Presumed Müller Cell Activation in Multiple Evanescent White Dot Syndrome

PurposeThe purpose of this study was to investigate the foveal changes occurring in multiple evanescent white dot syndrome (MEWDS) using multimodal imaging techniques with a specific focus on hyper-reflective dots (HRDs).MethodsThis was a retro-prospective observational study including 35 eyes with...

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Veröffentlicht in:Investigative ophthalmology & visual science 2023-10, Vol.64 (13), p.20-20
Hauptverfasser: Cicinelli, Maria Vittoria, Menean, Matteo, Apuzzo, Aurelio, Scandale, Pierluigi, Marchese, Alessandro, Introini, Ugo, Battaglia Parodi, Maurizio, Bandello, Francesco, Miserocchi, Elisabetta
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container_end_page 20
container_issue 13
container_start_page 20
container_title Investigative ophthalmology & visual science
container_volume 64
creator Cicinelli, Maria Vittoria
Menean, Matteo
Apuzzo, Aurelio
Scandale, Pierluigi
Marchese, Alessandro
Introini, Ugo
Battaglia Parodi, Maurizio
Bandello, Francesco
Miserocchi, Elisabetta
description PurposeThe purpose of this study was to investigate the foveal changes occurring in multiple evanescent white dot syndrome (MEWDS) using multimodal imaging techniques with a specific focus on hyper-reflective dots (HRDs).MethodsThis was a retro-prospective observational study including 35 eyes with active MEWDS. Structural and en face optical coherence tomography (OCT) was performed, with follow-up visits at 2 weeks, 6 weeks, and 2 months from baseline. HRD percentage area (HRD % area) was calculated in a 600 µm fovea centered circle on en face OCT, after background subtraction and image binarization. HRD % area was compared with 23 fellow control eyes. Longitudinal changes in the HRD % areas were assessed using repeated-measure statistics.ResultsHRDs were observed as scattered hyper-reflective spots on the vitreoretinal interface on en face OCT images, colocalizing with HRDs or vertical hyper-reflective lines on structural OCT images. The baseline evaluation showed a significantly higher HRD % area in MEWDS eyes compared to fellow eyes (0.10 ± 0.03 vs. 0.08 ± 0.04, P = 0.01). The HRD % area correlated positively with LogMAR visual acuity and inversely with the duration of symptoms. Longitudinal analysis revealed a significant reduction in the HRD % area over time. There was no significant interaction between the rate of HRD disappearance and clinical or demographic factors at baseline.ConclusionsAs HRD potentially represents the end-feet projections of activated Müller cells on the retinal surface, this study supports the involvement of Müller cells in the pathogenesis of the disease. The findings highlight the potential of en face OCT imaging for monitoring the progression of MEWDS.
doi_str_mv 10.1167/iovs.64.13.20
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Structural and en face optical coherence tomography (OCT) was performed, with follow-up visits at 2 weeks, 6 weeks, and 2 months from baseline. HRD percentage area (HRD % area) was calculated in a 600 µm fovea centered circle on en face OCT, after background subtraction and image binarization. HRD % area was compared with 23 fellow control eyes. Longitudinal changes in the HRD % areas were assessed using repeated-measure statistics.ResultsHRDs were observed as scattered hyper-reflective spots on the vitreoretinal interface on en face OCT images, colocalizing with HRDs or vertical hyper-reflective lines on structural OCT images. The baseline evaluation showed a significantly higher HRD % area in MEWDS eyes compared to fellow eyes (0.10 ± 0.03 vs. 0.08 ± 0.04, P = 0.01). The HRD % area correlated positively with LogMAR visual acuity and inversely with the duration of symptoms. Longitudinal analysis revealed a significant reduction in the HRD % area over time. There was no significant interaction between the rate of HRD disappearance and clinical or demographic factors at baseline.ConclusionsAs HRD potentially represents the end-feet projections of activated Müller cells on the retinal surface, this study supports the involvement of Müller cells in the pathogenesis of the disease. The findings highlight the potential of en face OCT imaging for monitoring the progression of MEWDS.