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Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study
OBJECTIVE: The immune response assumes a pivotal role in the underlying mechanisms of urticaria pathogenesis. The present study delves into an investigation of the genetic causal connections between urticaria and prevalent autoimmune afflictions, notably rheumatoid arthritis (RA), systemic lupus ery...
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/PMC10652397/ https://www.ncbi.nlm.nih.gov/pubmed/38022623 http://dx.doi.org/10.3389/fimmu.2023.1280135 |
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author | Yang, Mingyi Su, Yani Xu, Ke Wen, Pengfei Zhang, Binfei Guo, Jianbin Nan, Kai Yang, Peng Shao, Xiaolong Liu, Lin Yang, Zhi Xu, Peng |
author_facet | Yang, Mingyi Su, Yani Xu, Ke Wen, Pengfei Zhang, Binfei Guo, Jianbin Nan, Kai Yang, Peng Shao, Xiaolong Liu, Lin Yang, Zhi Xu, Peng |
author_sort | Yang, Mingyi |
collection | PubMed |
description | OBJECTIVE: The immune response assumes a pivotal role in the underlying mechanisms of urticaria pathogenesis. The present study delves into an investigation of the genetic causal connections between urticaria and prevalent autoimmune afflictions, notably rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), ulcerative colitis (UC), and Crohn’s disease (CD). METHODS: A bidirectional two-sample Mendelian randomization (MR) analysis was conducted to investigate the causal relationships involving four autoimmune diseases and urticaria. The genome-wide association study (GWAS) summary data of four autoimmune disease were sourced from the IEU OpenGWAS database. The GWAS summary data for urticaria were derived from the Finnish consortium dataset. The principal analytical approach employed in this study was the random-effects inverse variance weighted (IVW) method. Subsequently, a series of sensitivity analyses were performed, encompassing assessments of heterogeneity, horizontal pleiotropy, outliers, “Leave-one-out” analyses, and tests for adherence to the assumption of normal distribution. RESULTS: The random-effects IVW analysis indicate a positive genetic causal association between RA and urticaria (P < 0.001, OR 95% CI = 1.091 [1.051-1.133]). Conversely, SLE, UC, and CD do not exhibit a significant genetic causal relationship with urticaria. The reverse MR analysis reveals a positive genetic causal linkage between urticaria and SLE (P = 0.026, OR 95% CI = 1.289 [1.031-1.612]). However, the analysis demonstrates no substantial genetic causal relationship between urticaria and RA, UC, or CD. Importantly, the genetic causal assessment absence of heterogeneity, horizontal pleiotropy, and outliers. Furthermore, it remains unaffected by any individual single nucleotide polymorphism (SNP), demonstrating adherence to a normal distribution. CONCLUSION: This investigation establishing RA as a predisposing factor for urticaria. Moreover, urticaria as a plausible risk determinant for SLE. Heightened vigilance is recommended among RA patients to monitor the manifestation of urticaria within clinical settings. Similarly, individuals afflicted by urticaria should duly acknowledge the prospective susceptibility to SLE. |
format | Online Article Text |
id | pubmed-10652397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106523972023-01-01 Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study Yang, Mingyi Su, Yani Xu, Ke Wen, Pengfei Zhang, Binfei Guo, Jianbin Nan, Kai Yang, Peng Shao, Xiaolong Liu, Lin Yang, Zhi Xu, Peng Front Immunol Immunology OBJECTIVE: The immune response assumes a pivotal role in the underlying mechanisms of urticaria pathogenesis. The present study delves into an investigation of the genetic causal connections between urticaria and prevalent autoimmune afflictions, notably rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), ulcerative colitis (UC), and Crohn’s disease (CD). METHODS: A bidirectional two-sample Mendelian randomization (MR) analysis was conducted to investigate the causal relationships involving four autoimmune diseases and urticaria. The genome-wide association study (GWAS) summary data of four autoimmune disease were sourced from the IEU OpenGWAS database. The GWAS summary data for urticaria were derived from the Finnish consortium dataset. The principal analytical approach employed in this study was the random-effects inverse variance weighted (IVW) method. Subsequently, a series of sensitivity analyses were performed, encompassing assessments of heterogeneity, horizontal pleiotropy, outliers, “Leave-one-out” analyses, and tests for adherence to the assumption of normal distribution. RESULTS: The random-effects IVW analysis indicate a positive genetic causal association between RA and urticaria (P < 0.001, OR 95% CI = 1.091 [1.051-1.133]). Conversely, SLE, UC, and CD do not exhibit a significant genetic causal relationship with urticaria. The reverse MR analysis reveals a positive genetic causal linkage between urticaria and SLE (P = 0.026, OR 95% CI = 1.289 [1.031-1.612]). However, the analysis demonstrates no substantial genetic causal relationship between urticaria and RA, UC, or CD. Importantly, the genetic causal assessment absence of heterogeneity, horizontal pleiotropy, and outliers. Furthermore, it remains unaffected by any individual single nucleotide polymorphism (SNP), demonstrating adherence to a normal distribution. CONCLUSION: This investigation establishing RA as a predisposing factor for urticaria. Moreover, urticaria as a plausible risk determinant for SLE. Heightened vigilance is recommended among RA patients to monitor the manifestation of urticaria within clinical settings. Similarly, individuals afflicted by urticaria should duly acknowledge the prospective susceptibility to SLE. Frontiers Media S.A. 2023-11-02 /pmc/articles/PMC10652397/ /pubmed/38022623 http://dx.doi.org/10.3389/fimmu.2023.1280135 Text en Copyright © 2023 Yang, Su, Xu, Wen, Zhang, Guo, Nan, Yang, Shao, Liu, Yang and Xu 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 | Immunology Yang, Mingyi Su, Yani Xu, Ke Wen, Pengfei Zhang, Binfei Guo, Jianbin Nan, Kai Yang, Peng Shao, Xiaolong Liu, Lin Yang, Zhi Xu, Peng Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study |
title | Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study |
title_full | Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study |
title_fullStr | Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study |
title_full_unstemmed | Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study |
title_short | Common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study |
title_sort | common autoimmune diseases and urticaria: the causal relationship from a bidirectional two-sample mendelian randomization study |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652397/ https://www.ncbi.nlm.nih.gov/pubmed/38022623 http://dx.doi.org/10.3389/fimmu.2023.1280135 |
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