Sodium MRI of the Hip
髋关节钠 MRI
基本信息
- 批准号:8897271
- 负责人:
- 金额:$ 8.48万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-08-01 至 2017-05-31
- 项目状态:已结题
- 来源:
- 关键词:AffectAmericanArthritisBiochemicalBiochemical MarkersCartilageChemicalsChronicClinicalCoiled BodiesCollagen FiberComplementConcentration measurementConeDataDegenerative DisorderDegenerative polyarthritisDetectionDevelopmentDiagnosisDiagnostic ImagingDiffusionDiffusion Magnetic Resonance ImagingDisadvantagedDiseaseDisease ProgressionEarly DiagnosisElderlyEtiologyFutureGadoliniumGeometryGlycosaminoglycansGoalsGoldGrantHealthHeterogeneityHip JointHip OsteoarthritisHip PainHip region structureImageImaging TechniquesIndividualJointsLiquid substanceMagnetic Resonance ImagingMapsMeasurementMeasuresMethodsNoiseNuclear Magnetic ResonancePain managementPatientsPerformancePharmaceutical PreparationsPhysiologic pulsePilot ProjectsPopulationPrevalenceProtonsPublishingRadialRecoveryRelaxationReplacement ArthroplastyResearchResolutionRiskScanningSensitivity and SpecificitySignal TransductionSodiumSodium ChannelSpeedSynovial FluidTechniquesTimeTissuesWaterarticular cartilagebasecartilage degradationdata acquisitiondisabilityfollow-upgadolinium oxidehealthy volunteerhigh riskimaging modalityimprovedin vivomagnetic fieldnovelradiofrequencyreconstruction
项目摘要
DESCRIPTION (provided by applicant): Osteoarthritis (OA) is the most common form of arthritis in synovial joints and a leading cause of chronic disability, mainly in the elderly population. It currently affects 9% of the US population and is expected to affect 19% of Americans by 2030. OA is a degenerative disease of articular cartilage and is mainly characterized by a loss of glycosaminoglycans (GAG), change in size and organization of collagen fibers, and increased water content. There is no known cure for OA and present treatments focus mainly on pain management and ultimately, joint replacement. There are many obstacles to studying OA (heterogeneity in etiology, variability in progression of disease, long time periods required to see morphological joint changes), and consequently we currently lack the ability to predict the course of the disease. The limitation of identifying OA patients at riskfor progression and the lack of available non-invasive early biochemical markers have impeded the clinical development of potential disease modifying OA drugs (DMOAD). Specifically, hip osteoarthritis has a prevalence from 3 to 11% in Western population over 35 years old, and it is the main cause of hip pain in older adults. Quantitative sodium magnetic resonance imaging (MRI) is a non-invasive technique that is highly specific to the GAG content in cartilage that could be used to assess the degree of biochemical degradation of cartilage in OA. However, due to the low sodium concentration in vivo, its low sensitivity and fast relaxation, detecting the
sodium signal in cartilage requires high fields (>3T), specific coils and specific 3D non-Cartesian
sequences with ultrashort echo time. To the best of our knowledge, no study on sodium MRI of the hip was published to date. The recent acquisition of a dual-tuned body coil for imaging at 3T by our research team will allow us to acquire co-registered proton and sodium images of the hip within the same session. Quantitative sodium MRI could therefore provide a unique endogenous assessment of cartilage GAG content in clinically feasible scan times (20-25 min), and allow detection of OA in articular cartilage before morphological damage occurs and help assessing the effect of DMOAD treatments. The aims of this pilot study are: 1) to develop and optimize the acquisition and reconstruction of quantitative sodium MRI of the hip joint in vivo (to optimize the
acquisition sequence parameters for minimizing the acquisition time, increasing the signal-to-noise ratio and spatial resolution, to measure relaxation times and B1 maps, and to optimize synovial fluid suppression) and, 2) to apply quantitative sodium MRI to subjects with and without hip OA (to assess repeatability, sensitivity, specificity of the method, with and without fluid suppression). This method could profoundly affect how we diagnose OA in the hip joint and may allow the identification of high risk individuals and also assess DMOAD treatment follow-ups. Successful completion of this pilot project would allow us to apply to a R01 grant for improving the speed of sodium data acquisition (using compressed sensing) and investigating the clinical value of quantitative sodium MRI for assessing different degrees of OA in comparison to other proton-based imaging techniques such as dGEMRIC, T1 mapping or diffusion imaging.
描述(由申请人提供):骨关节炎(OA)是滑膜关节中最常见的关节炎形式,也是慢性残疾的主要原因,主要发生在老年人群中。它目前影响着9%的美国人口,预计到2030年将影响19%的美国人。OA是一种关节软骨退行性疾病,主要特征是糖胺聚糖(GAG)丢失、胶原纤维大小和组织变化以及含水量增加。OA没有已知的治愈方法,目前的治疗主要集中在疼痛管理和最终的关节置换。研究OA存在许多障碍(病因学的异质性、疾病进展的可变性、观察形态学关节变化所需的长时间),因此我们目前缺乏预测疾病进程的能力。由于OA患者病情进展风险的识别存在局限性,且缺乏无创性早期生化标志物,阻碍了潜在疾病缓解OA药物(DMOAD)的临床开发。具体而言,髋关节骨关节炎在35岁以上的西方人群中的患病率为3%至11%,是老年人髋关节疼痛的主要原因。定量钠磁共振成像(MRI)是一种非侵入性技术,对软骨中的GAG含量具有高度特异性,可用于评估OA中软骨的生化降解程度。然而,由于体内钠浓度低,其灵敏度低,弛豫快,检测到
软骨中钠信号需要高场(> 3 T)、特定线圈和特定3D非笛卡尔
超短回波序列据我们所知,迄今为止尚未发表关于髋关节钠MRI的研究。我们的研究团队最近获得了一个用于3 T成像的双调谐体线圈,这将使我们能够在同一会话中获得髋关节的共同配准质子和钠图像。因此,定量钠MRI可以在临床可行的扫描时间(20-25分钟)内提供软骨GAG含量的独特内源性评估,并允许在形态学损伤发生之前检测关节软骨中的OA,并帮助评估DMOAD治疗的效果。本初步研究的目的是:1)开发和优化体内髋关节定量钠MRI的采集和重建(以优化
用于最小化采集时间、增加信噪比和空间分辨率的采集序列参数,以测量弛豫时间和B1图,并优化滑液抑制)和,2)对患有和不患有髋关节OA的受试者应用定量钠MRI(以评估该方法的可重复性、灵敏度、特异性,有和没有液体抑制)。这种方法可能会深刻影响我们如何诊断髋关节OA,并可能允许识别高风险个体,并评估DMOAD治疗随访。该试点项目的成功完成将使我们能够申请R 01资助,以提高钠数据采集的速度(使用压缩感知),并研究定量钠MRI与其他基于质子的成像技术(如dGEMRIC,T1映射或扩散成像)相比评估不同程度OA的临床价值。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Guillaume MADELIN其他文献
Guillaume MADELIN的其他文献
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{{ truncateString('Guillaume MADELIN', 18)}}的其他基金
Multinuclear MRI to Assess Joint Homeostasis after Knee Injury
多核 MRI 评估膝关节损伤后的关节稳态
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10390153 - 财政年份:2022
- 资助金额:
$ 8.48万 - 项目类别:
Multinuclear MRI to Assess Joint Homeostasis after Knee Injury
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- 批准号:
9889957 - 财政年份:2018
- 资助金额:
$ 8.48万 - 项目类别:
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