UTE MR Imaging of the Cartilaginous Endplate in the Lumbar Spine
腰椎软骨终板的 UTE MR 成像
基本信息
- 批准号:8274445
- 负责人:
- 金额:$ 12.02万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-07-01 至 2014-06-30
- 项目状态:已结题
- 来源:
- 关键词:AffectAgeAgingAppearanceBack PainBiochemicalBiologicalBiological AssayBiological Response Modifier TherapyBiomechanicsBlood VesselsCalcifiedCalciumCartilageCell physiologyCellsChemicalsChondroitin ABC LyaseContrast MediaDepositionDiseaseEarly treatmentEdetic AcidEtiologyEvaluationExhibitsGoalsGrowth FactorHistologyHomeostasisHumanImageImaging TechniquesImmunohistochemistryImplantIntervertebral disc structureInvestigationLeadLiquid substanceLow Back PainMagnetic Resonance ImagingMatched GroupMorphologyNutrientNutritionalPathogenesisPatient SelectionPatientsPerfusionPlayPopulationPreparationPropertyPublic HealthResearchRoleSamplingSignal TransductionStructureSymptomsTechniquesTestingTherapeuticThickTimeTissuesVertebral columnbasebonecalcificationcollagenaseintervertebral disk degenerationnovelnutritionpatient populationvertebra body
项目摘要
DESCRIPTION (provided by applicant): Degeneration of intervertebral discs is associated with low back pain, which affects a large proportion of the U.S. population. Treatments for back pain, such as therapeutics (e.g., growth factors) to alter cell function and biological implants aimed at modifying symptoms and the morphology of intervertebral discs are topics of active investigation at present. The cartilaginous endplate (CEP), which is a part of the intervertebral disc and is situated between the avascular disc proper and the bony vertebral body, plays an important role in the function and homeostasis of the disc. Vascular canals are found in calcified portions of the CEP and facilitate the supply of nutrients to the disc. Past studies have noted structural and compositional changes such as thinning and calcification of cartilage with aging and these may change the transport properties of the endplate. Such changes may lead to subsequent disc degeneration, and ultimately back pain. Additionally, hindered transport through the CEP may render biologic treatment options ineffective, if cells do not receive sufficient concentration of the active agent. Non-invasive evaluation of cartilaginous endplate, and its association with disc degeneration, is likely to be of critical importance in selecting patients for various treatments, as well as in understanding disc degeneration. The long-term goal of our study is to evaluate changes in the cartilaginous endplates of the disc using novel magnetic resonance imaging (MRI) approaches. The overall hypothesis is that ultra short time-to-echo (UTE) MR imaging will be sensitive to abnormal changes in structure, composition and transport properties of the cartilaginous endplate (CEP) of human spine, and that abnormalities will be associated with disc degeneration. The UTE sequence captures short T2 signals intrinsic to the CEP, parts of which are invisible using conventional sequences. I propose to perform UTE MRI on experimentally prepared CEP samples to determine the structural and compositional basis underlying the signal change, and use these findings to help understand signal changes seen in abnormal endplates. Transport properties of normal and abnormal cartilaginous endplates will be correlated with UTE MRI signals, to establish the functional basis of fluid transfer with and without loading. Lastly, the association between UTE MRI signals and disc degeneration will be assessed. The proposed research will provide a non-invasive means of evaluating disease of the cartilaginous endplates of human spines and increase our understanding of the relationship between UTE MRI appearances, endplate structure, composition, and function. This is likely to be useful for early intervention in treatment of disc degeneration and selection of patients suitable for biological therapy.
