{"title":"Genetic Predictive Association Between Inflammatory Cytokines and Vitiligo: A Bidirectional Mendelian Randomization Study","authors":"Tianbing Lei, Yao Ni","doi":"10.1155/ijcp/1093015","DOIUrl":null,"url":null,"abstract":"<div>\n <p><b>Background:</b> Previous studies have indicated a close association between vitiligo and inflammatory cytokines, yet the genetic predictive association remains unclear. The study aimed to predict the relationship between vitiligo and inflammatory cytokines in genetics.</p>\n <p><b>Methods:</b> A bidirectional analysis was conducted by the two-sample MR. We selected independent genetic tools for significant levels associated with inflammatory cytokines and vitiligo from corresponding meta-analyses of genome-wide association study (GWAS). The summary data for inflammatory cytokines were derived from a GWAS meta-analysis conducted on three separate Finnish population cohorts, comprising a total of 8293 individuals (<i>N</i> = 8293). The vitiligo data, on the other hand, were extracted from a GWAS meta-analysis conducted on individuals of European ancestry, totaling 44,266 individuals (<i>N</i> = 44,266). As the primary analytical approach, we employed the inverse variance weighted (IVW) method, and to ensure the reliability of our main findings, we also performed sensitivity analysis to evaluate the robustness.</p>\n <p><b>Results:</b> Compelling evidence indicated a causal association between genetically predicted IL-18 and IL-8 with vitiligo (odds ratio, OR: 1.162, 95% CI: 1.043–1.295, <i>p</i> = 0.006, and <i>p</i><sub>fdr</sub> = 0.020 and OR: 0.726, 95% CI: 0.602–0.876, <i>p</i> = 0.001, and <i>p</i><sub>fdr</sub> = 0.004). In addition, cytokines including stromal cell-derived factor-1 alpha (SDF1a) (Beta: 0.032, <i>p</i> = 0.016, and <i>p</i><sub>fdr</sub> = 0.039), IL-17 (Beta: 0.038, <i>p</i> = 0.005, and <i>p</i><sub>fdr</sub> = 0.027), basic fibroblast growth factor (FGFBasic) (Beta: 0.028, <i>p</i> = 0.034, and <i>p</i><sub>fdr</sub> = 0.170), monocyte chemoattractant protein-1(MCP1) (Beta: 0.026, <i>p</i> = 0.046, and <i>p</i><sub>fdr</sub> = 0.189), and platelet-derived growth factor BB (PDGFbb) (Beta: 0.026, <i>p</i> = 0.040, and <i>p</i><sub>fdr</sub> = 0.198) were suggested to be the consequences of vitiligo.</p>\n <p><b>Conclusions:</b> According to this investigation, it has been proposed that the etiology of vitiligo is likely associated with IL-18 and IL-8, whereas the downstream progression of vitiligo can be attributed to several inflammatory cytokines such as IL-17, SDF1a, PDGFbb, MCP1, and FGFBasic.</p>\n </div>","PeriodicalId":13782,"journal":{"name":"International Journal of Clinical Practice","volume":"2025 1","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/ijcp/1093015","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Clinical Practice","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1155/ijcp/1093015","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Previous studies have indicated a close association between vitiligo and inflammatory cytokines, yet the genetic predictive association remains unclear. The study aimed to predict the relationship between vitiligo and inflammatory cytokines in genetics.
Methods: A bidirectional analysis was conducted by the two-sample MR. We selected independent genetic tools for significant levels associated with inflammatory cytokines and vitiligo from corresponding meta-analyses of genome-wide association study (GWAS). The summary data for inflammatory cytokines were derived from a GWAS meta-analysis conducted on three separate Finnish population cohorts, comprising a total of 8293 individuals (N = 8293). The vitiligo data, on the other hand, were extracted from a GWAS meta-analysis conducted on individuals of European ancestry, totaling 44,266 individuals (N = 44,266). As the primary analytical approach, we employed the inverse variance weighted (IVW) method, and to ensure the reliability of our main findings, we also performed sensitivity analysis to evaluate the robustness.
Results: Compelling evidence indicated a causal association between genetically predicted IL-18 and IL-8 with vitiligo (odds ratio, OR: 1.162, 95% CI: 1.043–1.295, p = 0.006, and pfdr = 0.020 and OR: 0.726, 95% CI: 0.602–0.876, p = 0.001, and pfdr = 0.004). In addition, cytokines including stromal cell-derived factor-1 alpha (SDF1a) (Beta: 0.032, p = 0.016, and pfdr = 0.039), IL-17 (Beta: 0.038, p = 0.005, and pfdr = 0.027), basic fibroblast growth factor (FGFBasic) (Beta: 0.028, p = 0.034, and pfdr = 0.170), monocyte chemoattractant protein-1(MCP1) (Beta: 0.026, p = 0.046, and pfdr = 0.189), and platelet-derived growth factor BB (PDGFbb) (Beta: 0.026, p = 0.040, and pfdr = 0.198) were suggested to be the consequences of vitiligo.
Conclusions: According to this investigation, it has been proposed that the etiology of vitiligo is likely associated with IL-18 and IL-8, whereas the downstream progression of vitiligo can be attributed to several inflammatory cytokines such as IL-17, SDF1a, PDGFbb, MCP1, and FGFBasic.
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