Yeh Yen-Ting, Yin Wei-Hsian, Tseng Wei-Kung, Lin Fang-Ju, Yeh Hung-I, Chen Jaw-Wen, Wu Yen-Wen, Wu Chau-Chung
Cardiology Division, Cardiovascular Medical Center, Far Eastern Memorial Hospital, New Taipei City, Taiwan.
National Yang-Ming University School of Medicine, Taipei, Taiwan.
PLoS One. 2017 Oct 26;12(10):e0186861. doi: 10.1371/journal.pone.0186861. eCollection 2017.
Whether a low-density lipoprotein cholesterol (LDL-C) goal is essential in secondary prevention is still being debated. The aim of our study was to investigate whether achieving particular LDL-C level goals is associated with the reduction in the risk of major adverse cardiac events (MACEs) in patients with atherosclerotic cardiovascular diseases (ASCVD) on statin therapy.
From January 2010 to August 2014, a total of 4099 patients with ASCVD in the Taiwan Secondary Prevention for patients with AtheRosCLErotic disease (T-SPARCLE) registry were analyzed. The risk of a MACE was lower in patients with LDL-C level under control at < 100 mg/dL by statins than in patients with LDL-C level ≥100 mg/dL whether on statin therapy (hazard ratio [HR] 1.66, 95% confidence interval [CI] 1.04‒2.63, p = 0.03) or not (HR 2.04, 95% CI 1.06‒3.94, p = 0.03). In multivariate Cox model analyses, statin intensity had no significant predictive value, and LDL-C ≥ 100 mg/dL was associated with a slight but not significant trend toward increased risk of MACEs (HR 1.41, 95% CI 0.96‒2.07, p = 0.08).
For patients with ASCVD on statin therapy guided by a target-driven strategy, failure to control LDL-C levels to < 100 mg/dL was associated with higher risk of MACEs. Statin intensity alone had no significant impact on the risk of MACEs after multivariate adjustment.
低密度脂蛋白胆固醇(LDL-C)目标在二级预防中是否至关重要仍存在争议。我们研究的目的是调查在接受他汀类药物治疗的动脉粥样硬化性心血管疾病(ASCVD)患者中,实现特定的LDL-C水平目标是否与主要不良心脏事件(MACE)风险的降低相关。
对2010年1月至2014年8月期间台湾动脉粥样硬化疾病患者二级预防(T-SPARCLE)登记处的4099例ASCVD患者进行分析。无论是否接受他汀类药物治疗,他汀类药物将LDL-C水平控制在<100mg/dL的患者发生MACE的风险低于LDL-C水平≥100mg/dL的患者(风险比[HR]1.66,95%置信区间[CI]1.04‒2.63,p = 0.03)或未接受他汀类药物治疗的患者(HR 2.04,95%CI 1.06‒3.94,p = 0.03)。在多变量Cox模型分析中,他汀类药物强度没有显著的预测价值,LDL-C≥100mg/dL与MACE风险增加的轻微但不显著趋势相关(HR 1.41,95%CI 0.96‒2.07,p = 0.08)。
对于采用目标驱动策略接受他汀类药物治疗的ASCVD患者,未能将LDL-C水平控制在<100mg/dL与更高的MACE风险相关。多变量调整后,单独的他汀类药物强度对MACE风险没有显著影响。