• 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

细胞毒性T淋巴细胞相关抗原4基因中rs3087243和rs231775多态性与格雷夫斯病的关联:一项病例/对照研究及荟萃分析

Association between rs3087243 and rs231775 polymorphism within the cytotoxic T-lymphocyte antigen 4 gene and Graves' disease: a case/control study combined with meta-analyses.

作者信息

Tu Yaqin, Fan Guorun, Dai Yu, Zeng Tianshu, Xiao Fei, Chen Lulu, Kong Wen

机构信息

Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

出版信息

Oncotarget. 2017 Nov 27;8(66):110614-110624. doi: 10.18632/oncotarget.22702. eCollection 2017 Dec 15.

DOI:10.18632/oncotarget.22702
PMID:29299173
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5746408/
Abstract

We conducted a case/control study to assess the impact of SNP rs3087243 and rs231775 within the gene, on the susceptibility to Graves' disease (GD) in a Chinese Han dataset (271 cases and 298 controls). The frequency of G allele for rs3087243 and rs231775 was observed to be significantly higher in subjects with GD than in control subjects ( = 0.005 and = 0.000, respectively). After logistic regression analysis, a significant association was detected between SNP rs3087243 and GD in the additive and recessive models. Similarly, association for the SNP rs231775 could also be detected in the additive model, dominant model and recessive model. A meta-analysis, including 27 published datasets along with the current dataset, was performed to further confirm the association. Consistent with our case/control results, rs3087243 and rs231775 showed a significant association with GD in all genetic models. Of note, ethnic stratification revealed that these two SNPs were associated with susceptibility to GD in populations of both Asian and European descent. In conclusion, our data support that the rs3087243 and rs231775 polymorphisms within the gene confer genetic susceptibility to GD.

摘要

我们进行了一项病例/对照研究,以评估该基因内的单核苷酸多态性(SNP)rs3087243和rs231775对中国汉族人群(271例病例和298例对照)Graves病(GD)易感性的影响。观察到rs3087243和rs231775的G等位基因频率在GD患者中显著高于对照受试者(分别为 = 0.005和 = 0.000)。经过逻辑回归分析,在加性和隐性模型中检测到SNP rs3087243与GD之间存在显著关联。同样,在加性模型、显性模型和隐性模型中也可检测到SNP rs231775的关联。进行了一项荟萃分析,纳入了27个已发表的数据集以及当前数据集,以进一步证实这种关联。与我们的病例/对照结果一致,rs3087243和rs231775在所有遗传模型中均显示与GD存在显著关联。值得注意的是,种族分层显示这两个SNP与亚洲和欧洲血统人群的GD易感性相关。总之,我们的数据支持该基因内的rs3087243和rs231775多态性赋予了GD遗传易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/108f3be6d2e1/oncotarget-08-110614-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/b37d79d052bb/oncotarget-08-110614-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/1f3b785d9abe/oncotarget-08-110614-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/715af31772b0/oncotarget-08-110614-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/4a5226f4dbf2/oncotarget-08-110614-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/108f3be6d2e1/oncotarget-08-110614-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/b37d79d052bb/oncotarget-08-110614-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/1f3b785d9abe/oncotarget-08-110614-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/715af31772b0/oncotarget-08-110614-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/4a5226f4dbf2/oncotarget-08-110614-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/5746408/108f3be6d2e1/oncotarget-08-110614-g005.jpg

