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Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases

It is difficult to get evidence from randomized trials of a causal relationship between steroid hormones produced by the adrenal gland and gonad and retinal neurodegenerative disorders (RND). In this study, genetic variations of aldosterone (Aldo), androstenedione (A4), progesterone (P4), hydroxypro...

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Autores principales: Liu, Kangcheng, Fan, Huimin, Hu, Hanying, Cheng, Yanhua, Liu, Jingying, You, Zhipeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871487/
https://www.ncbi.nlm.nih.gov/pubmed/36704044
http://dx.doi.org/10.3389/fendo.2022.1088557
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author Liu, Kangcheng
Fan, Huimin
Hu, Hanying
Cheng, Yanhua
Liu, Jingying
You, Zhipeng
author_facet Liu, Kangcheng
Fan, Huimin
Hu, Hanying
Cheng, Yanhua
Liu, Jingying
You, Zhipeng
author_sort Liu, Kangcheng
collection PubMed
description It is difficult to get evidence from randomized trials of a causal relationship between steroid hormones produced by the adrenal gland and gonad and retinal neurodegenerative disorders (RND). In this study, genetic variations of aldosterone (Aldo), androstenedione (A4), progesterone (P4), hydroxyprogesterone (17-OHP), and testosterone/17β-estradiol (T/E2) were obtained from genome-wide association studies as instrumental variables. Mendelian randomization (MR) analysis was used to assess the impact on the risk of RND, including glaucoma (8,591 cases and 210,201 controls), diabetic retinopathy (DR, 14,584 cases and 202,082 controls) and age-related macular degeneration (AMD, 14,034 cases and 91,214 controls). As the main method, inverse variance weighted results suggest that the increased glaucoma risk was affected by T/E2 (OR = 1.11, 95% CI, 1.01–1.22, P = 0.03), which was further validated by other methods (P(WM) = 0.03, P(MLE) = 0.03, P(MR-RAPS) (=) 0.03). In the replicated stage, the causal relationship between T/E2 and glaucoma was verified based on the MRC-IEU consortium (P = 0.04). No impact of Aldo, A4, P4, 17-OHP, and T/E2 was observed for the risk of DR (P > 0.05) and AMD (P > 0.05). The heterogeneity test (P > 0.05) and pleiotropy test (P > 0.05) verified the robustness of the results. Our results suggest that T/E2 has a suggestive effect on the glaucoma risk. However, the genetic evidence based on a large sample does not support the effect of steroid hormones on DR and AMD risk. Further studies are vital to assess the possibility of steroid hormones as targets for prevention and treatment.
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spelling pubmed-98714872023-01-25 Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases Liu, Kangcheng Fan, Huimin Hu, Hanying Cheng, Yanhua Liu, Jingying You, Zhipeng Front Endocrinol (Lausanne) Endocrinology It is difficult to get evidence from randomized trials of a causal relationship between steroid hormones produced by the adrenal gland and gonad and retinal neurodegenerative disorders (RND). In this study, genetic variations of aldosterone (Aldo), androstenedione (A4), progesterone (P4), hydroxyprogesterone (17-OHP), and testosterone/17β-estradiol (T/E2) were obtained from genome-wide association studies as instrumental variables. Mendelian randomization (MR) analysis was used to assess the impact on the risk of RND, including glaucoma (8,591 cases and 210,201 controls), diabetic retinopathy (DR, 14,584 cases and 202,082 controls) and age-related macular degeneration (AMD, 14,034 cases and 91,214 controls). As the main method, inverse variance weighted results suggest that the increased glaucoma risk was affected by T/E2 (OR = 1.11, 95% CI, 1.01–1.22, P = 0.03), which was further validated by other methods (P(WM) = 0.03, P(MLE) = 0.03, P(MR-RAPS) (=) 0.03). In the replicated stage, the causal relationship between T/E2 and glaucoma was verified based on the MRC-IEU consortium (P = 0.04). No impact of Aldo, A4, P4, 17-OHP, and T/E2 was observed for the risk of DR (P > 0.05) and AMD (P > 0.05). The heterogeneity test (P > 0.05) and pleiotropy test (P > 0.05) verified the robustness of the results. Our results suggest that T/E2 has a suggestive effect on the glaucoma risk. However, the genetic evidence based on a large sample does not support the effect of steroid hormones on DR and AMD risk. Further studies are vital to assess the possibility of steroid hormones as targets for prevention and treatment. Frontiers Media S.A. 2023-01-10 /pmc/articles/PMC9871487/ /pubmed/36704044 http://dx.doi.org/10.3389/fendo.2022.1088557 Text en Copyright © 2023 Liu, Fan, Hu, Cheng, Liu and You https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Liu, Kangcheng
Fan, Huimin
Hu, Hanying
Cheng, Yanhua
Liu, Jingying
You, Zhipeng
Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases
title Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases
title_full Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases
title_fullStr Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases
title_full_unstemmed Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases
title_short Genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases
title_sort genetic variation reveals the influence of steroid hormones on the risk of retinal neurodegenerative diseases
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871487/
https://www.ncbi.nlm.nih.gov/pubmed/36704044
http://dx.doi.org/10.3389/fendo.2022.1088557
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