Hu Cheng-Lin, Li Yan-Bo, Tang Yan-Hong, Chen Jiang-Bing, Liu Jun, Tang Qi-Zhu, Zhang Qing-Hua, Huang Cong-Xing
Department of Cardiology, Renmin Hospital of Wuhan University, 238 Jiefang Road, Wuchang District, Wuhan 430060, PR China.
Cardiovasc Drugs Ther. 2006 Jun;20(3):185-91. doi: 10.1007/s10557-006-7947-x.
C-reactive protein (CRP) is considered a risk factor for coronary artery disease. In addition to its lipid-lowering properties, statin decreases the level of CRP. Abrupt cessation of statin therapy during treatment could increase CRP level independently of the elevation of serum lipids and the incidence of cardiac events in patients with atherosclerotic heart disease. Xuezhikang (XZK), an extract of cholestin, has a marked modulating effect on lipid and CRP concentrations in different study time course. However, no attention has been paid to the changes of lipid profile and CRP concentrations after withdrawal of XZK treatment. This study was designed to explore short-term time course effects on lipid profile and CRP concentrations after withdrawal of XZK treatment in coronary heart disease patients.
Seventy-five consecutive patients with documented coronary heart disease were randomly divided into three groups: 1. Pretreatment with XZK 1,200 mg daily for 6 weeks and then replaced by placebo (XZK discontinued group; n = 25); 2. Treatment with XZK 1,200 mg daily throughout the study (XZK continued group; n = 25); or 3. Placebo (no XZK group; n = 25). Lipid levels (total cholesterol, HDL-C, LDL-C and triglycerides) and CRP were assessed before receiving the XZK therapy, 1 day before discontinuation of XZK, and on days 1, 2, 3, 7 and 14 after discontinuation of XZK, respectively.
After 6-week XZK treatment, the fasting total cholesterol, LDL-C, triglyceride and median hs-CRP concentrations decreased, whereas HDL-C concentration increased significantly (p < 0.001, respectively). At day 14 after discontinuation of XZK therapy, total cholesterol (15%), LDL-C (17%) and triglyceride (20%) significantly increased (p < 0.001, respectively), whereas HDL-C level (15%) significantly decreased (p < 0.05). The median level of CRP increased by 11, 65, 128, 103 and 101% on the first, second, third, seventh, and fourteenth day after withdrawal of XZK therapy (p > 0.05, <0.05, <0.001, <0.001, <0.001, compared with 1 day before withdrawal of XZK therapy, respectively). There was a prominent rebound of CRP concentration 3 days after discontinuation of XZK therapy. At this time point, hs-CRP concentration was higher than in the placebo group (p < 0.05). Seven to 14 days after discontinuation of XZK therapy, the hs-CRP concentration declined to a similar level as in the placebo group. No significant correlation was seen between the changes in hs-CRP and lipid profile at all time points.
The level of hs-CRP increases on the second day after withdrawal of XZK and there is a prominent rebound 3 days after discontinuation of XZK therapy. The increase of CRP ends within 7 days, where lipids increase at 14 days after discontinuation of XZK therapy. The results may be clinically important for patients with coronary artery disease.
C反应蛋白(CRP)被认为是冠状动脉疾病的一个危险因素。他汀类药物除具有降脂特性外,还可降低CRP水平。在治疗期间突然停用他汀类药物治疗,可能会使CRP水平升高,这与血清脂质升高及动脉粥样硬化性心脏病患者心脏事件的发生率无关。血脂康(XZK)是红曲提取物,在不同研究时间进程中对脂质和CRP浓度有显著的调节作用。然而,尚未有人关注停用XZK治疗后脂质谱和CRP浓度的变化。本研究旨在探讨冠心病患者停用XZK治疗后对脂质谱和CRP浓度的短期时间进程影响。
75例确诊为冠心病的连续患者被随机分为三组:1. 每天服用1200mg XZK预处理6周,然后换用安慰剂(XZK停药组;n = 25);2. 在整个研究期间每天服用1200mg XZK(XZK持续用药组;n = 25);或3. 安慰剂(无XZK组;n = 25)。分别在接受XZK治疗前、停用XZK前1天以及停用XZK后第1、2、3、7和14天评估脂质水平(总胆固醇、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇和甘油三酯)和CRP。
经过6周的XZK治疗后,空腹总胆固醇、低密度脂蛋白胆固醇、甘油三酯和hs-CRP中位数浓度降低,而高密度脂蛋白胆固醇浓度显著升高(分别为p < 0.001)。在停用XZK治疗后第14天,总胆固醇(15%)、低密度脂蛋白胆固醇(17%)和甘油三酯(20%)显著升高(分别为p < 0.001),而高密度脂蛋白胆固醇水平(15%)显著降低(p < 0.05)。在停用XZK治疗后的第1、2、3、7和14天,CRP中位数水平分别升高了11%、65%、128%、103%和101%(与停用XZK治疗前1天相比,分别为p > 0.05、<0.05、<0.001、<0.001、<0.001)。停用XZK治疗后3天,CRP浓度出现明显反弹。此时,hs-CRP浓度高于安慰剂组(p < 0.05)。在停用XZK治疗7至14天后,hs-CRP浓度降至与安慰剂组相似的水平。在所有时间点,hs-CRP变化与脂质谱之间均未发现显著相关性。
停用XZK后第2天hs-CRP水平升高,停用XZK治疗后3天出现明显反弹。CRP的升高在7天内结束,而脂质在停用XZK治疗后14天升高。这些结果对于冠心病患者可能具有临床重要性。