Quantitative multimodal retinal imaging
Quantitative multimodal retinal imaging
批准号:
10625417
负责人:
Shuliang Jiao
金额:
$50.09万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-07-01 至 2025-04-30
关键词:
AddressAgeAge related macular degenerationAlgorithmsAnimalsAnteriorAxonBiological MarkersCalibrationClinicalClinical ResearchClinical TrialsCompensationConfocal MicroscopyCytoskeletonDataDegenerative DisorderDetectionDiagnosisDiseaseEarly DiagnosisEarly treatmentEyeFeedbackFiberFluorescenceFunctional ImagingFundusGlaucomaGoalsImageImaging technologyIndividualLearningLightLight CoagulationLipofuscinMass Spectrum AnalysisMeasuresMelaninsMelanosomesModelingMolecularMonitorMultimodal ImagingNerve FibersNonexudative age-related macular degenerationOphthalmologistOptical Coherence TomographyOpticsPathogenesisPatient CarePatientsPhysiologic Intraocular PressurePolymethyl MethacrylatePredispositionRattusReference StandardsResearchRetinaRetinal DegenerationRetinal DiseasesRetinal Ganglion CellsSignal TransductionSlideSolidSourceStagingStainsStargardt&aposs diseaseStructure of retinal pigment epitheliumSystemTechnologyTestingTheoretical modelThickThinnessTimeTrabecular meshwork structureVisible RadiationWorkabsorptionage groupanimal imagingattenuationclinically significantcontrast imagingfollow-upfrontierfundus imaginghuman imaginghuman subjectimaging studyimprovedinterestmultimodalitynew technologynovelnovel imaging technologyquantitative imagingretinal damageretinal imagingretinal nerve fiber layertherapy developmenttitanium dioxidetooltreatment strategy
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary-Abstract
Our ultimate goal is to develop a multimodal VIS-OCT platform for retinal imaging to improve patient care and to
advance clinical research. We proposed to develop a visible-light optical coherence tomography (VIS-OCT)
platform for multimodal multifunctional imaging of the retina. Two novel VIS-OCT based imaging technologies
will be built in this platform: quantitative fundus autofluorescence (FAF) or VIS-OCT-FAF, and retinal nerve fiber
layer (RNFL) spectral contrast OCT or DUAL-OCT-RNFL. The two new technologies will add new tools for
ophthalmologists to make early diagnosis and better monitor retinal diseases. The proposed work is based on
hypotheses that are strongly supported by our theoretical modeling and solid preliminary data. We hypothesize
that 1) Quantification of absolute FAF intensity can be achieved by normalizing raw FAF signals with an
internal reference and an external standard fluorescence reference; 2) RPE OCT signals
simultaneously acquired with FAF can serve as an internal reference; and 3) The spectral contrast of
the RNFL can be used as a biomarker for RNFL damage by elevated IOP. Three Specific Aims are
proposed. Aim 1: To develop a VIS-OCT platform for VIS-OCT-FAF and DUAL-OCT-RNFL imaging. We will
develop and refine the VIS-OCT platform consisting of a VIS-OCT centered at 480 nm, a NIR-OCT centered at
840 nm, and a FAF detection module. A reference target with known fluorescence efficiency and reflectance
placed in the intermediate retinal imaging plane will serve as a reference to normalize raw data to obtain absolute
FAF intensity and quantitative RNFL spectral reflectance. The reference target will use a PMMA slide stained
with A2E as fluorescent molecule. We will introduce the A2E equivalent unit (AEU) as a measure of FAF. Aim 2:
To study VIS-OCT-FAF and DUAL-OCT-RNFL imaging in phantom and animals. We will test the system in
phantom and animals to verify the capabilities of the VIS-OCT platform, to calibrate and obtain feedback for
fine-tuning the hardware and algorithms. Phantom studies will use a model eye with A2E, melanosome and TiO2
to simulate lipofuscin, absorption and scattering in RPE. FAF images from albino and pigmented rats of different
ages will be studied. A2E in each imaged eye will be quantified by mass-spectroscopy to verify the accuracy of
FAF signals. Elevated IOP will be induced on rats by photocoagulation to the trabecular meshwork. RNFL
spectral contrast images from eyes with or without increased IOP will be compared. Aim 3: To study
VIS-OCT-FAF and DUAL-OCT-RNFL imaging in human subjects. Our ultimate goal is to develop a
multimodal VIS-OCT platform for retinal imaging to improve patient care and to advance clinical research.
Studies in this Aim will allow us to learn how the systems behave in a real clinical setting. We will image normal
subjects of 6 age groups to establish age-based normative data. Patients with early dry AMD and Stargardt’s
disease will also be studied. In the RNFL imaging studies, we will image 6 age groups of normal individuals to
establish age-based normative data. Patients with early stage glaucoma will be studied.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
Quantitative multimodal retinal imaging
-
批准号:10211698
-
项目类别:
-
资助金额:$50.23万
-
财政年份:2021
-
负责人:Shuliang Jiao
-
依托单位:
Quantitative multimodal retinal imaging
-
批准号:10436240
-
项目类别:
-
资助金额:$46.78万
-
财政年份:2021
-
负责人:Shuliang Jiao
-
依托单位:
Imaging the functional biomarker of photoreceptors
-
批准号:9239662
-
项目类别:
-
资助金额:$49.52万
-
财政年份:2017
-
负责人:Shuliang Jiao
-
依托单位:
Imaging the functional biomarker of photoreceptors
-
批准号:9893878
-
项目类别:
-
资助金额:$48.56万
-
财政年份:2017
-
负责人:Shuliang Jiao
-
依托单位:
Ophthalmic imaging of small animal models of ocular diseases
-
批准号:7512280
-
项目类别:
-
资助金额:$2.64万
-
财政年份:2008
-
负责人:Shuliang Jiao
-
依托单位:
Ophthalmic imaging of small animal models of ocular diseases
-
批准号:7755760
-
项目类别:
-
资助金额:$18.82万
-
财政年份:2008
-
负责人:Shuliang Jiao
-
依托单位:
Ophthalmic imaging of small animal models of ocular diseases
-
批准号:7681660
-
项目类别:
-
资助金额:$19.13万
-
财政年份:2008
-
负责人:Shuliang Jiao
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
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
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
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
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
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:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
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
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
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:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
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:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
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:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
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
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
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
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: