Sugihara Makoto, Miura Shin-Ichiro, Takamiya Yosuke, Kiya Yoshihiro, Arimura Tadaaki, Iwata Atsushi, Kawamura Akira, Nishikawa Hiroaki, Uehara Yoshinari, Saku Keijiro
Department of Cardiology, Fukuoka University School of Medicine, Fukuoka, Japan.
Hypertens Res. 2009 Jul;32(7):625-30. doi: 10.1038/hr.2009.66. Epub 2009 May 22.
This study was performed to evaluate the safety and efficacy of additional antihypertensive therapy with angiotensin II type 1 receptor blocker (ARB; olmesartan or valsartan) after successful stent implantation in patients with coronary artery disease (CAD). Fifty patients with CAD after successful stent implantation were included in this study. They were divided into an ARB group, which initially received olmesartan (n=20, 14+/-8 mg day(-1)) or valsartan (n=20, 60+/-23 mg day(-1)) immediately after stent implantation, and a non-ARB group (n=10) according to their blood pressure (BP). Follow-up coronary angiography, measurement of BP and blood sampling were performed before (at baseline) and 6-8 months after stent implantation (at follow-up). There were no significant differences in the baseline characteristics between the groups, except for BP. Although there were no changes in % diameter restenosis between the groups, the BP level in the ARB group at follow-up showed a significant reduction (125+/-12/69+/-9 mm Hg) and reached the target BP. There were no critical adverse effects in the ARB group throughout the study period. In addition, serum high-sensitive C-reactive protein (hs-CRP) and pentraxin 3 were significantly decreased in the ARB group but not in the non-ARB group. Although olmesartan and valsartan induced similar BP-lowering effects, olmesartan but not valsartan induced a significant decrease in hs-CRP, but did not increase serum uric acid. In conclusion, antihypertensive therapy with add-on low-dose ARB after stent implantation was safe and achieved the target BP. In particular, olmesartan had an anti-inflammatory effect.
本研究旨在评估在冠状动脉疾病(CAD)患者成功植入支架后,加用1型血管紧张素II受体阻滞剂(ARB;奥美沙坦或缬沙坦)进行降压治疗的安全性和有效性。本研究纳入了50例成功植入支架后的CAD患者。根据血压情况,将他们分为ARB组(n = 20)和非ARB组(n = 10),其中ARB组在支架植入后立即开始接受奥美沙坦(n = 20,14±8 mg/天)或缬沙坦(n = 20,60±23 mg/天)治疗。在支架植入前(基线时)和植入后6 - 8个月(随访时)进行随访冠状动脉造影、血压测量和血液采样。除血压外,两组间基线特征无显著差异。尽管两组间直径狭窄百分比无变化,但ARB组随访时血压水平显著降低(125±12/69±9 mmHg)并达到目标血压。在整个研究期间,ARB组未出现严重不良反应。此外,ARB组血清高敏C反应蛋白(hs-CRP)和五聚素3显著降低,而非ARB组未降低。尽管奥美沙坦和缬沙坦的降压效果相似,但奥美沙坦可显著降低hs-CRP,且不增加血清尿酸,而缬沙坦无此作用。总之,支架植入后加用小剂量ARB进行降压治疗是安全的,并达到了目标血压。特别是,奥美沙坦具有抗炎作用。