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颈动脉粥样硬化的 microRNA 和止血谱。

MicroRNA and Hemostasis Profile of Carotid Atherosclerosis.

机构信息

Research Center of Neurology, 125367 Moscow, Russia.

出版信息

Int J Mol Sci. 2022 Sep 19;23(18):10974. doi: 10.3390/ijms231810974.

Abstract

Carotid atherosclerosis (CA) is an important risk factor for ischemic stroke. We described the miRNA and hemostasis profile of patients with moderate and advanced stages of carotid atherosclerosis and elucidated potential correlations with hemostatic activation. A prospective case-control study included 61 patients with evidence of carotid atherosclerosis (via ultrasound). The study population was divided into groups depending on the degree of carotid artery stenosis: 60% or more (advanced) and <60% (moderate). All patients underwent the following blood tests: general blood test, hemostatic parameters and microRNA. Extraction of microRNA was performed using Leukocyte RNA Purification Kit (NORGEN Biotec Corp., Thorold, ON, Canada); miRNA quantification was performed via RT-PCR. Statistical analysis was performed in R programming language (v. 4.1.0) using RSudio. MicroRNA expression profile was different depending on CA degree. MiR-33a-5p/3p levels were higher in patients with ≥60% carotid stenosis (42.70 and 42.45 versus 38.50 and 38.50, respectively, p < 0.05). Almost complete separation can be visualized with the levels of miR-126-5p: 9.50 in the moderate CA group versus 5.25 in the advanced CA (p < 0.001). MiR-29-5p was higher in the moderate CA group: 28.60 [25.50;33.05] than in advanced CA group: 25.75 [24.38;29.50] (p = 0.086); miR-29-3p was also higher in the moderate CA group: 10.36 [8.60;14.99] than in advanced CA group: 8.46 [7.47;10.3] (p = 0.001). By-group pairwise correlation analyses revealed at least three clusters with significant positive correlations in the moderate CA group: miR-29-3p with factors V and XII (r = 0.53 and r = 0.37, respectively, p < 0.05); miR-21-5p with ADAMTS13, erythrocyte sedimentation rate and D-dimer (r = 0.42, r = 0.36 and r = 0.44, respectively, p < 0.05); stenosis degree with miR-33a-5p/3p and factor VIII levels (r = 0.43 (both) and r = 0.62, respectively, p < 0.05). Hemostasis parameters did not reveal significant changes in CA patients: the only statistically significant differences concerned factor VIII, plasminogen and (marginally significant) ADAMTS-13 and protein C. Down-regulation of miR-126-5p expression has been identified as a promising biomarker of advanced carotid atherosclerosis with high specificity and sensitivity. Correlation cluster analysis showed potential interplay between miRNAs and hemostatic activation in the setting of carotid atherosclerosis.

摘要

颈动脉粥样硬化(CA)是缺血性中风的重要危险因素。我们描述了中重度颈动脉粥样硬化患者的 miRNA 和止血谱,并阐明了与止血激活的潜在相关性。一项前瞻性病例对照研究纳入了 61 名有颈动脉粥样硬化证据的患者(通过超声检查)。根据颈动脉狭窄程度将研究人群分为两组:≥60%(进展期)和<60%(中度)。所有患者均接受以下血液检查:一般血液检查、止血参数和 microRNA。使用白细胞 RNA 纯化试剂盒(NORGEN Biotec Corp.,安大略省托罗尔德)提取 microRNA;通过 RT-PCR 进行 miRNA 定量。使用 R 编程语言(v. 4.1.0)在 RSudio 中进行统计分析。miRNA 表达谱因 CA 程度而异。miR-33a-5p/3p 在颈动脉狭窄≥60%的患者中水平较高(分别为 42.70 和 42.45 与 38.50 和 38.50,p<0.05)。miR-126-5p 的水平几乎可以完全分离:中度 CA 组为 9.50,进展性 CA 组为 5.25(p<0.001)。miR-29-5p 在中度 CA 组中更高:28.60 [25.50;33.05] 比进展性 CA 组高:25.75 [24.38;29.50](p=0.086);miR-29-3p 在中度 CA 组中也更高:10.36 [8.60;14.99] 比进展性 CA 组高:8.46 [7.47;10.3](p=0.001)。按组的两两相关分析显示,中度 CA 组有至少三个具有显著正相关的聚类:miR-29-3p 与因子 V 和 XII(r=0.53 和 r=0.37,分别,p<0.05);miR-21-5p 与 ADAMTS13、红细胞沉降率和 D-二聚体(r=0.42、r=0.36 和 r=0.44,分别,p<0.05);狭窄程度与 miR-33a-5p/3p 和因子 VIII 水平(r=0.43(均)和 r=0.62,分别,p<0.05)。CA 患者的止血参数未发生显著变化:唯一具有统计学意义的差异涉及因子 VIII、纤溶酶原和(边缘显著)ADAMTS-13 和蛋白 C。miR-126-5p 表达下调被鉴定为一种有前途的高级颈动脉粥样硬化生物标志物,具有高特异性和灵敏度。相关性聚类分析显示,在颈动脉粥样硬化背景下,miRNA 与止血激活之间存在潜在的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d53/9500617/e703ad3a6e04/ijms-23-10974-g001.jpg

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