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Diffuse Optical Brain Imaging

Diffuse Optical Brain Imaging
漫射光学脑成像
批准号:
8351241
负责人:
Amir H Gandjbakhche
金额:
$18.2万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
3-DimensionalAddressAdultAgeAreaAtlasesBehaviorBiophotonicsBlood VesselsBrainBrain PartBrain imagingBrain regionChildChildhoodChronicClinicalCognitiveCollaborationsCollectionConflict (Psychology)CouplingDataData CorrelationsDevelopmentDevicesDiffuseElectroencephalographyEpilepsyEvaluationEventFiberFrequenciesFunctional ImagingFunctional Magnetic Resonance ImagingFundingGrantHelmetHematomaHemispherectomyHourImageImaging TechniquesImaging technologyInstitutional Review BoardsJudgmentKnowledgeLasersLegal patentMagnetic Resonance ImagingMapsMedicineMethodsModelingMonitorMorphologic artifactsMotionMotor CortexNational Institute of Child Health and Human DevelopmentNational Institute of Mental HealthNational Institute of Neurological Disorders and StrokeNatureNeurosciencesNoiseOperative Surgical ProceduresOptical Image ReconstructionOpticsPaperPatientsPhysiologicalPopulationPrefrontal CortexProcessRehabilitation therapyRelative (related person)ResearchRestScientistSecureShort-Term MemorySideSignal TransductionSocietiesSoldierSourceSurfaceSystemTBI PatientsTechniquesTechnologyTestingTimeTissuesTraumatic Brain InjuryTriageUniversitiesVeteransVisual CortexWorkautism spectrum disorderbasebench to bedsideclinical applicationcohortdensitydesigndetectorhealthy volunteerhemodynamicsindexinginstrumentinterestlensminiaturizemultitaskneuropsychologicalnovelnovel strategiesoptical imagingpatient populationphotonicsprototyperesearch clinical testingresearch studyresponsetechnique developmenttool

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中文摘要
翻译
漫射光学成像(DOI)使我们能够获得组织中的血流动力学反应。研究表明,我们可以通过检测神经血管耦合的影响,将其与大脑中的功能事件联系起来。DOI中的现有技术受到许多因素的限制,但最强烈的是缺乏可行的临床应用。在这个项目中,我们的目标是退伍军人(在儿科人口的上端)与穿透性创伤性脑损伤(TBI)和自闭症谱系障碍(ASD)患者。这些患者是低功能和典型的儿科人群。 在2011财年的过程中,我们已经获得了一个板凳到床边补助金,以资助后者的研究,并延长了神经修复医学中心下的前一项研究的资金。我们再次在神经科学学会接受了几次演讲,并就我们的各种项目提交了几篇关键论文。我们已经完成了基于光纤的仪器的开发,并正在通过我们在德雷克塞尔的合作者完成第二台仪器的组装。我们已经开始在我们的实验室和乔治敦的其他合作者实验室使用仪器进行研究。后者是一种结合脑电图的DOI仪器。 在临床上,我们正在继续对健康志愿者进行测试,并从TBI受试者那里获得了一些初步数据。我们有一个通过NICHD的IRB来测试我们在NICHD的原型系统,包括神经心理学评估。除了我们的认知任务(事件复杂性判断任务,言语工作记忆任务和多任务)的测试外,我们还进一步开发了一种用于静息状态和功能连接的方法。对于休息/功能状态连接性,用于评估功能连接性的现有技术(诸如相关性和数据驱动的分解)通常假设大脑信号在记录的持续时间内是时间静止的。这样的假设会导致无法检测到大脑参与区域之间功能连接的动态变化。我们一直在研究时频分析技术,以捕捉在静息状态和基于任务的实验中,前额叶皮层连接的动态行为。随着神经心理学评估的纳入,我们正在为我们的ASD研究提供基础,一旦完成,我们将能够使用NIMH的现有数据来确定与我们的健康受试者人群密切匹配的患者队列。 从理论上讲,我们目前正在完成技术的发展,以处理当前DOI技术的缺点。我们已经确定了一种使用立体定向成像的方法,该方法允许我们将光学数据与MNI图谱配准,其精度与类似MRI实验的精度相匹配。目前,这需要存在患者特异性MRI,我们的重点是删除此要求的能力,因为这可能不适用于我们的目标患者人群。在发展新技术加速光学图像重建方面也取得了初步成果。目前,用于光学数据的三维成像的技术需要数天或最多数小时来由专家用户重建。我们正在开发新的方法,使用我们的图集方法和分析功能的组合,以解决这两个问题与DOI。 我们与NINDS的合作已经完全开发了一种基于光纤的成像仪,该成像仪已添加到我们的阵列设备中,用于DOI技术的比较和对比。这个特殊的系统还增加了我们的设备可以访问的大脑区域,将我们从前额叶皮层扩展到包括运动和视觉皮层。此外,我们正在与德雷克塞尔的合作者联合开发一个完全小型化的系统。光发射机和接收机的初步设计已经实现,每个模块的功能已经通过实验验证。发射机采用四腔垂直腔面发射半导体激光器,并利用折射率(GRIN)透镜技术实现了良好的光收集效率。我们目前正在致力于模块的集成。这些项目将联合收割机生产用于近红外功能成像的完全可穿戴DOI。我们的理论研究也将运动伪影视为信号而不是噪声。初步结果表明,如果我们能够通过头盔接口(我们的仪器人员正在进行的一个过程)对成像系统相对于受试者的运动进行建模,我们应该能够进一步将光学信号增强到该领域前所未有的准确性和定量水平。 大脑项目的最后一部分涉及结构成像。我们已经开发了一种新的方法来检测血肿在一个快速的手持设备。这种方法将极大地有助于血肿的分类,并大大提高使用更昂贵的有限进入技术(如CT或MRI)的效率。理论结果表明,该设备将工作,以检测硬膜血肿,也有可能映射他们与一个简单的手持设备存在。这种设备对于辅助CT或MRI不可用的外科手术干预至关重要。正在开发的方法已经经历了初步测试与原型成像幻影和初步结果表明,更多的源和更多的探测器在更高的密度范例更好的近红外成像可能是不正确的。事实上,用更小的设备实现类似质量的更快的结构成像是可能的。不幸的是,这种方法不能应用于功能成像。
英文摘要
Diffuse Optical Imaging (DOI) allows us access to the hemodynamic response in tissue. It has been shown that we can, by detecting the effects of neuro-vascular coupling, relate this to functional events in the brain. Existing technologies in DOI are limited by a number of factors, but most strongly by the absence of viable clinical applications where they may be applied. In this project we are targeting veterans (at the upper end of the pediatric population) with penetrating Traumatic Brain Injury (TBI) and Autistic Spectrum Disorder (ASD) patients. These patients are low-functioning and typically pediatric populations. Over the course of the 2011 fiscal year we have secured a Bench to Bedside grant to fund the latter study and extended the funding for the former study under the Center for Neuro-Rehabilitative Medicine. We have again had several presentations accepted at the Society for Neuroscience and have several key papers in submission on our various projects. We have completed the development of our fiber based instrument and are finishing assembling a second instrument through our collaborators at Drexel). We have commenced studies using instruments at our lab and at our other collaborators lab in Georgetown. The latter is a DOI instruments combined with EEG. Clinically we are continuing