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Choroidal vascularity index in type-2 diabetes analyzed by swept-source optical coherence tomography
The relationships between changes in choroidal vasculature and the severity of diabetic retinopathy (DR) remain unclear. We assessed choroidal changes in diabetic patients by measuring choroidal vascularity index (CVI) in conjunction with DR stage. In this study, patients with diabetes and healthy c...
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description | The relationships between changes in choroidal vasculature and the severity of diabetic retinopathy (DR) remain unclear. We assessed choroidal changes in diabetic patients by measuring choroidal vascularity index (CVI) in conjunction with DR stage. In this study, patients with diabetes and healthy controls were retrospectively analyzed. Subjects were divided into seven groups as follows: Healthy controls, no DR, mild/moderate non-proliferative DR (NPDR), severe NPDR, proliferative DR (PDR), panretinal photocoagulation-treated DR, and clinically significant macular edema. The mean CVI values in the above groups were 69.08, 67.07, 66.28, 66.20, 63.48, 65.38, and 66.28, respectively. The eyes of diabetic patients exhibited a significantly lower CVI value than those of healthy controls even without DR. The PDR group exhibited a significantly lower CVI value than the healthy control, no DR, and mild/moderate NPDR groups. Age, sex, disease duration, glycated hemoglobin, fasting blood sugar, or intraocular pressure had no correlation with CVI. In multivariate regression analysis, thicker subfoveal choroid and thinner central retina were significantly associated with higher CVI values. These findings carefully suggest that changes in choroidal vasculature could be the primary event in diabetes even where there is no DR. |
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We assessed choroidal changes in diabetic patients by measuring choroidal vascularity index (CVI) in conjunction with DR stage. In this study, patients with diabetes and healthy controls were retrospectively analyzed. Subjects were divided into seven groups as follows: Healthy controls, no DR, mild/moderate non-proliferative DR (NPDR), severe NPDR, proliferative DR (PDR), panretinal photocoagulation-treated DR, and clinically significant macular edema. The mean CVI values in the above groups were 69.08, 67.07, 66.28, 66.20, 63.48, 65.38, and 66.28, respectively. The eyes of diabetic patients exhibited a significantly lower CVI value than those of healthy controls even without DR. The PDR group exhibited a significantly lower CVI value than the healthy control, no DR, and mild/moderate NPDR groups. Age, sex, disease duration, glycated hemoglobin, fasting blood sugar, or intraocular pressure had no correlation with CVI. In multivariate regression analysis, thicker subfoveal choroid and thinner central retina were significantly associated with higher CVI values. These findings carefully suggest that changes in choroidal vasculature could be the primary event in diabetes even where there is no DR.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-017-18511-7</identifier><identifier>PMID: 29311618</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/699/2743/137 ; 692/699/3161/3175 ; Blood pressure ; Diabetes ; Diabetes mellitus ; Diabetic retinopathy ; Edema ; Hemoglobin ; Humanities and Social Sciences ; multidisciplinary ; Regression analysis ; Retina ; Retinopathy ; Science ; Science (multidisciplinary) ; Sugar</subject><ispartof>Scientific reports, 2018-01, Vol.8 (1), p.70-70, Article 70</ispartof><rights>The Author(s) 2017</rights><rights>2017. 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We assessed choroidal changes in diabetic patients by measuring choroidal vascularity index (CVI) in conjunction with DR stage. In this study, patients with diabetes and healthy controls were retrospectively analyzed. Subjects were divided into seven groups as follows: Healthy controls, no DR, mild/moderate non-proliferative DR (NPDR), severe NPDR, proliferative DR (PDR), panretinal photocoagulation-treated DR, and clinically significant macular edema. The mean CVI values in the above groups were 69.08, 67.07, 66.28, 66.20, 63.48, 65.38, and 66.28, respectively. The eyes of diabetic patients exhibited a significantly lower CVI value than those of healthy controls even without DR. The PDR group exhibited a significantly lower CVI value than the healthy control, no DR, and mild/moderate NPDR groups. Age, sex, disease duration, glycated hemoglobin, fasting blood sugar, or intraocular pressure had no correlation with CVI. In multivariate regression analysis, thicker subfoveal choroid and thinner central retina were significantly associated with higher CVI values. These findings carefully suggest that changes in choroidal vasculature could be the primary event in diabetes even where there is no DR.