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Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study
Primary open angle glaucoma (POAG) is a chronic, adult-onset optic neuropathy associated with characteristic optic disc and/or visual field changes. With a view to identifying modifiable risk factors for this common neurodegenerative condition, we performed a ‘phenome-wide’ univariable Mendelian ran...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282034/ https://www.ncbi.nlm.nih.gov/pubmed/37340071 http://dx.doi.org/10.1038/s41598-023-37144-7 |
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author | Julian, Thomas H. Girach, Zain Sanderson, Eleanor Guo, Hui Yu, Jonathan Cooper-Knock, Johnathan Black, Graeme C. Sergouniotis, Panagiotis I. |
author_facet | Julian, Thomas H. Girach, Zain Sanderson, Eleanor Guo, Hui Yu, Jonathan Cooper-Knock, Johnathan Black, Graeme C. Sergouniotis, Panagiotis I. |
author_sort | Julian, Thomas H. |
collection | PubMed |
description | Primary open angle glaucoma (POAG) is a chronic, adult-onset optic neuropathy associated with characteristic optic disc and/or visual field changes. With a view to identifying modifiable risk factors for this common neurodegenerative condition, we performed a ‘phenome-wide’ univariable Mendelian randomisation (MR) study that involved analysing the relationship between 9661 traits and POAG. Utilised analytical approaches included weighted mode based estimation, the weighted median method, the MR Egger method and the inverse variance weighted (IVW) approach. Eleven traits related to POAG risk were identified including: serum levels of the angiopoietin-1 receptor (OR [odds ratio] = 1.11, IVW p = 2.34E-06) and the cadherin 5 protein (OR = 1.06, IVW p = 1.31E-06); intraocular pressure (OR = 2.46–3.79, IVW p = 8.94E-44–3.00E-27); diabetes (OR = 5.17, beta = 1.64, IVW p = 9.68E-04); and waist circumference (OR = 0.79, IVW p = 1.66E-05). Future research focussing on the effects of adiposity, cadherin 5 and angiopoietin-1 receptor on POAG development and progression is expected to provide key insights that might inform the provision of lifestyle modification advice and/or the development of novel therapies. |
format | Online Article Text |
id | pubmed-10282034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102820342023-06-22 Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study Julian, Thomas H. Girach, Zain Sanderson, Eleanor Guo, Hui Yu, Jonathan Cooper-Knock, Johnathan Black, Graeme C. Sergouniotis, Panagiotis I. Sci Rep Article Primary open angle glaucoma (POAG) is a chronic, adult-onset optic neuropathy associated with characteristic optic disc and/or visual field changes. With a view to identifying modifiable risk factors for this common neurodegenerative condition, we performed a ‘phenome-wide’ univariable Mendelian randomisation (MR) study that involved analysing the relationship between 9661 traits and POAG. Utilised analytical approaches included weighted mode based estimation, the weighted median method, the MR Egger method and the inverse variance weighted (IVW) approach. Eleven traits related to POAG risk were identified including: serum levels of the angiopoietin-1 receptor (OR [odds ratio] = 1.11, IVW p = 2.34E-06) and the cadherin 5 protein (OR = 1.06, IVW p = 1.31E-06); intraocular pressure (OR = 2.46–3.79, IVW p = 8.94E-44–3.00E-27); diabetes (OR = 5.17, beta = 1.64, IVW p = 9.68E-04); and waist circumference (OR = 0.79, IVW p = 1.66E-05). Future research focussing on the effects of adiposity, cadherin 5 and angiopoietin-1 receptor on POAG development and progression is expected to provide key insights that might inform the provision of lifestyle modification advice and/or the development of novel therapies. Nature Publishing Group UK 2023-06-20 /pmc/articles/PMC10282034/ /pubmed/37340071 http://dx.doi.org/10.1038/s41598-023-37144-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Julian, Thomas H. Girach, Zain Sanderson, Eleanor Guo, Hui Yu, Jonathan Cooper-Knock, Johnathan Black, Graeme C. Sergouniotis, Panagiotis I. Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study |
title | Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study |
title_full | Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study |
title_fullStr | Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study |
title_full_unstemmed | Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study |
title_short | Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study |
title_sort | causal factors in primary open angle glaucoma: a phenome-wide mendelian randomisation study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282034/ https://www.ncbi.nlm.nih.gov/pubmed/37340071 http://dx.doi.org/10.1038/s41598-023-37144-7 |
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