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Anant Madabhushi

Publications and source records attributed to Anant Madabhushi.

6 recordsLinked to original sources

Comparing MR image intensity standardization against tissue characterizability of magnetization transfer ratio imaging.

PURPOSE: To evaluate existing methods of standardization by exploiting the well-known tissue characterizing property of magnetization transfer ratio (MTR) values obtained from MT imaging, and compare the tissue characterizability of standardized T2, proton density (PD), and T1 images against the MTR images. MATERIALS AND METHODS: Image intensity standardization is a postprocessing method that was designed to correct for acquisition-to-acquisition signal intensity variations (nonstandardness) inherent in magnetic resonance (MR) images. The main idea of this technique is to deform the volume image histogram of each study to match a standard histogram, and to utilize the resulting transformations to map the image intensities into a standard scale. The method has been shown to produce a significant gain in similarity of resulting images and to achieve numeric tissue characterization. In this work we compared PD-, T2-, and T1-weighted images before and after standardization with the corresponding MT images for 10 patient MRI studies of the brain, in terms of the normalized median values on the corresponding image histograms. RESULTS: No statistically significant difference was observed between the standardized PD-, T2-, and T1-weighted images and the corresponding MTR images. However, a statistically significant difference was found between the pre- and poststandardized PD-, T2-, and T1-weighted images, and between the prestandardized PD-, T2-, and T1-weighted images and the corresponding MTR images. CONCLUSION: These results suggest that standardized T2, PD, and T1 images and their tissue-specific intensity signatures may be useful for characterizing disease.

Brain↗

New methods of MR image intensity standardization via generalized scale.

Image intensity standardization is a post-acquisition processing operation designed for correcting acquisition-to-acquisition signal intensity variations (non-standardness) inherent in Magnetic Resonance (MR) images. While existing standardization methods based on histogram landmarks have been shown to produce a significant gain in the similarity of resulting image intensities, their weakness is that in some instances the same histogram-based landmark may represent one tissue, while in other cases it may represent different tissues. This is often true for diseased or abnormal patient studies in which significant changes in image intensity characteristics may occur. In an attempt to overcome this problem, in this paper, we present two new intensity standardization methods based on two scale concepts developed in Madabhushi et al. [Computer Vision Image Understanding 101, 100-121 (2006)] for image processing applications. These scale concepts are utilized in this paper to accurately determine principal tissue regions within MR images. Landmarks derived from these regions are used to perform intensity standardization. The new methods were qualitatively and quantitatively evaluated on a total of 67 clinical three dimensional (3D) MR images corresponding to four different protocols and to normal, Multiple Sclerosis (MS), and brain tumor patient studies. The new scale-based methods were found to be better than the existing methods, with a significant improvement observed for severely diseased and abnormal patient studies.

Algorithms↗

Graph embedding to improve supervised classification and novel class detection: application to prostate cancer.

Recently there has been a great deal of interest in algorithms for constructing low-dimensional feature-space embeddings of high dimensional data sets in order to visualize inter- and intra-class relationships. In this paper we present a novel application of graph embedding in improving the accuracy of supervised classification schemes, especially in cases where object class labels cannot be reliably ascertained. By refining the initial training set of class labels we seek to improve the prior class distributions and thus classification accuracy. We also present a novel way of visualizing the class embeddings which makes it easy to appreciate inter-class relationships and to infer the presence of new classes which were not part of the original classification. We demonstrate the utility of the method in detecting prostatic adenocarcinoma from high-resolution MRI.

Adenocarcinoma↗

Interplay between intensity standardization and inhomogeneity correction in MR image processing.

Image intensity standardization is a postprocessing method designed for correcting acquisition-to-acquisition signal intensity variations (nonstandardness) inherent in magnetic resonance (MR) images. Inhomogeneity correction is a process used to suppress the low frequency background nonuniformities (inhomogeneities) of the image domain that exist in MR images. Both these procedures have important implications in MR image analysis. The effects of these postprocessing operations on improvement of image quality in isolation has been well documented. However, the combined effects of these two processes on MR images and how the processes influence each other have not been studied thus far. In this paper, we evaluate the effect of inhomogeneity correction followed by standardization and vice-versa on MR images in order to determine the best sequence to follow for enhancing image quality. We conducted experiments on several clinical and phantom data sets (nearly 4000 three-dimensional MR images were analyzed) corresponding to four different MRI protocols. Different levels of artificial nonstandardness, and different models and levels of artificial background inhomogeneity were used in these experiments. Our results indicate that improved standardization can be achieved by preceding it with inhomogeneity correction. There is no statistically significant difference in image quality obtained between the results of standardization followed by correction and that of correction followed by standardization from the perspective of inhomogeneity correction. The correction operation is found to bias the effect of standardization. We demonstrate this bias both qualitatively and quantitatively by using two different methods of inhomogeneity correction. We also show that this bias in standardization is independent of the specific inhomogeneity correction method used. The effect of this bias due to correction was also seen in magnetization transfer ratio (MTR) images, which are naturally endowed with the standardness property. Standardization, on the other hand, does not seem to influence the correction operation. It is also found that longer sequences of repeated correction and standardization operations do not considerably improve image quality. These results were found to hold for the clinical and the phantom data sets, for different MRI protocols, for different levels of artificial nonstandardness, for different models and levels of artificial inhomogeneity, for different correction methods, and for images that were endowed with inherent standardness as well as for those that were standardized by using the intensity standardization method. Overall, we conclude that inhomogeneity correction followed by intensity standardization is the best sequence to follow from the perspective of both image quality and computational efficiency.

