• 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

TNF-α、IL-10 基因多态性与原发性干燥综合征的相关性:荟萃分析和系统评价。

The association between TNF-α, IL-10 gene polymorphisms and primary Sjögren's syndrome: a meta-analysis and systemic review.

机构信息

Department of Laboratory Diagnostics, Changzheng Hospital, Second Military Medical University, Shanghai, China.

出版信息

PLoS One. 2013 May 21;8(5):e63401. doi: 10.1371/journal.pone.0063401. Print 2013.

DOI:10.1371/journal.pone.0063401
PMID:23723980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3661073/
Abstract

OBJECTIVE

Previous studies have evaluated the associations of TNF-α, IL-10 gene polymorphisms and susceptibility to pSS, but the results remained controversial. To assess the associations between TNF-α-308, IL-10-1082, -819, -592 polymorphisms and pSS risk, a meta-analysis was conducted.

METHOD

The available articles were searched in PubMed, EMBASE and MEDLINE. ORs with 95% CIs were calculated to determine the strength of associations by fixed-effects or random-effects models. The data about IL-10-1082, -819, -592 polymorphisms were analyzed in the additive, dominant and recessive modes. The associations between haplotypes of IL-10 gene and susceptibility to pSS were also assessed.

RESULTS

A total of 9 relevant studies were identified in the meta-analyses. TNF-α-308 A allele was significantly associated with pSS (OR = 1.8, 95% CI: 1.53-2.13). The IL-10 -1082 G allele and the genotype "GCC/ATA" were identified as a candidate genetic risk factor for pSS. Under the dominant model for -819 and -582, the overall ORs suggested that individuals with genotype (CC+TC) or (CC+AC) may have a 59% increased risk of pSS in Caucasians population (OR = 1.59, 95% CI:1.09-1.23). Besides, the genotype "ATA/ATA" may be a protective factor against the development of pSS in Caucasians (OR = 0.40, 95% CI:0.19-0.84).

CONCLUSION

The meta-analysis demonstrated TNF-α-308 A, IL-10-1082 G allele were significantly associated with pSS susceptibility, supporting these alleles were predisposing factors for pSS. In Caucasian population, the genotype "ATA/ATA" may be a protective factors.

摘要

目的

先前的研究已经评估了 TNF-α、IL-10 基因多态性与 pSS 易感性的关联,但结果仍存在争议。为了评估 TNF-α-308、IL-10-1082、-819、-592 多态性与 pSS 风险之间的关联,进行了荟萃分析。

方法

在 PubMed、EMBASE 和 MEDLINE 中搜索可用的文章。使用固定效应或随机效应模型计算 ORs 及其 95%CI,以确定关联的强度。以加性、显性和隐性模式分析了 IL-10-1082、-819、-592 多态性的数据。还评估了 IL-10 基因单倍型与 pSS 易感性之间的关联。

结果

荟萃分析共确定了 9 项相关研究。TNF-α-308 A 等位基因与 pSS 显著相关(OR=1.8,95%CI:1.53-2.13)。IL-10-1082 G 等位基因和基因型“GCC/ATA”被鉴定为 pSS 的候选遗传风险因素。在 -819 和 -582 的显性模型下,总体 OR 表明,高加索人群中基因型(CC+TC)或(CC+AC)的个体可能有 59%的 pSS 风险增加(OR=1.59,95%CI:1.09-1.23)。此外,基因型“ATA/ATA”可能是高加索人群中 pSS 发病的保护因素(OR=0.40,95%CI:0.19-0.84)。

结论

荟萃分析表明 TNF-α-308 A、IL-10-1082 G 等位基因与 pSS 易感性显著相关,支持这些等位基因是 pSS 的易感因素。在高加索人群中,基因型“ATA/ATA”可能是一种保护因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73a8/3661073/dc512b51c225/pone.0063401.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73a8/3661073/dc512b51c225/pone.0063401.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73a8/3661073/dc512b51c225/pone.0063401.g001.jpg

