SBIR-STTR Award

Multiplexed Echo Planar Imaging for Neurosciences
Award last edited on: 1/26/15

Sponsored Program
SBIR
Awarding Agency
NIH : NINDS
Total Award Amount
$2,797,154
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
David A Feinberg

Company Information

Advanced MRI Technologies LLC (AKA: AMRIT~Advanced MRI Technology LLC)

652 Petaluma Avenue Suite J
Sebastopol, CA 95472
   (707) 829-2933
   david.feinberg@advancedmri.com
   www.advancedmri.com
Location: Single
Congr. District: 02
County: Sonoma

Phase I

Contract Number: 1R44NS073417-01
Start Date: 6/15/11    Completed: 12/14/11
Phase I year
2011
Phase I Amount
$287,441
MRI is a proven non-invasive technique that makes high resolution image of the brain. Echo planar imaging (EPI) is the most widely used MRI technique used for neurosciences due to its extremely fast imaging speed and unique contrast mechanisms. EPI combined with diffusion sensitive gradient pulses provides 3D visualization of axonal fibers, which reveals the connectional anatomy of the human brain. EPI is also nearly exclusively used for functional MRI (fMRI) given its extremely high sensitivity to changes in ""blood oxygen level dependent"" (BOLD) contrast in different regions of the brain, revealing maps of neuronal activity. We are proposing to develop a family of highly efficient new EPI sequences for diffusion and fMRI providing several times faster imaging of the brain. This new faster imaging technique works by multiplexing several images within the single-shot echo train, to produce several images instead of a single EPI image from a each train of signals, whereas only a single image is produced in the normal EPI pulse sequence. The new Multiplexed EPI imaging sequence will largely replace the use of the original EPI sequence invented by Peter Mansfield in 1978 that to date has been used for all neuroscience and clinical brain imaging. The availability of these Multiplexed EPI techniques will give researchers and clinicians the capability of performing high angular resolution diffusion imaging (HARDI) in scan times reduced from 25 minutes to 8 or 12 minutes scans and these scan times will be more tolerable by both patients and research subjects. The multiplexed EPI can scan many times faster or instead be used to provide more images that are thinner for higher resolution and reduced artifacts. The greatly accelerated scan times of the whole brain will enable new experiments in functional MRI at 7 Tesla and 3 Tesla. The sequence will be designed, implemented and evaluated on MRI scanners operating at 3T at University of California Berkeley and San Francisco and at 7T and 10.5T at University of Minnesota. Once the Multiplexed EPI sequence is fully evaluated and optimized, it will be made into a useful tool for basic and clinical neuroscience research, and for clinical diagnostic imaging.

Public Health Relevance:
Diffusion MRI based 3D images of axonal fibers is becoming widely used method to study the anatomy of the human brain. Functional MRI (fMRI)is used to study the brain while it is performing thinking tasks and thus to map regions of brain activity. We are proposing a much faster MRI pulse sequence technology to replace existing sub-second imaging sequences used for fMRI and diffusion imaging. The new multiplexed signal encoding technology will produce several times faster multi-slice 2D images, useful for obtaining images of neuronal fibers in times under 10 minutes, supplanting the currently used slower scans that can take over 30 minutes that may often be intolerable to patients and normal people. The novel multiplexed EPI images when used for fMRI at 7T will provide much higher data sampling rates and improved statistics in functional MRI studies which will contribute to new discoveries of how the brain works. These new measurements obtained in with diffusion and fMRI will be useful for studying neurodegenerative diseases of the brain including Alzheimer's disease and for evaluating people with stroke and cerebrovascular diseases.

Thesaurus Terms:
3-D Images;3-D Image;3d Image;3d Images;Abdomen;Abdominal;Acceleration;Algorithms;Alzheimer;Alzheimer Type Dementia;Alzheimer Disease;Alzheimer Sclerosis;Alzheimer Syndrome;Alzheimer's;Alzheimer's Disease;Alzheimers Dementia;Alzheimers Disease;Anatomic;Anatomical Sciences;Anatomy;Apoplexy;Artifacts;Brain;Brain Nervous System;Brain Vascular Accident;Brain Vascular Disorders;Brain Imaging;Brain Region;California;Cell Communication And Signaling;Cell Signaling;Cerebral Stroke;Cerebrovascular Apoplexy;Cerebrovascular Disease;Cerebrovascular Disorders;Cerebrovascular Stroke;Chemicals;Clinical;Code;Coding System;Computer Software;Data;Degenerative Neurologic Diseases;Degenerative Neurologic Disorders;Diagnostic;Diagnostic Imaging;Diffusion;Diffusion Mri;Diffusion Magnetic Resonance Imaging;Diffusion Weighted Mri;Echo-Planar Imaging;Echo-Planar Magnetic Resonance Imaging;Echoplanar Imaging;Echoplanar Magnetic Resonance Imaging;Encephalon;Family;Fats;Fatty Acid Glycerol Esters;Fiber;Functional Mri;Functional Magnetic Resonance Imaging;Human;Image;Image Reconstructions;Imagery;Imaging Procedures;Imaging Technics;Imaging Techniques;Intracellular Communication And Signaling;Intracranial Vascular Diseases;Intracranial Vascular Disorders;Investigators;Mr Imaging;Mr Tomography;Mri;Magnetic Resonance Imaging;Magnetic Resonance Imaging Scan;Man (Taxonomy);Maps;Measurement;Medical Imaging, Magnetic Resonance / Nuclear Magnetic Resonance;Methods;Minnesota;Modern Man;Morphologic Artifacts;Nmr Imaging;Nmr Tomography;Nerve Cells;Nerve Unit;Nervous System Degenerative Diseases;Neural Cell;Neurocyte;Neurodegenerative Diseases;Neurodegenerative Disorders;Neurologic Degenerative Conditions;Neurons;Neurosciences;Neurosciences Research;Noise;Nuclear Magnetic Resonance Imaging;Patients;Phase;Physiologic Pulse;Planar Medical Imaging;Predisposition;Primary Senile Degenerative Dementia;Program Development;Protocol;Protocols Documentation;Pulse;Research Personnel;Research Subjects;Researchers;Resolution;Sampling;San Francisco;Scanning;Scheme;Signal Transduction;Signal Transduction Systems;Signaling;Slice;Software;Sorting - Cell Movement;Speed;Speed (Motion);Spinal;Susceptibility;Techniques;Technology;Testing;Thinking;Thinking, Function;Three-Dimensional Image;Time;Training;Universities;Visualization;Work;Writing;Zeugmatography;Base;Biological Signal Transduction;Blood Oxygen Level Dependent;Blood Oxygenation Level Dependent;Brain Attack;Brain Visualization;Cerebral Vascular Accident;Cerebrovascular Accident;Computer Program/Software;Dementia Of The Alzheimer Type;Design;Designing;Diffusion Tensor Imaging;Experiment;Experimental Research;Experimental Study;Fmri;Imaging;Improved;Neurodegenerative Illness;Neuronal;Novel;Primary Degenerative Dementia;Prototype;Reconstruction;Research Study;Senile Dementia Of The Alzheimer Type;Sorting;Statistics;Stroke;Thoughts;Tool

