Alterations of choroidal thickness with diabetic neuropathy

dc.contributor.authorYazıcı, Alper
dc.contributor.authorSarı, Esin Söğütlü
dc.contributor.authorKoç, Emine Rabia
dc.contributor.authorŞahin, Gözde
dc.contributor.authorKurt, Hüseyin
dc.contributor.authorÖzdal, Pınar Çakar
dc.contributor.authorErmiş, Sıtkı Samet
dc.date.accessioned2019-10-17T11:39:17Z
dc.date.available2019-10-17T11:39:17Z
dc.date.issued2016en_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.descriptionYazıcı, Alper (Balikesir Author)en_US
dc.description.abstractPURPOSE. To evaluate the effect of diabetic polyneuropathy on choroidal thickness in type 2 diabetes patients. METHODS. Forty-one diabetic polyneuropathy (DPN) patients with no or mild retinopathy, 50 non-DPN diabetic patients with no or mild retinopathy, and 42 healthy controls without any retinal complaint were included in the study. All participants underwent detailed ophthalmic examinations. Choroidal thickness (CT) measurements were performed by the same independent technician in the morning between 9 and 11 AM to avoid diurnal variations. Perpendicular CT was measured from the outer edge of the hyperreflective retinal pigment epithelium to the inner sclera at seven locations: the fovea; and 500, 1000, and 1500 mu m temporally and nasally to the fovea. RESULTS. The groups were age and sex matched (P > 0.05). The mean subfoveal CT values were significantly different in groups with a thickening trend from control to non-DPN and DPN (P < 0.01). The mean values for subfoveal CT in control, non-DPN, and DPN groups were 241.12 +/- 52.71, 279.82 +/- 51.42, and 304.71 +/- 54.92 mu m, respectively. The same thickening trend was also evident in all other six measurement points with statistical significance (P < 0.01). CONCLUSIONS. Diabetic patients had increased CT compared to healthy controls. The presence of neuropathy in diabetes patients caused additional choroidal thickening, compared to nonneuropathic patients.en_US
dc.identifier.doi10.1167/iovs.15-17966
dc.identifier.endpage1522en_US
dc.identifier.issn0146-0404
dc.identifier.issn1552-5783
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-84962468692
dc.identifier.scopusqualityQ1
dc.identifier.startpage1518en_US
dc.identifier.urihttps://doi.org/10.1167/iovs.15-17966
dc.identifier.urihttps://hdl.handle.net/20.500.12462/8653
dc.identifier.volume57en_US
dc.identifier.wosWOS:000375926700002
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherAssoc Research Vision Ophthalmology Inc.en_US
dc.relation.ispartofInvestigative Ophthalmology & Visual Scienceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution‐NonCommercial‐NoDerivs 3.0 United Statesen_US
dc.rights.urihttp://creativecommons.org/licenses/by‐nc‐nd/3.0/us/en_US
dc.subjectChoroiden_US
dc.subjectDiabetesen_US
dc.subjectNeuropathyen_US
dc.subjectRetinopathyen_US
dc.subjectThicknessen_US
dc.titleAlterations of choroidal thickness with diabetic neuropathyen_US
dc.typeArticleen_US

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