Jianyu Liu, Da Liu, Xing Guo, Li Zhou, Zhiyao Xu, Hua Liu
{"title":"LINC01492与大动脉粥样硬化性卒中的易感性和炎症因子水平相关。","authors":"Jianyu Liu, Da Liu, Xing Guo, Li Zhou, Zhiyao Xu, Hua Liu","doi":"10.4103/bc.bc_42_24","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>LINC01492 polymorphism has been implicated in the susceptibility of large artery atherosclerotic (LAA) stroke; however, a dearth of systematic research exists regarding this association in the Asian population at present.</p><p><strong>Subjects and methods: </strong>This study enrolled Han Chinese patients with LAA stroke (n = 428) and age- and sex-matched controls (n = 434). We employed dominant, recessive, and codominant genetic models to analyze the distribution of alleles and genotypes for 14 tag single nucleotide polymorphisms (SNPs) in LINC01492. Furthermore, we quantified the transcript levels of LINC01492 as well as concentrations of inflammatory factors (interleukin [IL]-1β, IL-6, IL-8, IL-10, IL-18, tumor necrosis factor alpha, and CCL18). In addition, we explored the association between these SNPs and levels of inflammatory factors.</p><p><strong>Results: </strong>The rs10990654 AA genotype of LINC01492 was markedly associated with a heightened risk of LAA stroke (odds ratio [OR] = 6.403, 95% confidence interval [CI] = 1.180-34.734, <i>P</i> = 0.031). Conversely, both the GG genotype of rs10990654 (OR = 0.614, 95% CI = 0.384-0.980, <i>P</i> = 0.041) and the GG genotype of rs16922693 (OR = 0.518, 95% CI = 0.313-0.857, <i>P</i> = 0.010) were identified as being linked to a reduced risk in this study population. In addition, the transcription level of LINC01492 was markedly reduced in patients compared to controls. Furthermore, significant variations were observed in IL-10 and IL-18 levels across genotypes at LINC01492 polymorphism loci among patients.</p><p><strong>Conclusions: </strong>The genetic polymorphisms and transcript levels of LINC01492 exhibit an association with susceptibility to LAA stroke, and the available evidence suggests that this association may be mediated through IL-10 and IL-18.</p><p><strong>Trial registration: </strong>The trial was registered with the Chinese Clinical Trial Registry (www.chictr.org.cn) under trial registration number ChiCTR2000032684.</p>","PeriodicalId":9288,"journal":{"name":"Brain Circulation","volume":"11 1","pages":"48-56"},"PeriodicalIF":2.3000,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11984819/pdf/","citationCount":"0","resultStr":"{\"title\":\"LINC01492 is associated with susceptibility to large atherosclerotic stroke and levels of inflammatory factors.\",\"authors\":\"Jianyu Liu, Da Liu, Xing Guo, Li Zhou, Zhiyao Xu, Hua Liu\",\"doi\":\"10.4103/bc.bc_42_24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>LINC01492 polymorphism has been implicated in the susceptibility of large artery atherosclerotic (LAA) stroke; however, a dearth of systematic research exists regarding this association in the Asian population at present.</p><p><strong>Subjects and methods: </strong>This study enrolled Han Chinese patients with LAA stroke (n = 428) and age- and sex-matched controls (n = 434). We employed dominant, recessive, and codominant genetic models to analyze the distribution of alleles and genotypes for 14 tag single nucleotide polymorphisms (SNPs) in LINC01492. Furthermore, we quantified the transcript levels of LINC01492 as well as concentrations of inflammatory factors (interleukin [IL]-1β, IL-6, IL-8, IL-10, IL-18, tumor necrosis factor alpha, and CCL18). In addition, we explored the association between these SNPs and levels of inflammatory factors.</p><p><strong>Results: </strong>The rs10990654 AA genotype of LINC01492 was markedly associated with a heightened risk of LAA stroke (odds ratio [OR] = 6.403, 95% confidence interval [CI] = 1.180-34.734, <i>P</i> = 0.031). Conversely, both the GG genotype of rs10990654 (OR = 0.614, 95% CI = 0.384-0.980, <i>P</i> = 0.041) and the GG genotype of rs16922693 (OR = 0.518, 95% CI = 0.313-0.857, <i>P</i> = 0.010) were identified as being linked to a reduced risk in this study population. In addition, the transcription level of LINC01492 was markedly reduced in patients compared to controls. Furthermore, significant variations were observed in IL-10 and IL-18 levels across genotypes at LINC01492 polymorphism loci among patients.