• 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

相似文献

1
Interleukin-10 genotype correlated to deficiency syndrome in hepatitis B cirrhosis.白细胞介素-10 基因型与乙型肝炎肝硬化缺乏综合征相关。
Evid Based Complement Alternat Med. 2012;2012:298925. doi: 10.1155/2012/298925. Epub 2012 May 28.
2
[Relationship between gene polymorphisms of interleukin-10 and syndrome types of traditional Chinese medicine in post-hepatitis B cirrhosis].
Zhong Xi Yi Jie He Xue Bao. 2009 Nov;7(11):1052-6. doi: 10.3736/jcim20091106.
3
Investigation on the association between inerleukin-10 -592C/A, 819C/T and -1082A/G gene polymorphisms and development of diabetic nephrophathy.白细胞介素-10基因-592C/A、819C/T和-1082A/G多态性与糖尿病肾病发生之间的关联研究。
Int J Clin Exp Pathol. 2015 Nov 1;8(11):15216-21. eCollection 2015.
4
Association of -592C/A, -819C/T and -1082A/G interleukin-10 promoter polymorphisms with idiopathic recurrent spontaneous abortion.白细胞介素-10启动子-592C/A、-819C/T和-1082A/G多态性与特发性复发性自然流产的关联
Mol Hum Reprod. 2006 Dec;12(12):771-6. doi: 10.1093/molehr/gal084. Epub 2006 Oct 13.
5
Association of IL10 and TGFB single nucleotide polymorphisms with intervertebral disc degeneration in Iranian population: a case control study.白细胞介素10和转化生长因子β单核苷酸多态性与伊朗人群椎间盘退变的关联:一项病例对照研究
BMC Med Genet. 2018 Apr 10;19(1):59. doi: 10.1186/s12881-018-0572-2.
6
MiRNA-target network analysis identifies potential biomarkers for Traditional Chinese Medicine (TCM) syndrome development evaluation in hepatitis B caused liver cirrhosis.miRNA 靶标网络分析鉴定乙型肝炎肝硬化中医证候发展评价的潜在生物标志物。
Sci Rep. 2017 Sep 8;7(1):11054. doi: 10.1038/s41598-017-11351-5.
7
Association of IL-10 gene (-1082A>G, -819C>T and -592C>A) polymorphism and its serum level with metabolic syndrome of north Indian subjects.白细胞介素-10基因(-1082A>G、-819C>T和-592C>A)多态性及其血清水平与北印度人群代谢综合征的关联
J Genet. 2017 Mar;96(1):53-64. doi: 10.1007/s12041-016-0738-7.
8
Curative Effects of ZHENG-Based Fuzheng-Huayu Tablet on Hepatitis B Caused Cirrhosis Related to CYP1A2 Genetic Polymorphism.基于证型的扶正化瘀片对 CYP1A2 基因多态性相关乙型肝炎肝硬化的疗效。
Evid Based Complement Alternat Med. 2013;2013:302131. doi: 10.1155/2013/302131. Epub 2013 Oct 24.
9
Interleukin 10 gene -1082A/G polymorphism is associated with osteosarcoma risk and poor outcomes in the Chinese population.白细胞介素10基因-1082A/G多态性与中国人群骨肉瘤风险及不良预后相关。
Tumour Biol. 2016 Apr;37(4):4517-22. doi: 10.1007/s13277-015-4238-9. Epub 2015 Oct 27.
10
[Basic pathogenesis of asthenia of healthy energy and blood stasis in liver cirrhosis studied by serum proteomics].血清蛋白质组学研究肝硬化正气亏虚血瘀证的基本发病机制
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2011 May;31(5):595-602.

引用本文的文献

1
Relationship between EGF, TGFA, and EGFR Gene Polymorphisms and Traditional Chinese Medicine ZHENG in Gastric Cancer.EGF、TGFA 和 EGFR 基因多态性与胃癌中医证型的关系。
Evid Based Complement Alternat Med. 2013;2013:731071. doi: 10.1155/2013/731071. Epub 2013 Dec 16.
2
Curative Effects of ZHENG-Based Fuzheng-Huayu Tablet on Hepatitis B Caused Cirrhosis Related to CYP1A2 Genetic Polymorphism.基于证型的扶正化瘀片对 CYP1A2 基因多态性相关乙型肝炎肝硬化的疗效。
Evid Based Complement Alternat Med. 2013;2013:302131. doi: 10.1155/2013/302131. Epub 2013 Oct 24.
3
Clinical Applications of Omics Technologies on ZHENG Differentiation Research in Traditional Chinese Medicine.组学技术在中医“证”研究中的临床应用。
Evid Based Complement Alternat Med. 2013;2013:989618. doi: 10.1155/2013/989618. Epub 2013 Jun 18.
4
Differences of excess and deficiency zheng in patients with chronic hepatitis B by urinary metabonomics.尿代谢组学探讨慢性乙型肝炎患者的虚实证差异。
Evid Based Complement Alternat Med. 2013;2013:738245. doi: 10.1155/2013/738245. Epub 2013 Apr 24.
5
ZHENG-Omics Application in ZHENG Classification and Treatment: Chinese Personalized Medicine.ZHENG 组学在 ZHENG 分类与治疗中的应用:中医个体化医学。
Evid Based Complement Alternat Med. 2013;2013:235969. doi: 10.1155/2013/235969. Epub 2013 Apr 3.

