Takamiya Yosuke, Miura Shin-Ichiro, Kawamura Akira, Tanigawa Hiroyuki, Zhang Bo, Iwata Atsushi, Nishikawa Hiroaki, Matsuo Kunihiro, Shirai Kazuyuki, Saku Keijiro
Department of Cardiology, Fukuoka University School of Medicine, Fukuoka, Japan.
Coron Artery Dis. 2009 Jun;20(4):288-94. doi: 10.1097/MCA.0b013e32832c4538.
This prospective study was carried out to evaluate the benefits of intensive lowering of low-density lipoprotein cholesterol (LDL-C) with statin and intensive blood pressure (BP)-lowering therapy as aggressive medical interventions after stent implantation.
Fifty-four patients with coronary artery disease initially received statin immediately after successful stent implantation. They were divided into intensive therapy (IT group, n = 27; therapeutic target levels of LDL-C and BP were 60 mg/dl and <120/80 mmHg at follow-up coronary angiography, respectively, 6-8 months after stent implantation) and conventional therapy groups (CT group, n = 27; target levels of LDL-C and BP were 100 mg/dl and <130/85 mmHg, respectively). Additional antihypertensive therapy with angiotensin II type 1 receptor blockers was begun according to the BP levels.
There were significant differences in the levels of LDL-C at follow-up between the IT and CT groups [average, 68+/-10 (cut-off value,>or=83.4) mg/dl and 102+/-14 (<83.4) mg/dl, respectively]. Percentage diameter stenosis (P = 0.039) and diastolic BP (P = 0.005) in the IT group were significantly decreased compared with those in the CT group at follow-up. In addition, percentage diameter stenosis was most significantly related to the level of LDL-C (P = 0.03) among other metabolic factors (BP, body mass index, triglyceride, high-density lipoprotein cholesterol, hemoglobin A1c, and adiponectin) at follow-up as assessed by a stepwise multivariable regression analysis.
These results suggest that intensive lowering of LDL-C by statin decreased the neointimal formation after stent implantation, and an LDL-C level of at least 83.4 mg/dl was the most acceptable clinical therapeutic target at follow-up.
本前瞻性研究旨在评估他汀类药物强化降低低密度脂蛋白胆固醇(LDL-C)及强化降压治疗作为支架植入术后积极药物干预措施的益处。
54例冠心病患者在成功植入支架后立即开始接受他汀类药物治疗。他们被分为强化治疗组(IT组,n = 27;在支架植入后6 - 8个月的随访冠状动脉造影中,LDL-C和血压的治疗目标水平分别为60 mg/dl和<120/80 mmHg)和常规治疗组(CT组,n = 27;LDL-C和血压的目标水平分别为100 mg/dl和<130/85 mmHg)。根据血压水平开始使用1型血管紧张素II受体阻滞剂进行额外的降压治疗。
IT组和CT组随访时LDL-C水平存在显著差异[平均值分别为68±10(临界值,≥83.4)mg/dl和102±14(<83.4)mg/dl]。随访时,IT组的直径狭窄百分比(P = 0.039)和舒张压(P = 0.005)与CT组相比显著降低。此外,通过逐步多变量回归分析评估,在随访时的其他代谢因素(血压、体重指数、甘油三酯、高密度脂蛋白胆固醇、糖化血红蛋白和脂联素)中,直径狭窄百分比与LDL-C水平的相关性最为显著(P = 0.03)。
这些结果表明,他汀类药物强化降低LDL-C可减少支架植入术后的新生内膜形成,随访时LDL-C水平至少83.4 mg/dl是最可接受的临床治疗目标。