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Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study
OBJECTIVE: Systemic lupus erythematosus (SLE) has been observationally associated with endometrial cancer, but the causality remains unclear. Here, we investigated for the first time the causal links between SLE and endometrial cancer risk. METHODS: Univariable and multivariable Mendelian randomizat...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575983/ https://www.ncbi.nlm.nih.gov/pubmed/36263221 http://dx.doi.org/10.3389/fonc.2022.930243 |
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author | Wan, An Zhao, Wei-Dong Tao, Jin-Hui |
author_facet | Wan, An Zhao, Wei-Dong Tao, Jin-Hui |
author_sort | Wan, An |
collection | PubMed |
description | OBJECTIVE: Systemic lupus erythematosus (SLE) has been observationally associated with endometrial cancer, but the causality remains unclear. Here, we investigated for the first time the causal links between SLE and endometrial cancer risk. METHODS: Univariable and multivariable Mendelian randomization (MR) analyses were conducted to disentangle the causality of SLE with endometrial cancer. Apart from the inverse-variance weighted (IVW) method as the primary MR estimate, three complementary MR techniques including weighted median, weighted mode, and MR-Egger regression in univariable MR were conducted to clarify the robustness of the causal estimate and mediation effects of the body mass index (BMI) and were investigated within multivariable MR-IVW and MR-Egger analyses. RESULTS: All univariable MR analyses consistently suggested that SLE has a protective effect on the risk of overall endometrial cancer (IVW: OR = 0.956, 95% CI = 0.932-0.981, P = 0.001) and endometrioid endometrial cancer (IVW: OR = 0.965, 95% CI = 0.933-0.999, P = 0.043). More compelling, after adjustment for BMI within the multivariable MR setting, the association between SLE and decreased risk of overall endometrial cancer was significantly stronger (IVW: OR = 0.952, 95% CI = 0.931-0.973, P = 9.58E-06). CONCLUSIONS: Our findings provide evidence of a significant causal relationship between SLE and decreased endometrial cancer risk. Further understanding of the underlying mechanisms linking SLE with endometrial cancer is therefore needed. |
format | Online Article Text |
id | pubmed-9575983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95759832022-10-18 Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study Wan, An Zhao, Wei-Dong Tao, Jin-Hui Front Oncol Oncology OBJECTIVE: Systemic lupus erythematosus (SLE) has been observationally associated with endometrial cancer, but the causality remains unclear. Here, we investigated for the first time the causal links between SLE and endometrial cancer risk. METHODS: Univariable and multivariable Mendelian randomization (MR) analyses were conducted to disentangle the causality of SLE with endometrial cancer. Apart from the inverse-variance weighted (IVW) method as the primary MR estimate, three complementary MR techniques including weighted median, weighted mode, and MR-Egger regression in univariable MR were conducted to clarify the robustness of the causal estimate and mediation effects of the body mass index (BMI) and were investigated within multivariable MR-IVW and MR-Egger analyses. RESULTS: All univariable MR analyses consistently suggested that SLE has a protective effect on the risk of overall endometrial cancer (IVW: OR = 0.956, 95% CI = 0.932-0.981, P = 0.001) and endometrioid endometrial cancer (IVW: OR = 0.965, 95% CI = 0.933-0.999, P = 0.043). More compelling, after adjustment for BMI within the multivariable MR setting, the association between SLE and decreased risk of overall endometrial cancer was significantly stronger (IVW: OR = 0.952, 95% CI = 0.931-0.973, P = 9.58E-06). CONCLUSIONS: Our findings provide evidence of a significant causal relationship between SLE and decreased endometrial cancer risk. Further understanding of the underlying mechanisms linking SLE with endometrial cancer is therefore needed. Frontiers Media S.A. 2022-10-03 /pmc/articles/PMC9575983/ /pubmed/36263221 http://dx.doi.org/10.3389/fonc.2022.930243 Text en Copyright © 2022 Wan, Zhao and Tao 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 | Oncology Wan, An Zhao, Wei-Dong Tao, Jin-Hui Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study |
title | Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study |
title_full | Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study |
title_fullStr | Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study |
title_full_unstemmed | Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study |
title_short | Causal effects of systemic lupus erythematosus on endometrial cancer: A univariable and multivariable Mendelian randomization study |
title_sort | causal effects of systemic lupus erythematosus on endometrial cancer: a univariable and multivariable mendelian randomization study |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575983/ https://www.ncbi.nlm.nih.gov/pubmed/36263221 http://dx.doi.org/10.3389/fonc.2022.930243 |
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