This proposal is a resubmission of a competing renewal application for an ongoing collaborative program among investigators at the Massachusetts Institute of Technology, New England Eye Center and University of Pittsburgh Medical Center Eye Center. This is a multidisciplinary program which integrates imaging technology research, clinical and small animal imaging studies.
The specific aims are:
Aim 1. Next generation OCT technology and methods for structural and functional imaging. We propose to develop ultrahigh speed swept source OCT (SSOCT) at 1050nm which will enable wide field volumetric retinal and choroidal structural imaging, OCT angiography of retinal and choroidal microvasculature as well as Doppler OCT to measure total retinal blood flow and functional stimulus response. In parallel, we will continue development of ultrahigh resolution (UHR) spectral domain OCT (SDOCT) with 2-3?m axial resolution to visualize and measure outer retinal structures. We will also develop 3D image processing techniques to correct motion artifacts, enable volumetric data averaging and quantitatively analyze 3D data. Volumetric data from different patient visits will be registered to track disease progression and measure subtle changes in pathology.
Aim 2. Structural and functional imaging of age-related macular degeneration (AMD), diabetic retinopathy (DR) and glaucoma. Cross sectional and longitudinal structural and functional clinical imaging studies will be performed in patients with AMD, DR and glaucoma. Changes in photoreceptors, RPE and Bruch's membrane are possible markers of disease in AMD and will be investigated using UHR SDOCT. Volumetric structural imaging of the retina and choroid will be performed using ultrahigh speed SSOCT. 3D vascular and capillary structure in the retina, ONH, choriocapillaris and choroid, potential markers of AMD, DR, and glaucoma will be investigated using OCT angiography. Alterations in blood flow and functional flicker stimulus response (neurovascular coupling) will be investigated in DR and glaucoma patients using Doppler OCT and OCT angiography. Studies will include patients with different levels of disease as well as normal controls. The objective is to identify new structural and functional markers for early diagnosis, monitoring progression and response to therapy.
Aim 3. New OCT techniques for structural and functional imaging in small animals. We propose to develop ultrahigh speed OCT methods for structural and functional hemodynamic imaging in small animals. Studies will investigate the streptozotocin-induced rat diabetes model compared to normal controls. We will also develop spectroscopic OCT techniques to measure retinal vascular permeability with Evans blue dye exogenous contrast. Spectroscopic OCT will provide 3D maps of retinal vascular permeability and will be more efficient than current ex vivo Evans blue vascular permeability assays. Advances in small animal imaging will be powerful tools for both fundamental studies of disease mechanisms and pharmaceutical development.

Public Health Relevance

This program is a multidisciplinary effort between investigators at the Massachusetts Institute of Technology, the New England Eye Center and the University of Pittsburgh Medical Center Eye Center which integrates fundamental studies, technology research and clinical studies. The objective is to develop advanced optical imaging technology using optical coherence tomography (OCT) to perform structural and functional imaging of the retina. We will investigate novel markers of age related macular degeneration, diabetic retinopathy and glaucoma for early diagnosis and improved monitoring of disease progression and treatment response.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY011289-33
Application #
9684616
Study Section
Neuroscience and Ophthalmic Imaging Technologies Study Section (NOIT)
Program Officer
Greenwell, Thomas
Project Start
1985-09-01
Project End
2020-03-31
Budget Start
2019-03-01
Budget End
2020-03-31
Support Year
33
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Miscellaneous
Type
Organized Research Units
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Arya, Malvika; Rashad, Ramy; Sorour, Osama et al. (2018) Optical coherence tomography angiography (OCTA) flow speed mapping technology for retinal diseases. Expert Rev Med Devices :1-8
Schirrmacher, Franziska; Köhler, Thomas; Endres, Jürgen et al. (2018) Temporal and volumetric denoising via quantile sparse image prior. Med Image Anal 48:131-146
Liang, Kaicheng; Wang, Zhao; Ahsen, Osman O et al. (2018) Cycloid scanning for wide field optical coherence tomography endomicroscopy and angiography in vivo. Optica 5:36-43
Wang, Bo; Lucy, Katie A; Schuman, Joel S et al. (2018) Tortuous Pore Path Through the Glaucomatous Lamina Cribrosa. Sci Rep 8:7281
Lee, Hsiang-Chieh; Ahsen, Osman O; Liang, Kaicheng et al. (2017) Endoscopic optical coherence tomography angiography microvascular features associated with dysplasia in Barrett's esophagus (with video). Gastrointest Endosc 86:476-484.e3
Rebhun, Carl B; Moult, Eric M; Novais, Eduardo A et al. (2017) Polypoidal Choroidal Vasculopathy on Swept-Source Optical Coherence Tomography Angiography with Variable Interscan Time Analysis. Transl Vis Sci Technol 6:4
Cole, Emily D; Moult, Eric M; Dang, Sabin et al. (2017) The Definition, Rationale, and Effects of Thresholding in OCT Angiography. Ophthalmol Retina 1:435-447
Lucy, Katie A; Wang, Bo; Schuman, Joel S et al. (2017) Thick Prelaminar Tissue Decreases Lamina Cribrosa Visibility. Invest Ophthalmol Vis Sci 58:1751-1757
Tieger, Marisa G; Hedges 3rd, Thomas R; Ho, Joseph et al. (2017) Ganglion Cell Complex Loss in Chiasmal Compression by Brain Tumors. J Neuroophthalmol 37:7-12
Skalet, Alison H; Li, Yan; Lu, Chen D et al. (2017) Optical Coherence Tomography Angiography Characteristics of Iris Melanocytic Tumors. Ophthalmology 124:197-204

Showing the most recent 10 out of 300 publications