testing with healthy volunteers and have some initial data from TBI subjects. We have an in-place IRB through NICHD to test our prototype systems here at NICHD for both projects including a neuropsychological evaluation. Alongside our tests for cognitive tasks (event complexity judgment task, a verbal working memory task, and a multi-task) we have further developed an approach for resting state and functional connectivity. For the resting/functional state connectivity existing techniques such as correlation and data-driven decompositions, for assessing functional connectivity, generally assume temporal stationary for the brain signals over the duration of the recording. Such an assumption would result in not detecting the dynamic changes that exist in functional connectivity between engaged regions of the brain. We have been investigating time-frequency analysis techniques to capture the dynamic behavior of connectivity across the prefrontal cortex, at both resting-state and task-based experiments. With the inclusion of neuropsychological evaluation we are well on our way to providing the basis for our ASD study, once complete we will be able to use the existing data from NIMH to identify a patient cohort to closely match our healthy subject population. Theoretically we are currently finishing the development of techniques to handle the shortcomings of current DOI techniques. We have identified an approach using stereotactic imaging that allows us to co-register our optical data to the MNI atlas with accuracy matching that of similar MRI experiments. Currently this requires the existence of a patient specific MRI and our focus is on the ability to remove this requirement as this may not be available for our target patient populations. Initial results have also been done on developing novel techniques to accelerate optical image reconstruction. Currently techniques for 3 dimensional imaging of optical data require days or at best hours to reconstruct by expert users. We are developing novel approaches using a combination of our atlasing approach and analytical functions to address both these issues with DOI. Our collaboration with NINDS has fully developed a fiber based imager which has added to our array devices for comparison and contrast of DOI techniques. This particular system has also increased the areas of the brain accessible to our devices expanding us away from the prefrontal cortex to include motor and visual cortices. Also we have a fully miniaturized system under development in association with our collaborators at Drexel. Initial designs for optical transmitter and receiver have been implemented and the functionality of each module has been verified experimentally. Quad vertical cavity surface emitting laser diodes are used in the transmitter, and the system takes advantage of Gradient-Index (GRIN) lens technology to achieve excellent optical collection efficiency. We are currently working on the integration of the modules. These projects will combine to produce fully wearable DOI for Near Infrared functional imaging. Our theoretical research is also examining motion artifact as a signal instead of noise. Initial results suggest that if we can model the motion of our imaging system relative to the subject via the helmet interface (a process being worked on by our instrumentalists), we should further be able to enhance optical signals to an unprecedented level of accuracy and quantitation in the field. The final part of the brain project involves structural imaging. We have developed a novel approach to detect hematomas in a rapid handheld device. This approach would greatly help for the triaging for the presence of hematomas and greatly increase the efficiency of use of more expensive limited access technologies such as CT or MRI. Theoretical results indicate the device will work to detect Dural hematomas and also that the potential to map them with a simple handheld device exists. Such a device could be critical to aiding in surgical interventions where CT or MRI is unavailable. The approach being developed has undergone initial testing with a prototype imager on phantoms and initial results suggest that the more sources and more detectors at higher density paradigm for better near infra-red imaging may not be correct. In fact it may be possible to achieve faster structural imaging of similar quality with smaller devices. Unfortunately such approaches cannot be applied to functional imaging.
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Functional and Structural Optical Brain Imaging
Functional and Structural Optical Brain Imaging
Quantitative Biophotonics for Tissue Characterization and Function
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