房颤或心力衰竭患者的循环富玻璃蛋白与冠状动脉钙和心血管病理有关吗?一项初步研究

D. Vankova, M. Pasheva, A. Angelov, Y. Yotov, B. Galunska
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引用次数: 1

摘要

目前,富玻璃蛋白(GRP)被认为是一种新的生物标志物,在慢性炎症和血管钙化之间的相互作用中起着关键作用。目的:本文的目的是研究循环GRP、心血管病理和动脉钙化程度之间的联系,通过冠状动脉钙化评分(CACS)评估保加利亚人群样本。材料和方法:男女成年参与者(n = 81)被分为:对照组(n = 41) -无已知心血管疾病(CVD)的估计中至高风险受试者和合并CVD组(n = 40) -阵发性或持续性心房颤动伴有窦性心律的患者,以及保留射血分数的心力衰竭受试者。进行结构化访谈以评估经典心血管疾病危险因素。CACS采用多层计算机断层扫描测定。从病历中提取常规实验室参数。血清总GRP、基质Gla蛋白和骨钙素水平用商用ELISA试剂盒测定。采用标准统计方法(描述性统计、学生t检验和Spearman相关)。p<0.05认为差异有统计学意义。结果:冠脉钙化患者的GRP水平明显低于无钙沉积的患者。与对照组相比,合并CVD组GRP水平有明显下降趋势。循环GRP与未羧化基质Gla蛋白显著相关。血清GRP、CRP和低密度脂蛋白(ldl)之间存在关联。结论:本研究为循环GRP在钙化抑制中的作用提供了新的信息。我们的研究结果阐明了循环总GRP、CVD病理和冠状动脉钙化程度之间的联系。
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Is circulating Gla-rich protein linked with coronary calcium and cardiovascular pathology in patients with atrial fibrillation or heart failure? A pilot study
Introduction: Nowadays Gla-rich protein (GRP) is recognized as a novel biomarker playing a pivotal role in the crosstalk between chronic inflammation and vascular calcification. Aim: The aim of this article is to study the link between circulating GRP, cardiovascular pathology, and the degree of arterial calcification evaluated by the coronary arterial calcium score (CACS) in a Bulgarian population sample. Materials and Methods: Adult participants (n = 81) of both genders were divided into: controls (n = 41)—subjects with estimated moderate-to-high risk without known cardiovascular diseases (CVDs) and a combined CVD group (n = 40)—patients with paroxysmal or persistent atrial fibrillation in sinus rhythm, and heart failure subjects with preserved ejection fraction. A structured interview was carried out for evaluation of the classical CVD risk factors. CACS was determined by multislice computed tomography. Routine laboratory parameters were extracted from medical records. Serum levels of total GRP, matrix Gla protein, and osteocalcin were estimated by commercial ELISA kits. Standard statistical methods (descriptive statistics, Student’s t-test and Spearman’s correlation) were applied. Statistical significance was considered at p<0.05. Results: Significantly lower GRP levels were established in patients with coronary calcium compared to those without calcium deposits. Clear tendency for decreased levels of GRP was observed in the combined CVD group vs controls. Circulating GRP significantly correlates with uncarboxylated matrix Gla protein. An association between serum GRP, CRP, and low-density lipoproteins (LDLs) was demonstrated. Conclusion: This study adds new information regarding the role of circulating GRP as a new player in calcification inhibition. Our findings illuminate the link between total circulating GRP, CVD pathology, and the degree of coronary calcification.
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