{"title":"探讨特应性皮炎与恶性肿瘤的因果关系:一项综合观察和遗传研究。","authors":"Yang He, Abai Xu, Xiangbin Mi, Nina Tang","doi":"10.1177/17103568251384311","DOIUrl":null,"url":null,"abstract":"<p><p><u><b><i></i></b></u> <u><b><i>Background:</i></b></u> Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by immune dysregulation. The global rise in the incidence of both AD and cancer suggests a potential link through shared immune-inflammatory pathways. <u><b><i>Objective:</i></b></u> This study aimed to investigate the causal relationship between AD and multiple cancer types and to explore potential underlying biological mechanisms. <u><b><i>Methods:</i></b></u> A two-sample Mendelian randomization (MR) analysis was conducted using data from a genome-wide association study of 6,224 AD patients. Seventeen cancer types were assessed. Additionally, expression quantitative trait loci analysis, pathway enrichment, and survival analyses were performed. <u><b><i>Results</i>:</b></u> MR analysis identified a significant causal relationship between AD and the risk of esophageal cancer (odds ratio [OR] = 0.88, <i>P</i> = 0.0247) as well as colorectal cancer (OR = 0.94, <i>P</i> = 0.0154). Subsequent research revealed differential expression between tumor and normal tissues, with pathway enrichment highlighting immune processes. No survival association was found in esophageal cancer, but <i>MFN2</i> and <i>SIPA1</i> expression levels could affect outcomes in colorectal cancer. <u><b><i>Conclusion:</i></b></u> This study provides evidence for a protective causal relationship between AD and the risks of esophageal and colorectal cancers. Immune and inflammatory pathways may mediate this link.</p>","PeriodicalId":93974,"journal":{"name":"Dermatitis : contact, atopic, occupational, drug","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exploring the Causal Relationship Between Atopic Dermatitis and Malignancies: A Comprehensive Observational and Genetic Study.\",\"authors\":\"Yang He, Abai Xu, Xiangbin Mi, Nina Tang\",\"doi\":\"10.1177/17103568251384311\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><u><b><i></i></b></u> <u><b><i>Background:</i></b></u> Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by immune dysregulation. The global rise in the incidence of both AD and cancer suggests a potential link through shared immune-inflammatory pathways. <u><b><i>Objective:</i></b></u> This study aimed to investigate the causal relationship between AD and multiple cancer types and to explore potential underlying biological mechanisms. <u><b><i>Methods:</i></b></u> A two-sample Mendelian randomization (MR) analysis was conducted using data from a genome-wide association study of 6,224 AD patients. Seventeen cancer types were assessed. Additionally, expression quantitative trait loci analysis, pathway enrichment, and survival analyses were performed. <u><b><i>Results</i>:</b></u> MR analysis identified a significant causal relationship between AD and the risk of esophageal cancer (odds ratio [OR] = 0.88, <i>P</i> = 0.0247) as well as colorectal cancer (OR = 0.94, <i>P</i> = 0.0154). Subsequent research revealed differential expression between tumor and normal tissues, with pathway enrichment highlighting immune processes. No survival association was found in esophageal cancer, but <i>MFN2</i> and <i>SIPA1</i> expression levels could affect outcomes in colorectal cancer. <u><b><i>Conclusion:</i></b></u> This study provides evidence for a protective causal relationship between AD and the risks of esophageal and colorectal cancers. Immune and inflammatory pathways may mediate this link.</p>\",\"PeriodicalId\":93974,\"journal\":{\"name\":\"Dermatitis : contact, atopic, occupational, drug\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-10-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dermatitis : contact, atopic, occupational, drug\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/17103568251384311\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dermatitis : contact, atopic, occupational, drug","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/17103568251384311","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:特应性皮炎(AD)是一种以免疫失调为特征的慢性炎症性皮肤病。阿尔茨海默病和癌症发病率的全球上升表明,它们之间存在着共同的免疫炎症途径的潜在联系。目的:本研究旨在探讨AD与多种癌症类型之间的因果关系,并探讨潜在的生物学机制。方法:对6224例AD患者的全基因组关联研究数据进行双样本孟德尔随机化(MR)分析。评估了17种癌症类型。此外,还进行了表达数量性状位点分析、途径富集和生存分析。结果:MR分析发现AD与食管癌(比值比[OR] = 0.88, P = 0.0247)和结直肠癌(OR = 0.94, P = 0.0154)存在显著的因果关系。随后的研究揭示了肿瘤和正常组织之间的差异表达,途径富集突出免疫过程。在食管癌中未发现生存相关,但MFN2和SIPA1表达水平可能影响结直肠癌的预后。结论:本研究为AD与食管癌和结直肠癌风险之间的保护性因果关系提供了证据。免疫和炎症途径可能介导这种联系。
Exploring the Causal Relationship Between Atopic Dermatitis and Malignancies: A Comprehensive Observational and Genetic Study.
Background: Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by immune dysregulation. The global rise in the incidence of both AD and cancer suggests a potential link through shared immune-inflammatory pathways. Objective: This study aimed to investigate the causal relationship between AD and multiple cancer types and to explore potential underlying biological mechanisms. Methods: A two-sample Mendelian randomization (MR) analysis was conducted using data from a genome-wide association study of 6,224 AD patients. Seventeen cancer types were assessed. Additionally, expression quantitative trait loci analysis, pathway enrichment, and survival analyses were performed. Results: MR analysis identified a significant causal relationship between AD and the risk of esophageal cancer (odds ratio [OR] = 0.88, P = 0.0247) as well as colorectal cancer (OR = 0.94, P = 0.0154). Subsequent research revealed differential expression between tumor and normal tissues, with pathway enrichment highlighting immune processes. No survival association was found in esophageal cancer, but MFN2 and SIPA1 expression levels could affect outcomes in colorectal cancer. Conclusion: This study provides evidence for a protective causal relationship between AD and the risks of esophageal and colorectal cancers. Immune and inflammatory pathways may mediate this link.