Ultrashort Echo Time (UTE) Magnetic Resonance Imaging of Bone
骨超短回波时间 (UTE) 磁共振成像
基本信息
- 批准号:9005600
- 负责人:
- 金额:$ 51.96万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2015
- 资助国家:美国
- 起止时间:2015-09-17 至 2019-08-31
- 项目状态:已结题
- 来源:
- 关键词:AffectAgeBindingBiochemicalBiochemical MarkersBiological MarkersBiomechanicsBody mass indexBone DensityBone MarrowBone MatrixCattleCollagenControl GroupsDiagnosisDual-Energy X-Ray AbsorptiometryElderlyEthnic OriginEvaluationFatty acid glycerol estersFractureGoalsGoldHead and neck structureHumanImageImaging TechniquesIsotopesLegMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMarrowMeasurementMeasuresMechanicsMedicineMineralsModelingMonitorNMR SpectroscopyNeckObesityOsteoporosisPhysiologic pulsePlayPorosityPostmenopausePremenopausePropertyQuantitative EvaluationsReference StandardsRelaxationRiskRisk FactorsRoleSamplingScanningSignal TransductionSoft Tissue DisorderSpecimenStagingStructure of greater trochanter of femurTechniquesTestingTherapeuticTimeTriglyceridesUnsaturated FatsWaterWomanWorkX-Ray Computed Tomographyage groupbasebonebone lossbone qualityclinical sequencingcohortdensityimprovedin vivoin vivo imaginginsightinterestmillisecondnovelosteoporosis with pathological fracturepublic health relevancequantitative imagingsubstantia spongiosatemporal measurementtwo-dimensional
项目摘要
DESCRIPTION (provided by applicant): Quantitative imaging of bone has been of central importance in medicine since Roentgen produced the first radiograph in 1895. The current gold standard technique DEXA measures bone mineral density (BMD). However, the majority of bone, including the organic matrix and bone water which together occupy ~60% of bone by volume is inaccessible. BMD by itself only predicts osteoporotic fractures with an accuracy of 30-50%. The overall fracture risk increases 13-fold from ages 60 to 80, but BMD alone only predicts a doubling of the fracture risk. In addition, recent studies demonstrate that bone marrow adiposity plays an active role in affecting bone quantity and quality. There is considerable interest in more comprehensive evaluation of bone quality using information not only about bone mineral, but organic matrix, bone water and marrow fat. All of these factors may play a role in maintaining the biomechanical integrity of cortical and trabecular bone. Magnetic resonance imaging (MRI) is routinely used in the diagnosis of soft tissue disease. However, bone is "invisible" using all clinical sequences due to its short T2*. We have developed 2D and 3D UTE sequences with TEs of 8 µs that are ~1000 times shorter than conventional TEs. This makes it possible to detect multiple water components in cortical bone, and fat content and composition in trabecular bone. The pore water content provides a surrogate measure of cortical porosity. Collagen-bound water provides an indirect measure of organic matrix density. Marrow fat content and composition provide BMD independent fracture risk factors. It would be a major advance to develop UTE MRI techniques to evaluate porosity and organic matrix density in cortical bone, as well as marrow fat content and composition in trabecular bone. This study aims to develop and combine novel 3D UTE MRI techniques to evaluate cortical and trabecular bone offering full insight into bone characterization and correlation with function. To achieve thi goal, in Aim 1 we will evaluate 3D UTE MRI techniques for assessment of cortical bone. We will determine the accuracy of UTE measurement of collagen-bound and pore water, and correlate UTE MRI metrics (collagen-bound and pore water content, T1, T2* and MTR) with biomechanical properties of cortical bone. In Aim 2 we will evaluate 3D UTE MRI techniques for evaluation of trabecular bone. We will determine the accuracy of 3D UTE MRI measurement of marrow fat content and composition and correlate 3D UTE MRI metrics with those from MR spectroscopy (MRS) as well as biomechanical properties of trabecular bone. In Aim 3 we will apply the validated 3D UTE MRI techniques to study one group of premenopausal women and two groups of postmenopausal women with slow or fast bone loss. We will compare the 3D UTE MRI and MRS metrics in different groups and correlate the results with BMD and biochemical markers. This work will provide accurate panels of 3D UTE MRI and MRS based biomarkers which may be important for assessing bone quality, and may have a major impact on the diagnosis and therapeutic monitoring of OP.
