Przybyłowski P, Wasilewski G, Koc-Żórawska E, Małyszko J
Jagiellonian University, Medical College, Krakow, Poland; Silesian Center for Heart Diseases, Zabrze, Poland.
Department of Cardiovascular Surgery and Transplantology, Jagiellonian University, Medical College, John Paul II Hospital, Krakow, Poland.
Transplant Proc. 2018 Sep;50(7):2105-2109. doi: 10.1016/j.transproceed.2018.02.167. Epub 2018 Mar 13.
Development of arterial hypertension is to some extent related to decreased activity of the kallikrein-kinin system. This poorly understood hormonal system consists of blood proteins playing a role in the process of inflammation, coagulation, blood pressure control, and pain conduction. The system consists of kallikreins (plasma and tissue), kallistatin, kininogens, kinins (bradykinin, kallidin-lizynobradykinin), kininases (I and II), and membrane receptors of bradykinin. The aim of the study was the assessment of kallistatin in correlation to blood pressure value in heart transplant recipients.
Kallistatin level was estimated in 131 heart transplant recipients on standard 3 drugs immunosuppressive regimens (calcineurin inhibitor, mycophenolate mofetil/mycophenolic acid, and steroids) in correlation to inflammation markers and blood pressure values. Additionally, 22 healthy volunteers served as controls. In cross-sectional study, kallistatin and catecholamine concentrations were assessed using commercially available assays.
Kallistatin concentration did not differ significantly among heart transplant recipients in comparison with controls; serum noradrenaline concentration was lower in the study group. In the orthotopic heart transplant group, kallistatin correlated with renal function; estimated glomerular filtration rate was calculated by Modification of Diet in Renal Disease formula (r = -0.28, P < .01; hemoglobin r = -0.19, P < .05; cholesterol level r = -0.23, P < .01; low-density lipoprotein r = 0.25, P < .01; ferritin r = 0.21, P < .05; noradrenaline r = -0.28, P < .01). No correlation with blood pressure values were revealed. In multivariate analysis, cholesterol serum level and age predicted 32% of variability of kallistatin concentration.
Kallistatin among heart transplant recipients does not seem to be the pathogenetic factor of arterial hypertension but may be involved in the development of hyperlipidemia often present in this group of patients.
动脉高血压的发生在一定程度上与激肽释放酶-激肽系统活性降低有关。这个了解甚少的激素系统由在炎症、凝血、血压控制和疼痛传导过程中起作用的血液蛋白组成。该系统包括激肽释放酶(血浆和组织型)、激肽抑制蛋白、激肽原、激肽(缓激肽、胰激肽-赖氨酰缓激肽)、激肽酶(I和II)以及缓激肽的膜受体。本研究的目的是评估心脏移植受者中激肽抑制蛋白与血压值的相关性。
对131名接受标准三联免疫抑制方案(钙调神经磷酸酶抑制剂、霉酚酸酯/霉酚酸和类固醇)治疗的心脏移植受者的激肽抑制蛋白水平进行评估,并与炎症标志物和血压值进行相关性分析。另外,22名健康志愿者作为对照。在横断面研究中,使用市售检测方法评估激肽抑制蛋白和儿茶酚胺浓度。
与对照组相比,心脏移植受者的激肽抑制蛋白浓度无显著差异;研究组血清去甲肾上腺素浓度较低。在原位心脏移植组中,激肽抑制蛋白与肾功能相关;估算肾小球滤过率采用肾脏病饮食改良公式计算(r = -0.28,P < 0.01;血红蛋白r = -0.19,P < 0.05;胆固醇水平r = -0.23,P < 0.01;低密度脂蛋白r = 0.25,P < 0.01;铁蛋白r = 0.21,P < 0.05;去甲肾上腺素r = -0.28,P < 0.01)。未发现与血压值相关。在多变量分析中,血清胆固醇水平和年龄可预测激肽抑制蛋白浓度变异性的32%。
心脏移植受者中的激肽抑制蛋白似乎不是动脉高血压的致病因素,但可能参与了该组患者中常见的高脂血症的发生。