Kasprzak Magdalena P, Iskra Maria, Majewski Wacław, Budzyń-Napierała Magdalena, Gryszczyńska Bogna, Strzyżewski Krzysztof, Kasprzak Jakub
Department of General Chemistry, Chair of Chemistry and Clinical Biochemistry, Poznan University of Medical Sciences, Poznan, Poland.
Department of General and Vascular Surgery, Poznan University of Medical Sciences, Poznan, Poland.
Arch Med Sci. 2014 Dec 22;10(6):1101-8. doi: 10.5114/aoms.2014.41348.
Human paraoxonase (PON1) is a calcium-dependent enzyme physically associated with HDL, and it is believed to contribute to the atheroprotective effect of HDL. The aim of the study was to evaluate PON1 status in patients with atherosclerosis obliterans as an effect of ischemia regarding its activity and phenotype distribution.
The study group consisted of patients with chronic arterial occlusion of the lower limbs due to atherosclerosis obliterans (AO). The patients were divided into two groups according to the degree of ischemia: moderate (MI), and critical (CI). The ratio of the hydrolysis of salt-stimulated PON1 activity to the hydrolysis of phenylacetate was used to assign individuals to one of three possible phenotypes (low activity - A, medium activity - AB, high activity - B). It was observed that PON1 arylesterase activity was affected by ischemia of the lower limbs depending on its degree.
The odds ratio and the relative risk analysis showed that the patients with moderate ischemia are much more often characterized by phenotype A than by phenotype B. The low activity phenotype A occurs over twice as often in patients with chronic ischemia of the lower limbs as in individuals from the control group (OR = 2.125; 1.96 to 3.776, p = 0.0143).
This study presents the low activity phenotype A in relation to the risk of ischemia of the lower limbs due to atherosclerosis and shows the potentially important role of PON1 in conclusion of the process leading to intensification of ischemia degree.
人对氧磷酶(PON1)是一种与高密度脂蛋白(HDL)物理相关的钙依赖性酶,据信它有助于HDL的抗动脉粥样硬化作用。本研究的目的是评估闭塞性动脉硬化患者的PON1状态,作为缺血对其活性和表型分布影响的结果。
研究组由因闭塞性动脉硬化(AO)导致下肢慢性动脉闭塞的患者组成。根据缺血程度将患者分为两组:中度(MI)和重度(CI)。用盐刺激的PON1活性水解与苯乙酸水解的比率将个体分为三种可能的表型之一(低活性 - A、中等活性 - AB、高活性 - B)。观察到PON1芳基酯酶活性受下肢缺血程度的影响。
优势比和相对风险分析表明,中度缺血患者的表型A比表型B更为常见。下肢慢性缺血患者中低活性表型A的发生率是对照组个体的两倍多(OR = 2.125;1.96至3.776,p = 0.0143)。
本研究提出了与因动脉粥样硬化导致下肢缺血风险相关的低活性表型A,并表明PON1在导致缺血程度加重的过程中可能具有重要作用。