</description><identifier>ISSN: 1552-5783</identifier><identifier>ISSN: 0146-0404</identifier><identifier>EISSN: 1552-5783</identifier><identifier>DOI: 10.1167/iovs.64.13.20</identifier><identifier>PMID: 37824135</identifier><language>eng</language><publisher>The Association for Research in Vision and Ophthalmology</publisher><subject>Retina</subject><ispartof>Investigative ophthalmology &amp; visual science, 2023-10, Vol.64 (13), p.20-20</ispartof><rights>Copyright 2023 The Authors 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-4aa00607a312bf58031472253baeb2a2aae564aa586a6cbaa6587ab8518117e53</citedby><cites>FETCH-LOGICAL-c365t-4aa00607a312bf58031472253baeb2a2aae564aa586a6cbaa6587ab8518117e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587856/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587856/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Cicinelli, Maria Vittoria</creatorcontrib><creatorcontrib>Menean, Matteo</creatorcontrib><creatorcontrib>Apuzzo, Aurelio</creatorcontrib><creatorcontrib>Scandale, Pierluigi</creatorcontrib><creatorcontrib>Marchese, Alessandro</creatorcontrib><creatorcontrib>Introini, Ugo</creatorcontrib><creatorcontrib>Battaglia Parodi, Maurizio</creatorcontrib><creatorcontrib>Bandello, Francesco</creatorcontrib><creatorcontrib>Miserocchi, Elisabetta</creatorcontrib><title>Presumed Müller Cell Activation in Multiple Evanescent White Dot Syndrome</title><title>Investigative ophthalmology &amp; visual science</title><description>PurposeThe purpose of this study was to investigate the foveal changes occurring in multiple evanescent white dot syndrome (MEWDS) using multimodal imaging techniques with a specific focus on hyper-reflective dots (HRDs).MethodsThis was a retro-prospective observational study including 35 eyes with active MEWDS. Structural and en face optical coherence tomography (OCT) was performed, with follow-up visits at 2 weeks, 6 weeks, and 2 months from baseline. HRD percentage area (HRD % area) was calculated in a 600 µm fovea centered circle on en face OCT, after background subtraction and image binarization. HRD % area was compared with 23 fellow control eyes. Longitudinal changes in the HRD % areas were assessed using repeated-measure statistics.ResultsHRDs were observed as scattered hyper-reflective spots on the vitreoretinal interface on en face OCT images, colocalizing with HRDs or vertical hyper-reflective lines on structural OCT images. The baseline evaluation showed a significantly higher HRD % area in MEWDS eyes compared to fellow eyes (0.10 ± 0.03 vs. 0.08 ± 0.04, P = 0.01). The HRD % area correlated positively with LogMAR visual acuity and inversely with the duration of symptoms. Longitudinal analysis revealed a significant reduction in the HRD % area over time. There was no significant interaction between the rate of HRD disappearance and clinical or demographic factors at baseline.ConclusionsAs HRD potentially represents the end-feet projections of activated Müller cells on the retinal surface, this study supports the involvement of Müller cells in the pathogenesis of the disease. The findings highlight the potential of en face OCT imaging for monitoring the progression of MEWDS.</description><subject>Retina</subject><issn>1552-5783</issn><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpVkUtPwzAQhC0EoqVw5O4jlwQ_Ysc3VJXyUiuQAHG0NqlLjZy42Emk_jdu_DFStUJw2pV29O2MBqFzSlJKZX5pfRdTmaWUp4wcoCEVgiUiV_zwzz5AJzF-EMIoZeQYDXiuWEa5GKKHp2BiW5kFnn9_OWcCnhjn8LhsbAeN9TW2NZ63rrFrZ_C0g9rE0tQNflvZxuBr3-DnTb0IvjKn6GgJLpqz_Ryh15vpy-QumT3e3k_Gs6TkUjRJBkCIJDlwyoqlUITTLGdM8AJMwYABGCF7kVASZFkASKFyKJSgitLcCD5CVzvuui1641s3AZxeB1tB2GgPVv-_1Hal332nKelJSsiecLEnBP_ZmtjoyvapnOvT-TZqpnIpeaZk1kuTnbQMPsZglr9_KNHbAvS2AC0zTblmhP8AoJ95ew</recordid><startdate>20231012</startdate><enddate>20231012</enddate><creator>Cicinelli, Maria Vittoria</creator><creator>Menean, Matteo</creator><creator>Apuzzo, Aurelio</creator><creator>Scandale, Pierluigi</creator><creator>Marchese, Alessandro</creator><creator>Introini, Ugo</creator><creator>Battaglia