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Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction
BACKGROUND: Several studies have found that erectile dysfunction (ED) is associated with interstitial lung disease. However, the causal relationship between idiopathic pulmonary fibrosis (IPF) and ED risk remains unclear. The present two-sample Mendelian randomization (MR) study aimed to reveal the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370277/ https://www.ncbi.nlm.nih.gov/pubmed/37502356 http://dx.doi.org/10.3389/fmed.2023.1162153 |
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author | Zhang, Kun Zhou, Jiejun Li, Anqi Chen, Mingwei |
author_facet | Zhang, Kun Zhou, Jiejun Li, Anqi Chen, Mingwei |
author_sort | Zhang, Kun |
collection | PubMed |
description | BACKGROUND: Several studies have found that erectile dysfunction (ED) is associated with interstitial lung disease. However, the causal relationship between idiopathic pulmonary fibrosis (IPF) and ED risk remains unclear. The present two-sample Mendelian randomization (MR) study aimed to reveal the causal effect of IPF on ED risk. METHODS: This study included two GWAS summary statistics of IPF (1,028 cases and 196,986 controls) and ED (6,175 cases and 217,630 controls) of European ancestry. The inverse-variance weighted (IVW) was applied as the primary method, and MR-Egger, weighted median, weighted mode, and simple mode were applied as complementary methods to estimate the causal impact of IPF on ED risk. The MR-PRESSO global test and MR-Egger regression were applied to evaluate the pleiotropy. The Cochran’s Q test was applied to examine heterogeneity. The leave-one-out analysis ensured the robustness and reliability of the results. RESULTS: Twenty-one genetic variants were obtained as IPF instrumental variables without pleiotropy and heterogeneity. MR analysis using the IVW showed a potential causal relationship between IPF and increased ED risk (OR(IVW) = 1.046, 95% CI: 1.020–1.073, p = 0.001), and consistent results were obtained with MR-Egger, weighted median, and weighted mode. The leave-one-out analysis showed that no instrumental variables unduly influenced the results. CONCLUSION: This study suggested that IPF may increase the ED risk of the European population. |
format | Online Article Text |
id | pubmed-10370277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103702772023-07-27 Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction Zhang, Kun Zhou, Jiejun Li, Anqi Chen, Mingwei Front Med (Lausanne) Medicine BACKGROUND: Several studies have found that erectile dysfunction (ED) is associated with interstitial lung disease. However, the causal relationship between idiopathic pulmonary fibrosis (IPF) and ED risk remains unclear. The present two-sample Mendelian randomization (MR) study aimed to reveal the causal effect of IPF on ED risk. METHODS: This study included two GWAS summary statistics of IPF (1,028 cases and 196,986 controls) and ED (6,175 cases and 217,630 controls) of European ancestry. The inverse-variance weighted (IVW) was applied as the primary method, and MR-Egger, weighted median, weighted mode, and simple mode were applied as complementary methods to estimate the causal impact of IPF on ED risk. The MR-PRESSO global test and MR-Egger regression were applied to evaluate the pleiotropy. The Cochran’s Q test was applied to examine heterogeneity. The leave-one-out analysis ensured the robustness and reliability of the results. RESULTS: Twenty-one genetic variants were obtained as IPF instrumental variables without pleiotropy and heterogeneity. MR analysis using the IVW showed a potential causal relationship between IPF and increased ED risk (OR(IVW) = 1.046, 95% CI: 1.020–1.073, p = 0.001), and consistent results were obtained with MR-Egger, weighted median, and weighted mode. The leave-one-out analysis showed that no instrumental variables unduly influenced the results. CONCLUSION: This study suggested that IPF may increase the ED risk of the European population. Frontiers Media S.A. 2023-07-12 /pmc/articles/PMC10370277/ /pubmed/37502356 http://dx.doi.org/10.3389/fmed.2023.1162153 Text en Copyright © 2023 Zhang, Zhou, Li and Chen. 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 | Medicine Zhang, Kun Zhou, Jiejun Li, Anqi Chen, Mingwei Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction |
title | Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction |
title_full | Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction |
title_fullStr | Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction |
title_full_unstemmed | Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction |
title_short | Mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction |
title_sort | mendelian randomization study reveals the effect of idiopathic pulmonary fibrosis on the risk of erectile dysfunction |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370277/ https://www.ncbi.nlm.nih.gov/pubmed/37502356 http://dx.doi.org/10.3389/fmed.2023.1162153 |
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