• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

CARD8 基因多态性与强直性脊柱炎易感性的关系:一项病例对照研究。

Relationship of CARD8 Gene Polymorphisms with Susceptibility to Ankylosing Spondylitis: A Case-Control Study.

机构信息

Department of Orthopaedic, The Yongchuan Hospital of Chongqing Medical University, Chongqing, China (mainland).

出版信息

Med Sci Monit. 2020 Feb 21;26:e916935. doi: 10.12659/MSM.916935.

DOI:10.12659/MSM.916935
PMID:32080163
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7055193/
Abstract

BACKGROUND The aim of this case-control study was to evaluate the correlation of caspase recruitment domain-containing protein 8 (CARD8) gene rs2043211 (exon) and rs7253718 (intron) polymorphisms with the susceptibility of ankylosing spondylitis (AS) in the Chinese Han population. MATERIAL AND METHODS CARD8 polymorphisms were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 118 AS patients and 122 healthy persons. Linkage disequilibrium (LD) and haplotype analysis were carried out using Haploview software. Distribution differences of genotypes, alleles and haplotypes between the case and control groups were tested by chi-square test. Relative risk of AS was expressed by odds ratios (ORs) and 95% confidence intervals (CIs). Logistic regression analysis was used to adjust the results of association by clinical parameters. RESULTS For rs2043211, distribution of variant allele T was obviously different between AS patients and healthy controls (P=0.046). It indicated that T allele might increase the susceptibility of AS (OR=1.441, 95%CI=1.006-2.065). Adjusted by clinical characteristics, the significance of difference was slightly decreased (P=0.050, OR=1.439, 95%CI=0.999-2.072). Strong LD existed between rs2043211 and rs7253718 polymorphisms, and rs2043211T-rs7253718G haplotype was significantly associated with increased AS susceptibility (OR=1.787, 95%CI=1.165-2.740). In subgroup analysis, we found that the TT genotype and T allele of rs2043211 significantly increased the risk of AS in males (TT versus AA: OR=2.554, 95%CI=1.079-6.049; T versus A: OR=1.661, 95%CI=1.067-2.586), but not females. CONCLUSIONS CARD8 polymorphisms are likely to be associated with the elevated susceptibility of AS. Present results should be confirmed in the future studies.

摘要

背景

本病例对照研究旨在评估半胱氨酸天冬氨酸蛋白酶募集域蛋白 8(CARD8)基因 rs2043211(外显子)和 rs7253718(内含子)多态性与中国汉族人群强直性脊柱炎(AS)易感性的相关性。

材料与方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对 118 例 AS 患者和 122 例健康对照者的 CARD8 多态性进行基因分型。采用 Haploview 软件进行连锁不平衡(LD)和单倍型分析。采用卡方检验比较病例组和对照组基因型、等位基因和单倍型的分布差异。采用比值比(ORs)和 95%置信区间(CIs)表示 AS 的相对风险。采用 logistic 回归分析调整临床参数对关联结果的影响。

结果

rs2043211 中,变异等位基因 T 在 AS 患者和健康对照组中的分布差异有统计学意义(P=0.046)。这表明 T 等位基因可能增加 AS 的易感性(OR=1.441,95%CI=1.006-2.065)。调整临床特征后,差异的显著性略有降低(P=0.050,OR=1.439,95%CI=0.999-2.072)。rs2043211 与 rs7253718 多态性之间存在强连锁不平衡,rs2043211T-rs7253718G 单倍型与 AS 易感性增加显著相关(OR=1.787,95%CI=1.165-2.740)。在亚组分析中,我们发现 rs2043211 的 TT 基因型和 T 等位基因显著增加了男性 AS 的发病风险(TT 与 AA:OR=2.554,95%CI=1.079-6.049;T 与 A:OR=1.661,95%CI=1.067-2.586),但在女性中无此相关性。

结论

CARD8 多态性可能与 AS 易感性升高有关。本研究结果有待进一步研究验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e004/7055193/b608353f1320/medscimonit-26-e916935-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e004/7055193/b608353f1320/medscimonit-26-e916935-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e004/7055193/b608353f1320/medscimonit-26-e916935-g001.jpg

