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The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome
PURPOSE : There is conflicting evidence whether components of metabolic syndrome (MetS) increase or decrease the risk of primary open-angle glaucoma (POAG). The aim of the present study was to determine the association between metabolic syndrome and primary open-angle glaucoma. METHODS : A total of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Open
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627385/ https://www.ncbi.nlm.nih.gov/pubmed/26535072 http://dx.doi.org/10.2174/1874364101509010149 |
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author | Rasoulinejad, Seyed Ahmad Kasiri, Ali Montazeri, Mahdi Rashidi, Negin Montazeri, Maryam Montazeri, Mohammad Hedayati, Hesam |
author_facet | Rasoulinejad, Seyed Ahmad Kasiri, Ali Montazeri, Mahdi Rashidi, Negin Montazeri, Maryam Montazeri, Mohammad Hedayati, Hesam |
author_sort | Rasoulinejad, Seyed Ahmad |
collection | PubMed |
description | PURPOSE : There is conflicting evidence whether components of metabolic syndrome (MetS) increase or decrease the risk of primary open-angle glaucoma (POAG). The aim of the present study was to determine the association between metabolic syndrome and primary open-angle glaucoma. METHODS : A total of 200 participants comprising 100 controls and 100 patients with POAG documented by clinical tests and examined by an experienced ophthalmologist using standard ophthalmologic equipment were included in the study. MetS was defined and based on ATP III criteria and POAG was defined by the criteria of the International Society of Geographic and Epidemiological Ophthalmology (ISGEO). The data were entered into the SPSS software and analyzed. RESULTS : The prevalence of MetS in the glaucoma group was 53% in comparison to 38% in the control group (p=0.037). MetS was associated with an increased odds ratio for an IOP higher than 21 mmHg (OR: 1.72; 95% CI 1.03-2.79; p=0.034). The mean IOP was 24.91±4.29 mmHg in the patients without MetS, and 27.23±4.81 mmHg in those with MetS (p=0.027). The mean values of CCT were 603.64±63.16 µm in MetS patients and 579.27±72.87 µm in controls (p=0.018). CONCLUSION : Data showed an increased prevalence of components of metabolic syndrome in patients with glaucoma. The mechanisms underlying these associations need to be established in future studies. Our results support the recommendation that patients with metabolic syndrome undergo regular ophthalmological exams to monitor for the onset or progression of glaucoma. |
format | Online Article Text |
id | pubmed-4627385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-46273852015-11-03 The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome Rasoulinejad, Seyed Ahmad Kasiri, Ali Montazeri, Mahdi Rashidi, Negin Montazeri, Maryam Montazeri, Mohammad Hedayati, Hesam Open Ophthalmol J Article PURPOSE : There is conflicting evidence whether components of metabolic syndrome (MetS) increase or decrease the risk of primary open-angle glaucoma (POAG). The aim of the present study was to determine the association between metabolic syndrome and primary open-angle glaucoma. METHODS : A total of 200 participants comprising 100 controls and 100 patients with POAG documented by clinical tests and examined by an experienced ophthalmologist using standard ophthalmologic equipment were included in the study. MetS was defined and based on ATP III criteria and POAG was defined by the criteria of the International Society of Geographic and Epidemiological Ophthalmology (ISGEO). The data were entered into the SPSS software and analyzed. RESULTS : The prevalence of MetS in the glaucoma group was 53% in comparison to 38% in the control group (p=0.037). MetS was associated with an increased odds ratio for an IOP higher than 21 mmHg (OR: 1.72; 95% CI 1.03-2.79; p=0.034). The mean IOP was 24.91±4.29 mmHg in the patients without MetS, and 27.23±4.81 mmHg in those with MetS (p=0.027). The mean values of CCT were 603.64±63.16 µm in MetS patients and 579.27±72.87 µm in controls (p=0.018). CONCLUSION : Data showed an increased prevalence of components of metabolic syndrome in patients with glaucoma. The mechanisms underlying these associations need to be established in future studies. Our results support the recommendation that patients with metabolic syndrome undergo regular ophthalmological exams to monitor for the onset or progression of glaucoma. Bentham Open 2015-10-06 /pmc/articles/PMC4627385/ /pubmed/26535072 http://dx.doi.org/10.2174/1874364101509010149 Text en © Rasoulinejad et al.; Licensee Bentham Open. https://creativecommons.org/licenses/by/4.0/legalcode This is an open access article licensed under the terms of the (https://creativecommons.org/licenses/by/4.0/legalcode), which permits unrestricted, noncommercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Rasoulinejad, Seyed Ahmad Kasiri, Ali Montazeri, Mahdi Rashidi, Negin Montazeri, Maryam Montazeri, Mohammad Hedayati, Hesam The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome |
title | The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome |
title_full | The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome |
title_fullStr | The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome |
title_full_unstemmed | The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome |
title_short | The Association Between Primary Open Angle Glaucoma and Clustered Components of Metabolic Syndrome |
title_sort | association between primary open angle glaucoma and clustered components of metabolic syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627385/ https://www.ncbi.nlm.nih.gov/pubmed/26535072 http://dx.doi.org/10.2174/1874364101509010149 |
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