Expression of Tissue microRNAs in Ascending Aortic Aneurysms and Dissections

Author:

Goliopoulou Athina1ORCID,Oikonomou Evangelos1ORCID,Antonopoulos Alexis2,Koumallos Nikolaos2,Gazouli Maria3,Theofilis Panagiotis2ORCID,Mystakidi Vasiliki-Chara1,Pantelidis Panteleimon1ORCID,Vavuranakis Michael-Andrew1,Siasos Gerasimos1,Tousoulis Dimitris2

Affiliation:

1. 3rd Department of Cardiology, National and Kapodistrian University of Athens, Medical School, “Sotiria” Chest Disease Hospital, Athens, Greece

2. 1st Department of Cardiology, “Hippokration” General Hospital of Athens, National & Kapodistrian University of Athens, School of Medicine, Athens, Greece

3. National & Kapodistrian University of Athens, School of Medicine, Athens, Greece

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 MMP2 and MMP9 levels. hsCRP was higher in the dissection group ( P = .03). Tissue expression of microRNA 29 was 2.11-fold higher in the dissection ( P = .001) and 2.99-fold higher in the aneurysm group ( P < .001), compared with the control group. Tissue expression of microRNA 195 was 2.72-fold higher in the dissection ( P < .001) and 2.00-fold lower in the aneurysm group ( P = .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.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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