このアイテムのアクセス数: 116

このアイテムのファイル:
ファイル 記述 サイズフォーマット 
j.xops.2022.100241.pdf5.32 MBAdobe PDF見る/開く
完全メタデータレコード
DCフィールド言語
dc.contributor.authorKawai, Kentaroen
dc.contributor.authorMurakami, Tomoakien
dc.contributor.authorMori, Yukien
dc.contributor.authorIshihara, Kenjien
dc.contributor.authorDodo, Yokoen
dc.contributor.authorTerada, Norikoen
dc.contributor.authorNishikawa, Keiichien
dc.contributor.authorMorino, Kazuyaen
dc.contributor.authorTsujikawa, Akitakaen
dc.contributor.alternative河合, 健太郎ja
dc.contributor.alternative村上, 智昭ja
dc.contributor.alternative森, 雄貴ja
dc.contributor.alternative石原, 健司ja
dc.contributor.alternative百々, 蓉子ja
dc.contributor.alternative寺田, 紀子ja
dc.contributor.alternative西川, 慶一ja
dc.contributor.alternative森野, 数哉ja
dc.contributor.alternative辻川, 明孝ja
dc.date.accessioned2023-06-21T04:18:16Z-
dc.date.available2023-06-21T04:18:16Z-
dc.date.issued2023-03-
dc.identifier.urihttp://hdl.handle.net/2433/283370-
dc.description.abstract[Purpose] To investigate the distribution of clinically significant nonperfusion areas (NPAs) on widefield OCT angiography (OCTA) images in patients with diabetes. [Design] Prospective, cross-sectional, observational study. [Participants] One hundred and forty-four eyes of 114 patients with diabetes. [Methods] Nominal 20 × 23 mm OCTA images were obtained using a swept-source OCTA device (Xephilio OCT-S1), followed by the creation of en face images 20-mm (1614 pixels) in diameter centering on the fovea. The nonperfusion squares (NPSs) were defined as the 10 × 10 pixel squares without retinal vessels, and the ratio of eyes with the NPSs to all eyes in each square was referred to as the NPS ratio. The areas with probabilistic differences (APD) for proliferative diabetic retinopathy (PDR) and nonproliferative diabetic retinopathy (NPDR) (APD[PDR] and APD[NPDR]) were defined as sets of squares with higher NPS ratios in eyes with PDR and NPDR, respectively. The P ratio (NPSs within APD[PDR] but not APD[NPDR]/all NPSs) was also calculated. [Main Outcome Measures] The probabilistic distribution of the NPSs and the association with diabetic retinopathy (DR) severity. [Results] The NPSs developed randomly in eyes with mild and moderate NPDR and were more prevalent in the extramacular areas and the temporal quadrant in eyes with severe NPDR and PDR. The APD(PDR) was distributed mainly in the extramacular areas, sparing the areas around the vascular arcades and radially peripapillary capillaries. The APD(PDR) contained retinal neovascularization more frequently than the non-APD(PDR) (P = 0.023). The P ratio was higher in eyes with PDR than in those with NPDR (P < 0.001). The multivariate analysis designated the P ratio (odds ratio, 8.293 × 107; 95% confidence interval, 6.529 × 102–1.053 × 1013; P = 0.002) and the total NPSs (odds ratio, 1.002; 95% confidence interval, 1.001–1.003; P < 0.001) as independent risk factors of PDR. Most eyes with NPDR and 4-2-1 rule findings of DR severity had higher P ratios but not necessarily greater NPS numbers. [Conclusions] The APD(PDR) is uniquely distributed on widefield OCTA images, and the NPA location patterns are associated with DR severity, independent of the entire area of NPAs. [Financial Disclosure(s)] Proprietary or commercial disclosure may be found after the references.en
dc.language.isoeng-
dc.publisherElsevier BVen
dc.rights© 2022 Published by Elsevier Inc. on behalf of American Academy of Ophthalmology.en
dc.rightsThis is an open access article under the CC BY-NC-ND license.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectDiabetic retinopathyen
dc.subjectNonperfusion areasen
dc.subjectNeovascularizationen
dc.subjectSemiautomatic quantificationen
dc.subjectWidefield OCT angiographyen
dc.titleClinically Significant Nonperfusion Areas on Widefield OCT Angiography in Diabetic Retinopathyen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleOphthalmology Scienceen
dc.identifier.volume3-
dc.identifier.issue1-
dc.relation.doi10.1016/j.xops.2022.100241-
dc.textversionpublisher-
dc.identifier.artnum100241-
dc.identifier.pmid36545265-
dcterms.accessRightsopen access-
datacite.awardNumber20K09788-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20K09788/-
dc.identifier.eissn2666-9145-
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle糖尿病網膜症における自己免疫による神経障害を標的とした新規治療法の開発ja
出現コレクション:学術雑誌掲載論文等

アイテムの簡略レコードを表示する

Export to RefWorks


出力フォーマット 


このアイテムは次のライセンスが設定されています: クリエイティブ・コモンズ・ライセンス Creative Commons