Patent classifications
G01R33/485
Magnetic resonance spectroscopy system and method for diagnosing pain or infection associated with propionic acid
An MR Spectroscopy (MRS) system and approach is provided for measuring spectral information corresponding with propionic acid (PA), either alone or in combination with other measurements corresponding with other chemicals, to diagnose and/or monitor at least one of bacterial infection, such as associated with P. acnes, or conditions related thereto such as nociceptive pain associated with tissue acidity. An interfacing DDD-MRS signal processor receives output signals to produce a post-processed spectrum, with spectral regions corresponding with certain chemicals, including PA, then measured as biomarkers. A diagnostic processor derives a diagnostic value for each disc, and performs certain normalizations, based upon ratios of the spectral regions related to chemicals implicated in degenerative painful tissue pathology, such as PA and hypoxia markers of lactic acid (LA) and alanine (AL), and structural chemicals of proteoglycan (PG) and collagen or carbohydrate (CA).
Magnetic resonance spectroscopy system and method for diagnosing pain or infection associated with propionic acid
An MR Spectroscopy (MRS) system and approach is provided for measuring spectral information corresponding with propionic acid (PA), either alone or in combination with other measurements corresponding with other chemicals, to diagnose and/or monitor at least one of bacterial infection, such as associated with P. acnes, or conditions related thereto such as nociceptive pain associated with tissue acidity. An interfacing DDD-MRS signal processor receives output signals to produce a post-processed spectrum, with spectral regions corresponding with certain chemicals, including PA, then measured as biomarkers. A diagnostic processor derives a diagnostic value for each disc, and performs certain normalizations, based upon ratios of the spectral regions related to chemicals implicated in degenerative painful tissue pathology, such as PA and hypoxia markers of lactic acid (LA) and alanine (AL), and structural chemicals of proteoglycan (PG) and collagen or carbohydrate (CA).
Deep learning-based water-fat separation from dual-echo chemical shift encoded imaging
A method for magnetic resonance imaging performs chemical shift encoded imaging to produce complex dual-echo images which are then applied (with imaging parameters) as input to a deep neural network to produce as output water-only and fat-only images. The deep neural network can be trained with ground truth water/fat images derived from chemical shift encoded images using a conventional water-fat separation algorithm such as projected power approach, IDEAL, or VARPRO. The chemical shift encoded imaging comprises performing an image acquisition with the MRI scanner via a spoiled-gradient echo sequence or a spin-echo sequence.
Deep learning-based water-fat separation from dual-echo chemical shift encoded imaging
A method for magnetic resonance imaging performs chemical shift encoded imaging to produce complex dual-echo images which are then applied (with imaging parameters) as input to a deep neural network to produce as output water-only and fat-only images. The deep neural network can be trained with ground truth water/fat images derived from chemical shift encoded images using a conventional water-fat separation algorithm such as projected power approach, IDEAL, or VARPRO. The chemical shift encoded imaging comprises performing an image acquisition with the MRI scanner via a spoiled-gradient echo sequence or a spin-echo sequence.
MRI apparatus
An MRI system coil insert 2 for use within a bore B of a main MRI system 1, the coil insert 2 comprising at least one gradient coil, for creating a spatially varying magnetic field along a respective axis and being arranged to be electrically driven at an ultrasonic frequency.
DIXON-TYPE WATER/FAT SEPARATION MR IMAGING
The invention relates to a method of Dixon-type MR imaging of an object (10) placed in an examination volume of a MR device (1). It is an object of the invention to provide a method that enables an improved Dixon water/fat separation in combination with a dual-acquisition gradient-echo imaging sequence. The method comprises the steps of: subjecting the object (10) to a dual-acquisition gradient-echo imaging sequence comprising a series of temporally equidistant RF excitations, wherein one gradient echo is generated in each repetition time between successive RF excitations with the echo time alternating between a first and a second value (TE1, TE2), and wherein phase-encoding magnetic field gradients (P, S) are switched in each repetition time to sample a pre-defined region of k-space; acquiring echo signals from the object (10), wherein each gradient echo associated with either the first or the second echo time value (TE1, TE2) is sampled as a partial echo, and—reconstructing an MR image from the acquired echo signals, whereby signal contributions from water and fat are separated. Moreover the invention relates to an MR device (1) and to a computer program to be run on an MR device (1).
DIXON-TYPE WATER/FAT SEPARATION MR IMAGING
The invention relates to a method of Dixon-type MR imaging of an object (10) placed in an examination volume of a MR device (1). It is an object of the invention to provide a method that enables an improved Dixon water/fat separation in combination with a dual-acquisition gradient-echo imaging sequence. The method comprises the steps of: subjecting the object (10) to a dual-acquisition gradient-echo imaging sequence comprising a series of temporally equidistant RF excitations, wherein one gradient echo is generated in each repetition time between successive RF excitations with the echo time alternating between a first and a second value (TE1, TE2), and wherein phase-encoding magnetic field gradients (P, S) are switched in each repetition time to sample a pre-defined region of k-space; acquiring echo signals from the object (10), wherein each gradient echo associated with either the first or the second echo time value (TE1, TE2) is sampled as a partial echo, and—reconstructing an MR image from the acquired echo signals, whereby signal contributions from water and fat are separated. Moreover the invention relates to an MR device (1) and to a computer program to be run on an MR device (1).
Method for detecting tumor tissue boundaries or tumor stromal cell distribution range
A method for detecting tumor tissue boundaries or a tumor stromal cell distribution range, more specifically, a diagnostic or non-diagnostic method for determining the boundaries of a tumor tissue; the boundaries of the tumor tissue are determined by means of determining the boundaries of the tumor stromal cells in the tumor tissue. The present method can more accurately determine the boundaries of tumor tissue, which serves to more accurately instruct the treatment of tumors, especially with respect to surgical treatment.
SYSTEM AND METHOD FOR CONTROLLING CONCOMITANT GRADIENT PHASE ERRORS IN CHEMICAL-SHIFT ENCODED IMAGING
A system and method are provided for magnetic resonance imaging (MRI) and/or image reconstruction that includes acquiring multi-pass, chemical shift-encoded (CSE)-MRI imaging data of a subject. The method further includes performing a complex, joint estimation of phase terms in the imaging data for each pass of the multi-pass, CSE-MRI imaging data to account for concomitant gradient (CG)-induced phase errors of different passes. The method also includes generating at least one of a proton density fat fraction (PDFF) estimate or an R*2 estimate that is unbiased by CG-induced phase errors using the phase terms and communicating a report that includes at least one of the PDFF estimate or the R*2 estimate.
SYSTEM AND METHOD FOR CONTROLLING CONCOMITANT GRADIENT PHASE ERRORS IN CHEMICAL-SHIFT ENCODED IMAGING
A system and method are provided for magnetic resonance imaging (MRI) and/or image reconstruction that includes acquiring multi-pass, chemical shift-encoded (CSE)-MRI imaging data of a subject. The method further includes performing a complex, joint estimation of phase terms in the imaging data for each pass of the multi-pass, CSE-MRI imaging data to account for concomitant gradient (CG)-induced phase errors of different passes. The method also includes generating at least one of a proton density fat fraction (PDFF) estimate or an R*2 estimate that is unbiased by CG-induced phase errors using the phase terms and communicating a report that includes at least one of the PDFF estimate or the R*2 estimate.