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Novel grading system for quantification of cystic macular lesions in Usher syndrome
BACKGROUND: To evaluate novel grading system used to quantify optical coherence tomography (OCT) scans for cystic macular lesions (CML) in Usher syndrome (USH) patients, focusing on CML associated alterations in MOY7A and USH2A mutations. METHODS: Two readers evaluated 76 patients’ (mean age 42 ± 14...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676164/ https://www.ncbi.nlm.nih.gov/pubmed/26654877 http://dx.doi.org/10.1186/s13023-015-0372-0 |
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author | Sliesoraityte, Ieva Peto, Tunde Mohand-Said, Saddek Sahel, Jose Alain |
author_facet | Sliesoraityte, Ieva Peto, Tunde Mohand-Said, Saddek Sahel, Jose Alain |
author_sort | Sliesoraityte, Ieva |
collection | PubMed |
description | BACKGROUND: To evaluate novel grading system used to quantify optical coherence tomography (OCT) scans for cystic macular lesions (CML) in Usher syndrome (USH) patients, focusing on CML associated alterations in MOY7A and USH2A mutations. METHODS: Two readers evaluated 76 patients’ (mean age 42 ± 14 years) data prospectively uploaded on Eurush database. OCT was used to obtain high quality cross-sectional images through the fovea. The CML was graded as none, mild, moderate or severe, depending on the following features set: subretinal fluid without clearly detectable CML boundaries; central macular thickness; largest diameter of CML; calculated mean of all detectable CML; total number of detectable CML; retinal layers affected by CML. Intra-and inter-grader reproducibility was evaluated. RESULTS: CML were observed in 37 % of USH eyes, while 45 % were observed in MYO7A and 29 % in USH2A cases. Of those with CML: 52 % had mild, 22 % had moderate and 26 % had severe changes, respectively. CML were found in following retinal layers: 50 % inner nuclear layer, 44 % outer nuclear layer, 6 % retinal ganglion cell layer. For the inter-grader repeatability analysis, agreements rates for CML were 97 % and kappa statistics was 0.91 (95 % CI 0.83-0.99). For the intra-grader analysis, agreement rates for CML were 98 %, while kappa statistics was 0.96 (95 % CI 0.92-0.99). CONCLUSIONS: The novel grading system is a reproducible tool for grading OCT images in USH complicated by CML, and potentially could be used for objective tracking of macular pathology in clinical therapy trials. |
format | Online Article Text |
id | pubmed-4676164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46761642015-12-12 Novel grading system for quantification of cystic macular lesions in Usher syndrome Sliesoraityte, Ieva Peto, Tunde Mohand-Said, Saddek Sahel, Jose Alain Orphanet J Rare Dis Research BACKGROUND: To evaluate novel grading system used to quantify optical coherence tomography (OCT) scans for cystic macular lesions (CML) in Usher syndrome (USH) patients, focusing on CML associated alterations in MOY7A and USH2A mutations. METHODS: Two readers evaluated 76 patients’ (mean age 42 ± 14 years) data prospectively uploaded on Eurush database. OCT was used to obtain high quality cross-sectional images through the fovea. The CML was graded as none, mild, moderate or severe, depending on the following features set: subretinal fluid without clearly detectable CML boundaries; central macular thickness; largest diameter of CML; calculated mean of all detectable CML; total number of detectable CML; retinal layers affected by CML. Intra-and inter-grader reproducibility was evaluated. RESULTS: CML were observed in 37 % of USH eyes, while 45 % were observed in MYO7A and 29 % in USH2A cases. Of those with CML: 52 % had mild, 22 % had moderate and 26 % had severe changes, respectively. CML were found in following retinal layers: 50 % inner nuclear layer, 44 % outer nuclear layer, 6 % retinal ganglion cell layer. For the inter-grader repeatability analysis, agreements rates for CML were 97 % and kappa statistics was 0.91 (95 % CI 0.83-0.99). For the intra-grader analysis, agreement rates for CML were 98 %, while kappa statistics was 0.96 (95 % CI 0.92-0.99). CONCLUSIONS: The novel grading system is a reproducible tool for grading OCT images in USH complicated by CML, and potentially could be used for objective tracking of macular pathology in clinical therapy trials. BioMed Central 2015-12-10 /pmc/articles/PMC4676164/ /pubmed/26654877 http://dx.doi.org/10.1186/s13023-015-0372-0 Text en © Sliesoraityte et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Sliesoraityte, Ieva Peto, Tunde Mohand-Said, Saddek Sahel, Jose Alain Novel grading system for quantification of cystic macular lesions in Usher syndrome |
title | Novel grading system for quantification of cystic macular lesions in Usher syndrome |
title_full | Novel grading system for quantification of cystic macular lesions in Usher syndrome |
title_fullStr | Novel grading system for quantification of cystic macular lesions in Usher syndrome |
title_full_unstemmed | Novel grading system for quantification of cystic macular lesions in Usher syndrome |
title_short | Novel grading system for quantification of cystic macular lesions in Usher syndrome |
title_sort | novel grading system for quantification of cystic macular lesions in usher syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676164/ https://www.ncbi.nlm.nih.gov/pubmed/26654877 http://dx.doi.org/10.1186/s13023-015-0372-0 |
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