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血清维生素 A、D 和 E 水平升高与多发性硬化症患者不同炎症标志物的改变有关。

Increasing serum levels of vitamin A, D and E are associated with alterations of different inflammation markers in patients with multiple sclerosis.

机构信息

Department of Neurology, Akershus University Hospital, Lørenskog, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Norwegian Multiple Sclerosis Registry and Biobank, Department of Neurology, Haukeland University Hospital, Bergen, Norway; KG Jebsen MS Research Centre, Department of Clinical Medicine, University of Bergen, Bergen, Norway.

出版信息

J Neuroimmunol. 2014 Jun 15;271(1-2):60-5. doi: 10.1016/j.jneuroim.2014.03.014. Epub 2014 Mar 24.

Abstract

To explore the relationships between vitamin A, D and E and inflammation in relapsing remitting multiple sclerosis, we assessed their associations with 11 inflammation markers in 9 serial serum samples from 85 patients, before and during interferon-β1a treatment. A negative association was found between vitamin A and pentraxin 3 independent of interferon-β1a use, whereas positive associations between vitamin D and interleukin-1 receptor antagonist and secreted frizzled-related protein 3 were seen before, and between vitamin E and chemokine (C-X-C motif) ligand 16 during interferon-β1a treatment. These findings suggest associations with diverse inflammatory pathways, which may be differentially influenced by interferon-β1a treatment.

摘要

为了探究维生素 A、D 和 E 与复发性缓解型多发性硬化症中的炎症之间的关系,我们评估了它们与 85 名患者的 9 个连续血清样本中的 11 个炎症标志物之间的关联,这些患者在接受干扰素-β1a 治疗前后均接受了评估。结果发现,维生素 A 与 pentraxin 3 之间存在负相关,与干扰素-β1a 的使用无关,而维生素 D 与白细胞介素-1 受体拮抗剂和分泌卷曲相关蛋白 3 之间存在正相关,维生素 E 与干扰素-β1a 治疗期间的趋化因子(C-X-C 基序)配体 16 之间存在正相关。这些发现表明与多种炎症途径有关,这些途径可能受到干扰素-β1a 治疗的不同影响。

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