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类风湿性关节炎与阿尔茨海默病:炎症调节中的遗传与表观遗传联系

Rheumatoid arthritis and Alzheimer's disease: genetic and epigenetic links in inflammatory regulation.

作者信息

Ferraccioli Gianfranco, Carbonella Angela, Gremese Elisa, Alivernini Stefano

机构信息

Division of Rheumatology, Institute of Rheumatology and Affine Sciences, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

Discov Med. 2012 Dec;14(79):379-88.

Abstract

Controversial data are available about the relationship between Alzheimer's disease (AD) and rheumatoid arthritis (RA). An inverse relationship between AD and RA, due to different factors, was previously described. Similarly to RA, AD pathogenesis is multifactorial and different findings support the inflammatory pathogenetic hypothesis. Several inflammatory mediators are involved in the disease onset and progression regulated by genetic and epigenetic mechanisms. Among them, inteleukin-6 (IL-6) and interleukin-1 (IL-1) as pro-inflammatory soluble factors produced by monocytes-macrophages and tumor necrosis factor alpha (TNF-α) produced by activated macrophages and mononuclear cells represent key molecules in the induction and maintenance of chronic inflammation in RA. In particular a link with the T allele of the SNP 3953 T/C in the IL-1 gene and an overexpression of miR-146a appears to be common to both RA and AD. In this review we will discuss the genetic and epigenetic regulation of the inflammatory cascade in RA and AD to find out the possible links between RA and AD onset.

摘要

关于阿尔茨海默病(AD)与类风湿关节炎(RA)之间的关系,存在有争议的数据。先前曾描述过由于不同因素导致的AD与RA之间的负相关关系。与RA类似,AD的发病机制是多因素的,并且不同的研究结果支持炎症发病假说。几种炎症介质参与了由遗传和表观遗传机制调节的疾病发生和发展过程。其中,单核细胞 - 巨噬细胞产生的促炎可溶性因子白细胞介素 - 6(IL - 6)和白细胞介素 - 1(IL - 1),以及活化的巨噬细胞和单核细胞产生的肿瘤坏死因子α(TNF - α),是RA中慢性炎症诱导和维持的关键分子。特别是,IL - 1基因中SNP 3953 T/C的T等位基因与miR - 146a的过表达之间的联系似乎在RA和AD中都很常见。在这篇综述中,我们将讨论RA和AD中炎症级联反应的遗传和表观遗传调控,以找出RA和AD发病之间可能存在的联系。

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