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纤溶酶原激活物抑制剂-1与低密度脂蛋白异质性作为动脉粥样硬化性心血管疾病合并甘油三酯代谢紊乱的危险因素:一项前瞻性横断面研究。

Association of plasminogen activator inhibitor-1 and low-density lipoprotein heterogeneity as a risk factor of atherosclerotic cardiovascular disease with triglyceride metabolic disorder: a pilot cross-sectional study.

作者信息

Iida Kiyoshi, Tani Shigemasa, Atsumi Wataru, Yagi Tsukasa, Kawauchi Kenji, Matsumoto Naoya, Hirayama Atsushi

机构信息

aDepartment of Health Planning Center bDepartment of Cardiology, Nihon University Hospital cDivision of Cardiology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Coron Artery Dis. 2017 Nov;28(7):577-587. doi: 10.1097/MCA.0000000000000521.

Abstract

BACKGROUND

We hypothesized that an increase in plasminogen activator inhibitor 1 (PAI-1) might reduce low-density lipoprotein (LDL) particle size in conjunction with triglyceride (TG) metabolism disorder, resulting in an increased risk of atherosclerotic cardiovascular disease (ASCVD).

METHODS

This study was carried out as a hospital-based cross-sectional study in 537 consecutive outpatients (mean age: 64 years; men: 71%) with one or more risk factors for ASCVD from April 2014 to October 2014 at the Cardiovascular Center of Nihon University Surugadai Hospital. The estimated LDL-particle size was measured as relative LDL migration using polyacrylamide gel electrophoresis with the LipoPhor system.The plasma PAI-1 level, including the tissue PA/PAI-1 complex and the active and latent forms of PAI-1, was determined using a latex photometric immunoassay method.

RESULTS

A multivariate regression analysis after adjustments for ASCVD risk factors showed that an elevated PAI-1 level was an independent predictor of smaller-sized LDL-particle in both the overall patients population (β=0.209, P<0.0001) and a subset of patients with a serum low-density lipoprotein cholesterol (LDL-C) level lower than 100 mg/dl (β=0.276, P<0.0001). Furthermore, an increased BMI and TG-rich lipoprotein related markers [TG, remnant-like particle cholesterol, apolipoprotein (apo) B, apo C-II, and apo C-III] were found to be independent variables associated with an increased PAI-1 level in multivariate regression models. A statistical analysis of data from nondiabetic patients with well-controlled serum LDL-C levels yielded similar findings. Furthermore, in the 310 patients followed up for at least 6 months, a multiple-logistic regression analysis after adjustments for ASCVD risk factors identified the percent changes of the plasma PAI-1 level in the third tertile compared with those in the first tertile as being independently predictive of decreased LDL-particle size [odds ratio (95% confidence interval): 2.11 (1.12/3.40), P=0.02].

CONCLUSION

The plasma PAI-1 levels may be determined by the degree of obesity and TG metabolic disorders. These factors were also shown to be correlated with a decreased LDL-particle size, increasing the risk of ASCVD, even in nondiabetic patients with well-controlled serum LDL-C levels.

摘要

背景

我们推测纤溶酶原激活物抑制剂1(PAI-1)水平升高可能会与甘油三酯(TG)代谢紊乱共同作用,使低密度脂蛋白(LDL)颗粒大小减小,从而增加动脉粥样硬化性心血管疾病(ASCVD)的风险。

方法

本研究于2014年4月至2014年10月在日本大学巢鸭医院心血管中心对537例连续门诊患者(平均年龄:64岁;男性:71%)进行了一项基于医院的横断面研究,这些患者具有一项或多项ASCVD危险因素。使用LipoPhor系统通过聚丙烯酰胺凝胶电泳将估计的LDL颗粒大小作为相对LDL迁移率进行测量。采用乳胶比浊免疫测定法测定血浆PAI-1水平,包括组织型纤溶酶原激活物/PAI-1复合物以及PAI-1的活性和潜伏形式。

结果

在对ASCVD危险因素进行调整后的多因素回归分析显示,PAI-1水平升高是总体患者人群中较小LDL颗粒大小的独立预测因素(β=0.209,P<0.0001),也是血清低密度脂蛋白胆固醇(LDL-C)水平低于100mg/dl的患者亚组中较小LDL颗粒大小的独立预测因素(β=0.276,P<0.0001)。此外,在多因素回归模型中,体重指数增加以及富含TG的脂蛋白相关标志物[TG、残粒样颗粒胆固醇、载脂蛋白(apo)B、apo C-II和apo C-III]被发现是与PAI-1水平升高相关的独立变量。对血清LDL-C水平控制良好的非糖尿病患者的数据进行统计分析也得出了类似的结果。此外,在310例至少随访6个月的患者中,在对ASCVD危险因素进行调整后的多因素逻辑回归分析确定,与第一三分位数相比,第三三分位数血浆PAI-1水平的百分比变化可独立预测LDL颗粒大小减小[比值比(95%置信区间):2.11(1.12/3.40),P=0.02]。

结论

血浆PAI-1水平可能由肥胖程度和TG代谢紊乱程度决定。这些因素也与LDL颗粒大小减小相关,即使在血清LDL-C水平控制良好的非糖尿病患者中,也会增加ASCVD的风险。

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