An imaging-based method of mapping multi-echo BOLD intracranial pulsatility.

PURPOSE: Cardiac-related intracranial pulsatility may relate to cerebrovascular health, and this information is contained in BOLD MRI data. There is broad interest in methods to isolate BOLD pulsatility, and the current study examines a deep learning approach. METHODS: Multi-echo BOLD images, respiratory, and cardiac recordings were measured in 55 adults. Ground truth BOLD pulsatility maps were calculated with an established method. BOLD fast Fourier transform magnitude images were used as temporal-frequency image inputs to a U-Net deep learning model. Model performance was evaluated by mean squared error (MSE), mean absolute error (MAE), structural similarity index (SSIM), and mutual information (MI). Experiments evaluated the influence of input channel size, an age group effect during training, dependence on TE, performance without the U-Net architecture, and importance of respiratory preprocessing. RESULTS: The U-Net model generated BOLD pulsatility maps with lower MSE as additional fast Fourier transform input images were used. There was no age group effect for MSE (P > 0.14). MAE and SSIM metrics did not vary across TE (P > 0.36), whereas MI showed a significant TE dependence (P < 0.05). The U-Net versus no U-Net comparison showed no significant difference for MAE (P = 0.059); however, SSIM and MI were significantly different between models (P < 0.001). Within the insula, the cross-correlation values were high (r > 0.90) when comparing the U-Net model trained with/without respiratory preprocessing. CONCLUSION: Multi-echo BOLD pulsatility maps were synthesized from a U-net model that was trained to use temporal-frequency BOLD image inputs. This work adds to the deep learning methods that characterize BOLD physiological signals.

A deep community based approach for large scale content based X-ray image retrieval.

A computer assisted system for automatic retrieval of medical images with similar image contents can serve as an efficient management tool for handling and mining large scale data, and can also be used as a tool in clinical decision support systems. In this paper, we propose a deep community based automated medical image retrieval framework for extracting similar images from a large scale X-ray database. The framework integrates a deep learning-based image feature generation approach and a network community detection technique to extract similar images. When compared with the state-of-the-art medical image retrieval techniques, the proposed approach demonstrated improved performance. We evaluated the performance of the proposed method on two large scale chest X-ray datasets, where given a query image, the proposed approach was able to extract images with similar disease labels with a precision of 85%. To the best of our knowledge, this is the first deep community based image retrieval application on large scale chest X-ray database.

A data-driven approach to prostate cancer detection from dynamic contrast enhanced MRI.

Magnetic resonance imaging (MRI), particularly dynamic contrast enhanced (DCE) imaging, has shown great potential in prostate cancer diagnosis and staging. In the current practice of DCE-MRI, diagnosis is based on quantitative parameters extracted from the series of T1-weighted images acquired after the injection of a contrast agent. To calculate these parameters, a pharmacokinetic model is fitted to the T1-weighted intensities. Most models make simplistic assumptions about the perfusion process. Moreover, these models require accurate estimation of the arterial input function, which is challenging. In this work we propose a data-driven approach to characterization of the prostate tissue that uses the time series of DCE T1-weighted images without pharmacokinetic modeling. This approach uses a number of model-free empirical parameters and also the principal component analysis (PCA) of the normalized T1-weighted intensities, as features for cancer detection from DCE MRI. The optimal set of principal components is extracted with sparse regularized regression through least absolute shrinkage and selection operator (LASSO). A support vector machine classifier was used with leave-one-patient-out cross validation to determine the ability of this set of features in cancer detection. Our data is obtained from patients prior to radical prostatectomy and the results are validated based on histological evaluation of the extracted specimens. Our results, obtained on 449 tissue regions from 16 patients, show that the proposed data-driven features outperform the traditional pharmacokinetic parameters with an area under ROC of 0.86 for LASSO-isolated PCA parameters, compared to 0.78 for pharmacokinetic parameters. This shows that our novel approach to the analysis of DCE data has the potential to improve the multiparametric MRI protocol for prostate cancer detection.