描述(由申请人提供):自1895年伦琴拍摄第一张X线照片以来,骨的定量成像在医学中一直具有核心重要性。目前的金标准技术DEXA测量骨矿物质密度(BMD)。然而,大部分骨,包括有机基质和骨水,它们一起占骨体积的约60%,是不可接近的。BMD本身仅能以30- 50%的准确率预测骨质疏松性骨折。从60岁到80岁,整体骨折风险增加了13倍,但单独的BMD只能预测骨折风险增加一倍。此外,最近的研究表明,骨髓肥胖在影响骨的数量和质量方面起着积极的作用。有相当大的兴趣,更全面的评价骨质量,不仅使用有关骨矿物质,但有机基质,骨水和骨髓脂肪的信息。所有这些因素都可能在维持皮质骨和松质骨的生物力学完整性方面发挥作用。 磁共振成像(MRI)通常用于诊断软组织疾病。然而,由于其短T2*,使用所有临床序列,骨是“不可见的”。我们开发了TE为8 µs的2D和3D UTE序列,比传统TE短约1000倍。这使得可以检测皮质骨中的多种水成分以及松质骨中的脂肪含量和组成。孔隙水含量提供了皮质孔隙度的替代测量。胶原结合水提供了有机基质密度的间接测量。骨髓脂肪含量和组成提供了与骨密度无关的骨折危险因素。这将是一个重大的进展,发展UTE MRI技术,以评估孔隙率和有机基质密度的皮质骨,以及骨髓脂肪含量和组成的松质骨。 本研究旨在开发并联合收割机新型3D UTE MRI技术,以评价皮质骨和松质骨,从而全面了解骨表征及其与功能的相关性。为了实现这一目标,在目标1中,我们将评价3D UTE MRI技术用于评估皮质骨。我们将确定UTE测量胶原结合水和孔隙水的准确性,并将UTE MRI指标(胶原结合水和孔隙水含量、T1、T2* 和MTR)与皮质骨的生物力学特性相关联。在目标2中,我们将评价3D UTE MRI技术用于评价骨小梁。我们将确定骨髓脂肪含量和组成的3D UTE MRI测量的准确性,并将3D UTE MRI指标与MR波谱(MRS)指标以及松质骨的生物力学特性相关联。在目标3中,我们将应用经验证的3D UTE MRI技术研究一组绝经前妇女和两组绝经后妇女的缓慢或快速骨丢失。我们将比较不同组的3D UTE MRI和MRS指标,并将结果与BMD和生化标志物相关联。这项工作将提供准确的3D UTE MRI和MRS生物标志物,这可能是重要的评估骨质量,并可能有重大影响的诊断和治疗监测的OP。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Jiang Du其他文献
Jiang Du的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Jiang Du', 18)}}的其他基金
Quantitative UTE MR Imaging of Myelin: Novel Biomarkers for Alzheimer's Disease
髓鞘质的定量 UTE MR 成像:阿尔茨海默病的新型生物标志物
- 批准号:
10525525 - 财政年份:2022
- 资助金额:
$ 51.96万 - 项目类别:
Developing MRI Biomarkers of Myelin and Iron in Veterans with Traumatic Brain Injury
开发患有创伤性脑损伤的退伍军人的髓磷脂和铁的 MRI 生物标志物
- 批准号:
10246748 - 财政年份:2021
- 资助金额:
$ 51.96万 - 项目类别:
Developing MRI Biomarkers of Myelin and Iron in Veterans with Traumatic Brain Injury
开发患有创伤性脑损伤的退伍军人的髓磷脂和铁的 MRI 生物标志物
- 批准号:
10426261 - 财政年份:2021
- 资助金额:
$ 51.96万 - 项目类别:
Ultrashort Echo Time (UTE) Magnetic Resonance Imaging of Bone
骨超短回波时间 (UTE) 磁共振成像
- 批准号:
10379443 - 财政年份:2015
- 资助金额:
$ 51.96万 - 项目类别:
Ultrashort Echo Time (UTE) Magnetic Resonance Imaging of Bone
骨超短回波时间 (UTE) 磁共振成像
- 批准号:
9344532 - 财政年份:2015
- 资助金额:
$ 51.96万 - 项目类别:
UTE Magnetic Resonance Imaging: New Biomarkers for Multiple Sclerosis
UTE 磁共振成像:多发性硬化症的新生物标志物
- 批准号:
9095465 - 财政年份:2015
- 资助金额:
$ 51.96万 - 项目类别:
Ultrashort Echo Time (UTE) Magnetic Resonance Imaging of Bone
骨超短回波时间 (UTE) 磁共振成像
- 批准号:
10132985 - 财政年份:2015
- 资助金额:
$ 51.96万 - 项目类别:
Ultrashort Echo Time (UTE) Magnetic Resonance Imaging of Bone
骨超短回波时间 (UTE) 磁共振成像
- 批准号:
10613881 - 财政年份:2015
- 资助金额:
$ 51.96万 - 项目类别:
Ultrashort Echo Time (UTE) Magnetic Resonance Imaging of Bone
骨超短回波时间 (UTE) 磁共振成像
- 批准号:
9981928 - 财政年份:2015
- 资助金额:
$ 51.96万 - 项目类别:
Quantitative UTE MR Imaging: Sensitive Biomarkers for Osteoarthritis
定量 UTE MR 成像:骨关节炎的敏感生物标志物
- 批准号:
8728743 - 财政年份:2013
- 资助金额:
$ 51.96万 - 项目类别:
相似国自然基金
