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Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney)
PURPOSE: The population prevalence of diabetic macular oedema (DME) is unclear. Previous estimates have depended on photographic grading of clinically significant macular oedema, which is subjective and has resulted in widely varying estimates. With the advent of optical coherence tomography (OCT),...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347905/ https://www.ncbi.nlm.nih.gov/pubmed/30679285 http://dx.doi.org/10.1136/bmjopen-2018-021884 |
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author | Liew, Gerald Wong, Vincent W Saw, Mercy Tsang, Tania E Nolan, Tim Ong, Stephen Ho, I-Van |
author_facet | Liew, Gerald Wong, Vincent W Saw, Mercy Tsang, Tania E Nolan, Tim Ong, Stephen Ho, I-Van |
author_sort | Liew, Gerald |
collection | PubMed |
description | PURPOSE: The population prevalence of diabetic macular oedema (DME) is unclear. Previous estimates have depended on photographic grading of clinically significant macular oedema, which is subjective and has resulted in widely varying estimates. With the advent of optical coherence tomography (OCT), the presence and severity of DME can now be assessed objectively and accurately. METHODS: The Liverpool Eye and Diabetes Study (LEADS) is a cross-sectional population-based study of patients with type 1 and type 2 diabetes in a multi-ethnic region of Sydney, Australia, to determine the population prevalence of OCT-defined DME, how this varies by ethnicity and association with systemic factors. This report describes the rationale, methodology and study aims. RESULTS: To date 646 patients out of an expected sample size of 2000 have been recruited. Baseline data are presented for patients with type 1 (n=75, 11.8%) and type 2 (n=562, 88.2%) diabetes recruited to date. Patients with type 1 diabetes were younger (39.5vs60.7 years), with longer duration of diabetes (18.1vs11.7 years), slightly worse glycaemic control (HbA1c 9.0vs8.3), and less likely to have hypertension (30.7vs71.4%), hypercholesterolaemia (33.3vs74.6%) and obesity (31.1vs51.5%, respectively, all p<0.05). CONCLUSIONS: The LEADS will provide objective estimates of the population prevalence of DME, how this varies with ethnicity and associations with systemic disease. |
format | Online Article Text |
id | pubmed-6347905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-63479052019-02-08 Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney) Liew, Gerald Wong, Vincent W Saw, Mercy Tsang, Tania E Nolan, Tim Ong, Stephen Ho, I-Van BMJ Open Diabetes and Endocrinology PURPOSE: The population prevalence of diabetic macular oedema (DME) is unclear. Previous estimates have depended on photographic grading of clinically significant macular oedema, which is subjective and has resulted in widely varying estimates. With the advent of optical coherence tomography (OCT), the presence and severity of DME can now be assessed objectively and accurately. METHODS: The Liverpool Eye and Diabetes Study (LEADS) is a cross-sectional population-based study of patients with type 1 and type 2 diabetes in a multi-ethnic region of Sydney, Australia, to determine the population prevalence of OCT-defined DME, how this varies by ethnicity and association with systemic factors. This report describes the rationale, methodology and study aims. RESULTS: To date 646 patients out of an expected sample size of 2000 have been recruited. Baseline data are presented for patients with type 1 (n=75, 11.8%) and type 2 (n=562, 88.2%) diabetes recruited to date. Patients with type 1 diabetes were younger (39.5vs60.7 years), with longer duration of diabetes (18.1vs11.7 years), slightly worse glycaemic control (HbA1c 9.0vs8.3), and less likely to have hypertension (30.7vs71.4%), hypercholesterolaemia (33.3vs74.6%) and obesity (31.1vs51.5%, respectively, all p<0.05). CONCLUSIONS: The LEADS will provide objective estimates of the population prevalence of DME, how this varies with ethnicity and associations with systemic disease. BMJ Publishing Group 2019-01-24 /pmc/articles/PMC6347905/ /pubmed/30679285 http://dx.doi.org/10.1136/bmjopen-2018-021884 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Diabetes and Endocrinology Liew, Gerald Wong, Vincent W Saw, Mercy Tsang, Tania E Nolan, Tim Ong, Stephen Ho, I-Van Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney) |
title | Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney) |
title_full | Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney) |
title_fullStr | Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney) |
title_full_unstemmed | Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney) |
title_short | Profile of a population-based diabetic macular oedema study: the Liverpool Eye and Diabetes Study (Sydney) |
title_sort | profile of a population-based diabetic macular oedema study: the liverpool eye and diabetes study (sydney) |
topic | Diabetes and Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347905/ https://www.ncbi.nlm.nih.gov/pubmed/30679285 http://dx.doi.org/10.1136/bmjopen-2018-021884 |
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