描述(由申请人提供):椎间盘退变与腰痛相关,影响了很大一部分美国人群。治疗背痛的方法,如改变细胞功能的疗法(如生长因子)和旨在改变症状和椎间盘形态的生物植入物,是目前积极研究的主题。软骨终板(CEP)是椎间盘的一部分,位于无血管椎间盘和骨性椎体之间,对椎间盘的功能和内部平衡起着重要作用。在CEP钙化部分发现血管管,促进向椎间盘提供营养。过去的研究指出,随着年龄的增长,软骨变薄和钙化等结构和成分的变化可能会改变终板的运输特性。这些变化可能导致随后的椎间盘退变,最终导致背痛。此外,如果细胞没有获得足够浓度的活性剂,通过CEP的运输受阻可能会使生物治疗方案无效。无创评估软骨终板及其与椎间盘退变的关系,可能对选择各种治疗方法的患者以及了解椎间盘退变具有至关重要的意义。我们研究的长期目标是利用新型磁共振成像(MRI)方法评估椎间盘软骨终板的变化。总的假设是,超短时间回声(UTE) MR成像对人类脊柱软骨终板(CEP)的结构、组成和运输特性的异常变化敏感,并且异常与椎间盘退变有关。UTE序列捕获CEP固有的短T2信号,其中部分信号使用常规序列是不可见的。我建议对实验制备的CEP样品进行UTE MRI,以确定信号变化的结构和成分基础,并利用这些发现来帮助理解异常终板中所见的信号变化。正常和异常软骨终板的输运特性将与UTE MRI信号相关联,建立有载荷和无载荷流体输运的功能基础。最后,将评估UTE MRI信号与椎间盘退变之间的关系。本研究将提供一种评估人类脊柱软骨终板疾病的非侵入性方法,并增加我们对UTE MRI表现、终板结构、组成和功能之间关系的理解。这可能有助于椎间盘退变的早期干预治疗和选择适合生物治疗的患者。
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 }}
Won C Bae其他文献
Won C Bae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('Won C Bae', 18)}}的其他基金
Ultrashort Time to Echo MRI of Disco Vertebral Junction
迪斯科椎体交界处的超短时间回波 MRI
- 批准号:
8886674 - 财政年份:2015
- 资助金额:
$ 12.02万 - 项目类别:
UTE MR Imaging of the Cartilaginous Endplate in the Lumbar Spine
腰椎软骨终板的 UTE MR 成像
- 批准号:
8103908 - 财政年份:2010
- 资助金额:
$ 12.02万 - 项目类别:
UTE MR Imaging of the Cartilaginous Endplate in the Lumbar Spine
腰椎软骨终板的 UTE MR 成像
- 批准号:
8496718 - 财政年份:2010
- 资助金额:
$ 12.02万 - 项目类别:
UTE MR Imaging of the Cartilaginous Endplate in the Lumbar Spine
腰椎软骨终板的 UTE MR 成像
- 批准号:
7962968 - 财政年份:2010
- 资助金额:
$ 12.02万 - 项目类别:
Biomechanical Basis for Treatment of Cartilage defects
软骨缺损治疗的生物力学基础
- 批准号:
7156450 - 财政年份:2006
- 资助金额:
$ 12.02万 - 项目类别:
Biomechanical Basis for Treatment of Cartilage defects
软骨缺损治疗的生物力学基础
- 批准号:
7494460 - 财政年份:2006
- 资助金额:
$ 12.02万 - 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:n/a
- 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 Phenomenon of Stem Cell Aging according to Methylation Estimates of Age After Hematopoietic Stem Cell Transplantation
根据造血干细胞移植后甲基化年龄估算干细胞衰老现象
- 批准号:
23K07844 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Analysis of Age-dependent Functional Changes in Skeletal Muscle CB1 Receptors by an in Vitro Model of Aging-related Muscle Atrophy
通过衰老相关性肌肉萎缩的体外模型分析骨骼肌 CB1 受体的年龄依赖性功能变化
- 批准号:
22KJ2960 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Grant-in-Aid for JSPS Fellows
Joint U.S.-Japan Measures for Aging and Dementia Derived from the Prevention of Age-Related and Noise-induced Hearing Loss
美日针对预防与年龄相关和噪声引起的听力损失而导致的老龄化和痴呆症联合措施
- 批准号:
23KK0156 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Fund for the Promotion of Joint International Research (International Collaborative Research)
The Effects of Muscle Fatigability on Gait Instability in Aging and Age-Related Falls Risk
肌肉疲劳对衰老步态不稳定性和年龄相关跌倒风险的影响
- 批准号:
10677409 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Characterizing gut physiology by age, frailty, and sex: assessing the role of the aging gut in "inflamm-aging"
按年龄、虚弱和性别表征肠道生理学特征:评估衰老肠道在“炎症衰老”中的作用
- 批准号:
497927 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
- 批准号:
10679287 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Role of AGE/RAGEsignaling as a driver of pathological aging in the brain
AGE/RAGE信号传导作为大脑病理性衰老驱动因素的作用
- 批准号:
10836835 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Elucidation of the protein kinase NLK-mediated aging mechanisms and treatment of age-related diseases
阐明蛋白激酶NLK介导的衰老机制及年龄相关疾病的治疗
- 批准号:
23K06378 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Underlying mechanisms of age-related changes in ingestive behaviors: From the perspective of the aging brain and deterioration of the gustatory system.
与年龄相关的摄入行为变化的潜在机制:从大脑老化和味觉系统退化的角度来看。
- 批准号:
23K10845 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Targeting Age-Activated Proinflammatory Chemokine Signaling by CCL2/11 to Enhance Skeletal Muscle Regeneration in Aging
通过 CCL2/11 靶向年龄激活的促炎趋化因子信号传导以增强衰老过程中的骨骼肌再生
- 批准号:
478877 - 财政年份:2023
- 资助金额:
$ 12.02万 - 项目类别:
Operating Grants