相似文献

1
The association between TNF-α, IL-10 gene polymorphisms and primary Sjögren's syndrome: a meta-analysis and systemic review.TNF-α、IL-10 基因多态性与原发性干燥综合征的相关性:荟萃分析和系统评价。
PLoS One. 2013 May 21;8(5):e63401. doi: 10.1371/journal.pone.0063401. Print 2013.
2
Associations between TNF-α and interleukin gene polymorphisms with polycystic ovary syndrome risk: a systematic review and meta-analysis.肿瘤坏死因子-α和白细胞介素基因多态性与多囊卵巢综合征风险的关联:一项系统评价和荟萃分析。
J Assist Reprod Genet. 2015 Apr;32(4):625-34. doi: 10.1007/s10815-015-0449-7. Epub 2015 Feb 18.
3
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.慢性斑块状银屑病的全身药理学治疗:一项网状荟萃分析。
Cochrane Database Syst Rev. 2017 Dec 22;12(12):CD011535. doi: 10.1002/14651858.CD011535.pub2.
4
Cytokine Gene Variants as Predisposing Factors for the Development and Progression of Coronary Artery Disease: A Systematic Review.细胞因子基因变异作为冠状动脉疾病发生和进展的易感因素:一项系统综述
Biomolecules. 2024 Dec 19;14(12):1631. doi: 10.3390/biom14121631.
5
Tumor necrosis factor and interleukin-6 gene polymorphisms and endometriosis risk in Asians: a systematic review and meta-analysis.亚洲人中肿瘤坏死因子和白细胞介素-6基因多态性与子宫内膜异位症风险:一项系统评价和荟萃分析
Ann Hum Genet. 2014 Mar;78(2):104-16. doi: 10.1111/ahg.12048. Epub 2013 Dec 6.
6
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.慢性斑块状银屑病的全身药理学治疗:一项网状Meta分析。
Cochrane Database Syst Rev. 2020 Jan 9;1(1):CD011535. doi: 10.1002/14651858.CD011535.pub3.
7
Associations between interleukin-10 polymorphisms and susceptibility to juvenile idiopathic arthritis: a systematic review and meta-analysis.白细胞介素-10基因多态性与幼年特发性关节炎易感性的关联:一项系统综述和荟萃分析
Eur Cytokine Netw. 2018 Mar 1;29(1):16-26. doi: 10.1684/ecn.2018.0404.
8
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.系统性药理学治疗慢性斑块状银屑病:网络荟萃分析。
Cochrane Database Syst Rev. 2021 Apr 19;4(4):CD011535. doi: 10.1002/14651858.CD011535.pub4.
9
The Association between ANXA11 Gene Polymorphisms and Sarcoidosis: a Meta-Analysis and systematic review.膜联蛋白A11基因多态性与结节病的关联:一项荟萃分析与系统评价
Sarcoidosis Vasc Diffuse Lung Dis. 2016 Aug 1;33(2):102-11.
10
Risk factors for primary Sjögren's Syndrome: a systematic review and meta-analysis.原发性干燥综合征的危险因素:系统评价和荟萃分析。
Clin Rheumatol. 2023 Feb;42(2):327-338. doi: 10.1007/s10067-022-06474-8. Epub 2022 Dec 19.

引用本文的文献

1
Association of endometriosis with Sjögren's syndrome: Genetic insights (Review).子宫内膜异位症与干燥综合征的关联:遗传见解(综述)。
Int J Mol Med. 2024 Feb;53(2). doi: 10.3892/ijmm.2024.5344. Epub 2024 Jan 8.
2
rs1800629 Polymorphism and Response to Anti- Treatment in Behçet Syndrome: Data from an Italian Cohort Study.rs1800629多态性与白塞病抗治疗反应:来自一项意大利队列研究的数据。
J Pers Med. 2023 Aug 31;13(9):1347. doi: 10.3390/jpm13091347.
3
Interferon Gamma Targeted Therapy: Is It Justified in Primary Sjögren's Syndrome?干扰素γ靶向治疗:在原发性干燥综合征中是否合理?

