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正常受试者和类风湿性关节炎患者甲氨蝶呤通路的单核苷酸多态性分析

Single nucleotide polymorphism profiling across the methotrexate pathway in normal subjects and patients with rheumatoid arthritis.

作者信息

Ranganathan Prabha, Culverhouse Robert, Marsh Sharon, Ahluwalia Ranjeet, Shannon William D, Eisen Seth, McLeod Howard L

机构信息

Department of Medicine, Washington University School of Medicine, St Louis, Missouri 63110, USA. prangana @im.wustl.edu

出版信息

Pharmacogenomics. 2004 Jul;5(5):559-69. doi: 10.1517/14622416.5.5.559.

DOI:10.1517/14622416.5.5.559
PMID:15212592
Abstract

Methotrexate (MTX) is a commonly used disease-modifying antirheumatic drug in rheumatoid arthritis (RA). Polymorphisms occur in several genes encoding key enzymes in the folic acid pathway, which is influenced by MTX, but have not been evaluated in patients with RA. The effect of race on allele frequency has also not been evaluated. In this study, the allele frequencies of polymorphisms in six key enzymes in the MTX-folate pathway in patients with RA and healthy controls, including several common racial groups were studied. European- and African-American patients with RA and European and African healthy controls were genotyped for 22 genetic loci in six genes in the MTX cellular pathway. Differences in genotype distributions between the different racial groups were evaluated using chi(2) tests. Allele frequencies were significantly different (p < 0.001) for eight single nucleotide polymorphisms between the European and African controls. The allele frequencies of two polymorphisms showed significant differences (p < 0.001) between the African- and European-American patients with RA. Thus, racial differences exist between the allele frequencies of several polymorphisms in enzymes in the MTX-folate pathway in patients with RA and healthy controls. Whether such differences contribute to a differential response to MTX in patients with RA deserves to be investigated.

摘要

甲氨蝶呤(MTX)是类风湿关节炎(RA)中常用的改善病情抗风湿药物。叶酸途径中编码关键酶的几个基因存在多态性,该途径受MTX影响,但尚未在RA患者中进行评估。种族对等位基因频率的影响也未得到评估。在本研究中,对包括几个常见种族群体在内的RA患者和健康对照者的MTX-叶酸途径中六种关键酶的多态性等位基因频率进行了研究。对欧洲裔和非裔美国RA患者以及欧洲裔和非裔健康对照者的MTX细胞途径中六个基因的22个基因位点进行基因分型。使用卡方检验评估不同种族群体之间基因型分布的差异。欧洲裔和非裔对照者之间的八个单核苷酸多态性的等位基因频率存在显著差异(p < 0.001)。非裔和欧洲裔美国RA患者之间的两个多态性的等位基因频率存在显著差异(p < 0.001)。因此,RA患者和健康对照者的MTX-叶酸途径中几种酶的多态性等位基因频率存在种族差异。这种差异是否导致RA患者对MTX的反应不同值得研究。

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引用本文的文献

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Effect of thymidylate synthase (TYMS) gene polymorphisms with methotrexate treatment outcome in south Indian Tamil patients with rheumatoid arthritis.在印度南部泰米尔族类风湿关节炎患者中,胸苷酸合成酶(TYMS)基因多态性对甲氨蝶呤治疗效果的影响。
Clin Rheumatol. 2017 Jun;36(6):1253-1259. doi: 10.1007/s10067-017-3608-7. Epub 2017 Mar 27.
2
Old drugs, old problems: where do we stand in prediction of rheumatoid arthritis responsiveness to methotrexate and other synthetic DMARDs?旧药,老问题:我们在预测甲氨蝶呤和其他合成 DMARDs 治疗类风湿关节炎的反应方面处于什么位置?
BMC Med. 2013 Jan 23;11:17. doi: 10.1186/1741-7015-11-17.
3
Profiling single nucleotide polymorphisms (SNPs) across intracellular folate metabolic pathway in healthy Indians.
在健康的印度人群体中分析细胞内叶酸代谢途径中的单核苷酸多态性(SNPs)。
Indian J Med Res. 2011 Mar;133(3):274-9.
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Functional polymorphisms of folate-metabolizing enzymes in relation to homocysteine concentrations in systemic lupus erythematosus.系统性红斑狼疮中叶酸代谢酶功能多态性与同型半胱氨酸浓度的关系
J Rheumatol. 2008 Nov;35(11):2179-86. doi: 10.3899/jrheum.080071. Epub 2008 Sep 1.
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Racial or ethnic differences in allele frequencies of single-nucleotide polymorphisms in the methylenetetrahydrofolate reductase gene and their influence on response to methotrexate in rheumatoid arthritis.亚甲基四氢叶酸还原酶基因单核苷酸多态性的等位基因频率的种族或民族差异及其对类风湿关节炎中甲氨蝶呤反应的影响。
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