相似文献

1
Relationship of CARD8 Gene Polymorphisms with Susceptibility to Ankylosing Spondylitis: A Case-Control Study.CARD8 基因多态性与强直性脊柱炎易感性的关系:一项病例对照研究。
Med Sci Monit. 2020 Feb 21;26:e916935. doi: 10.12659/MSM.916935.
2
Genetic variants in CARD8 but not in NLRP3 are associated with ankylosing spondylitis.CARD8 中的遗传变异与强直性脊柱炎相关,但 NLRP3 中的遗传变异则不然。
Scand J Rheumatol. 2013;42(6):465-8. doi: 10.3109/03009742.2013.779020. Epub 2013 Apr 2.
3
CARD8 rs2043211 polymorphism is associated with gout in a Chinese male population.CARD8基因rs2043211多态性与中国男性人群的痛风有关。
Cell Physiol Biochem. 2015;35(4):1394-400. doi: 10.1159/000373960. Epub 2015 Mar 12.
4
The Association between Polymorphism of CARD8 rs2043211 and Susceptibility to Arteriosclerosis Obliterans in Chinese Han Male Population.CARD8基因rs2043211多态性与中国汉族男性人群闭塞性动脉硬化易感性的关联
Cell Physiol Biochem. 2017;41(1):173-180. doi: 10.1159/000455986. Epub 2017 Jan 18.
5
rs2043211 polymorphism in CARD8 is not associated with Tourette syndrome in a family-based association study in the Chinese Han population.在中国汉族人群的一项基于家系的关联研究中,CARD8基因中的rs2043211多态性与抽动秽语综合征无关。
Int J Psychiatry Med. 2015;49(3):208-14. doi: 10.1177/0091217415582190. Epub 2015 Apr 28.
6
Association between HRH4 polymorphisms and ankylosing spondylitis susceptibility.HRH4基因多态性与强直性脊柱炎易感性之间的关联。
Int J Clin Exp Pathol. 2015 Nov 1;8(11):15265-9. eCollection 2015.
7
Genetic Association for P2X7R rs3751142 and CARD8 rs2043211 Polymorphisms for Susceptibility of Gout in Korean Men: Multi-Center Study.韩国男性中P2X7R基因rs3751142和CARD8基因rs2043211多态性与痛风易感性的遗传关联:多中心研究
J Korean Med Sci. 2016 Oct;31(10):1566-70. doi: 10.3346/jkms.2016.31.10.1566.
8
Combined polymorphisms in genes encoding the inflammasome components NLRP3 and CARD8 confer risk of ischemic stroke in men.编码炎症小体成分 NLRP3 和 CARD8 的基因联合多态性与男性缺血性卒中风险相关。
J Stroke Cerebrovasc Dis. 2020 Aug;29(8):104874. doi: 10.1016/j.jstrokecerebrovasdis.2020.104874. Epub 2020 Jun 5.
9
CARD8 rs2043211 (p.C10X) polymorphism is not associated with disease susceptibility or cardiovascular events in Spanish rheumatoid arthritis patients.CARD8 rs2043211(p.C10X)多态性与西班牙类风湿关节炎患者的疾病易感性或心血管事件无关。
DNA Cell Biol. 2013 Jan;32(1):28-33. doi: 10.1089/dna.2012.1836. Epub 2012 Oct 22.
10
The Association of CARD8 rs2043211 Polymorphism with Preeclampsia in the Chinese Han Population.中国汉族人群中CARD8基因rs2043211多态性与子痫前期的关联
Gynecol Obstet Invest. 2015;80(3):193-8. doi: 10.1159/000377630. Epub 2015 Apr 17.

引用本文的文献

1
CARD8: A Novel Inflammasome Sensor with Well-Known Anti-Inflammatory and Anti-Apoptotic Activity.CARD8:一种具有良好抗炎和抗凋亡活性的新型炎症小体传感器。
Cells. 2024 Jun 13;13(12):1032. doi: 10.3390/cells13121032.

本文引用的文献

1
and Polymorphisms Influence Higher Disease Activity in Rheumatoid Arthritis.多态性影响类风湿关节炎更高的疾病活动度。
J Med Biochem. 2016 Sep;35(3):319-323. doi: 10.1515/jomb-2016-0008. Epub 2016 Jul 6.
2
Signaling Pathways and Emerging Therapies in Multiple Myeloma.多发性骨髓瘤中的信号通路与新兴疗法
Curr Hematol Malig Rep. 2016 Apr;11(2):156-64. doi: 10.1007/s11899-016-0315-4.
3
Cell intrinsic role of NF-κB-inducing kinase in regulating T cell-mediated immune and autoimmune responses.核因子κB诱导激酶在调节T细胞介导的免疫和自身免疫反应中的细胞内在作用。
Sci Rep. 2016 Feb 25;6:22115. doi: 10.1038/srep22115.
4
The preventative effect of Akt knockout on liver cancer through modulating NF-κB-regulated inflammation and Bad-related apoptosis signaling pathway.Akt 敲除通过调节 NF-κB 调控的炎症和 Bad 相关凋亡信号通路对肝癌的预防作用。
Int J Oncol. 2016 Apr;48(4):1467-76. doi: 10.3892/ijo.2016.3383. Epub 2016 Feb 8.
5
Global Prevalence of Spondyloarthritis: A Systematic Review and Meta-Regression Analysis.脊柱关节炎的全球患病率:一项系统评价和Meta回归分析
Arthritis Care Res (Hoboken). 2016 Sep;68(9):1320-31. doi: 10.1002/acr.22831. Epub 2016 Jul 27.
6
The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis.急性前葡萄膜炎的遗传相关性及其与强直性脊柱炎遗传相关性的重叠。
Genes Immun. 2016 Jan-Feb;17(1):46-51. doi: 10.1038/gene.2015.49. Epub 2015 Nov 26.
7
Genetics of ankylosing spondylitis--insights into pathogenesis.强直性脊柱炎的遗传学——发病机制的研究进展。
Nat Rev Rheumatol. 2016 Feb;12(2):81-91. doi: 10.1038/nrrheum.2015.133. Epub 2015 Oct 6.
8
Bilateral sacroiliitis and uveitis comorbidity: brucellosis? Ankylosing spondylitis?双侧骶髂关节炎与葡萄膜炎合并症:布鲁氏菌病?强直性脊柱炎?
BMJ Case Rep. 2015 Sep 22;2015:bcr2015211461. doi: 10.1136/bcr-2015-211461.
9
Mortality in ankylosing spondylitis: results from a nationwide population-based study.强直性脊柱炎的死亡率:一项全国范围内基于人群的研究结果。
Ann Rheum Dis. 2016 Aug;75(8):1466-72. doi: 10.1136/annrheumdis-2015-207688. Epub 2015 Sep 2.
10
Inflammasome polymorphisms in juvenile systemic lupus erythematosus.青少年系统性红斑狼疮中的炎性小体多态性
Autoimmunity. 2015;48(7):434-7. doi: 10.3109/08916934.2015.1064399. Epub 2015 Jul 16.