Zeyu Xu, Yi Fang, Yong Peng, Chunhua Zhang, Chunhua Zheng
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引用次数: 0
摘要
虽然PCSK9抑制已被证明是安全有效的,但使用血管内超声(IVUS)评估阿托伐他汀联合PCSK9抑制剂对临界冠状动脉病变的影响的研究有限。方法对2022年6月~ 2025年6月69例经不同治疗的边缘性冠状动脉病变患者进行生化指标、冠状动脉造影(CAG)、静脉造影(IVUS)等详细分析。结果在69例入组患者中,60例完成了为期48周的研究。所有组均显示低密度脂蛋白胆固醇(LDL-C)显著降低,其中C组(Alirocumab +阿托伐他汀)从3.64降至1.48,降幅最大(P P = 0.038)。与a组和B组相比,C组的斑块体积也有更大的减少(P = 0.041)。结论阿利rocumab和阿托伐他汀联合治疗可显著降低LDL-C水平,改善血管环境,显著逆转边缘性冠状动脉病变患者的斑块。
Clinical Efficacy of Atorvastatin and PCSK9 Inhibitors in Patients With Borderline Coronary Lesions: An Intravascular Ultrasound Assessment.
BackgroundWhile PCSK9 inhibition has proven safe and effective, there is limited research on using intravascular ultrasound (IVUS) to assess the impact of atorvastatin combined with PCSK9 inhibitors on borderline coronary lesions.MethodsFrom June 2022 to June 2025, a detailed analysis of biochemical markers, coronary angiography (CAG), and IVUS was conducted on 69 patients with borderline coronary lesions after different treatments.ResultsOf the 69 patients enrolled, 60 completed the 48-week study. All groups showed significant low-density lipoprotein cholesterol (LDL-C) reductions, with Group C (Alirocumab + Atorvastatin) having the largest decrease from 3.64 to 1.48 (P < .001). At 48 weeks, arterial lumen volumes increased in all groups, but Group C's was significantly larger than Groups A (Alirocumab + placebo) and B (Atorvastatin + placebo) (P = .038). Group C also had a greater reduction in plaque volume compared to Groups A and B (P = .041).ConclusionAlirocumab and Atorvastatin together significantly lowered LDL-C levels and improved the vascular environment, notably reversing plaque in patients with borderline coronary lesions.
期刊介绍:
Journal of Cardiovascular Pharmacology and Therapeutics (JCPT) is a peer-reviewed journal that publishes original basic human studies, animal studies, and bench research with potential clinical application to cardiovascular pharmacology and therapeutics. Experimental studies focus on translational research. This journal is a member of the Committee on Publication Ethics (COPE).