Phase II

Contract Number: 4R44NS073417-02
Start Date: 6/15/11    Completed: 2/28/15
Phase II year
2012
(last award dollars: 2014)
Phase II Amount
$2,509,713

MRI is a proven non-invasive technique that makes high resolution image of the brain. Echo planar imaging (EPI) is the most widely used MRI technique used for neurosciences due to its extremely fast imaging speed and unique contrast mechanisms. EPI combined with diffusion sensitive gradient pulses provides 3D visualization of axonal fibers, which reveals the connectional anatomy of the human brain. EPI is also nearly exclusively used for functional MRI (fMRI) given its extremely high sensitivity to changes in "blood oxygen level dependent" (BOLD) contrast in different regions of the brain, revealing maps of neuronal activity. We are proposing to develop a family of highly efficient new EPI sequences for diffusion and fMRI providing several times faster imaging of the brain. This new faster imaging technique works by multiplexing several images within the single-shot echo train, to produce several images instead of a single EPI image from a each train of signals, whereas only a single image is produced in the normal EPI pulse sequence. The new Multiplexed EPI imaging sequence will largely replace the use of the original EPI sequence invented by Peter Mansfield in 1978 that to date has been used for all neuroscience and clinical brain imaging. The availability of these Multiplexed EPI techniques will give researchers and clinicians the capability of performing high angular resolution diffusion imaging (HARDI) in scan times reduced from 25 minutes to 8 or 12 minutes scans and these scan times will be more tolerable by both patients and research subjects. The multiplexed EPI can scan many times faster or instead be used to provide more images that are thinner for higher resolution and reduced artifacts. The greatly accelerated scan times of the whole brain will enable new experiments in functional MRI at 7 Tesla and 3 Tesla. The sequence will be designed, implemented and evaluated on MRI scanners operating at 3T at University of California Berkeley and San Francisco and at 7T and 10.5T at University of Minnesota. Once the Multiplexed EPI sequence is fully evaluated and optimized, it will be made into a useful tool for basic and clinical neuroscience research, and for clinical diagnostic imaging.

Public Health Relevance Statement:
Diffusion MRI based 3D images of axonal fibers is becoming widely used method to study the anatomy of the human brain. Functional MRI (fMRI)is used to study the brain while it is performing thinking tasks and thus to map regions of brain activity. We are proposing a much faster MRI pulse sequence technology to replace existing sub-second imaging sequences used for fMRI and diffusion imaging. The new multiplexed signal encoding technology will produce several times faster multi-slice 2D images, useful for obtaining images of neuronal fibers in times under 10 minutes, supplanting the currently used slower scans that can take over 30 minutes that may often be intolerable to patients and normal people. The novel multiplexed EPI images when used for fMRI at 7T will provide much higher data sampling rates and improved statistics in functional MRI studies which will contribute to new discoveries of how the brain works. These new measurements obtained in with diffusion and fMRI will be useful for studying neurodegenerative diseases of the brain including Alzheimer's disease and for evaluating people with stroke and cerebrovascular diseases.

Project Terms:
Abdomen; Acceleration; Algorithms; Alzheimer's Disease; Anatomy; base; blood oxygen level dependent; Brain; Brain imaging; Brain region; California; Cerebrovascular Disorders; Chemicals; Clinical; Code; Computer software; Data; design; Diagnostic; Diagnostic Imaging; Diffusion; Diffusion Magnetic Resonance Imaging; Echo-Planar Imaging; Family; Fatty acid glycerol esters; Fiber; Functional Magnetic Resonance Imaging; Human; Image; Image Reconstructions; Imagery; Imaging Techniques; improved; Magnetic Resonance Imaging; Maps; Measurement; Methods; Minnesota; Morphologic artifacts; Neurodegenerative Disorders; Neurons; Neurosciences; Neurosciences Research; Noise; novel; Patients; Phase; Physiologic pulse; Predisposition; Program Development; Protocols documentation; prototype; reconstruction; Research Personnel; research study; Research Subjects; Resolution; Sampling; San Francisco; Scanning; Scheme; Signal Transduction; Slice; Sorting - Cell Movement; Speed (motion); Spinal; statistics; stroke; Techniques; Technology; Testing; Thinking, function; Three-Dimensional Image; Time; tool; Training; Universities; Work; Writing