TY - JOUR
T1 - Identification of epiretinal proliferation in various retinal diseases and vitreoretinal interface disorders
AU - Chehaibou, Ismael
AU - Pettenkofer, Moritz
AU - Govetto, Andrea
AU - Rabina, Gilad
AU - Sadda, Srini Vas R.
AU - Hubschman, Jean Pierre
N1 - Publisher Copyright:
© 2020 The Author(s).
PY - 2020/7/10
Y1 - 2020/7/10
N2 - Background: To describe the presence of epiretinal proliferation in eyes with various retinal and vitreoretinal interface conditions. Methods: Consecutive patients seen at the Stein Eye Institute, by one retina specialist, from December 2018 to March 2019, and demonstrating epiretinal proliferation on optical coherence tomography (OCT) were enrolled in this cross-sectional study. Included patients were divided into two groups: vitreoretinal interface pathologies group or retinal diseases group. Presence of epiretinal proliferation and its localization within the 9 macular sectors, as defined by the Early Treatment Diabetic Retinopathy Study (ETDRS), were assessed on OCT. Results: 77 eyes from 69 patients demonstrated epiretinal proliferation on OCT. The most frequently involved ETDRS sector was the 1-mm central subfield, followed by inner temporal and inner nasal sectors. Localization of epiretinal proliferation correlated with the presence of any retinal abnormalities in the same quadrant (r = 0.962; P < 0.0001). 31 eyes (40.3%) demonstrated symptomatic vitreoretinal interface pathologies including lamellar macular hole, full-thickness macular hole, epiretinal membrane and history of macular peeling. 46 eyes (59.7%) manifested various retinal diseases, including age-related macular degeneration, diabetic retinopathy, refractory macular edema, vein occlusion and high myopia. Conclusions: Epiretinal proliferation was noted in several retinal conditions and not limited only to full-thickness and lamellar macular holes. Different mechanisms affecting retinal homeostasis might trigger Müller cells dysregulation, potentially leading to abnormal retinal remodeling.
AB - Background: To describe the presence of epiretinal proliferation in eyes with various retinal and vitreoretinal interface conditions. Methods: Consecutive patients seen at the Stein Eye Institute, by one retina specialist, from December 2018 to March 2019, and demonstrating epiretinal proliferation on optical coherence tomography (OCT) were enrolled in this cross-sectional study. Included patients were divided into two groups: vitreoretinal interface pathologies group or retinal diseases group. Presence of epiretinal proliferation and its localization within the 9 macular sectors, as defined by the Early Treatment Diabetic Retinopathy Study (ETDRS), were assessed on OCT. Results: 77 eyes from 69 patients demonstrated epiretinal proliferation on OCT. The most frequently involved ETDRS sector was the 1-mm central subfield, followed by inner temporal and inner nasal sectors. Localization of epiretinal proliferation correlated with the presence of any retinal abnormalities in the same quadrant (r = 0.962; P < 0.0001). 31 eyes (40.3%) demonstrated symptomatic vitreoretinal interface pathologies including lamellar macular hole, full-thickness macular hole, epiretinal membrane and history of macular peeling. 46 eyes (59.7%) manifested various retinal diseases, including age-related macular degeneration, diabetic retinopathy, refractory macular edema, vein occlusion and high myopia. Conclusions: Epiretinal proliferation was noted in several retinal conditions and not limited only to full-thickness and lamellar macular holes. Different mechanisms affecting retinal homeostasis might trigger Müller cells dysregulation, potentially leading to abnormal retinal remodeling.
KW - Epiretinal membrane
KW - Epiretinal proliferation
KW - Full-thickness macular holes
KW - Lamellar hole-associated epiretinal proliferation
KW - Lamellar macular holes
KW - Macular edema
KW - Müller glial cells
KW - Spectral-domain optical coherence tomography
UR - http://www.scopus.com/inward/record.url?scp=85088014694&partnerID=8YFLogxK
U2 - 10.1186/s40942-020-00233-0
DO - 10.1186/s40942-020-00233-0
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AN - SCOPUS:85088014694
SN - 2056-9920
VL - 6
JO - International Journal of Retina and Vitreous
JF - International Journal of Retina and Vitreous
IS - 1
M1 - 31
ER -