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首页> 外文期刊>Clinical and experimental medicine >Relationship between lipoprotein(a) levels, oxidative stress, and blood pressure levels in patients with essential hypertension.
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Relationship between lipoprotein(a) levels, oxidative stress, and blood pressure levels in patients with essential hypertension.

机译:原发性高血压患者脂蛋白(a)水平,氧化应激和血压水平之间的关系。

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High plasma levels of lipoprotein(a) [Lp(a)] are considered a risk factor for the development of coronary artery disease. In vitro experiments have shown that oxidized Lp(a) is able to impair the arterial endothelium-dependent dilation, thus suggesting a possible role of Lp(a) in the genesis of essential hypertension. The aim of our work was to investigate the correlation of blood pressure levels with plasma Lp(a) concentration, apo(a) isoform size, and peroxidative stress in patients with essential hypertension. The study was performed in 54 untreated hypertensive patients whose blood pressure was monitored for 24 h by ambulatory blood pressure monitoring. Lp(a) concentration was measured by a double monoclonal antibody-based enzyme immunoassay demonstrated to be insensitive to apo(a) size heterogeneity. Apo(a) isoforms were determined by a high-resolution SDS-agarose gel electrophoresis followed by immunoblotting. A significant correlation was found between Lp(a) levels and the night-time systolic and diastolic pressures (r=0.32, P<0.05 and r=0.30, P<0.05, respectively), as well as with the mean night-time fall in systolic and diastolic blood pressures (r=-0.28, P<0.05 and r=-0.29, P<0.05, respectively). These relationships were further potentiated when peroxidative stress data were taken into consideration (r=0.37 and r=0.40, P<0.01 for the night-time systolic and diastolic pressures, respectively and r=-0.34 and r=-0.38, P<0.01 for the night-time fall in systolic and diastolic blood pressures, respectively). Apo(a) isoform size did not affect these relationships. Our data suggest that Lp(a) and peroxidative stress may be involved as cofactors in essential hypertension, with a mechanism that remains to be elucidated.
机译:血浆高水平的脂蛋白(a)[Lp(a)]被认为是发展冠心病的危险因素。体外实验表明,氧化的Lp(a)能够损害动脉内皮依赖性的扩张,从而提示Lp(a)在原发性高血压的发生中可能发挥作用。我们的工作目的是研究原发性高血压患者的血压水平与血浆Lp(a)浓度,apo(a)亚型大小和过氧化应激的相关性。这项研究是在54名未经治疗的高血压患者中进行的,他们通过动态血压监测对血压进行了24小时监测。 Lp(a)浓度是通过基于双单克隆抗体的酶免疫分析法测定的,该酶联免疫法对apo(a)大小异质性不敏感。 Apo(a)亚型通过高分辨率SDS-琼脂糖凝胶电泳,然后进行免疫印迹测定。发现Lp(a)水平与夜间收缩压和舒张压之间存在显着相关性(分别为r = 0.32,P <0.05和r = 0.30,P <0.05)以及平均夜间下降收缩压和舒张压分别为(r = -0.28,P <0.05和r = -0.29,P <0.05)。当考虑过氧化应激数据时,这些关系得到进一步加强(夜间收缩压和舒张压的r = 0.37和r = 0.40,P <0.01,r = -0.34和r = -0.38,P <0.01夜间收缩压和舒张压分别下降)。 Apo(a)亚型的大小不影响这些关系。我们的数据表明,Lp(a)和过氧化应激可能是原发性高血压的辅助因子,其机制尚待阐明。

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