Identifying the genetic association between systemic lupus erythematosus and the risk of autoimmune liver diseases
Copyright © 2024 Elsevier Ltd. All rights reserved..
BACKGROUND: Previous studies on the relationship between systemic lupus erythematosus (SLE) and autoimmune liver diseases (AILDs) are inconclusive. Therefore, we employed Mendelian randomization (MR) to explore the causal associations between SLE and AILDs.
METHODS: A two-sample MR analysis was performed using summary-level statistics sourced from genome-wide association study (GWAS) datasets. Inverse-variance weighting (IVW), MR‒Egger, and weighted median (WM) were further supported by several sensitivity analyses.
RESULTS: We detected causal genetic associations between SLE and primary biliary cholangitis (PBC) (odds ratio (OR) = 1.31, 95% CI = 1.15-1.51, P < 0.01; adjusted OR = 1.63, 95% CI = 1.39-1.90, P < 0.01) and between SLE and primary sclerosing cholangitis (PSC) (OR = 1.09, 95% CI = 1.01-1.08, P = 0.03; adjusted OR = 1.10, 95% CI = 1.00-1.21, P = 0.04). No causal association was found between SLE and autoimmune hepatitis.
CONCLUSIONS: We are the first to use MR analysis to explore the causal relationships between SLE and various AILDs, revealing an increased risk of PBC and PSC in individuals with SLE.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:145 |
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Enthalten in: |
Journal of autoimmunity - 145(2024) vom: 07. März, Seite 103188 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Huang, Wei [VerfasserIn] |
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Links: |
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Themen: |
Autoimmune liver diseases |
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Anmerkungen: |
Date Revised 08.03.2024 published: Print-Electronic Citation Status Publisher |
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doi: |
10.1016/j.jaut.2024.103188 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM36947807X |
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500 | |a published: Print-Electronic | ||
500 | |a Citation Status Publisher | ||
520 | |a Copyright © 2024 Elsevier Ltd. All rights reserved. | ||
520 | |a BACKGROUND: Previous studies on the relationship between systemic lupus erythematosus (SLE) and autoimmune liver diseases (AILDs) are inconclusive. Therefore, we employed Mendelian randomization (MR) to explore the causal associations between SLE and AILDs | ||
520 | |a METHODS: A two-sample MR analysis was performed using summary-level statistics sourced from genome-wide association study (GWAS) datasets. Inverse-variance weighting (IVW), MR‒Egger, and weighted median (WM) were further supported by several sensitivity analyses | ||
520 | |a RESULTS: We detected causal genetic associations between SLE and primary biliary cholangitis (PBC) (odds ratio (OR) = 1.31, 95% CI = 1.15-1.51, P < 0.01; adjusted OR = 1.63, 95% CI = 1.39-1.90, P < 0.01) and between SLE and primary sclerosing cholangitis (PSC) (OR = 1.09, 95% CI = 1.01-1.08, P = 0.03; adjusted OR = 1.10, 95% CI = 1.00-1.21, P = 0.04). No causal association was found between SLE and autoimmune hepatitis | ||
520 | |a CONCLUSIONS: We are the first to use MR analysis to explore the causal relationships between SLE and various AILDs, revealing an increased risk of PBC and PSC in individuals with SLE | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Review | |
650 | 4 | |a Autoimmune liver diseases | |
650 | 4 | |a Genetics | |
650 | 4 | |a Systemic lupus erythematosus | |
700 | 1 | |a Jin, Tianyu |e verfasserin |4 aut | |
700 | 1 | |a Zheng, Wei |e verfasserin |4 aut | |
700 | 1 | |a Yin, Qiaoqiao |e verfasserin |4 aut | |
700 | 1 | |a Yan, Qiqi |e verfasserin |4 aut | |
700 | 1 | |a Pan, Hongying |e verfasserin |4 aut | |
700 | 1 | |a Xu, Chengan |e verfasserin |4 aut | |
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