Algorithms↗

Automated detection of prostatic adenocarcinoma from high-resolution ex vivo MRI.

Prostatic adenocarcinoma is the most commonly occurring cancer among men in the United States, second only to skin cancer. Currently, the only definitive method to ascertain the presence of prostatic cancer is by trans-rectal ultrasound (TRUS) directed biopsy. Owing to the poor image quality of ultrasound, the accuracy of TRUS is only 20%-25%. High-resolution magnetic resonance imaging (MRI) has been shown to have a higher accuracy of prostate cancer detection compared to ultrasound. Consequently, several researchers have been exploring the use of high resolution MRI in performing prostate biopsies. Visual detection of prostate cancer, however, continues to be difficult owing to its apparent lack of shape, and the fact that several malignant and benign structures have overlapping intensity and texture characteristics. In this paper, we present a fully automated computer-aided detection (CAD) system for detecting prostatic adenocarcinoma from 4 Tesla ex vivo magnetic resonance (MR) imagery of the prostate. After the acquired MR images have been corrected for background inhomogeneity and nonstandardness, novel three-dimensional (3-D) texture features are extracted from the 3-D MRI scene. A Bayesian classifier then assigns each image voxel a "likelihood" of malignancy for each feature independently. The "likelihood" images generated in this fashion are then combined using an optimally weighted feature combination scheme. Quantitative evaluation was performed by comparing the CAD results with the manually ascertained ground truth for the tumor on the MRI. The tumor labels on the MR slices were determined manually by an expert by visually registering the MR slices with the corresponding regions on the histology slices. We evaluated our CAD system on a total of 33 two-dimensional (2-D) MR slices from five different 3-D MR prostate studies. Five slices from two different glands were used for training. Our feature combination scheme was found to outperform the individual texture features, and also other popularly used feature combination methods, including AdaBoost, ensemble averaging, and majority voting. Further, in several instances our CAD system performed better than the experts in terms of accuracy, the expert segmentations being determined solely from visual inspection of the MRI data. In addition, the intrasystem variability (changes in CAD accuracy with changes in values of system parameters) was significantly lower than the corresponding intraobserver and interobserver variability. CAD performance was found to be very similar for different training sets. Future work will focus on extending the methodology to guide high-resolution MRI-assisted in vivo prostate biopsies.

Adenocarcinoma↗

Combining low-, high-level and empirical domain knowledge for automated segmentation of ultrasonic breast lesions.

Breast cancer is the most frequently diagnosed malignancy and the second leading cause of mortality in women. In the last decade, ultrasound along with digital mammography has come to be regarded as the gold standard for breast cancer diagnosis. Automatically detecting tumors and extracting lesion boundaries in ultrasound images is difficult due to their specular nature and the variance in shape and appearance of sonographic lesions. Past work on automated ultrasonic breast lesion segmentation has not addressed important issues such as shadowing artifacts or dealing with similar tumor like structures in the sonogram. Algorithms that claim to automatically classify ultrasonic breast lesions, rely on manual delineation of the tumor boundaries. In this paper, we present a novel technique to automatically find lesion margins in ultrasound images, by combining intensity and texture with empirical domain specific knowledge along with directional gradient and a deformable shape-based model. The images are first filtered to remove speckle noise and then contrast enhanced to emphasize the tumor regions. For the first time, a mathematical formulation of the empirical rules used by radiologists in detecting ultrasonic breast lesions, popularly known as the "Stavros Criteria" is presented in this paper. We have applied this formulation to automatically determine a seed point within the image. Probabilistic classification of image pixels based on intensity and texture is followed by region growing using the automatically determined seed point to obtain an initial segmentation of the lesion. Boundary points are found on the directional gradient of the image. Outliers are removed by a process of recursive refinement. These boundary points are then supplied as an initial estimate to a deformable model. Incorporating empirical domain specific knowledge along with low and high-level knowledge makes it possible to avoid shadowing artifacts and lowers the chance of confusing similar tumor like structures for the lesion. The system was validated on a database of breast sonograms for 42 patients. The average mean boundary error between manual and automated segmentation was 6.6 pixels and the normalized true positive area overlap was 75.1%. The algorithm was found to be robust to 1) variations in system parameters, 2) number of training samples used, and 3) the position of the seed point within the tumor. Running time for segmenting a single sonogram was 18 s on a 1.8-GHz Pentium machine.

Algorithms↗