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干扰素β治疗的多发性硬化症患者中MXA单核苷酸多态性的药物遗传学

Pharmacogenetics of MXA SNPs in interferon-beta treated multiple sclerosis patients.

作者信息

Weinstock-Guttman Bianca, Tamaño-Blanco Miriam, Bhasi Kavitha, Zivadinov Robert, Ramanathan Murali

机构信息

Jacobs Neurological Institute, Buffalo General Hospital, Buffalo, NY 14203, United States.

出版信息

J Neuroimmunol. 2007 Jan;182(1-2):236-9. doi: 10.1016/j.jneuroim.2006.10.011. Epub 2006 Nov 27.

Abstract

The myxovirus resistance A (MXA) mRNA has been extensively investigated for assessing the biologic responses of multiple sclerosis (MS) patients to interferon-beta (IFN-beta) therapy. The objective of this study was to evaluate the associations between two MXA promoter region single nucleotide polymorphisms (rs2071430 and rs17000900) and the gene expression responses, clinical and MRI phenotypes in IFN-beta treated MS patients. The rs2071430 and rs17000900 SNPs, which are located in or near an interferon-stimulated response element (ISRE), were genotyped in 179 relapsing MS patients. Quantitative MRI measurements were available for 101 patients on IFN-beta monotherapy. Gene expression was assessed in 22 anti-interferon-beta neutralizing antibody negative patients. No significant association was found between the MXA genotype at these two SNPs and clinical, MRI and MXA gene expression in MS patients treated with IFN-beta therapy.

摘要

为评估多发性硬化症(MS)患者对β-干扰素(IFN-β)治疗的生物学反应,已对黏病毒抗性A(MXA)mRNA进行了广泛研究。本研究的目的是评估两个MXA启动子区域单核苷酸多态性(rs2071430和rs17000900)与IFN-β治疗的MS患者的基因表达反应、临床和MRI表型之间的关联。对179例复发型MS患者的位于干扰素刺激反应元件(ISRE)内或附近的rs2071430和rs17000900单核苷酸多态性(SNP)进行了基因分型。101例接受IFN-β单一疗法的患者可进行定量MRI测量。对22例抗β-干扰素中和抗体阴性的患者进行了基因表达评估。在接受IFN-β治疗的MS患者中,未发现这两个SNP处的MXA基因型与临床、MRI和MXA基因表达之间存在显著关联。

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