Parodi, Maurizio</creator><creator>Bandello, Francesco</creator><creator>Miserocchi, Elisabetta</creator><general>The Association for Research in Vision and Ophthalmology</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20231012</creationdate><title>Presumed Müller Cell Activation in Multiple Evanescent White Dot Syndrome</title><author>Cicinelli, Maria Vittoria ; Menean, Matteo ; Apuzzo, Aurelio ; Scandale, Pierluigi ; Marchese, Alessandro ; Introini, Ugo ; Battaglia Parodi, Maurizio ; Bandello, Francesco ; Miserocchi, Elisabetta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-4aa00607a312bf58031472253baeb2a2aae564aa586a6cbaa6587ab8518117e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Retina</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cicinelli, Maria Vittoria</creatorcontrib><creatorcontrib>Menean, Matteo</creatorcontrib><creatorcontrib>Apuzzo, Aurelio</creatorcontrib><creatorcontrib>Scandale, Pierluigi</creatorcontrib><creatorcontrib>Marchese, Alessandro</creatorcontrib><creatorcontrib>Introini, Ugo</creatorcontrib><creatorcontrib>Battaglia Parodi, Maurizio</creatorcontrib><creatorcontrib>Bandello, Francesco</creatorcontrib><creatorcontrib>Miserocchi, Elisabetta</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Investigative ophthalmology &amp; visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cicinelli, Maria Vittoria</au><au>Menean, Matteo</au><au>Apuzzo, Aurelio</au><au>Scandale, Pierluigi</au><au>Marchese, Alessandro</au><au>Introini, Ugo</au><au>Battaglia Parodi, Maurizio</au><au>Bandello, Francesco</au><au>Miserocchi, Elisabetta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Presumed Müller Cell Activation in Multiple Evanescent White Dot Syndrome</atitle><jtitle>Investigative ophthalmology &amp; visual science</jtitle><date>2023-10-12</date><risdate>2023</risdate><volume>64</volume><issue>13</issue><spage>20</spage><epage>20</epage><pages>20-20</pages><issn>1552-5783</issn><issn>0146-0404</issn><eissn>1552-5783</eissn><abstract>PurposeThe purpose of this study was to investigate the foveal changes occurring in multiple evanescent white dot syndrome (MEWDS) using multimodal imaging techniques with a specific focus on hyper-reflective dots (HRDs).MethodsThis was a retro-prospective observational study including 35 eyes with active MEWDS. Structural and en face optical coherence tomography (OCT) was performed, with follow-up visits at 2 weeks, 6 weeks, and 2 months from baseline. HRD percentage area (HRD % area) was calculated in a 600 µm fovea centered circle on en face OCT, after background subtraction and image binarization. HRD % area was compared with 23 fellow control eyes. Longitudinal changes in the HRD % areas were assessed using repeated-measure statistics.ResultsHRDs were observed as scattered hyper-reflective spots on the vitreoretinal interface on en face OCT images, colocalizing with HRDs or vertical hyper-reflective lines on structural OCT images. The baseline evaluation showed a significantly higher HRD % area in MEWDS eyes compared to fellow eyes (0.10 ± 0.03 vs. 0.08 ± 0.04, P = 0.01). The HRD % area correlated positively with LogMAR visual acuity and inversely with the duration of symptoms. Longitudinal analysis revealed a significant reduction in the HRD % area over time. There was no significant interaction between the rate of HRD disappearance and clinical or demographic factors at baseline.ConclusionsAs HRD potentially represents the end-feet projections of activated Müller cells on the retinal surface, this study supports the involvement of Müller cells in the pathogenesis of the disease. The findings highlight the potential of en face OCT imaging for monitoring the progression of MEWDS.</abstract><pub>The Association for Research in Vision and Ophthalmology</pub><pmid>37824135</pmid><doi>10.1167/iovs.64.13.20</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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title Presumed Müller Cell Activation in Multiple Evanescent White Dot Syndrome
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