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Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma
Glaucoma is a leading cause of irreversible blindness worldwide and is characterized by progressive loss of visual function and retinal ganglion cells (RGC). Current epidemiological, clinical, and basic science evidence suggest that estrogen plays a role in the aging of the optic nerve. Menopause, a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250947/ https://www.ncbi.nlm.nih.gov/pubmed/34981287 http://dx.doi.org/10.1007/s10571-021-01179-z |
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author | Douglass, Amber Dattilo, Michael Feola, Andrew J. |
author_facet | Douglass, Amber Dattilo, Michael Feola, Andrew J. |
author_sort | Douglass, Amber |
collection | PubMed |
description | Glaucoma is a leading cause of irreversible blindness worldwide and is characterized by progressive loss of visual function and retinal ganglion cells (RGC). Current epidemiological, clinical, and basic science evidence suggest that estrogen plays a role in the aging of the optic nerve. Menopause, a major biological life event affecting all women, coincides with a decrease in circulating sex hormones, such as estrogen. While 59% of the glaucomatous population are females, sex is not considered a risk factor for developing glaucoma. In this review, we explore whether menopause is a sex-specific risk factor for glaucoma. First, we investigate how menopause is defined as a sex-specific risk factor for other pathologies, including cardiovascular disease, osteoarthritis, and bone health. Next, we discuss clinical evidence that highlights the potential role of menopause in glaucoma. We also highlight preclinical studies that demonstrate larger vision and RGC loss following surgical menopause and how estrogen is protective in models of RGC injury. Lastly, we explore how surgical menopause and estrogen signaling are related to risk factors associated with developing glaucoma (e.g., intraocular pressure, aqueous outflow resistance, and ocular biomechanics). We hypothesize that menopause potentially sets the stage to develop glaucoma and therefore is a sex-specific risk factor for this disease. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-9250947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-92509472023-01-06 Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma Douglass, Amber Dattilo, Michael Feola, Andrew J. Cell Mol Neurobiol Review Paper Glaucoma is a leading cause of irreversible blindness worldwide and is characterized by progressive loss of visual function and retinal ganglion cells (RGC). Current epidemiological, clinical, and basic science evidence suggest that estrogen plays a role in the aging of the optic nerve. Menopause, a major biological life event affecting all women, coincides with a decrease in circulating sex hormones, such as estrogen. While 59% of the glaucomatous population are females, sex is not considered a risk factor for developing glaucoma. In this review, we explore whether menopause is a sex-specific risk factor for glaucoma. First, we investigate how menopause is defined as a sex-specific risk factor for other pathologies, including cardiovascular disease, osteoarthritis, and bone health. Next, we discuss clinical evidence that highlights the potential role of menopause in glaucoma. We also highlight preclinical studies that demonstrate larger vision and RGC loss following surgical menopause and how estrogen is protective in models of RGC injury. Lastly, we explore how surgical menopause and estrogen signaling are related to risk factors associated with developing glaucoma (e.g., intraocular pressure, aqueous outflow resistance, and ocular biomechanics). We hypothesize that menopause potentially sets the stage to develop glaucoma and therefore is a sex-specific risk factor for this disease. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2022-01-04 2023 /pmc/articles/PMC9250947/ /pubmed/34981287 http://dx.doi.org/10.1007/s10571-021-01179-z Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Review Paper Douglass, Amber Dattilo, Michael Feola, Andrew J. Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma |
title | Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma |
title_full | Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma |
title_fullStr | Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma |
title_full_unstemmed | Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma |
title_short | Evidence for Menopause as a Sex-Specific Risk Factor for Glaucoma |
title_sort | evidence for menopause as a sex-specific risk factor for glaucoma |
topic | Review Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250947/ https://www.ncbi.nlm.nih.gov/pubmed/34981287 http://dx.doi.org/10.1007/s10571-021-01179-z |
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