Fieseler H G, Armstrong V W, Wieland E, Thiery J, Schütz E, Walli A K, Seidel D
Department of Clinical Chemistry, University Hospital of Göttingen, FRG.
Clin Chim Acta. 1991 Dec 31;204(1-3):291-300. doi: 10.1016/0009-8981(91)90239-9.
The concentration of lipoprotein (a) in plasma is under stringent genetic control and raised concentrations are strongly linked to coronary heart disease, in particular when low density lipoprotein levels are also increased. We serially monitored serum Lp(a) in 14 hypercholesterolemic patients who were treated with Pravastatin over a period of two years. C-reactive protein levels were also quantified to exclude a possible 'acute-phase' response as a reason for a sudden increase in the Lp(a) concentration. No significant changes were seen in mean Lp(a) levels after 24 months of therapy. Considerable fluctuations of serum Lp(a) levels occurred during the course of treatment. These were in some cases associated with raised C-reactive protein concentrations and might therefore be attributable to an 'acute-phase' response. We conclude that the HMG-CoA reductase inhibitor Pravastatin has no long-lasting effects on Lp(a) levels in hypercholesterolemic patients suffering from coronary heart disease.
血浆中脂蛋白(a)的浓度受到严格的基因控制,浓度升高与冠心病密切相关,尤其是在低密度脂蛋白水平也升高时。我们对14名接受普伐他汀治疗两年的高胆固醇血症患者的血清脂蛋白(a)进行了连续监测。还对C反应蛋白水平进行了定量,以排除可能的“急性期”反应作为脂蛋白(a)浓度突然升高的原因。治疗24个月后,平均脂蛋白(a)水平未见明显变化。在治疗过程中,血清脂蛋白(a)水平出现了相当大的波动。在某些情况下,这些波动与C反应蛋白浓度升高有关,因此可能归因于“急性期”反应。我们得出结论,HMG-CoA还原酶抑制剂普伐他汀对患有冠心病的高胆固醇血症患者的脂蛋白(a)水平没有长期影响。