Tu Kuan-Chieh, Chang Wei-Ting, Lin Hui-Wen, Lin Po-Lin, Wu Yen-Wen, Lin Chao-Feng, Yeh Hung-I, Charng Min-Ji, Huang Po-Hsun, Lin Tsung-Hsien, Lin Wei-Wen, Hsieh I-Chang, Kuo Feng-Yu, Chen Ching-Pei, Lin Sheng-Hsiang, Li Yi-Heng
Division of Cardiology, Department of Internal Medicine, Chi Mei Medical Center, Tainan, Taiwan.
Department of Cardiology, Chi Mei Medical Center, Tainan, 710, Taiwan.
Eur J Med Res. 2025 Mar 15;30(1):176. doi: 10.1186/s40001-025-02431-8.
Proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors are a standard therapy for patients who respond poorly to or cannot tolerate statins. However, identifying responders to PCSK9 inhibitors remains unclear. This study investigates the characteristics of patients who achieve target LDL-C reduction (< 70 mg/dl) after PCSK9 inhibitor therapy.
A multicenter, retrospective cohort study included patients initiating PCSK9 inhibitors at 11 teaching hospitals in Taiwan (2017-2021). Baseline characteristics, lipid-lowering therapies, and lipid profile changes were analyzed.
Among 211 patients (mean age 57.2 ± 13.1 years, 72.0% male), 73.5% used alirocumab and 26.5% used evolocumab. More than half had coronary artery disease and/or hypertension. Of these, 120 patients achieved the LDL-C target. Target achievers had a lower baseline BMI (25.8 ± 3.7 vs. 27.4 ± 4.5 kg/m, P = 0.028) and a higher incidence of myocardial infarction and anti-platelet use compared to non-achievers. Baseline cholesterol and LDL-C levels were similar, but target achievers experienced greater LDL-C reductions (- 71.5; IQR - 81.8, - 62.2 vs. - 29.4; IQR - 38, - 10.5 mg/dl, P < 0.001), as well as decreases in triglycerides and increases in HDL-C. Glucose levels and liver enzymes did not differ significantly. Logistic regression revealed BMI as the only independent predictor of LDL-C target achievement (odds ratio: 0.899, 95% CI 0.821-0.984, P = 0.021).
Lower BMI at baseline was associated with a higher likelihood of achieving LDL-C < 70 mg/dl after 12 weeks of PCSK9 inhibitor therapy. These findings support personalized strategies for optimizing cholesterol management in statin-intolerant patients while further investigations are required.
前蛋白转化酶枯草溶菌素9型(PCSK9)抑制剂是对他汀类药物反应不佳或不耐受患者的标准治疗方法。然而,确定PCSK9抑制剂的反应者仍不明确。本研究调查了接受PCSK9抑制剂治疗后实现低密度脂蛋白胆固醇(LDL-C)降低目标(<70mg/dl)的患者特征。
一项多中心回顾性队列研究纳入了台湾11家教学医院中开始使用PCSK9抑制剂的患者(2017 - 2021年)。分析了基线特征、降脂治疗方法和血脂谱变化。
在211例患者(平均年龄57.2±13.1岁,72.0%为男性)中,73.5%使用阿利西尤单抗,26.5%使用依洛尤单抗。超过一半的患者患有冠状动脉疾病和/或高血压。其中,120例患者实现了LDL-C目标。与未实现目标者相比,实现目标者的基线体重指数较低(25.8±3.7 vs. 27.4±4.5kg/m²,P = 0.028),心肌梗死发生率和使用抗血小板药物的比例更高。基线胆固醇和LDL-C水平相似,但实现目标者的LDL-C降低幅度更大(-71.5;四分位间距-81.8,-62.2 vs. -29.4;四分位间距-38,-10.5mg/dl,P < 0.001),甘油三酯降低,高密度脂蛋白胆固醇升高。血糖水平和肝酶无显著差异。逻辑回归显示体重指数是LDL-C目标实现的唯一独立预测因素(比值比:0.899,95%置信区间0.821 - 0.984,P = 0.021)。
基线体重指数较低与PCSK9抑制剂治疗12周后实现LDL-C < 70mg/dl的可能性较高相关。这些发现支持在他汀类药物不耐受患者中优化胆固醇管理的个性化策略,同时还需要进一步研究。