本文引用的文献

1
Association of interleukin-10 gene polymorphisms with breast cancer in a Chinese population.白细胞介素-10 基因多态性与中国人群乳腺癌的相关性研究。
J Exp Clin Cancer Res. 2010 Jun 17;29(1):72. doi: 10.1186/1756-9966-29-72.
2
Polymorphisms of some cytokines and chronic hepatitis B and C virus infection.某些细胞因子的多态性与慢性乙型和丙型肝炎病毒感染。
World J Gastroenterol. 2009 Nov 28;15(44):5610-9. doi: 10.3748/wjg.15.5610.
3
[Relationship between gene polymorphisms of interleukin-10 and syndrome types of traditional Chinese medicine in post-hepatitis B cirrhosis].
Zhong Xi Yi Jie He Xue Bao. 2009 Nov;7(11):1052-6. doi: 10.3736/jcim20091106.
4
Identification of Linkage Disequilibrium SNPs from a Kidney-Yang Deficiency Syndrome Pedigree.从肾阳虚证家系中鉴定连锁不平衡单核苷酸多态性
Am J Chin Med. 2009;37(3):427-38. doi: 10.1142/S0192415X09006953.
5
Genomewide association studies and human disease.全基因组关联研究与人类疾病
N Engl J Med. 2009 Apr 23;360(17):1759-68. doi: 10.1056/NEJMra0808700. Epub 2009 Apr 15.
6
Understanding ZHENG in traditional Chinese medicine in the context of neuro-endocrine-immune network.从神经-内分泌-免疫网络角度理解中医的证。
IET Syst Biol. 2007 Jan;1(1):51-60. doi: 10.1049/iet-syb:20060032.
7
A novel method based on ligase detection reaction for low abundant YIDD mutants detection in hepatitis B virus.基于连接酶检测反应的新型方法用于检测乙型肝炎病毒中低丰度 YIDD 突变体。
Hepatol Res. 2006 Mar;34(3):150-5. doi: 10.1016/j.hepres.2005.12.007. Epub 2006 Feb 24.
8
Effects of hepatitis B virus X protein on the development of liver cancer.乙型肝炎病毒X蛋白对肝癌发生发展的影响。
J Lab Clin Med. 2006 Feb;147(2):58-66. doi: 10.1016/j.lab.2005.10.003.
9
Systematic review: The model for end-stage liver disease--should it replace Child-Pugh's classification for assessing prognosis in cirrhosis?系统评价:终末期肝病模型——它是否应取代Child-Pugh分级来评估肝硬化的预后?
Aliment Pharmacol Ther. 2005 Dec;22(11-12):1079-89. doi: 10.1111/j.1365-2036.2005.02691.x.
10
Interleukin-10 and the immune response against cancer: a counterpoint.白细胞介素-10与抗癌免疫反应:一种不同观点
J Leukoc Biol. 2005 Nov;78(5):1043-51. doi: 10.1189/jlb.0705358. Epub 2005 Oct 4.

白细胞介素-10 基因型与乙型肝炎肝硬化缺乏综合征相关。

Interleukin-10 genotype correlated to deficiency syndrome in hepatitis B cirrhosis.

机构信息

Research Center for TCM Complexity System, Shanghai University of TCM, Shanghai 201203, China.

出版信息

Evid Based Complement Alternat Med. 2012;2012:298925. doi: 10.1155/2012/298925. Epub 2012 May 28.

DOI:10.1155/2012/298925
PMID:22690243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3368439/
Abstract

Traditional Chinese medicine (TCM) syndrome is an important basis for TCM diagnosis and treatment. As Child-Pugh classification as well as compensation and decompensation phase in liver cirrhosis, it is also an underlying clinical classification. In this paper, we investigated the correlation between single nucleotide polymorphisms (SNPs) of Interleukin-10 (IL-10) and TCM syndromes in patients with hepatitis B cirrhosis (HBC). Samples were obtained from 343 HBC patients in China. Three SNPs of IL-10 (-592A/C, -819C/T, and -1082A/G) were detected with polymerase chain-reaction-ligase detection reaction (PCR-LDR). The result showed the SNP-819C/T was significantly correlated with Deficiency syndrome (P = 0.031), but none of the 3 loci showed correlation either with Child-Pugh classification and phase in HBC patients. The logistic regression analysis showed that the Excess syndrome was associated with dizzy and spider nevus, and the Deficiency syndrome was associated with dry eyes, aversion to cold, IL-10-819C/T loci, and IL-10-1082A/G loci. The odds ratio (OR) value at IL-10-819C/T was 4.022. The research results suggested that IL-10-819C/T locus (TC plus CC genotype) is probably a risk factor in the occurrence of Deficiency syndrome in HBC patients.

摘要

中医证候是中医诊断和治疗的重要依据。正如 Child-Pugh 分类以及肝硬化的代偿和失代偿期一样,它也是一种潜在的临床分类。在本文中,我们研究了乙型肝炎肝硬化(HBC)患者白细胞介素 10(IL-10)单核苷酸多态性(SNP)与中医证候之间的相关性。在中国,我们从 343 名 HBC 患者中获得了样本。使用聚合酶链反应-连接酶检测反应(PCR-LDR)检测了 IL-10 的三个 SNP(-592A/C、-819C/T 和-1082A/G)。结果表明,SNP-819C/T 与虚证显著相关(P=0.031),但这 3 个位点均与 HBC 患者的 Child-Pugh 分类和分期无相关性。逻辑回归分析显示,实证与头晕、蜘蛛痣有关,虚证与眼睛干涩、恶寒、IL-10-819C/T 位点、IL-10-1082A/G 位点有关。在 IL-10-819C/T 处的比值比(OR)值为 4.022。研究结果表明,IL-10-819C/T 位点(TC 加 CC 基因型)可能是 HBC 患者虚证发生的危险因素。