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Inflammatory bowel disease and prostate cancer risk: a two-sample Mendelian randomization analysis
Previous epidemiological observational studies have reported an association between inflammatory bowel disease (IBD) and prostate cancer (PCa), but the causality is inconclusive. The purpose of this study was to evaluate the causality of IBD on PCa using the mendelian randomization (MR) analysis. We...
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Published in: | Frontiers in immunology 2023-06, Vol.14, p.1157313-1157313 |
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description | Previous epidemiological observational studies have reported an association between inflammatory bowel disease (IBD) and prostate cancer (PCa), but the causality is inconclusive. The purpose of this study was to evaluate the causality of IBD on PCa using the mendelian randomization (MR) analysis.
We performed a two-sample MR analysis with public genome-wide association studies (GWAS) data. Eligible instrumental variables (IVs) were selected according to the three assumptions of MR analysis. The inverse-variance weighted (IVW) method was the main method. Complementary methods included the MR-Egger regression, the Weighted Median, the Simple Mode, the Weighted Mode and MR pleiotropy residual sum and outlier (MR-PRESSO) methods.
Genetically determined IBD did not have a causal effect on PCa (IVW
> 0.05). Additionally, there was no causal effect of Crohn's disease (CD) and ulcerative colitis (UC) on PCa in the MR analysis (IVW
> 0.05). Results of complementary methods were consistent with those of the IVW method.
This study does not support a causal association of IBD on PCa, which is in contrast to most observational studies. |
doi_str_mv | 10.3389/fimmu.2023.1157313 |
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We performed a two-sample MR analysis with public genome-wide association studies (GWAS) data. Eligible instrumental variables (IVs) were selected according to the three assumptions of MR analysis. The inverse-variance weighted (IVW) method was the main method. Complementary methods included the MR-Egger regression, the Weighted Median, the Simple Mode, the Weighted Mode and MR pleiotropy residual sum and outlier (MR-PRESSO) methods.
Genetically determined IBD did not have a causal effect on PCa (IVW
> 0.05). Additionally, there was no causal effect of Crohn's disease (CD) and ulcerative colitis (UC) on PCa in the MR analysis (IVW
> 0.05). Results of complementary methods were consistent with those of the IVW method.
This study does not support a causal association of IBD on PCa, which is in contrast to most observational studies.</description><identifier>ISSN: 1664-3224</identifier><identifier>EISSN: 1664-3224</identifier><identifier>DOI: 10.3389/fimmu.2023.1157313</identifier><identifier>PMID: 37409117</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>causality ; Colitis, Ulcerative ; Crohn ‘s disease ; Genome-Wide Association Study ; Humans ; Immunology ; inflammatory bowel disease ; Inflammatory Bowel Diseases - epidemiology ; Inflammatory Bowel Diseases - genetics ; Male ; Mendelian randomization ; Mendelian Randomization Analysis ; prostate cancer ; Prostatic Neoplasms - epidemiology ; Prostatic Neoplasms - genetics ; ulcerative colitis</subject><ispartof>Frontiers in immunology, 2023-06, Vol.14, p.1157313-1157313</ispartof><rights>Copyright © 2023 Cheng, Liao, Mou, Xiao and Jia.</rights><rights>Copyright © 2023 Cheng, Liao, Mou, Xiao and Jia 2023 Cheng, Liao, Mou, Xiao and Jia</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-1f2a768f3cf17f3244814ae213259c85eef0551c04f2c685bd56c4d62d5a6b353</citedby><cites>FETCH-LOGICAL-c469t-1f2a768f3cf17f3244814ae213259c85eef0551c04f2c685bd56c4d62d5a6b353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318899/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318899/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37409117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheng, Wen</creatorcontrib><creatorcontrib>Liao, Yang</creatorcontrib><creatorcontrib>Mou, Ruiyu</creatorcontrib><creatorcontrib>Xiao, Xian</creatorcontrib><creatorcontrib>Jia, Yingjie</creatorcontrib><title>Inflammatory bowel disease and prostate cancer risk: a two-sample Mendelian randomization analysis</title><title>Frontiers in immunology</title><addtitle>Front Immunol</addtitle><description>Previous epidemiological observational studies have reported an association between inflammatory bowel disease (IBD) and prostate cancer (PCa), but the causality is inconclusive. The purpose of this study was to evaluate the causality of IBD on PCa using the mendelian randomization (MR) analysis.
We performed a two-sample MR analysis with public genome-wide association studies (GWAS) data. Eligible instrumental variables (IVs) were selected according to the three assumptions of MR analysis. The inverse-variance weighted (IVW) method was the main method. Complementary methods included the MR-Egger regression, the Weighted Median, the Simple Mode, the Weighted Mode and MR pleiotropy residual sum and outlier (MR-PRESSO) methods.
Genetically determined IBD did not have a causal effect on PCa (IVW
> 0.05). Additionally, there was no causal effect of Crohn's disease (CD) and ulcerative colitis (UC) on PCa in the MR analysis (IVW
> 0.05). Results of complementary methods were consistent with those of the IVW method.