相似文献

1
Association between rs3087243 and rs231775 polymorphism within the cytotoxic T-lymphocyte antigen 4 gene and Graves' disease: a case/control study combined with meta-analyses.细胞毒性T淋巴细胞相关抗原4基因中rs3087243和rs231775多态性与格雷夫斯病的关联:一项病例/对照研究及荟萃分析
Oncotarget. 2017 Nov 27;8(66):110614-110624. doi: 10.18632/oncotarget.22702. eCollection 2017 Dec 15.
2
Correlation between CTLA-4 and CD40 gene polymorphisms and their interaction in graves' disease in a Chinese Han population.中国汉族人群中CTLA-4和CD40基因多态性及其相互作用与格雷夫斯病的相关性
BMC Med Genet. 2018 Sep 17;19(1):171. doi: 10.1186/s12881-018-0665-y.
3
The Association of CTLA-4 rs231775 and rs3087243 Polymorphisms with Latent Autoimmune Diabetes in Adults: A Meta-Analysis.CTLA-4 rs231775 和 rs3087243 多态性与成人潜伏自身免疫性糖尿病的关联:一项荟萃分析。
Biochem Genet. 2022 Aug;60(4):1222-1235. doi: 10.1007/s10528-021-10152-w. Epub 2021 Nov 25.
4
Cytotoxic T-lymphocyte antigen 4 gene polymorphism influences the incidence of symptomatic human cytomegalovirus infection after renal transplantation.细胞毒性T淋巴细胞抗原4基因多态性影响肾移植后有症状的人巨细胞病毒感染的发生率。
Pharmacogenet Genomics. 2015 Jan;25(1):19-29. doi: 10.1097/FPC.0000000000000102.
5
Association of the gene CT60/rs3087243 single-nucleotide polymorphisms with Graves' disease.CT60/rs3087243基因单核苷酸多态性与格雷夫斯病的关联。
Biomed Rep. 2015 Sep;3(5):691-696. doi: 10.3892/br.2015.493. Epub 2015 Jul 27.
6
CTLA-4 CT60 (rs3087243) polymorphism and autoimmune thyroid diseases susceptibility: a comprehensive meta-analysis.细胞毒性T淋巴细胞相关抗原4基因CT60(rs3087243)多态性与自身免疫性甲状腺疾病易感性:一项全面的荟萃分析。
Endocr Res. 2014;39(4):180-8. doi: 10.3109/07435800.2013.879167. Epub 2014 Apr 3.
7
CTLA-4 and MDR1 polymorphisms increase the risk for ulcerative colitis: A meta-analysis.细胞毒性T淋巴细胞相关抗原4(CTLA-4)和多药耐药基因1(MDR1)多态性增加溃疡性结肠炎风险:一项荟萃分析。
World J Gastroenterol. 2015 Sep 14;21(34):10025-40. doi: 10.3748/wjg.v21.i34.10025.
8
[Association of CTLA4 and TNF gene polymorphisms with endocrine ophthalmopathy in ethnic Russian patients with Graves' disease].[俄罗斯族格雷夫斯病患者中CTLA4和TNF基因多态性与内分泌性眼病的关联]
Ter Arkh. 2015;87(10):67-71. doi: 10.17116/terarkh2015871067-71.
9
CTLA4 polymorphisms and ophthalmopathy in Graves' disease patients: association study and meta-analysis.格雷夫斯病患者中CTLA4基因多态性与眼病:关联研究与荟萃分析
Hum Immunol. 2006 Aug;67(8):618-26. doi: 10.1016/j.humimm.2006.05.003. Epub 2006 Jun 8.
10
Meta-analysis of the rs231775 locus polymorphism in the CTLA-4 gene and the susceptibility to Graves' disease in children.CTLA-4基因rs231775位点多态性与儿童Graves病易感性的Meta分析。
Open Life Sci. 2023 Apr 28;18(1):20220589. doi: 10.1515/biol-2022-0589. eCollection 2023.

引用本文的文献

1
Investigating the functional and structural effect of non-synonymous single nucleotide polymorphisms in the cytotoxic T-lymphocyte antigen-4 gene: An in-silico study.研究细胞毒性T淋巴细胞抗原4基因非同义单核苷酸多态性的功能和结构效应:一项计算机模拟研究。
PLoS One. 2025 Jan 24;20(1):e0316465. doi: 10.1371/journal.pone.0316465. eCollection 2025.
2
Single Nucleotide Polymorphisms Associated with Rheumatoid Arthritis in Saudi Patients.沙特患者中与类风湿性关节炎相关的单核苷酸多态性
J Clin Med. 2023 Jul 27;12(15):4944. doi: 10.3390/jcm12154944.
3
Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study.