本文引用的文献

1
Association of STAT4 rs7574865 polymorphism with autoimmune diseases: a meta-analysis.STAT4 rs7574865 多态性与自身免疫性疾病的关联:荟萃分析。
Mol Biol Rep. 2012 Sep;39(9):8873-82. doi: 10.1007/s11033-012-1754-1. Epub 2012 Jun 20.
2
Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjogren's syndrome in Scandinavian samples.肿瘤坏死因子/淋巴毒素α/淋巴毒素β基因座内的遗传变异与斯堪的纳维亚样本原发性干燥综合征的关联。
Ann Rheum Dis. 2012 Jun;71(6):981-8. doi: 10.1136/annrheumdis-2011-200446. Epub 2012 Jan 30.
3
Genetics of Sjögren's syndrome in the genome-wide association era.
J Clin Med. 2022 Sep 14;11(18):5405. doi: 10.3390/jcm11185405.
4
Gene Variation at Immunomodulatory and Cell Adhesion Molecules Loci Impacts Primary Sjögren's Syndrome.免疫调节和细胞黏附分子位点的基因变异影响原发性干燥综合征。
Front Med (Lausanne). 2022 Mar 18;9:822290. doi: 10.3389/fmed.2022.822290. eCollection 2022.
5
Musculoskeletal Manifestations in Sjogren's Syndrome: An Orthopedic Point of View.干燥综合征的肌肉骨骼表现:骨科视角
J Clin Med. 2021 Apr 8;10(8):1574. doi: 10.3390/jcm10081574.
6
Current State of Knowledge on Primary Sjögren's Syndrome, an Autoimmune Exocrinopathy.原发性干燥综合征(一种自身免疫性外分泌腺病)的当前知识状态
J Clin Med. 2020 Jul 20;9(7):2299. doi: 10.3390/jcm9072299.
7
Vitamin C and B as new biomaterials to alter intestinal stem cells.维生素 C 和 B 作为改变肠道干细胞的新型生物材料。
J Biomed Mater Res A. 2019 Sep;107(9):1886-1897. doi: 10.1002/jbm.a.36715. Epub 2019 May 23.
8
SNP variations in IL10, TNFα and TNFAIP3 genes in patients with dry eye syndrome and Sjogren's syndrome.干眼症和干燥综合征患者中白细胞介素10、肿瘤坏死因子α和肿瘤坏死因子α诱导蛋白3基因的单核苷酸多态性变异
J Inflamm (Lond). 2019 Mar 18;16:6. doi: 10.1186/s12950-019-0209-z. eCollection 2019.
9
, , , and Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects.干燥综合征的基因多态性:与疾病易感性和临床特征的相关性。
J Immunol Res. 2019 Feb 10;2019:7682827. doi: 10.1155/2019/7682827. eCollection 2019.
10
The association between MTHFR gene polymorphisms (C677T, A1298C) and oral squamous cell carcinoma: A systematic review and meta-analysis.亚甲基四氢叶酸还原酶基因多态性(C677T、A1298C)与口腔鳞状细胞癌的关系:系统评价和荟萃分析。
PLoS One. 2018 Aug 24;13(8):e0202959. doi: 10.1371/journal.pone.0202959. eCollection 2018.
在全基因组关联研究时代的干燥综合征遗传学。
J Autoimmun. 2012 Aug;39(1-2):57-63. doi: 10.1016/j.jaut.2012.01.008. Epub 2012 Jan 29.
4
HLA and Sjögren's syndrome susceptibility. A meta-analysis of worldwide studies.HLA 与干燥综合征易感性:全球研究的荟萃分析。
Autoimmun Rev. 2012 Feb;11(4):281-7. doi: 10.1016/j.autrev.2011.10.002. Epub 2011 Oct 7.
5
Meta-analysis of the association between single nucleotide polymorphisms in TGF-β receptor genes and abdominal aortic aneurysm.TGF-β 受体基因单核苷酸多态性与腹主动脉瘤关联性的荟萃分析
Atherosclerosis. 2011 Nov;219(1):218-23. doi: 10.1016/j.atherosclerosis.2011.07.105. Epub 2011 Jul 30.
6
Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses.纽卡斯尔-渥太华量表在荟萃分析中评估非随机研究质量的批判性评价。
Eur J Epidemiol. 2010 Sep;25(9):603-5. doi: 10.1007/s10654-010-9491-z. Epub 2010 Jul 22.
7
The geoepidemiology of Sjögren's syndrome.干燥综合征的地理流行病学。
Autoimmun Rev. 2010 Mar;9(5):A305-10. doi: 10.1016/j.autrev.2009.11.004. Epub 2009 Nov 10.
8
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.系统评价与Meta分析的首选报告项目:PRISMA声明。
J Clin Epidemiol. 2009 Oct;62(10):1006-12. doi: 10.1016/j.jclinepi.2009.06.005. Epub 2009 Jul 23.
9
The role of interleukin-10 promoter polymorphisms in primary Sjogren's syndrome.白细胞介素-10启动子多态性在原发性干燥综合征中的作用。
Scand J Rheumatol. 2008 Jul-Aug;37(4):293-9. doi: 10.1080/03009740801910353.
10
Non-HLA associations with autoimmune diseases.非HLA与自身免疫性疾病的关联。
Autoimmun Rev. 2006 Mar;5(3):209-14. doi: 10.1016/j.autrev.2005.06.009. Epub 2005 Aug 8.