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
- 批准号:JCZRQN202500010
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
- 批准号:2025JJ70209
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
- 批准号:
- 批准年份:2024
- 资助金额:0 万元
- 项目类别:面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
- 批准号:2023JJ50274
- 批准年份:2023
- 资助金额:0.0 万元
- 项目类别:省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
- 批准号:
- 批准年份:2022
- 资助金额:33 万元
- 项目类别:地区科学基金项目
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
- 批准号:
- 批准年份:2022
- 资助金额:52 万元
- 项目类别:面上项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
- 批准号:
- 批准年份:2022
- 资助金额:10.0 万元
- 项目类别:省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
- 批准号:81973577
- 批准年份:2019
- 资助金额:55.0 万元
- 项目类别:面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
- 批准号:81602908
- 批准年份:2016
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
- 批准号:81501928
- 批准年份:2015
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
相似海外基金
The role of intermittent binge ethanol, sex, and age on memory and CREB binding protein (CBP) expression
间歇性酗酒、性别和年龄对记忆和 CREB 结合蛋白 (CBP) 表达的影响
- 批准号:
10429943 - 财政年份:2021
- 资助金额:
$ 51.96万 - 项目类别:
The role of intermittent binge ethanol, sex, and age on memory and CREB binding protein (CBP) expression
间歇性酗酒、性别和年龄对记忆和 CREB 结合蛋白 (CBP) 表达的影响
- 批准号:
10315664 - 财政年份:2021
- 资助金额:
$ 51.96万 - 项目类别:
The role of intermittent binge ethanol, sex, and age on memory and CREB binding protein (CBP) expression
间歇性酗酒、性别和年龄对记忆和 CREB 结合蛋白 (CBP) 表达的影响
- 批准号:
10618314 - 财政年份:2021
- 资助金额:
$ 51.96万 - 项目类别:
The role of hypothalamic RNA binding protein Caprin2 in osmoregulatory dysfunction in old age
下丘脑RNA结合蛋白Caprin2在老年渗透压调节功能障碍中的作用
- 批准号:
BB/R016879/1 - 财政年份:2018
- 资助金额:
$ 51.96万 - 项目类别:
Research Grant
Procollagen Binding Proteins in Age-Dependent LV Remodeling
年龄依赖性左心室重塑中的原胶原结合蛋白
- 批准号:
8795683 - 财政年份:2012
- 资助金额:
$ 51.96万 - 项目类别:
Procollagen Binding Proteins in Age-Dependent LV Remodeling
年龄依赖性左心室重塑中的原胶原结合蛋白
- 批准号:
8326830 - 财政年份:2012
- 资助金额:
$ 51.96万 - 项目类别:
Procollagen Binding Proteins in Age-Dependent LV Remodeling
年龄依赖性左心室重塑中的原胶原结合蛋白
- 批准号:
8698295 - 财政年份:2012
- 资助金额:
$ 51.96万 - 项目类别:
Procollagen Binding Proteins in Age-Dependent LV Remodeling
年龄依赖性左心室重塑中的原胶原结合蛋白
- 批准号:
8440206 - 财政年份:2012
- 资助金额:
$ 51.96万 - 项目类别:
Adult Age Differences in Binding Actors and Actions
约束演员和动作的成人年龄差异
- 批准号:
6757012 - 财政年份:2004
- 资助金额:
$ 51.96万 - 项目类别:
Characterisation of Novel AGE Binding Proteins: Implications for Diabetic Vascular Complications.
新型 AGE 结合蛋白的表征:对糖尿病血管并发症的影响。
- 批准号:
nhmrc : 208940 - 财政年份:2002
- 资助金额:
$ 51.96万 - 项目类别:
NHMRC Project Grants














{{item.name}}会员




