performed. Differentiating between benign and malignant bile duct stricture is also difficult, except when metastases are observed. The sensitivity of fluorodeoxyglucose positron emission tomography is limited in small, infiltrative, and mucinous cholangiocarcinomas. When the diagnosis of a biliary stenosis remains indeterminate at MRI or CT, endoscopic imaging (endoscopic or intraductal ultrasound, cholangioscopy, or optical coherence tomography) and tissue sampling should be carried out. Tissue sampling has a high specificity for diagnosing malignant biliary strictures, but sensitivity is low. The diagnosis of cholangiocarcinoma is particularly challenging in patients with primary sclerosing cholangitis. These patients should be followed with yearly tumor markers, CT, or MRI. In the case of dominant stricture, histological or cytological confirmation of cholangiocarcinoma should be obtained. More studies are needed to compare the accuracy of the various imaging methods, especially the new intraductal methods, and the imaging features of malignancy should be standardized.

[Magnetic resonance imaging of angiogenesis in tumors]. / Imagerie par résonance magnétique de l'angiogenèse tumorale.

Tumor angiogenesis induces the proliferation of immature blood vessels that are both heterogeneous and leaky. These characteristics can be demonstrated by measuring the perfusion parameters with MRI. Perfusion MRI is usually performed with in T1-weighted dynamic imaging after bolus injection of an exogenous contrast agent such as gadolinium chelate. The perfusion parameters are obtained by semi-quantitative or quantitative analysis of the enhancement curves in the tumor and the arterial input. Perfusion can also be assessed without injecting a contrast agent using arterial spin labeling techniques, diffusion MRI, or BOLD (blood oxygen level dependent) MRI. However, these latter methods are limited by a low signal-to-noise ratio and problems with quantification. The main indication for perfusion MRI is the assessment of antiangiogenic and antivascular treatments. New possibilities for demonstrating angiogenic blood vessels are being opened by molecular imaging.

Analysis of contrast-enhanced MR images to assess renal function.

The image analysis and kinetic modeling methods used in dynamic contrast-enhanced magnetic resonance imaging of the kidney are reviewed. Image analysis includes various techniques of coregistration and segmentation. Few methods have been completely implemented. Nevertheless, the use of coregistration may become a standard to decrease the effect of motion on abdominal images and improve the quality of the renal signals. Kinetic models are classified into three categories: enhancement-based, external and internal representations. Enhancement-based representations are limited to a basic analysis of the tracer concentration curves in the kidneys. Their relationship to the underlying physiology is complex and undefined. However, they can be used to evaluate the split renal function. External representations assess the kidney input and output. An external representation based on the up-slope of the renal enhancement to calculate the renal perfusion is commonly used because of its simplicity. In contrast, external representation based on deconvolution or identification methods remain underexploited. For glomerular filtration, an internal representation based on a two-compartmental model is mostly used. Internal representations based on multi-compartmental models describe the renal function in a more realistic way. Because of their numerical complexity, these models remain rarely used.

Focal bowel wall changes detected with colour Doppler ultrasound: diagnostic value in acute non-diverticular diseases of the colon.

We performed a study to determine if colour Doppler findings may help to identify the cause of wall thickening in acute non-diverticular diseases of the colon. The study group included 66 patients admitted to the emergency department with a final diagnosis of infectious colitis (n=23), inflammatory colitis (n=10), ischaemic colitis (n=23) and malignant tumours (n=10). The following ultrasound features were assessed: maximal wall thickness, wall stratification, arterial flow in the colonic wall and arteriolar resistive index. Higher values of wall thickness were observed in malignant tumour (18.2+/-6.2 mm, p<0.001). Moderately thickened wall (6.6+/-1.3 mm, p< or =0.06), preserved stratification (90% versus 46% in the remainder of the study population) and lower resistive index (0.51+/-0.10, p< or =0.05) were significantly related to inflammatory colitis. Absence of arterial flow was more frequently observed in ischaemia (43% versus 12% in the remainder of the study population). In conclusion, despite some overlap, both ultrasound and colour Doppler features are helpful in the differential diagnosis of colonic thickening related to non-diverticular colonic lesions.

MR imaging findings in a patient with hepatic veno-occlusive disease.

We report the MRI findings in a 31-year-old woman with veno-occlusive disease. MRI demonstrated patent hepatic veins and patchy signal enhancement of the liver after gadolinium chelate injection. This enhancement was compatible with sinusoidal congestion. The diagnosis of veno-occlusive disease was confirmed by histological examination of liver biopsy. The diagnosis of veno-occlusive disease should be evoked when patchy liver enhancement suggestive of sinusoidal congestion is observed in the absence of hepatic vein thrombosis and congestive heart failure.

[Imaging of intestinal ischemia]. / Imagerie des ischémies intestinales.

Ischemic bowel disease includes acute and chronic mesenteric ischemia, and colon ischemia. Cross-sectional imaging, and more particularly computed tomography, has an increasing role in the detection of acute and chronic mesenteric ischemia. Vascular obstructions or stenoses and changes in the bowel wall can be observed. Functional information can be added with MRI by using sequences that are sensitive to oxygen saturation in the superior mesenteric vein. Arteriography remains the reference examination in patients with acute mesenteric ischemia.

Calculation of the renal perfusion and glomerular filtration rate from the renal impulse response obtained with MRI.

