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Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer
A risk association between membranous nephropathy (MN) and lung cancer is reported, but traditional observational studies cannot provide strong evidence of its causality. This study aimed to assess genome-wide association studies data for a causal relationship between MN and lung cancer using a two-...
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/PMC10474265/ https://www.ncbi.nlm.nih.gov/pubmed/37658161 http://dx.doi.org/10.1038/s42003-023-05111-7 |
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author | Yang, Kezhen Ding, Xiaofeng Liu, Jipeng Liu, Saisai Liu, Qingguo Li, Jianhua Zhang, Pingna |
author_facet | Yang, Kezhen Ding, Xiaofeng Liu, Jipeng Liu, Saisai Liu, Qingguo Li, Jianhua Zhang, Pingna |
author_sort | Yang, Kezhen |
collection | PubMed |
description | A risk association between membranous nephropathy (MN) and lung cancer is reported, but traditional observational studies cannot provide strong evidence of its causality. This study aimed to assess genome-wide association studies data for a causal relationship between MN and lung cancer using a two-sample Mendelian randomization (MR) approach. Inverse-variance weighted, and MR Egger regression techniques were used to determine the association of genetic variants from cohorts of MN and lung cancer patients. Independent genetic variants with genome-wide significance (P < 5×10(–8)) were used to determine the direction of chance. Sensitivity analyses confirmed the accuracy of the results. The results suggest that MN is an exposure factor for lung cancer, validated using a second cohort of lung cancer patients (P < 0.001). There is insufficient evidence to suggest a causal relationship between lung cancer and MN; however, cigarette smoking may be a confounding factor for lung cancer due to MN. The findings provide causal evidence for the effect of MN on lung cancer risk and may be useful for patient management, especially in older patients with MN who should be systematically screened regularly. |
format | Online Article Text |
id | pubmed-10474265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104742652023-09-03 Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer Yang, Kezhen Ding, Xiaofeng Liu, Jipeng Liu, Saisai Liu, Qingguo Li, Jianhua Zhang, Pingna Commun Biol Article A risk association between membranous nephropathy (MN) and lung cancer is reported, but traditional observational studies cannot provide strong evidence of its causality. This study aimed to assess genome-wide association studies data for a causal relationship between MN and lung cancer using a two-sample Mendelian randomization (MR) approach. Inverse-variance weighted, and MR Egger regression techniques were used to determine the association of genetic variants from cohorts of MN and lung cancer patients. Independent genetic variants with genome-wide significance (P < 5×10(–8)) were used to determine the direction of chance. Sensitivity analyses confirmed the accuracy of the results. The results suggest that MN is an exposure factor for lung cancer, validated using a second cohort of lung cancer patients (P < 0.001). There is insufficient evidence to suggest a causal relationship between lung cancer and MN; however, cigarette smoking may be a confounding factor for lung cancer due to MN. The findings provide causal evidence for the effect of MN on lung cancer risk and may be useful for patient management, especially in older patients with MN who should be systematically screened regularly. Nature Publishing Group UK 2023-09-01 /pmc/articles/PMC10474265/ /pubmed/37658161 http://dx.doi.org/10.1038/s42003-023-05111-7 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 Yang, Kezhen Ding, Xiaofeng Liu, Jipeng Liu, Saisai Liu, Qingguo Li, Jianhua Zhang, Pingna Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer |
title | Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer |
title_full | Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer |
title_fullStr | Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer |
title_full_unstemmed | Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer |
title_short | Two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer |
title_sort | two-sample mendelian randomization reveals a causal association between membranous nephropathy and lung cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474265/ https://www.ncbi.nlm.nih.gov/pubmed/37658161 http://dx.doi.org/10.1038/s42003-023-05111-7 |
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