利用免疫球蛋白游离轻链,新型炎症生物标志物治疗房颤。

IF 3.2 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Akira Matsumori
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引用次数: 2

摘要

房颤是最常见的心律失常。越来越多的证据表明炎症机制在其发病机制中起重要作用;炎症小体的激活有助于房颤的发生和进展。nod样受体-pyrin结构域-3 (NLRP3)炎症小体激活的增加释放促炎细胞因子,激活核因子(NF)-κB,从而调节免疫球蛋白游离轻链(FLCs)的产生。房颤患者血清FLC水平升高,FLC是炎症的生物标志物。当FLC水平升高时,炎性小体和NF-κB可能是预防和治疗房颤的抗炎策略的目标。这篇综述讨论了炎症在房颤发病机制中的作用,以及FLCs作为房颤治疗的新型炎症生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Management of Atrial Fibrillation Using Immunoglobulin Free Light Chains, Novel Biomarkers of Inflammation.

Management of Atrial Fibrillation Using Immunoglobulin Free Light Chains, Novel Biomarkers of Inflammation.

Management of Atrial Fibrillation Using Immunoglobulin Free Light Chains, Novel Biomarkers of Inflammation.

Management of Atrial Fibrillation Using Immunoglobulin Free Light Chains, Novel Biomarkers of Inflammation.

AF is the most common cardiac arrhythmia. There is growing evidence that inflammatory mechanisms play an important role in its pathogenesis; inflammasome activation contributes to the onset and progression of AF. An increase in NOD-like-receptor-pyrin domain-containing-3 (NLRP3) inflammasome activation releases proinflammatory cytokines that activate nuclear factor (NF)-κB, which regulates the production of immunoglobulin free light chains (FLCs). Serum FLC levels are increased in patients with AF, and FLCs are biomarkers of inflammation. Inflammasomes and NF-κB may be targets for anti-inflammatory strategies to prevent and treat AF when FLC levels are elevated. This review discusses the role of inflammation in the pathogenesis of AF, as well as FLCs as novel inflammatory biomarkers for the management of AF.

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来源期刊
European Cardiology Review
European Cardiology Review CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
5.40
自引率
0.00%
发文量
23
审稿时长
12 weeks
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