</p><p><strong>Conclusions: </strong>The genetic polymorphisms and transcript levels of LINC01492 exhibit an association with susceptibility to LAA stroke, and the available evidence suggests that this association may be mediated through IL-10 and IL-18.</p><p><strong>Trial registration: </strong>The trial was registered with the Chinese Clinical Trial Registry (www.chictr.org.cn) under trial registration number ChiCTR2000032684.</p>\",\"PeriodicalId\":9288,\"journal\":{\"name\":\"Brain Circulation\",\"volume\":\"11 1\",\"pages\":\"48-56\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-03-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11984819/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain Circulation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.4103/bc.bc_42_24\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Circulation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4103/bc.bc_42_24","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:LINC01492多态性与大动脉粥样硬化(LAA)卒中的易感性有关;然而,目前缺乏关于亚洲人群中这种关联的系统研究。对象和方法:本研究纳入了汉族LAA卒中患者(n = 428)和年龄和性别匹配的对照组(n = 434)。采用显性、隐性和共显性遗传模型分析了LINC01492中14个标签单核苷酸多态性(snp)的等位基因和基因型分布。此外,我们量化了LINC01492的转录水平以及炎症因子(白细胞介素[IL]-1β、IL-6、IL-8、IL-10、IL-18、肿瘤坏死因子α和CCL18)的浓度。此外,我们还探讨了这些snp与炎症因子水平之间的关系。结果:LINC01492的rs10990654 AA基因型与LAA卒中风险升高显著相关(优势比[OR] = 6.403, 95%可信区间[CI] = 1.180 ~ 34.734, P = 0.031)。相反,rs10990654的GG基因型(OR = 0.614, 95% CI = 0.384-0.980, P = 0.041)和rs16922693的GG基因型(OR = 0.518, 95% CI = 0.313-0.857, P = 0.010)被认为与该研究人群的风险降低有关。此外,与对照组相比,患者中LINC01492的转录水平明显降低。此外,在不同基因型的患者中,在LINC01492多态性位点上观察到IL-10和IL-18水平的显著差异。结论:LINC01492的遗传多态性和转录水平与LAA卒中易感性相关,现有证据表明这种关联可能通过IL-10和IL-18介导。试验注册:该试验已在中国临床试验注册中心(www.chictr.org.cn)注册,试验注册号为ChiCTR2000032684。
LINC01492 is associated with susceptibility to large atherosclerotic stroke and levels of inflammatory factors.
Background: LINC01492 polymorphism has been implicated in the susceptibility of large artery atherosclerotic (LAA) stroke; however, a dearth of systematic research exists regarding this association in the Asian population at present.
Subjects and methods: This study enrolled Han Chinese patients with LAA stroke (n = 428) and age- and sex-matched controls (n = 434). We employed dominant, recessive, and codominant genetic models to analyze the distribution of alleles and genotypes for 14 tag single nucleotide polymorphisms (SNPs) in LINC01492. Furthermore, we quantified the transcript levels of LINC01492 as well as concentrations of inflammatory factors (interleukin [IL]-1β, IL-6, IL-8, IL-10, IL-18, tumor necrosis factor alpha, and CCL18). In addition, we explored the association between these SNPs and levels of inflammatory factors.
Results: The rs10990654 AA genotype of LINC01492 was markedly associated with a heightened risk of LAA stroke (odds ratio [OR] = 6.403, 95% confidence interval [CI] = 1.180-34.734, P = 0.031). Conversely, both the GG genotype of rs10990654 (OR = 0.614, 95% CI = 0.384-0.980, P = 0.041) and the GG genotype of rs16922693 (OR = 0.518, 95% CI = 0.313-0.857, P = 0.010) were identified as being linked to a reduced risk in this study population. In addition, the transcription level of LINC01492 was markedly reduced in patients compared to controls. Furthermore, significant variations were observed in IL-10 and IL-18 levels across genotypes at LINC01492 polymorphism loci among patients.
Conclusions: The genetic polymorphisms and transcript levels of LINC01492 exhibit an association with susceptibility to LAA stroke, and the available evidence suggests that this association may be mediated through IL-10 and IL-18.
Trial registration: The trial was registered with the Chinese Clinical Trial Registry (www.chictr.org.cn) under trial registration number ChiCTR2000032684.