</description><subject>692/699/2743/137</subject><subject>692/699/3161/3175</subject><subject>Blood pressure</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetic retinopathy</subject><subject>Edema</subject><subject>Hemoglobin</subject><subject>Humanities and Social Sciences</subject><subject>multidisciplinary</subject><subject>Regression analysis</subject><subject>Retina</subject><subject>Retinopathy</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sugar</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp1kUFPHCEUx4mpUaN-AQ9mEi-9UIGBgbmYNJvaNjHx4p0wzJtdzOwwAmM7_fSyu2rWJnKAF97v_R-8P0IXlHyjpFTXkVNRK0yoxFQJSrE8QCeMcIFZydiXvfgYncf4SPISrOa0PkLHrC4prag6Qe1i5YN3remLZxPt1Jvg0ly4oYW_eS_SPAJmRetMAwliYQbTz_-gLZq5iH9gTDj6KVgo_JiczSrWryDAkG-SX_tlMONqPkOHnekjnL-ep-jh9sfD4he-u__5e_H9DlvBScJVJxvDO1FZLhtbAmGcK9vRxkpGBRNGCcnbirRGqUZZaRVjnagNq2wtBC9P0c1OdpyaNbQWhhRMr8fg1ibM2hunP2YGt9JL_6yFFKoiIgt8fRUI_mmCmPTaRQt9bwbwU9S0VttG215X_6GPeQ55OBuqLjmtBJOZYjvKBh9jgO79MZTojY16Z6PONuqtjXpTdLn_jfeSN9MyUO6AmFPDEsJe789lXwDzb6nV</recordid><startdate>20180108</startdate><enddate>20180108</enddate><creator>Kim, Mirinae</creator><creator>Ha, Min Ji</creator><creator>Choi, Seung Yong</creator><creator>Park, Young-Hoon</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180108</creationdate><title>Choroidal vascularity index in type-2 diabetes analyzed by swept-source optical coherence tomography</title><author>Kim, Mirinae ; Ha, Min Ji ; Choi, Seung Yong ; Park, Young-Hoon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-6f7ba4f56c47bc3e02448cf1bc721525a8574d60da88b8c7c822f59a26c95543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>692/699/2743/137</topic><topic>692/699/3161/3175</topic><topic>Blood pressure</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetic retinopathy</topic><topic>Edema</topic><topic>Hemoglobin</topic><topic>Humanities and Social Sciences</topic><topic>multidisciplinary</topic><topic>Regression analysis</topic><topic>Retina</topic><topic>Retinopathy</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Sugar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Mirinae</creatorcontrib><creatorcontrib>Ha, Min Ji</creatorcontrib><creatorcontrib>Choi, Seung Yong</creatorcontrib><creatorcontrib>Park, Young-Hoon</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Mirinae</au><au>Ha, Min Ji</au><au>Choi, Seung Yong</au><au>Park, Young-Hoon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Choroidal vascularity index in type-2 diabetes analyzed by swept-source optical coherence tomography</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-01-08</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>70</spage><epage>70</epage><pages>70-70</pages><artnum>70</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The relationships between changes in choroidal vasculature and the severity of diabetic retinopathy (DR) remain unclear. We assessed choroidal changes in diabetic patients by measuring choroidal vascularity index (CVI) in conjunction with DR stage. In this study, patients with diabetes and healthy controls were retrospectively analyzed. Subjects were divided into seven groups as follows: Healthy controls, no DR, mild/moderate non-proliferative DR (NPDR), severe NPDR, proliferative DR (PDR), panretinal photocoagulation-treated DR, and clinically significant macular edema. The mean CVI values in the above groups were 69.08, 67.07, 66.28, 66.20, 63.48, 65.38, and 66.28, respectively. The eyes of diabetic patients exhibited a significantly lower CVI value than those of healthy controls even without DR. The PDR group exhibited a significantly lower CVI value than the healthy control, no DR, and mild/moderate NPDR groups. Age, sex, disease duration, glycated hemoglobin, fasting blood sugar, or intraocular pressure had no correlation with CVI. In multivariate regression analysis, thicker subfoveal choroid and thinner central retina were significantly associated with higher CVI values. These findings carefully suggest that changes in choroidal vasculature could be the primary event in diabetes even where there is no DR.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29311618</pmid><doi>10.1038/s41598-017-18511-7</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 692/699/2743/137 692/699/3161/3175 Blood pressure Diabetes Diabetes mellitus Diabetic retinopathy Edema Hemoglobin Humanities and Social Sciences multidisciplinary Regression analysis Retina Retinopathy Science Science (multidisciplinary) Sugar |
title | Choroidal vascularity index in type-2 diabetes analyzed by swept-source optical coherence tomography |
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