The aim of this study was to assess the importance of deconvolution for the calculation of renal perfusion and glomerular filtration rate (GFR) on the basis of concentration-time curves as measured with perfusion MRI. Six rabbits were scanned dynamically after injection of a gadolinium chelate. Concentration-time curves were generated by manually drawing regions of interest in the aorta and the renal cortex. To remove the dependency on the arterial input function, a regularized structured total least-squares deconvolution algorithm was used to calculate the renal impulse response. This curve was fitted by the sum of two gamma variate functions, corresponding to the passage of the contrast agent in the glomeruli and the proximal convoluted tubules. Tracer kinetics models were applied to these two functions to obtain the renal perfusion and GFR. For comparison, these two parameters were also calculated on the basis of the renal concentration-time curve before deconvolution. The renal perfusion values correlated well (r = 0.9, P = 0.014) with the values calculated by a validated upslope method. The GFR values correlated well (r = 0.9, P = 0.014) with the values obtained from the clearance of (51)Cr-EDTA. A comparison of the values obtained with and without deconvolution demonstrated the necessity of deconvolution.

[Cardiac imaging by means of four-detector row computed tomography and cardiac gating]. / Imagerie cardiaque en tomodensitométrie à quatre canaux d'acquisition et synchronisation cardiaque.

Electrocardiographically-assisted imaging is a recent development in multislice spiral computed tomography. In this article, we summarize the principles of four-detector row CT for cardiac applications. Following is an overview of the potential of this technique to evaluate the heart, the thoracic aorta, and the paracardiac pulmonary parenchyma. Technical considerations for optimal imaging are highlighted.

Assessment of hepatic perfusion parameters with dynamic MRI.

Quantification of hepatic perfusion parameters greatly contributes to the assessment of liver function. The purpose of this study was to describe and validate the use of dynamic MRI for the noninvasive assessment of hepatic perfusion parameters. The signal from a fast T(1)-weighted spoiled gradient-echo sequence preceded by a nonslice-selective 90 degrees pulse and a spoiler gradient was calibrated in vitro with tubes filled with various gadolinium concentrations. Dynamic images of the liver were obtained after intravenous bolus administration of 0.05 mmol/kg of Gd-DOTA in rabbits with normal liver function. Hepatic, aortic, and portal venous signal intensities were converted to Gd-DOTA concentrations according to the in vitro calibration curve and fitted with a dual-input one-compartmental model. With MRI, hepatic blood flow was 100 +/- 35 mL min(-1) 100 mL(-1), the arterial fraction 24 +/- 11%, the distribution volume 13.0 +/- 3.7%, and the mean transit time 8.9 +/- 4.1 sec. A linear relationship was observed between perfusion values obtained with MRI and with radiolabeled microspheres (r = 0.93 for hepatic blood flow [P < 0.001], r = 0.79 for arterial blood flow [P = 0.01], and r = 0.91 for portal blood flow [P < 0.001]). Our results indicate that hepatic perfusion parameters can be assessed with dynamic MRI and compartmental modeling.

Vascular lesions of the liver and gastrointestinal tract.

In the liver, imaging can show lesions of large and medium-sized vessels, perfusion disorders related to vascular lesions, and parenchymal lesions including infarcts, regenerative nodules, and focal nodular hyperplasia. In the gastrointestinal tract, vascular lesions often result in bowel ischemia. Imaging can be used to show the vascular lesions and bowel wall abnormalities, including mural thickening, lack of perfusion, and pneumatosis. Doppler sonography, multislice helical computed tomography (CT), magnetic resonance (MR) imaging, and angiography are useful to demonstrate vascular lesions. Doppler sonography offers high spatial and temporal resolution. Information about blood flow and velocity can be obtained. However, the visualization of retroperitoneal vessels is often limited because of intestinal gas. A global view of the abdominal vasculature can be observed by using helical CT. High spatial and temporal resolution are obtained, especially when new multislice CT scanners are used. MR imaging has a better contrast resolution than CT, but its spatial resolution is lower. MR imaging can also be used to measure flow with phase contrast methods. The role of arteriography in the diagnosis of vascular lesions is decreasing. However, its role remains important to definitively demonstrate obstruction of the hepatic artery and to show arterial lesions in acute mesenteric ischemia. In addition, it is used as a problem-solving method to detect lesions in medium-sized vessels and to guide intravascular treatment.

Value of multislice helical CT scans and maximum-intensity-projection images to improve detection of ureteral stones at abdominal radiography.

OBJECTIVE: The purpose of this study was to assess the improvement in the detection of ureteral stones on abdominal radiographs when the stones were viewed on multislice helical CT scans and maximum-intensity-projection (MIP) images. SUBJECTS AND METHODS: The study included 72 patients with renal colic who underwent abdominal radiography and multislice helical CT. For each patient, a frontal MIP image was generated, and the stone, when present, was marked with a cross on the transverse CT scan. The cross appeared automatically on the corresponding MIP image. The CT examination was used as the standard of reference. The presence and location of ureteral stones on the abdominal radiographs were assessed during three interpretation sessions. In the first session, the abdominal radiographs were viewed alone. In the second, they were viewed with the transverse CT scans. In the third, the abdominal radiographs were viewed with the CT scans and the MIP images. RESULTS: Ureteral stones were present in 58 patients. The percentage of stones detected on the abdominal radiographs was 45% when the radiographs were viewed alone, 66% when they were viewed with the CT scans (p = 0.002 vs radiographs alone), and 78% when viewed with the CT scans and MIP images (p = 0.016 vs radiographs with CT scans). CONCLUSION: The sensitivity of stone detection on abdominal radiographs was greatest when the interpreters viewed the radiographs in conjunction with the CT scans and MIP images.