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dc.contributor.authorChoi, WooJhon
dc.contributor.authorMoult, Eric Michael
dc.contributor.authorLee, ByungKun
dc.contributor.authorFujimoto, James G
dc.date.accessioned2021-02-03T18:52:56Z
dc.date.available2021-02-03T18:52:56Z
dc.date.issued2017-01
dc.identifier.issn0275-004X
dc.identifier.urihttps://hdl.handle.net/1721.1/129650
dc.description.abstractPurpose: To investigate the utility of ultrahigh speed, swept source optical coherence tomography angiography in visualizing retinal microvascular and choriocapillaris (CC) changes in diabetic patients. Methods: The study was prospective and cross-sectional. A 1,050 nm wavelength, 400 kHz A-scan rate swept source optical coherence tomography prototype was used to perform volumetric optical coherence tomography angiography of the retinal and CC vasculatures in diabetic patients and normal subjects. Sixty-three eyes from 32 normal subjects, 9 eyes from 7 patients with proliferative diabetic retinopathy, 29 eyes from 16 patients with nonproliferative diabetic retinopathy, and 51 eyes from 28 diabetic patients without retinopathy were imaged. Results: Retinal and CC microvascular abnormalities were observed in all stages of diabetic retinopathy. In nonproliferative diabetic retinopathy and proliferative diabetic retinopathy, optical coherence tomography angiography visualized a variety of vascular abnormalities, including clustered capillaries, dilated capillary segments, tortuous capillaries, regions of capillary dropout, reduced capillary density, abnormal capillary loops, and foveal avascular zone enlargement. In proliferative diabetic retinopathy, retinal neovascularization above the inner limiting membrane was visualized. Regions of CC flow impairment in patients with proliferative diabetic retinopathy and nonproliferative diabetic retinopathy were also observed. In 18 of the 51 of eyes from diabetic patients without retinopathy, retinal mircrovascular abnormalities were observed and CC flow impairment was found in 24 of the 51 diabetic eyes without retinopathy. Conclusion: The ability of optical coherence tomography angiography to visualize retinal and CC microvascular abnormalities suggests it may be a useful tool for understanding pathogenesis, evaluating treatment response, and earlier detection of vascular abnormalities in patients with diabetes.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grants NIH R01-EY011289-28, R44-EY022864-03, R01-CA075289-17)en_US
dc.description.sponsorshipUnited States. Air Force. Office of Scientific Research (Grants AFOSR FA9550-10-1-0551 and FA9550-12-1-0499)en_US
dc.language.isoen
dc.publisherOvid Technologies (Wolters Kluwer Health)en_US
dc.relation.isversionof10.1097/IAE.0000000000001250en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleULTRAHIGH SPEED SWEPT SOURCE OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY OF RETINAL AND CHORIOCAPILLARIS ALTERATIONS IN DIABETIC PATIENTS WITH AND WITHOUT RETINOPATHYen_US
dc.title.alternativeUltrahigh Speed OCT Angiography of Retinal and Choriocapillaris Alterations in Diabetic Patients with and without Retinopathy Using Swept Source Optical Coherence Tomographyen_US
dc.typeArticleen_US
dc.identifier.citationChoi, WooJhon et al. “Ultrahigh Speed OCT Angiography of Retinal and Choriocapillaris Alterations in Diabetic Patients with and without Retinopathy Using Swept Source Optical Coherence Tomography.” Retina, 37, 1 (January 2017): 11-21 © 2017 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.relation.journalRetinaen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-12-11T19:30:12Z
dspace.orderedauthorsChoi, W; Waheed, NK; Moult, EM; Adhi, M; Lee, B; De Carlo, T; Jayaraman, V; Baumal, CR; Duker, JS; Fujimoto, JGen_US
dspace.date.submission2020-12-11T19:30:17Z
mit.journal.volume37en_US
mit.journal.issue1en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusComplete


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