Kim Changsoo, Kim Min Young, Kang Dae Ryong, Kim Jang-Young, Park Jeong Bae
Department of Preventive Medicine, and ; Division of Preventive Medicine, Brigham and Women's Hospital, Boston, Mass., USA.
Department of Medicine/Cardiology, Cheil General Hospital, Kwandong University College of Medicine, Seoul, Korea.
Pulse (Basel). 2014 May;1(3-4):177-85. doi: 10.1159/000360965. Epub 2014 Apr 23.
Fimasartan, the eighth angiotensin receptor blocker, was launched in March 2011 and was found to have an excellent efficacy and safety profile in a large cross-sectional population study [Safety and Efficacy of Fimasartan in Patients with Arterial Hypertension (Safe-KanArb); Park et al.: Am J Cardiovasc Drugs 2013;13:47-56]. However, there is no long-term study to evaluate its efficacy for major adverse cardiovascular events (MACE) and other effects. The purpose of this study (K-MetS study) was to evaluate whether the early reduction of blood pressure (BP) and/or correction of metabolic derangements with fimasartan will affect MACE and the development of diabetes after long-term use in patients with hypertension. A total of 10,734 patients were screened between October 2011 and October 2012. Of these, 10,601 patients from 582 private clinics and 11 university hospitals were enrolled and are currently treated with fimasartan. The primary endpoints are MACE (cardiovascular mortality, stroke, myocardial infarction, and hospitalization for heart failure) and the development of diabetes after 3 years of follow-up. In addition to BP monitoring in the clinic, home BP monitoring is performed in about two thirds of patients. The patients were 56.2 ± 10.9 years old (mean ± SD), with 48.4% being women. The mean clinic and home systolic/diastolic BP at baseline were 145.0 ± 17.0/88.8 ± 11.4 and 138.6 ± 14.8/82.6 ± 9.9 mm Hg, respectively. The metabolic syndrome was found in 56.4%, increased abdominal circumference in 52.8%, elevated fasting glucose in 46.8%, hypertriglyceridemia in 44.7%, and low high-density lipoprotein cholesterol in 33.3% of patients. Further, complicated hypertension with diabetes occurred in 15.1%, ischemic heart disease in 3.3%, stroke in 0.9%, heart failure in 0.7%, and atrial fibrillation in 0.4% of patients. Most participants in this study had a low-to-moderate risk for hypertension. The K-MetS study is expected to provide valuable information about the effects of early BP control and correction of metabolic abnormalities on future cardiovascular outcomes relative to low-risk hypertension.
第八种血管紧张素受体阻滞剂菲马沙坦于2011年3月上市,在一项大型横断面人群研究[菲马沙坦治疗动脉高血压患者的安全性和有效性(Safe-KanArb);Park等人:《美国心血管药物杂志》2013年;13:47 - 56]中发现其具有出色的疗效和安全性。然而,尚无长期研究评估其对主要不良心血管事件(MACE)及其他影响的疗效。本研究(K-MetS研究)的目的是评估在高血压患者长期使用菲马沙坦后,早期降低血压(BP)和/或纠正代谢紊乱是否会影响MACE及糖尿病的发生。2011年10月至2012年10月期间共筛查了10734例患者。其中,来自582家私人诊所和11所大学医院的10601例患者入组,目前正在接受菲马沙坦治疗。主要终点是随访3年后的MACE(心血管死亡、中风、心肌梗死和因心力衰竭住院)及糖尿病的发生。除了在诊所进行血压监测外,约三分之二的患者还进行家庭血压监测。患者年龄为56.2±10.9岁(均值±标准差),女性占48.4%。基线时诊所和家庭收缩压/舒张压的均值分别为145.0±17.0/88.8±11.4和138.6±14.8/82.6±9.9 mmHg。56.4%的患者存在代谢综合征,52.8%的患者腹围增加,46.8%的患者空腹血糖升高,44.7%的患者甘油三酯升高,33.3%的患者高密度脂蛋白胆固醇降低。此外,15.1%的患者患有合并糖尿病的高血压,3.3%的患者患有缺血性心脏病,0.9%的患者患有中风,0.7%的患者患有心力衰竭,0.4%的患者患有心房颤动。本研究中的大多数参与者高血压风险为低至中度。K-MetS研究有望提供有关早期血压控制和代谢异常纠正对低风险高血压患者未来心血管结局影响的有价值信息。