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抗磷脂综合征和血栓栓塞性疾病中常见 MicroRNAs 表达特征的鉴定:范围综述。

Identification of common MicroRNAs expression signatures in antiphospholipid syndrome and thromboembolic disease: A scoping review.

机构信息

School of Medical Sciences, University of Campinas, Campinas, Brazil.

Hospital das Clínicas of University of São Paulo Medical School, University of São Paulo, Sao Paulo, Brazil.

出版信息

Lupus. 2024 Nov;33(13):1455-1465. doi: 10.1177/09612033241286601. Epub 2024 Sep 27.

Abstract

BACKGROUND

Antiphospholipid syndrome (APS) is an acquired autoimmune disorder characterized by distinct pathophysiological mechanisms leading to heterogeneous manifestations, including venous and arterial thrombosis. Despite the lack of specific markers of thrombosis risk in APS, some of the mechanisms responsible for thrombosis in APS may overlap with those of other thromboembolic diseases. Understanding these similarities is important for improving the assessment of thrombosis risk in APS. MicroRNAs (MiRNAs) are RNA molecules that regulate gene expression and may influence the autoimmune response and coagulation.

PURPOSE

In this scoping review we aimed to investigate shared miRNAs profiles associated with APS and other thromboembolic diseases as a means of identifying markers indicative of a pro-thrombotic profile among patients with APS.

DATA COLLECTION AND RESULTS

Through a comprehensive search of scientific databases, 45 relevant studies were identified out of 1020 references. miRs-124-3p, 125b-5p, 125a-5p, and 17-5p, were associated with APS and arterial thrombosis, while miRs-106a-5p, 146b-5p, 15a-5p, 222-3p, and 451a were associated with APS and venous thrombosis. Additionally, miR-126a-3p was associated with APS and both arterial and venous thrombosis.

CONCLUSION

We observed that APS shares a common miRNAs signature with non-APS related thrombosis, suggesting that miRNA expression profiles may serve as markers of thrombotic risk in APS. Further validation of a pro-thrombotic miRNA signature in APS is warranted to improve risk assessment, diagnosis, and management of APS.

摘要

背景

抗磷脂综合征(APS)是一种获得性自身免疫性疾病,其特征为导致不同临床表现的独特病理生理机制,包括静脉和动脉血栓形成。尽管 APS 中缺乏血栓形成风险的特异性标志物,但 APS 中导致血栓形成的一些机制可能与其他血栓栓塞性疾病重叠。了解这些相似之处对于提高 APS 中血栓形成风险的评估很重要。微小 RNA(miRNA)是一种调节基因表达的 RNA 分子,可能影响自身免疫反应和凝血。

目的

在本次范围界定综述中,我们旨在研究与 APS 和其他血栓栓塞性疾病相关的共享 miRNA 谱,以确定 APS 患者中提示促血栓形成特征的标志物。

数据收集与结果

通过对科学数据库的全面检索,在 1020 篇参考文献中确定了 45 项相关研究。miR-124-3p、125b-5p、125a-5p 和 17-5p 与 APS 和动脉血栓形成相关,而 miR-106a-5p、146b-5p、15a-5p、222-3p 和 451a 与 APS 和静脉血栓形成相关。此外,miR-126a-3p 与 APS 以及动脉和静脉血栓形成均相关。

结论

我们发现 APS 与非 APS 相关的血栓形成具有共同的 miRNA 特征,提示 miRNA 表达谱可能作为 APS 血栓形成风险的标志物。需要进一步验证 APS 中促血栓形成 miRNA 特征,以改善 APS 的风险评估、诊断和管理。

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