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FOVEAL MULLER CELL CONE AS A PROGNOSTIC OPTICAL COHERENCE TOMOGRAPHY BIOMARKER FOR INITIAL RESPONSE TO ANTIVASCULAR ENDOTHELIAL GROWTH FACTOR TREATMENT IN CYSTOID DIABETIC MACULAR EDEMA

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dc.contributor.authorChoi, Mihyun-
dc.contributor.authorYun, Cheolmin-
dc.contributor.authorOh, Jong-Hyun-
dc.contributor.authorKim, Seong-Woo-
dc.date.accessioned2022-02-11T11:40:37Z-
dc.date.available2022-02-11T11:40:37Z-
dc.date.created2022-01-19-
dc.date.issued2022-01-
dc.identifier.issn0275-004X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/135331-
dc.description.abstractPurpose: To investigate the effect of the foveal Muller cell cone structure on the anatomical and functional response to intravitreal bevacizumab treatment in patients with diabetic macular edema. Methods: In 93 treatment-naive eyes with center-involved cystic type diabetic macular edema, spectral-domain optical coherence tomography scans of baseline were retrospectively evaluated to determine the foveal Muller cell cone structure and prognostic features including length of disorganization in the retinal inner layers and ellipsoid zone disruption. The area and circularity of the foveal avascular zone of the superficial and deep capillary plexus 1 month after intravitreal bevacizumab treatment were evaluated using optical coherence tomography angiography. Results: Destruction of the foveal Muller cell cone structure and a large foveal avascular zone in the deep capillary plexus (mm(2)) correlated strongly with a poor anatomical response (CST > 250 mm) at 1 month after first intravitreal bevacizumab (Exp [B] = 29.444, P = 0.002 and Exp [B] = 12.419, P = 0.013, respectively). A destroyed Muller cell cone structure (P = 0.008) and length of ellipsoid zone disruption (P < 0.001) at baseline were associated with poor visual acuity at 1 month after the first intravitreal bevacizumab. Conclusion: The foveal Muller cell cone structure correlates with the response to initial antivascular endothelial growth factor treatment.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherLIPPINCOTT WILLIAMS & WILKINS-
dc.subjectRANDOMIZED CLINICAL-TRIAL-
dc.subjectRETINAL INNER LAYERS-
dc.subjectDISORGANIZATION-
dc.subjectASSOCIATION-
dc.subjectBEVACIZUMAB-
dc.subjectRETINOPATHY-
dc.subjectPATHOGENESIS-
dc.subjectRANIBIZUMAB-
dc.subjectAFLIBERCEPT-
dc.subjectTHICKNESS-
dc.titleFOVEAL MULLER CELL CONE AS A PROGNOSTIC OPTICAL COHERENCE TOMOGRAPHY BIOMARKER FOR INITIAL RESPONSE TO ANTIVASCULAR ENDOTHELIAL GROWTH FACTOR TREATMENT IN CYSTOID DIABETIC MACULAR EDEMA-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Seong-Woo-
dc.identifier.doi10.1097/IAE.0000000000003271-
dc.identifier.scopusid2-s2.0-85122290857-
dc.identifier.wosid000732829100026-
dc.identifier.bibliographicCitationRETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, v.42, no.1, pp.129 - 137-
dc.relation.isPartOfRETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES-
dc.citation.titleRETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES-
dc.citation.volume42-
dc.citation.number1-
dc.citation.startPage129-
dc.citation.endPage137-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOphthalmology-
dc.relation.journalWebOfScienceCategoryOphthalmology-
dc.subject.keywordPlusRANDOMIZED CLINICAL-TRIAL-
dc.subject.keywordPlusRETINAL INNER LAYERS-
dc.subject.keywordPlusDISORGANIZATION-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusBEVACIZUMAB-
dc.subject.keywordPlusRETINOPATHY-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusRANIBIZUMAB-
dc.subject.keywordPlusAFLIBERCEPT-
dc.subject.keywordPlusTHICKNESS-
dc.subject.keywordAuthoranti-VEGF-
dc.subject.keywordAuthorbiomarker-
dc.subject.keywordAuthordiabetic retinopathy-
dc.subject.keywordAuthorDME-
dc.subject.keywordAuthorOCT-
dc.subject.keywordAuthoroptical coherence tomography angiography-
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