Differences in MicroRNA Expression in Pericoronary Adipose Tissue in Coronary Artery Disease Compared to Severe Valve Dysfunction

被引:4
|
作者
Marketou, Maria [1 ,7 ]
Kontaraki, Joanna [2 ]
Kalogerakos, Paris [3 ]
Plevritaki, Anthoula [1 ]
Chlouverakis, Gregory [4 ]
Kassotakis, Spyridon [1 ]
Maragkoudakis, Spyros [5 ]
Danelatos, Christos [1 ]
Zervakis, Stelios [1 ]
Savva, Eirini [1 ]
Vardas, Panos [6 ]
Kochiadakis, George [1 ]
Lazopoulos, George [3 ]
机构
[1] Heraklion Univ Gen Hosp, Cardiol Dept, Iraklion, Greece
[2] Univ Crete Univ, Sch Med, Mol Cardiol Lab, Iraklion, Greece
[3] Heraklion Univ Gen Hosp, Cardiovasc Surg Dept, Iraklion, Greece
[4] Univ Crete Univ, Sch Med, Dept Biostat, Iraklion, Greece
[5] Chania Gen Hosp, Cardiol Dept, Iraklion, Greece
[6] Mitera Hosp, Hygeia Grp, Athens, Greece
[7] Heraklion Univ Hosp, Cardiol Dept, Iraklion 71110, Greece
关键词
microRNAs; pericoronary adipose tissue; atherosclerosis; ATHEROSCLEROTIC PLAQUE; SMOOTH-MUSCLE; INFLAMMATION; OBESITY; ASSOCIATION; PROGRESSION; MIR-143; MIRNAS; TARGET;
D O I
10.1177/00033197221121617
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Pericoronary adipose tissue (PCAT) is a source of microRNAs (miRs) that act as messengers for intercellular communication. We investigated whether the PCAT surrounding significant coronary atherosclerotic lesions shows specific miR expression patterns compared with PCAT surrounding plaque-free segments. We included 49 patients with 3-vessel coronary artery disease (CAD) and 19 patients with severe valvular disease but no CAD, who underwent elective cardiac surgery. The PCAT was harvested from two sites: adjacent to a significant atherosclerotic coronary lesion and from plaque-free segments. miR-133a, miR-21, miR-26b, miR-9, and miR-143 levels in PCAT cells were quantified by real-time reverse transcription polymerase chain reaction (data expressed as arbitrary units). Expression of miR-133, miR-21, and miR-26b in adipose tissue at a site without atherosclerotic lesion was much lower in patients with CAD than in those without CAD (0.82 +/- 1.37 vs 1.86 +/- 0.52, P < .001, 0.45 +/- 1.3 vs 1.51 +/- 1.11, P < .001, 0.3 +/- 1.25 vs 1.2 +/- 0.73, P = .02, respectively). In addition, miR-133, miR-21, and miR-143 in CAD patients showed significantly greater expression in PCAT from atherosclerotic lesion compared with plaque-free segments (1.32 +/- 0.96 vs 0.82 +/- 0.37 (P = .011), 0.91 +/- 1.7 vs 0.3 +/- 1.25 (P = .012), 1.2 +/- 1.59 vs 0.43 +/- 0.54 (P < .001), respectively). Our findings open new perspectives for the role of PCAT in the pathophysiology of atherosclerosis and should be further investigated.
引用
收藏
页码:22 / 30
页数:9
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