This study does not support a causal association of IBD on PCa, which is in contrast to most observational studies.</description><subject>causality</subject><subject>Colitis, Ulcerative</subject><subject>Crohn ‘s disease</subject><subject>Genome-Wide Association Study</subject><subject>Humans</subject><subject>Immunology</subject><subject>inflammatory bowel disease</subject><subject>Inflammatory Bowel Diseases - epidemiology</subject><subject>Inflammatory Bowel Diseases - genetics</subject><subject>Male</subject><subject>Mendelian randomization</subject><subject>Mendelian Randomization Analysis</subject><subject>prostate cancer</subject><subject>Prostatic Neoplasms - epidemiology</subject><subject>Prostatic Neoplasms - genetics</subject><subject>ulcerative colitis</subject><issn>1664-3224</issn><issn>1664-3224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkcFu1DAQhiMEolXpC3BAOXLJYnvsxOaCUAXtSkVc4GxNnHFxceLFzrZanp5sd6laX2yN_X8z8ldVbzlbAWjzwYdx3K4EE7DiXHXA4UV1yttWNiCEfPnkfFKdl3LLliUNAKjX1Ql0khnOu9OqX08-4jjinPKu7tM9xXoIhbBQjdNQb3IqM85UO5wc5TqH8vtjjfV8n5qC4yZS_Y2mgWLAqc5LIo3hL84hTUsc466E8qZ65TEWOj_uZ9XPr19-XFw1198v1xefrxsnWzM33AvsWu3Bed55EFJqLpEEB6GM04rIM6W4Y9IL12rVD6p1cmjFoLDtQcFZtT5wh4S3dpPDiHlnEwb7UEj5xmKeg4tkSXcdovFKDiQBjDYtAxRMO68ZkFtYnw6szbYfaXA0zRnjM-jzmyn8sjfpznIGXGtjFsL7IyGnP1sqsx1DcRQjTpS2xQq99DWaif3g4vDULZ9dMvnHPpzZvWz7INvuZduj7CX07umEj5H_auEfJcGn4g</recordid><startdate>20230620</startdate><enddate>20230620</enddate><creator>Cheng, Wen</creator><creator>Liao, Yang</creator><creator>Mou, Ruiyu</creator><creator>Xiao, Xian</creator><creator>Jia, Yingjie</creator><general>Frontiers Media S.A</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><scope>DOA</scope></search><sort><creationdate>20230620</creationdate><title>Inflammatory bowel disease and prostate cancer risk: a two-sample Mendelian randomization analysis</title><author>Cheng, Wen ; Liao, Yang ; Mou, Ruiyu ; Xiao, Xian ; Jia, Yingjie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-1f2a768f3cf17f3244814ae213259c85eef0551c04f2c685bd56c4d62d5a6b353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>causality</topic><topic>Colitis, Ulcerative</topic><topic>Crohn ‘s disease</topic><topic>Genome-Wide Association Study</topic><topic>Humans</topic><topic>Immunology</topic><topic>inflammatory bowel disease</topic><topic>Inflammatory Bowel Diseases - epidemiology</topic><topic>Inflammatory Bowel Diseases - genetics</topic><topic>Male</topic><topic>Mendelian randomization</topic><topic>Mendelian Randomization Analysis</topic><topic>prostate cancer</topic><topic>Prostatic Neoplasms - epidemiology</topic><topic>Prostatic Neoplasms - genetics</topic><topic>ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Wen</creatorcontrib><creatorcontrib>Liao, Yang</creatorcontrib><creatorcontrib>Mou, Ruiyu</creatorcontrib><creatorcontrib>Xiao, Xian</creatorcontrib><creatorcontrib>Jia, Yingjie</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><collection>Directory of Open Access Journals</collection><jtitle>Frontiers in immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheng, Wen</au><au>Liao, Yang</au><au>Mou, Ruiyu</au><au>Xiao, Xian</au><au>Jia, Yingjie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inflammatory bowel disease and prostate cancer risk: a two-sample Mendelian randomization analysis</atitle><jtitle>Frontiers in immunology</jtitle><addtitle>Front Immunol</addtitle><date>2023-06-20</date><risdate>2023</risdate><volume>14</volume><spage>1157313</spage><epage>1157313</epage><pages>1157313-1157313</pages><issn>1664-3224</issn><eissn>1664-3224</eissn><abstract>Previous epidemiological observational studies have reported an association between inflammatory bowel disease (IBD) and prostate cancer (PCa), but the causality is inconclusive. The purpose of this study was to evaluate the causality of IBD on PCa using the mendelian randomization (MR) analysis.
We performed a two-sample MR analysis with public genome-wide association studies (GWAS) data. Eligible instrumental variables (IVs) were selected according to the three assumptions of MR analysis. The inverse-variance weighted (IVW) method was the main method. Complementary methods included the MR-Egger regression, the Weighted Median, the Simple Mode, the Weighted Mode and MR pleiotropy residual sum and outlier (MR-PRESSO) methods.
Genetically determined IBD did not have a causal effect on PCa (IVW
> 0.05). Additionally, there was no causal effect of Crohn's disease (CD) and ulcerative colitis (UC) on PCa in the MR analysis (IVW
> 0.05). Results of complementary methods were consistent with those of the IVW method.
This study does not support a causal association of IBD on PCa, which is in contrast to most observational studies.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>37409117</pmid><doi>10.3389/fimmu.2023.1157313</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | causality Colitis, Ulcerative Crohn ‘s disease Genome-Wide Association Study Humans Immunology inflammatory bowel disease Inflammatory Bowel Diseases - epidemiology Inflammatory Bowel Diseases - genetics Male Mendelian randomization Mendelian Randomization Analysis prostate cancer Prostatic Neoplasms - epidemiology Prostatic Neoplasms - genetics ulcerative colitis |
title | Inflammatory bowel disease and prostate cancer risk: a two-sample Mendelian randomization analysis |
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