本文引用的文献

1
CD28/CTLA-4/ICOS haplotypes confers susceptibility to Graves' disease and modulates clinical phenotype of disease.CD28/CTLA-4/ICOS单倍型赋予Graves病易感性并调节疾病的临床表型。
Endocrine. 2017 Jan;55(1):186-199. doi: 10.1007/s12020-016-1096-1. Epub 2016 Sep 16.
2
Association of Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4) Gene Polymorphisms with Autoimmune Thyroid Disease in Children and Adults: Case-Control Study.细胞毒性T淋巴细胞相关蛋白4(CTLA4)基因多态性与儿童及成人自身免疫性甲状腺疾病的关联:病例对照研究
PLoS One. 2016 Apr 25;11(4):e0154394. doi: 10.1371/journal.pone.0154394. eCollection 2016.
3
细胞毒性T淋巴细胞相关蛋白4基因多态性与复发性流产的关联:一项病例对照研究。
Int J Reprod Biomed. 2023 Feb 8;21(1):33-43. doi: 10.18502/ijrm.v21i1.12664. eCollection 2023 Jan.
4
Association between the side effect induced by COVID-19 vaccines and the immune regulatory gene polymorphism.COVID-19 疫苗引起的副作用与免疫调节基因多态性的关联。
Front Immunol. 2022 Oct 26;13:941497. doi: 10.3389/fimmu.2022.941497. eCollection 2022.
5
Increased risk of Graves´ophthalmopathy in patients with increasing TRAb after radioiodine treatment and the impact of CTLA4 on TRAb titres.放射性碘治疗后 TRAb 升高的 Graves 眼病风险增加及 CTLA4 对 TRAb 滴度的影响。
Endocrine. 2022 Mar;75(3):856-864. doi: 10.1007/s12020-021-02952-2. Epub 2021 Dec 2.
6
Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes.白细胞介素2受体α链(IL2RA)、干扰素诱导解旋酶C结构域蛋白1(IFIH1)和细胞毒性T淋巴细胞相关蛋白4(CTLA-4)基因多态性与自身免疫性甲状腺疾病和1型糖尿病的遗传关联研究
Front Pediatr. 2020 Aug 21;8:481. doi: 10.3389/fped.2020.00481. eCollection 2020.
7
Autoimmunity-Related Risk Variants in PTPN22 and CTLA4 Are Associated With ME/CFS With Infectious Onset.蛋白酪氨酸磷酸酶非受体型22(PTPN22)和细胞毒性T淋巴细胞相关抗原4(CTLA4)中与自身免疫相关的风险变异与感染性起病的肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)相关。
Front Immunol. 2020 Apr 9;11:578. doi: 10.3389/fimmu.2020.00578. eCollection 2020.
Association of single nucleotide polymorphism rs3792876 in SLC22A4 gene with autoimmune thyroid disease in a Chinese Han population.
中国汉族人群中SLC22A4基因单核苷酸多态性rs3792876与自身免疫性甲状腺疾病的关联
BMC Med Genet. 2015 Sep 2;16:76. doi: 10.1186/s12881-015-0222-x.
4
Synergistic combined effect between CD40-1C>T and CTLA-4+6230G>A polymorphisms in Graves' disease.Graves病中CD40基因1C>T多态性与CTLA-4基因+6230G>A多态性之间的协同联合效应。
Gene. 2015 Aug 10;567(2):154-8. doi: 10.1016/j.gene.2015.04.074. Epub 2015 Apr 30.
5
Association between age at diagnosis of Graves' disease and variants in genes involved in immune response.格雷夫斯病诊断年龄与免疫反应相关基因变异的关联。
PLoS One. 2013;8(3):e59349. doi: 10.1371/journal.pone.0059349. Epub 2013 Mar 27.
6
Association between CTLA-4 polymorphisms and the susceptibility to systemic lupus erythematosus and Graves' disease in Thai population.CTLA-4 多态性与泰国人群系统性红斑狼疮和格雷夫斯病易感性的关联。
Asian Pac J Allergy Immunol. 2011 Sep;29(3):229-35.
7
CD40 C/T(-1) and CTLA-4 A/G(49) SNPs are associated with autoimmune thyroid diseases in the Chinese population.CD40 C/T(-1) 和 CTLA-4 A/G(49) 单核苷酸多态性与中国人群自身免疫性甲状腺疾病相关。
Endocrine. 2012 Feb;41(1):111-5. doi: 10.1007/s12020-011-9510-1. Epub 2011 Aug 25.
8
Tumour necrosis factor-alpha gene polymorphisms and susceptibility to oral lichen planus.肿瘤坏死因子-α基因多态性与口腔扁平苔藓易感性的关系。
Oral Dis. 2011 Mar;17(2):206-9. doi: 10.1111/j.1601-0825.2010.01722.x. Epub 2010 Aug 27.
9
Soluble CTLA-4 receptor an immunological marker of Graves' disease and severity of ophthalmopathy is associated with CTLA-4 Jo31 and CT60 gene polymorphisms.可溶性CTLA-4受体作为Graves病和眼病严重程度的免疫标志物,与CTLA-4 Jo31和CT60基因多态性相关。
Eur J Endocrinol. 2009 Nov;161(5):787-93. doi: 10.1530/EJE-09-0600. Epub 2009 Sep 4.
10
Association of polymorphism at position 49 in exon 1 of the cytotoxic T-lymphocyte-associated factor 4 gene with Graves' disease refractory to medical treatment, but not with amiodarone-associated thyroid dysfunction.细胞毒性T淋巴细胞相关因子4基因第1外显子49位多态性与难治性Graves病相关,但与胺碘酮相关性甲状腺功能障碍无关。
Thyroid. 2009 Sep;19(9):975-81. doi: 10.1089/thy.2009.0066.