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Causal links between 13 autoimmune diseases and graft dysfunction: A Mendelian randomization study
Previous studies have suggested a possible link between autoimmune diseases and graft dysfunction; however, a causal link remains unclear. Exposure factors were set as 13 autoimmune diseases, and outcomes were set as graft dysfunction. Mendelian randomization was used to analyze the causal link betw...
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Published in: | Medicine (Baltimore) 2024-09, Vol.103 (37), p.e39666 |
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description | Previous studies have suggested a possible link between autoimmune diseases and graft dysfunction; however, a causal link remains unclear. Exposure factors were set as 13 autoimmune diseases, and outcomes were set as graft dysfunction. Mendelian randomization was used to analyze the causal link between exposure and outcome. Alopecia areata and asthma were linked to graft dysfunction (odds ratio 0.828; 95% confidence interval 0.699-0.980; P = .029; odds ratio 1.79; 95% confidence interval 1.069-2.996; P = .027). At the same time, primary sclerosing cholangitis was found to be heterogeneous as an exposure factor (P = .009), but no heterogeneity or pleiotropy was found in other exposure factors. Our preliminary findings show 2 autoimmune diseases as risk factors for graft dysfunction, 1 autoimmune disease as a protective factor for graft dysfunction and the mechanisms remain to be understood. |
doi_str_mv | 10.1097/MD.0000000000039666 |
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Exposure factors were set as 13 autoimmune diseases, and outcomes were set as graft dysfunction. Mendelian randomization was used to analyze the causal link between exposure and outcome. Alopecia areata and asthma were linked to graft dysfunction (odds ratio 0.828; 95% confidence interval 0.699-0.980; P = .029; odds ratio 1.79; 95% confidence interval 1.069-2.996; P = .027). At the same time, primary sclerosing cholangitis was found to be heterogeneous as an exposure factor (P = .009), but no heterogeneity or pleiotropy was found in other exposure factors. Our preliminary findings show 2 autoimmune diseases as risk factors for graft dysfunction, 1 autoimmune disease as a protective factor for graft dysfunction and the mechanisms remain to be understood.</description><identifier>ISSN: 0025-7974</identifier><identifier>ISSN: 1536-5964</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000039666</identifier><identifier>PMID: 39287258</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins</publisher><subject>Alopecia Areata - epidemiology ; Alopecia Areata - genetics ; Asthma - epidemiology ; Asthma - genetics ; Autoimmune Diseases - epidemiology ; Autoimmune Diseases - genetics ; Cholangitis, Sclerosing - genetics ; Cholangitis, Sclerosing - surgery ; Humans ; Mendelian Randomization Analysis ; Observational Study ; Primary Graft Dysfunction - epidemiology ; Primary Graft Dysfunction - genetics ; Risk Factors</subject><ispartof>Medicine (Baltimore), 2024-09, Vol.103 (37), p.e39666</ispartof><rights>Copyright © 2024 the Author(s). 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Published by Wolters Kluwer Health, Inc. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c286t-66975ecc7f68f07cbad8c5e78be29e7a4772eb819aa3b270006e08db41fc44443</cites><orcidid>0009-0004-5068-3943</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11404874/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11404874/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39287258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pan, Ziwen</creatorcontrib><creatorcontrib>Zhong, Lin</creatorcontrib><title>Causal links between 13 autoimmune diseases and graft dysfunction: A Mendelian randomization study</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>Previous studies have suggested a possible link between autoimmune diseases and graft dysfunction; however, a causal link remains unclear. Exposure factors were set as 13 autoimmune diseases, and outcomes were set as graft dysfunction. Mendelian randomization was used to analyze the causal link between exposure and outcome. Alopecia areata and asthma were linked to graft dysfunction (odds ratio 0.828; 95% confidence interval 0.699-0.980; P = .029; odds ratio 1.79; 95% confidence interval 1.069-2.996; P = .027). At the same time, primary sclerosing cholangitis was found to be heterogeneous as an exposure factor (P = .009), but no heterogeneity or pleiotropy was found in other exposure factors. Our preliminary findings show 2 autoimmune diseases as risk factors for graft dysfunction, 1 autoimmune disease as a protective factor for graft dysfunction and the mechanisms remain to be understood.