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dc.contributor.authorRegatieri, Caio V.
dc.contributor.authorBranchini, Lauren
dc.contributor.authorCarmody, Jill
dc.contributor.authorFujimoto, James G.
dc.contributor.authorDuker, Jay S.
dc.date.accessioned2014-05-05T17:14:08Z
dc.date.available2014-05-05T17:14:08Z
dc.date.issued2012-03
dc.identifier.issn0275-004X
dc.identifier.urihttp://hdl.handle.net/1721.1/86410
dc.description.abstractPurpose: This study was designed to examine choroidal thickness in patients with diabetes using spectral-domain optical coherence tomography. Methods: Forty-nine patients (49 eyes) with diabetes and 24 age-matched normal subjects underwent high-definition raster scanning using spectral-domain optical coherence tomography with frame enhancement software. Patients with diabetes were classified into 3 groups: 11 patients with mild or moderate nonproliferative diabetic retinopathy and no macular edema, 18 patients with nonproliferative diabetic retinopathy and diabetic macular edema, and 20 patients with treated proliferative diabetic retinopathy and no diabetic macular edema (treated proliferative diabetic retinopathy). Choroidal thickness was measured from the posterior edge of the retinal pigment epithelium to the choroid/sclera junction at 500-[mu]m intervals up to 2,500 [mu]m temporal and nasal to the fovea. Results: Reliable measurements of choroidal thickness were obtainable in 75.3% of eyes examined. Mean choroidal thickness showed a pattern of thinnest choroid nasally, thickening in the subfoveal region, and thinning again temporally in normal subjects and patients with diabetes. Mean subfoveal choroidal thickness was thinner in patients with diabetic macular edema (63.3 [mu]m, 27.2%, P < 0.05) or treated proliferative diabetic retinopathy (69.6 [mu]m, 30.0%, P < 0.01), compared with normal subjects. There was no difference between nonproliferative diabetic retinopathy and normal subjects. Conclusion: Choroidal thickness is altered in diabetes and may be related to the severity of retinopathy. Presence of diabetic macular edema is associated with a significant decrease in the choroidal thickness.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Contract RO1-EY11289-23)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Contract R01-EY13178-07)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Contract R01-EY013516-07)en_US
dc.description.sponsorshipUnited States. Air Force Office of Scientific Research (Grant FA9550-07-1-0101)en_US
dc.description.sponsorshipUnited States. Air Force Office of Scientific Research (Grant FA9550-07-1-0014)en_US
dc.language.isoen_US
dc.publisherOvid Technologies (Wolters Kluwer) - Lippincott Williams & Wilkinsen_US
dc.relation.isversionofhttp://dx.doi.org/10.1097/iae.0b013e31822f5678en_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.titleCHOROIDAL THICKNESS IN PATIENTS WITH DIABETIC RETINOPATHY ANALYZED BY SPECTRAL-DOMAIN OPTICAL COHERENCE TOMOGRAPHYen_US
dc.typeArticleen_US
dc.identifier.citationRegatieri, Caio V., Lauren Branchini, Jill Carmody, James G. Fujimoto, and Jay S. Duker. “CHOROIDAL THICKNESS IN PATIENTS WITH DIABETIC RETINOPATHY ANALYZED BY SPECTRAL-DOMAIN OPTICAL COHERENCE TOMOGRAPHY.” Retina (February 2012): 1.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.mitauthorFujimoto, James G.en_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
dspace.orderedauthorsRegatieri, Caio V.; Branchini, Lauren; Carmody, Jill; Fujimoto, James G.; Duker, Jay S.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-0828-4357
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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