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组织微小RNA在升主动脉瘤和夹层中的表达

Expression of Tissue microRNAs in Ascending Aortic Aneurysms and Dissections.

作者信息

Goliopoulou Athina, Oikonomou Evangelos, Antonopoulos Alexis, Koumallos Nikolaos, Gazouli Maria, Theofilis Panagiotis, Mystakidi Vasiliki-Chara, Pantelidis Panteleimon, Vavuranakis Michael-Andrew, Siasos Gerasimos, Tousoulis Dimitris

机构信息

3rd Department of Cardiology, National and Kapodistrian University of Athens, Medical School, "Sotiria" Chest Disease Hospital, Athens, Greece.

1st Department of Cardiology, "Hippokration" General Hospital of Athens, National & Kapodistrian University of Athens, School of Medicine, Athens, Greece.

出版信息

Angiology. 2023 Jan;74(1):88-94. doi: 10.1177/00033197221098295. Epub 2022 May 3.

Abstract

Little is known about the role of serum and tissue mediators in the progression of ascending aortic aneurysms and dissections. We examined how the tissue expression of microRNAs and matrix metalloproteinases (MMPs), as well as the serum levels of osteoprotegerin, adiponectin, and high sensitivity C-reactive protein (hsCRP) are associated with these entities. We enrolled 21 patients with ascending aortic aneurysm, 11 with acute Stanford type A aortic dissection and 18 controls. The serum levels of osteoprotegerin, adiponectin, and hsCRP, as well as the tissue expression of MMPs 2 and 9 and tissue microRNAs 29 and 195 were compared among groups. There was no difference regarding serum osteoprotegerin, adiponectin, and tissue and MMP9 levels. hsCRP was higher in the dissection group ( = .03). Tissue expression of microRNA 29 was 2.11-fold higher in the dissection ( = .001) and 2.99-fold higher in the aneurysm group ( < .001), compared with the control group. Tissue expression of microRNA 195 was 2.72-fold higher in the dissection ( < .001) and 2.00-fold lower in the aneurysm group ( = .08), compared with to the control group. These findings support the contribution of microRNAs in the progression of aneurysm formation and dissection, suggesting a role as potential biomarkers and future therapeutic targets.

摘要

关于血清和组织介质在升主动脉瘤和夹层形成过程中的作用,目前所知甚少。我们研究了微小RNA(microRNA)和基质金属蛋白酶(MMP)的组织表达,以及骨保护素、脂联素和高敏C反应蛋白(hsCRP)的血清水平与这些疾病的关联。我们纳入了21例升主动脉瘤患者、11例急性斯坦福A型主动脉夹层患者和18例对照。比较了各组骨保护素、脂联素和hsCRP的血清水平,以及MMP-2和MMP-9及组织微小RNA-29和微小RNA-195的组织表达。血清骨保护素、脂联素和组织MMP-9水平在各组间无差异。hsCRP在夹层组更高(P = .03)。与对照组相比,微小RNA-29的组织表达在夹层组高2.11倍(P = .001),在动脉瘤组高2.99倍(P < .001)。与对照组相比,微小RNA-195的组织表达在夹层组高2.72倍(P < .001),在动脉瘤组低2.00倍(P = .08)。这些发现支持了微小RNA在动脉瘤形成和夹层过程中的作用,提示其作为潜在生物标志物和未来治疗靶点的可能性。

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