</description><subject>Alopecia Areata - epidemiology</subject><subject>Alopecia Areata - genetics</subject><subject>Asthma - epidemiology</subject><subject>Asthma - genetics</subject><subject>Autoimmune Diseases - epidemiology</subject><subject>Autoimmune Diseases - genetics</subject><subject>Cholangitis, Sclerosing - genetics</subject><subject>Cholangitis, Sclerosing - surgery</subject><subject>Humans</subject><subject>Mendelian Randomization Analysis</subject><subject>Observational Study</subject><subject>Primary Graft Dysfunction - epidemiology</subject><subject>Primary Graft Dysfunction - genetics</subject><subject>Risk Factors</subject><issn>0025-7974</issn><issn>1536-5964</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdUblOxDAQtRAIluMLkJBLmoAdO7ZDg9Aul8SKBmpr4kzAkDgQJ6Dl68mKm9dM8Y6Z0SNkl7MDznJ9OJ8dsB-IXCm1QiY8EyrJciVXyYSxNEt0ruUG2YzxgTEudCrXyYbIU6PTzExIMYUhQk1rHx4jLbB_RQyUCwpD3_qmGQLS0keEiJFCKOldB1VPy0WshuB634YjekLnGEqsPQTajZq28W-wpGjsh3KxTdYqqCPufM4tcnt2ejO9SK6uzy-nJ1eJS43qE6VynaFzulKmYtoVUBqXoTYFpjlqkFqnWBieA4gi1ePLCpkpC8krJ0eILXL8kfs0FA2WDkPfQW2fOt9At7AtePuXCf7e3rUvlnPJpNHLhP3PhK59HjD2tvHRYV1DwHaIVnCmZKYVy0ap-JC6ro2xw-p7D2d2WY-dz-z_ekbX3u8Tvz1ffYh3c7-M_Q</recordid><startdate>20240913</startdate><enddate>20240913</enddate><creator>Pan, Ziwen</creator><creator>Zhong, Lin</creator><general>Lippincott Williams & Wilkins</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0009-0004-5068-3943</orcidid></search><sort><creationdate>20240913</creationdate><title>Causal links between 13 autoimmune diseases and graft dysfunction: A Mendelian randomization study</title><author>Pan, Ziwen ; Zhong, Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c286t-66975ecc7f68f07cbad8c5e78be29e7a4772eb819aa3b270006e08db41fc44443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Alopecia Areata - epidemiology</topic><topic>Alopecia Areata - genetics</topic><topic>Asthma - epidemiology</topic><topic>Asthma - genetics</topic><topic>Autoimmune Diseases - epidemiology</topic><topic>Autoimmune Diseases - genetics</topic><topic>Cholangitis, Sclerosing - genetics</topic><topic>Cholangitis, Sclerosing - surgery</topic><topic>Humans</topic><topic>Mendelian Randomization Analysis</topic><topic>Observational Study</topic><topic>Primary Graft Dysfunction - epidemiology</topic><topic>Primary Graft Dysfunction - genetics</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pan, Ziwen</creatorcontrib><creatorcontrib>Zhong, Lin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pan, Ziwen</au><au>Zhong, Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Causal links between 13 autoimmune diseases and graft dysfunction: A Mendelian randomization study</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2024-09-13</date><risdate>2024</risdate><volume>103</volume><issue>37</issue><spage>e39666</spage><pages>e39666-</pages><issn>0025-7974</issn><issn>1536-5964</issn><eissn>1536-5964</eissn><abstract>Previous studies have suggested a possible link between autoimmune diseases and graft dysfunction; however, a causal link remains unclear. Exposure factors were set as 13 autoimmune diseases, and outcomes were set as graft dysfunction. Mendelian randomization was used to analyze the causal link between exposure and outcome. Alopecia areata and asthma were linked to graft dysfunction (odds ratio 0.828; 95% confidence interval 0.699-0.980; P = .029; odds ratio 1.79; 95% confidence interval 1.069-2.996; P = .027). At the same time, primary sclerosing cholangitis was found to be heterogeneous as an exposure factor (P = .009), but no heterogeneity or pleiotropy was found in other exposure factors. Our preliminary findings show 2 autoimmune diseases as risk factors for graft dysfunction, 1 autoimmune disease as a protective factor for graft dysfunction and the mechanisms remain to be understood.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins</pub><pmid>39287258</pmid><doi>10.1097/MD.0000000000039666</doi><orcidid>https://orcid.org/0009-0004-5068-3943</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alopecia Areata - epidemiology Alopecia Areata - genetics Asthma - epidemiology Asthma - genetics Autoimmune Diseases - epidemiology Autoimmune Diseases - genetics Cholangitis, Sclerosing - genetics Cholangitis, Sclerosing - surgery Humans Mendelian Randomization Analysis Observational Study Primary Graft Dysfunction - epidemiology Primary Graft Dysfunction - genetics Risk Factors |
title | Causal links between 13 autoimmune diseases and graft dysfunction: A Mendelian randomization study |
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